Name: in situ neutron powder diffraction using custom-made lithium-ion batteries
Uploaded: 2014-11-10T15:00:00.000+00:00
Duration: 11 min 25 s
Description: Watch this Scientific Journal Video about In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries at JoVE.com

We thank AINSE Ltd for providing support through the research fellowship and postgraduate award scheme.

1. Cell Components Required Prior to Construction
NOTE: A vanadium can is conventionally used for NPD experiments and it is a wholly-vanadium tube that is sealed at one end and open at the other. There is virtually no signal in NPD data from vanadium.
<ol>
	<li>Cut a piece of lithium metal-foil to dimensions matching the volume of the vanadium can. For example, cut a piece approximately 120 x 35 mm for a 9&#160;mm diameter vanadium can. In addition, use thinner lithium foil to minimize neutron absorption, noting that thicknesses below 125 &#181;m may be difficult to handle without tearing.</li>
	<li>Pre-select the type of separator to be used. Cut a sheet of separator such that the dimensions are slightly larger than the electrodes, e.g. 140 x 40 mm. 
	NOTE: While porous polyvinyl-difluoride (PVDF) membrane readily soaks up electrolyte, it is expensive and can be easily damaged and torn if not handled carefully during construction. Alternatively, commercially available polyethylene-based sheets are more robust, however they do not soak up electrolyte as readily and generally reduce the signal-to-noise due to the larger hydrogen content.</li>
	<li>Make the positive electrode by following the guidelines set out by Marks et al.31 Namely, combine PVDF, carbon black, and the active material at a selected ratio. Typically, use a ratio of 10:10:80 of PVDF:carbon:active material, but adjust this depending on the material under investigation. Grind the mixture and add n-methyl pyrrolidone (NMP) dropwise until a slurry forms, then stir overnight.</li>
	<li>Spread the mixture onto aluminum foil (20 &#181;m thickness) using the doctor blade technique.
	<ol>
		<li>Adhere the current collector sheet of dimensions 200 x 70 mm to a smooth surface (e.g. glass) by applying a few drops of ethanol on to the surface and placing the current collector on the surface. Alternatively, use an instrument which can pull a slight vacuum on the current collector from the smooth surface. Smooth out the current collector to ensure that there are no crinkles or creases prior to applying the slurry.</li>
		<li>Place a tooth or wide semi-circle shaped puddle of the slurry on one end of the current collector. Using a notch bar, roller or specially designed coater (a notch bar with a pre-defined height above the current collector, e.g. 100 or 200 &#181;m is typically used) spread the slurry over the current collector by sliding the chosen device across the current collector and slurry, resulting in the spreading of the slurry onto the current collector surface.</li>
		<li>Gently remove the current collector from the smooth surface and place the current collector and spread slurry into a vacuum oven for drying. 
		NOTE: The spreading technique is described in greater detail in Marks et al.31</li>
	</ol>
	</li>
	<li>Cut the positive electrode prepared in step 1.3 such that the dimensions match the lithium foil. Ensure that there is a &#8220;tab&#8221; of uncoated metal current collector approximately 0.5 cm in length at one end. To improve battery performance, press the dried positive electrode film into the current collector using a flat plate press. 
	NOTE: Figure 1 shows the relative sizes of the separator and positive electrode components. Minimum active material quantity in the electrode is 300 mg, however, the larger the quantity (relative to other battery components), the better the NPD signal. A larger signal may allow more detailed information to be extracted from the NPD data and better temporal resolution.</li>
	<li>Pre-prepare 1 M lithium hexafluorophosphate in a 1/1 vol% mixture of deuterated ethylene carbonate and deuterated dimethyl carbonate. Ensure that all the LiPF6 is dissolved and the electrolyte is thoroughly mixed prior to use.</li>
	<li>Cut a piece of current collector of the same dimensions as the positive electrode in step 1.5 and weigh the current collector and positive electrode. Subtract these masses to obtain the mass of the electrode mixture. Multiply the mass of the electrode mixture by 0.8 to give the mass of the active material.</li>
</ol>
2. Cell Construction
<ol>
	<li>Prior to assembling the cell inside an argon filled glovebox, lay down either a plastic tray or some other non-metallic covering on the base of the gloxebox.</li>
	<li>Stack the individual components in the following order: A long strip of separator, positive electrode with the slurry facing up and aluminum rod (or copper wire) wound in the &#8220;tab&#8221; at one end, the second strip of separator, and finally the lithium metal with copper wire wound on the end of the lithium metal (the same end as the aluminum rod).</li>
	<li>Start rolling the layers from the end with the aluminum rod and copper wire, ensuring that the two electrodes do not come into contact.</li>
	<li>If a polyethylene-based sheet was selected as the separator, occasionally add several drops of electrolyte to the separator between the lithium metal and positive electrode along the entire length of the stack. Alternatively, add the drops gradually during the rolling process. If PVDF membrane was used as the separator this step is not necessary.</li>
	<li>Take care to ensure that the electrode is rolled tightly and that the layers remain aligned. 
	NOTE: If the layers become misaligned the rolling process may need to be restarted, however, caution must be taken as the electrolyte solution is highly volatile and more may need to be added.</li>
	<li>Ensure that the longer piece of separator completely wraps around the stack or roll such that the electrodes are not exposed (i.e. the electrodes don&#8217;t touch the vanadium housing).</li>
	<li>Insert the rolled stack into the vanadium can such that the copper wire and aluminum rod protrude 2-3 cm beyond the top of the vanadium can. Add the remaining electrolyte dropwise into the top of the vanadium can, use 1.5 ml in total.</li>
	<li>Add a rubber stopper with notches cut in the sides for the aluminum rod and copper wire into the top of the vanadium can. Seal the can by melting dental wax over the top of the can and around the end of the plastic sheath of the copper wire. Check that the final cell appears as shown in Figure 2.</li>
	<li>Allow the cell to &#8220;age&#8221; or &#8220;wet&#8221; horizontally for 12-24 hr. Prior to use, test the open-circuit potential by connecting the aluminum rod and the copper wire to the terminals of a multi-meter and measuring the potential of the constructed cell. Also ensure that there are no leaks by visual inspection.</li>
</ol>

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The authors have nothing to disclose.

When designing and performing an in situ experiment, either with the &#8220;roll-over&#8221; neutron diffraction cell or another design, there are a number of aspects that must be carefully controlled to ensure a successful experiment. These include careful choice of the type and quantity of cell components, ensuring that the prepared electrode and final constructed cell are of high quality, choosing appropriate diffraction conditions, planning the electrochemical cycling steps to be performed in advance, and finally understanding what the resulting data can and cannot tell one about the material being investigated.
The choice of cell components is vital to ensuring that the resulting diffraction pattern is able to be accurately modeled. In particular, minimizing the number of different phases present will reduce the complexity of the multiphase model. For instance, in the example here the binder used in the positive electrode mixture was PVDF and the separator was polyethylene. However, if the separator used was a PVDF membrane, the total number of components in the cell could have been reduced, simplifying analysis. Additionally, PVDF would decrease the total quantity of hydrogen in the cell, reducing the background contribution. Reducing the quantity of hydrogen containing materials in the cell is the reason why highly expensive deuterated electrolytes are employed for in situ NPD. Another alternative would be to replace both the binder in the positive electrode mixture and the separator with hydrogen-free materials (e.g. polytetrafluoroethylene). However, depending on the separator material, a larger volume of electrolyte may be required, rapidly increasing the cost of the cell. For example, glass fiber separator, which is hydrogen free, requires far more electrolyte than thin PVDF membranes or polyethylene-based sheets because of its comparatively larger volume. Glass fiber separators are also very difficult to roll.
The ability to prepare a high-quality electrode is essential to ensure that a large quantity of active material is in the beam, allowing fast cycling to be performed and ensuring that the electrode mixture does not detach from the current collector during the rolling process. In the first stage of preparing an electrode film, the positive electrode mixture is added to NMP to form a slurry. The consistency of this slurry is controlled through the mass ratio of NMP to electrode mixture. Obtaining a slurry of the appropriate consistency is essential for preparing a high quality electrode film, especially films that are both stable and large enough for in situ NPD. However, achieving the correct consistency may require a lot of testing as the quantity of NMP required is dependent on the morphology and particle size of the active electrode material. Fortunately, this step can be simplified greatly by ball-milling the NMP-electrode slurry. In this case the ratio of NMP to electrode powder mixture becomes less vital and a high-quality film can be readily prepared as long as the ball-milled slurry is spread into a film immediately. The reader is encouraged to also view the previously-reported recommended procedures for preparing a high-quality film.31 In this report the importance of pressing the electrodes prior to use is emphasized. In the case of the longer electrodes required for in situ NPD, applying homogeneous pressure to the entire electrode is best achieved using a rolling press. However, if a rolling press is not available, a flat-plate press can be used. Finally, the &#8220;roll-over&#8221; in situ cell design is compatible with a double-sided positive electrode without any additional changes made during construction. Using a double-sided electrode effectively doubles the quantity of the active material relative to the other battery components, leading to a higher quality diffraction pattern.
A common difficulty encountered is obtaining good pressure applied to the entire battery roll in the constructed cell. This can result in poor or inhomogeneous ionic diffusion through the cell, as shown for the Li0.18Sr0.66Ti0.5Nb0.5O3 results above, or a cell that does not function. Obtaining good pressure across to the stack is particularly difficult when winding the cell by hand. The process involves manual dexterity inside a glovebox and may not lead to consistent results. These difficulties can be overcome by using an automatic cell winding machine, although the amount of sample required may increase. Finally, the total mass of all cell components in the cell must be recorded in order to calculate the total neutron absorption. Without an appropriate absorption correction structural parameters, such as the atomic displacement parameters (ADPs), may refine to unrealistic values. In general it is good practice to measure and apply an appropriate absorption correction for NPD experiments.
Prior to beginning the in situ NPD experiment several experimental conditions must be considered and set. For example, the resulting angular resolution must be appropriate for the material investigated. If an electrode crystal structure adopts a low-symmetry space group reflections may not be resolved due to overlap with reflections from the same phase or the other phases present in the cell. To resolve certain reflections the wavelength of neutrons impinging on the sample may need to be adjusted, e.g. longer wavelengths can separate reflections in 2. Unfortunately, this reduces the Q-space range probed. This was potentially an issue for the Li0.18Sr0.66Ti0.5Nb0.5O3 results reported above. In this case reflections from planes with smaller d-spacings were previously determined to provide information of lithium ordering, and thus a shorter wavelength was selected. However, this also made it difficult to resolve the peak splitting due to the appearance of the second phase.
In addition to choosing the appropriate set of experimental parameters for the neutron diffractometer, the electrochemical cycling conditions should be pre-determined and not changed dramatically during the experiment. During cell cycling it is likely that the material exists in a metastable state which can subsequently relax once the cell is disconnected. If this is a particular property of the material which is being investigated then there should not be any issues, however, if the aim of the experiment is to investigate the rate of change of some structural parameter during charge or discharge then interruptions and the subsequent structural relaxation may influence the outcome. In addition, avoiding interruptions also simplifies the resulting sequential refinement by avoiding the need to restart the refinement at every break. It is also recommended that if the experimenter aims to determine the lithium position and occupancy at various stages of discharge then longer data collections at the end of each charge and discharge cycle is advised with an appropriate equilibration electrochemical step. The longer data collections may ensure that there is sufficient signal-to-noise to improve the chances of observing and modeling the lithium in addition to serving as a benchmark for how the lithium changes during cycling.
Once the data have been collected then there are a number of analysis methods which can be employed depending on the desired outcome of the experiment. Usually, the best form of analysis is Rietveld refinement with few constraints, although this is more difficult to perform than either a refinement with several constraints (such as fixed atomic co-ordinates, occupancies, or ADPs) or modeling the changes of a single reflection. Occasionally the information obtained from a more simple analysis is all that is desired from an in situ experiment, and so performing a more complex unconstrained Rietveld refinement is unnecessary.
To best judge what may be able to be accurately modeled during a sequential Rietveld refinement an initial refinement using a single dataset collected for a long period prior to discharge is often necessary. As was the case for Li0.18Sr0.66Ti0.5Nb0.5O3, if certain parameters are unable to be accurately determined in the initial refinement, it is unlikely that they will be accurately determined during the sequential refinement. However, being able to perform a successful sequential Rietveld refinement is one of the most desirable outcomes of an in situ NPD experiment. As the model is refined against every point within the diffraction pattern, highly accurate information of the change in the average structure for all phases during electrochemical cycling can be extracted and directly correlated to the potential profile. In addition, if rapid data collection was performed the rate of structural change during battery cycling can be investigated and the kinetics of lithium insertion determined. Obtaining a stable refinement with few constraints, such as fixing atomic co-ordinates, occupancies, and ADPs, requires high-quality data with good signal-to-noise, high angular-resolution, and access to a large d-space range. The specific data quality required depends in part on the material being investigated. For example, a more complex structure will need higher signal-to-noise to see weaker reflections and higher resolution in order to observe peak splitting. Thus, occasionally constraints may be necessary, as was the case for Li0.18Sr0.66Ti0.5Nb0.5O3, where certain parameters are held constant during a refinement. In addition, caution must always be taken to ensure that the resulting model is chemically reasonable. This can be performed by checking the visual fit of the model to the data to ensure that there are no systematic differences, checking that the refined parameters are physically reasonable, as well as monitoring the statistical measures of the quality of fit (such as RB or &#967;2). The observation of reproducible trends in the parameters between several electrochemical cycles can add more weight to a particular observation.
In addition to performing a Rietveld refinement using the data, changes occurring to characteristic reflections during battery cycling can be modeled.8,18,19 This is particularly useful if it is known in advance which reflections are influenced by either lithium ordering or a change in the host structure. The changes to these characteristic reflections can then be correlated to changes in the electrochemical potential-profile to build an understanding of structure-property relationships. The change in position or integrated intensity of a specific reflection can be modeled using programs such as LAMP33 or Origin. Finally, the appearance of characteristic reflections indicating the formation of new phases can be followed during electrochemical cycling.8,16,35,36 Similar to other changes observed in situ, their appearance and identity can be linked to the observed electrochemical properties. The reader is encouraged to view and read the article about in situ X-ray based studies by see Doeff et al.37
No matter what form of analysis is performed, if data were collected continuously during electrochemical cycling, information unique to in situ diffraction will be obtained. In particular, information regarding the formation of metastable phases and non-equilibrium processes from the whole cell can be extracted.11,28,29 Results for example cathode materials studied as a function of charge/discharge using in situ NPD cells are shown in Figure 5. Figure 5A shows a selected region of the in situ NPD patterns, voltage profiles, weight fractions, and lattice parameters of the active cathode material, LiFePO4 and FePO4.25 While Figure 5B shows a typical multiphase refinement using structural models of the components and an in situ NPD dataset.26
In situ NPD is a tool that is sensitive to lithium, the charge carrier in lithium-ion batteries. Thus, there is lithium-sensitive insight gained into the function of electrodes during battery operation. Charging processes can be related to how the electrode crystal-structure expands/contracts/forms new phases and to how lithium inserts/extracts from these electrodes. In situ NPD can uncover how lithium is inserted/extracted into electrodes, via one, two, or more crystallographic sites, and this directly influences the ease of charging/discharging a whole battery. By determining how and where lithium is inserted/extracted we can design new materials that can take advantage of this knowledge. For example, materials with larger voids for lithium to reside in can be designed such that more lithium can be inserted, leading to higher capacity batteries. In addition, knowledge of the crystallographic sites that lithium occupies during insertion/extraction can be used to direct the development of materials with larger &#8216;tunnels&#8217; for lithium, again potentially allowing more lithium to be reversibly inserted/extracted, especially at higher rates of discharge/charge. Although, these examples are based on insertion electrodes, in situ NPD may in the future provide valuable information for electrodes that undergo conversion reactions. Therefore, in situ NPD provides crucial information on electrode function that can be used to design the next generation of electrodes.
Future in situ NPD studies will tackle more complex systems, exhibiting lower symmetry space-groups and/or more complex lithium distributions. Additionally, these studies can be used to develop new materials for alternative applications &#8212; why use an electrode for a battery? We can use an electrode as a starting material, insert/extract a known amount of lithium (with information provided by in situ NPD), extract the electrode and use it for another application, e.g. taking advantage of another physical property. Further, electrochemical cells can be developed that allow in situ NPD to probe structural information on the processes occurring in speciation cells, lithium-air batteries, and fuel cells. Performing reactions in situ allows us to study functioning materials, and this is underpinned by having appropriate cells that merge the requirements of electrochemistry and structural characterization.

Rechargeable lithium-ion batteries provide portable energy for modern electronics and are important in high-energy applications such as electric vehicles and as energy storage devices for large-scale renewable energy generation.3-7 A number of challenges remain to achieve widespread use of rechargeable batteries in vehicular and large-scale storage, including energy densities and safety. The use of in situ methods to probe atomic and molecular-scale battery function during operation are becoming increasingly common as the information gained in such experiments can direct methods to improve existing battery materials, e.g. by identifying possible failure mechanisms,8-10 and by revealing crystal structures that could be considered for the next generation of materials.11
A primary goal of in situ NPD is to probe the crystal structure evolution of the components inside a battery as a function of charge/discharge. In order to measure the crystal structure evolution the components must be crystalline, which focuses such studies on crystallographically-ordered electrodes. It is at the electrodes that the charge carrier (lithium) is inserted/extracted and such changes are followed by NPD. In situ NPD offers the possibility to &#8220;track&#8221; not only the reaction mechanism and lattice parameter evolution of the electrodes, but also the insertion/extraction of lithium from the electrodes. Essentially the charge carrier in lithium-ion batteries can be followed. This gives a lithium-centered view of the battery function and has been recently demonstrated in only a few studies.11-13
NPD is an ideal technique to examine lithium-containing materials and lithium-ion batteries. This is because NPD relies on the interaction between a neutron beam and the sample. Unlike X-ray powder diffraction (XRD), where the interaction of the X-ray radiation is predominantly with the electrons of the sample and thus varies linearly with atomic number, in NPD the interaction is mediated by neutron-nuclei interactions that result in a more complex and apparently random variation with atomic number. Thus, in situ NPD is particularly promising for the study of lithium-ion battery materials due to factors such as the sensitivity of NPD towards lithium atoms in the presence of heavier elements, the non-destructive interaction of neutrons with the battery, and the high penetration depth of neutrons enabling the examination of the bulk crystal-structure of the battery components within whole batteries of the size used in commercial devices. Therefore, in situ NPD is particularly useful for the study of lithium-ion batteries as a result of these advantages. Despite this, the uptake of in situ NPD experiments by the battery-research community has been limited, accounting for only 25 publications since the first report of using in situ NPD for battery research in 1998.14 The limited uptake is due to some major experimental hurdles, such as the need to account for the large incoherent neutron-scattering cross section of hydrogen in the electrolyte solutions and separator in the battery, which is detrimental to the NPD signal. This is often overcome by substituting with deuterated (2H) electrolyte solutions and replacing the separator with alternate hydrogen-free or poor materials.15 Another hurdle is the need to have sufficient sample in the neutron beam, a requirement that often necessitates the use of thicker electrodes which in turn limits the maximum charging/discharging rate that can be applied to the battery. A more practical concern is the relatively small number of world-wide neutron diffractometers relative to X-ray diffractometers, and their capabilities &#8212; e.g. time and angular resolution. As new neutron diffractometers have come online and the abovementioned hurdles overcome, in situ NPD experiments have grown in number.
There are two options to conduct in situ NPD experiments, using either commercial or custom-built cells. Commercial cells have been demonstrated to reveal structural information, including the evolution of lithium content and distribution in electrodes.8-11,16-20 However, using commercial cells limits the number of electrodes that can be studied to those already commercially available, and where manufacturers or select research facilities are engaged to produce commercial-type cells with as yet un-commercialized materials. The production of the commercial-type cells is dependent on the availability of sufficient quantities of electrode material for cell manufacture, typically of the order of kilograms and significantly higher than that used in battery research, which can be a barrier to cell production. Commercial cells typically feature two electrodes that evolve during charge/discharge and the evolution of both electrodes will be captured in the resulting diffraction patterns. This is because the neutron beam is highly penetrating and can penetrate the single lithium-ion cells (e.g., the entire volume of 18,650 cells). The evolution of the two electrodes can make the data analysis complicated, but if sufficient Bragg reflections of both electrodes are observed these can be modeled using whole powder-pattern methods. Nonetheless, custom-made half cells can be constructed in which one electrode is lithium and should not structurally change during charge/discharge and therefore act as an (or another) internal standard. This leaves only one electrode that should exhibit structural change, simplifying data analysis. Care must also be taken to ensure that all electrode reflections of interest are not overlapping with reflections from other components undergoing structural change in the cell. The advantage of a custom-made cell is that components can be swapped to alter reflection positions in diffraction patterns. Furthermore, custom-made cells allow researchers the option to, in principle, improve signal-to-noise ratios and to investigate materials that are made in smaller-scale research batches and thereby permitting the in situ NPD study of a larger variety of materials.
To date there have been six electrochemical cell designs for in situ NPD studies reported, including three cylindrical designs,14,15,21,22 two coin-type cell designs23-26 and a pouch cell design.12,27 The first cylindrical cell design was limited in use to very low charging/discharging rates due to the large quantities of electrode materials used.14,21 The roll-over design,15 detailed below, and modified version of the original cylindrical cell,22 have overcome many of the problems associated with the first cylindrical design, and can be used for reliably correlating the structure of electrode materials with their electrochemistry. Coin-cell designs for in situ NPD also allow similar quantities of electrode materials to be probed relative to the roll-over cell, while featuring subtle differences in terms of construction, applicable charging rates, and cost.15 In particular, the coin-cell type was recently reported to have been constructed using a Ti-Zn alloy as the casing material (null-matrix) which produces no signal in the NPD patterns.26 This is similar to the use of vanadium cans in the roll-over design described below. A key factor that can influence applicable charge/discharge rates (and polarization) is electrode thickness, where typically thicker electrodes require the application of lower current. The cell designs that are now becoming more popular are the pouch cells with sheets of multiple individual cells connected in parallel, or sheets that are rolled in a similar manner to the construction of lithium-ion batteries found in mobile electronics.12,27 This cell is rectangular (a pouch) that can function at higher charge/discharge rates than the roll-over or coin-type cells. In this work, we focus on the &#8216;roll-over&#8217; cell design, illustrating the cell construction, use, and some results using the cell.
The electrode preparation for the roll-over design batteries is practically similar to the electrode preparation for use in conventional coin-cell batteries. The electrode can be cast onto the current collector by doctor blading, with the biggest difference being that the electrode needs to span dimensions larger than 35 x 120-150 mm. This can be hard to uniformly coat with every electrode material. Layers of the electrode on current collector, separator, and lithium metal-foil on current collector are arranged, rolled, and inserted into vanadium cans. The electrolyte used is LiPF6, one of the most commonly used salts in lithium-ion batteries with deuterated ethylene carbonate and deuterated dimethyl carbonate. This cell has been used successfully in four reported studies and will be described in greater detail below.15,28-30

<table><tbody><tr><td colspan="4">&lt;strong&gt;Slurry Preparation&lt;/strong&gt;</td></tr><tr><td>PVDF</td><td>MTI Corporation</td><td>EQ-Lib-PVDF</td><td>http://www.mtixtl.com/PVDFbinderforLi-ionbatteryelectrodes80g/bag-EQ-Lib-PVDF.aspx</td></tr><tr><td>Active Electrode Material</td><td>Researcher makes*</td><td></td><td>This is dependent on the electrode under investigation, typically made in-house by the researcher and varies every time</td></tr><tr><td>Carbon black</td><td>MTI Corporation</td><td>EQ-Lib-SuperC65</td><td>http://www.mtixtl.com/TimicalSUPERC65forLithium-IonBatteries80g/bag-EQ-Lib-SuperC65.aspx</td></tr><tr><td>NMP</td><td>MTI Corporation</td><td>EQ-Lib-NMP</td><td>http://www.mtixtl.com/N-Methyl-2-pyrrolidoneNMPsolventforPVDF&lt;br/&gt; 250g/bottleLib-NMP.aspx</td></tr><tr><td>Magnetic stirrer</td><td>IKA</td><td>C-MAG HS 7 IKAMAG</td><td>http://www.ika.in/owa/ika/catalog.product_detail?iProduct=3581200</td></tr><tr><td colspan="4">&lt;strong&gt;Electrode Fabrication&lt;/strong&gt;</td></tr><tr><td>Doctor blade (notch bar)</td><td>DPM Solutions Inc.</td><td>100, 200, 300 &amp;amp; 400 micron&amp;nbsp; 4-Sided Notch Bar</td><td></td></tr><tr><td>Al or Cu current collectors</td><td>MTI Corporation</td><td>EQ-bcaf-15u-280</td><td>http://www.mtixtl.com/AluminumFoilforBatteryCathodeSub&lt;br/&gt; strate-EQ-bcaf-15u-280.aspx</td></tr><tr><td>Vacuum Oven</td><td>Binder</td><td>&lt;em&gt;e.g.&lt;/em&gt; VD 53</td><td>http://www.binder-world.com/en/vacuum-drying-oven/vd-series/vd-53/</td></tr><tr><td>Flat-plate press</td><td>MTI Corporation</td><td>EQ-HP-88V-LD</td><td>http://www.mtixtl.com/25THydraulicFlat&lt;br/&gt; HotPress-EQ-HP-88V.aspx</td></tr><tr><td colspan="4">&lt;strong&gt;Roll-over cell construction&lt;/strong&gt;</td></tr><tr><td>V can</td><td></td><td></td><td></td></tr><tr><td>electrode on Al/Cu</td><td>MTI Corporation</td><td>EQ-bcaf-15u-280</td><td>http://www.mtixtl.com/AluminumFoilforBatteryCathodeSub&lt;br/&gt; strate-EQ-bcaf-15u-280.aspx</td></tr><tr><td>polyethylene-based or PVDF membrane</td><td>MTI Corporation</td><td>EQ-bsf-0025-400C</td><td>http://www.mtixtl.com/separatorfilm-EQ-bsf-0025-400C.aspx</td></tr><tr><td>LiPF&lt;sub&gt;6&lt;/sub&gt;</td><td>Sigma-Aldrich</td><td>450227</td><td>http://www.sigmaaldrich.com/catalog/product/aldrich/450227?lang=en&amp;amp;region=AU</td></tr><tr><td>deuterated dimethyl carbonate</td><td>Cambridge Isotopes</td><td>DLM-3903-PK&amp;nbsp;</td><td>http://shop.isotope.com/productdetails.aspx?id=10032379&amp;amp;itemno=DLM-3903-PK</td></tr><tr><td>deuterated ethylene carboante</td><td>CDN Isotopes</td><td>D-5489</td><td>https://www.cdnisotopes.com/as/products/specifications/D-5489.php?ei=YWVraWmjoJ1i0lZ7nkr0RpwHr&lt;br/&gt; Hxc9ornu14O4WUtZKbZWZrcq6j55&lt;br/&gt; G0lOab3Wi0dMZ7xc+0Yse1leWVtZ&lt;br/&gt; LnrGKvta7v591o4JrnkbRowHt/r</td></tr><tr><td>Li metal foil</td><td>MTI Corporation</td><td>Lib-LiF-30M</td><td>http://www.mtixtl.com/Li-Foil-30,000 ml-35 mmW-0.17 mm&lt;br/&gt; Th.aspx</td></tr><tr><td>Rubber stopper cut to size</td><td>generic eraser</td><td></td><td>cut a generic eraser to size</td></tr><tr><td>dental wax</td><td>Ainsworth Dental</td><td>AIW042</td><td>http://www.ainsworthdental.com.au/catalogue/Ainsworth-Modelling-Wax-500g.html</td></tr><tr><td>Copper wire (insulated)</td><td>generic</td><td></td><td>sheathed Cu wire that can be cut to size</td></tr><tr><td>Aluminum rod (&amp;lt;2 mm diameter)</td><td>generic</td><td></td><td>cut to size as required</td></tr><tr><td>Glovebox</td><td>Mbraun</td><td>UNILab</td><td>http://www.mbraun.com/products/glovebox-workstations/unilab-glovebox/</td></tr><tr><td>Scissors&amp;nbsp;</td><td>generic</td><td></td><td></td></tr><tr><td>Soldering iron</td><td>generic</td><td></td><td></td></tr><tr><td colspan="4">&lt;strong&gt;&lt;em&gt;In situ&lt;/em&gt; NPD&lt;/strong&gt;</td></tr><tr><td>Appropriate neutron diffractometer</td><td>ANSTO</td><td>Wombat</td><td>http://www.ansto.gov.au/ResearchHub/Bragg/Facilities/Instruments/Wombat/</td></tr><tr><td>Potentiostat/galvanostat</td><td>Autolab</td><td>PGSTAT302N</td><td>http://www.ecochemie.nl/Products/Echem/NSeriesFolder/PGSTAT302N</td></tr><tr><td>Connections to battery from potentiostat/galvanostat</td><td>generic</td><td></td><td></td></tr><tr><td>Training of NPD instrument and use</td><td></td><td></td><td></td></tr><tr><td colspan="4">&lt;strong&gt;Data analysis&lt;/strong&gt;</td></tr><tr><td>Data visualisation and peak fitting, .&lt;em&gt;e.g.&lt;/em&gt; LAMP suite</td><td>ILL</td><td>LAMP</td><td>http://www.ill.eu/instruments-support/computing-for-science/cs-software/all-software/lamp/</td></tr><tr><td>Rietveld analysis software, &lt;em&gt;e.g.&lt;/em&gt; GSAS</td><td>APS</td><td>GSAS</td><td>https://subversion.xray.aps.anl.gov/trac/EXPGUI</td></tr></tbody></table>

in situ neutron powder diffraction using custom-made lithium-ion batteries

Li-ion batteries are widely used in portable electronic devices and are considered as promising candidates for higher-energy applications such as electric vehicles.1,2 However, many challenges, such as energy density and battery lifetimes, need to be overcome before this particular battery technology can be widely implemented in such applications.3 This research is challenging, and we outline a method to address these challenges using in situ NPD to probe the crystal structure of electrodes undergoing electrochemical cycling (charge/discharge) in a battery. NPD data help determine the underlying structural mechanism responsible for a range of electrode properties, and this information can direct the development of better electrodes and batteries.
We briefly review six types of battery designs custom-made for NPD experiments and detail the method to construct the &#8216;roll-over&#8217; cell that we have successfully used on the high-intensity NPD instrument, WOMBAT, at the Australian Nuclear Science and Technology Organisation (ANSTO). The design considerations and materials used for cell construction are discussed in conjunction with aspects of the actual in situ NPD experiment and initial directions are presented on how to analyze such complex in situ data.

We have demonstrated the versatility in using this roll-over cell in the literature15,28-30 and here we present an example with the Li0.18Sr0.66Ti0.5Nb0.5O3 electrode.32
Prior to attempting a sequential Rietveld refinement (Rietveld refinements as a function of state-of-charge), a single refinement of a multiphase model to the first data set was performed, with this data collected for the pristine cell prior to current application. Several models were tested to determine which structural parameters could be accurately refined. Ideally, all structural parameters would be refined using the first pattern and also during the sequential refinements. However, occasionally this may not be possible due to factors such as a lower signal-to-noise, which is especially important for tracking small changes to the lithium position and occupancy, and peak overlap. In the present case to obtain a stable model parameters which were strongly correlated (based on the correlation matrix) were not refined. That is, all the cation atomic displacement parameters were fixed to values obtained from ex-situ measurements. Such restrictions have often been necessary for the &#8220;roll-over&#8221; in-situ cell design.11,29,30 The final outcome of the multiphase Rietveld refinement of the Li0.18Sr0.66Ti0.5Nb0.5O3, copper, and lithium metal structures is shown in Figure 3. The resulting structural data are provided in Table 1. The reason for the large Bragg R value in the refinement compared to the low &#967;2 value is likely due to the relatively large proportions of weak reflections in both the main and lithium-metal phase, which are strongly influenced by the background in the data. As the background is quite irregular, and therefore difficult to accurately model, these weaker reflections also become difficult to accurately model.
The refinement result prior to cell discharge provides a basic indication of what may be refined sequentially. However, following the progression of refineable parameters during cycling is not the only way to track structural change during discharge. Changes in intensity of specific characteristic reflections, the appearance of new reflections, and cell parameter variations as a function of discharge can provide significant information concerning the structural changes which take place during discharge. Sequential fitting of a single reflection within each diffraction pattern collected can be performed in programs such as LAMP33 and Origin. Further, as the diffraction patterns and electrochemical data are collected simultaneously they can both be plotted together as a function of time. The electrochemical procedure followed during the in situ experiment performed on Li0.18Sr0.66Ti0.5Nb0.5O3 is provided in Table 2. These conditions provide a reference for the changes observed during electrochemical cycling, as indicated within Figure 4.
The first three components from the top of Figure 4 display the various changes which occur to the 115 reflection during cycling. Under these plots are the change in cell parameter and electrochemical potential profile. An interesting aspect of lithium insertion into Li0.18Sr0.66Ti0.5Nb0.5O3 is that for potentials above 1 V it is reversible, however, discharge below 1 V results in irreversible lithium insertion. For lithium insertion above 1 V, 0.25 mol Li/formula unit can be reversibly inserted under constant current conditions and takes 1,257 min at 1.7(1) mA&#160;g-1.32,34 Under equilibrium conditions (lower current densities) up to 0.4 mol Li/formula unit can be inserted in 160 hr. The insertion of lithium within this region is known to proceed via a solid solution reaction with the unit-cell volume continuously expanding to 1.81(9)% larger following the insertion of 0.25 mol of lithium. In comparison, the volume of the electrode in the neutron cell expanded by only 0.61(6)% in 870 min at 2.5 mA g-1. However, on charging at 5.0 mA g-1 the cell contracted further than the initial values, suggesting that self-discharge had occurred before the start of the experiment. Comparing absolute values, the unit cell of a completely charged material (no lithium) was found to be 3.93190(2)&#160;&#197; from synchrotron X-ray diffraction data compared to 3.9345(5) &#197; from the in situ NPD data. Further, the material discharged to 1&#160;V was found to have a unit-cell length of 3.95640(2)&#160;&#197; from synchrotron X-ray diffraction data compared to 3.9454(7) &#197; from the in situ NPD data. Thus it appears as though the material did not completely react on discharge to 1&#160;V, nor on charging. Besides the higher applied current densities, a low pressure applied to the battery stack (or roll) can result in high area-specific impedances and so charge and discharge runs would end prematurely due to high polarization. The latter is a major factor in constructing these cells and it is crucial to obtain a good quality electrode roll for the in situ neutron diffraction cell. Further, if the applied pressure is uneven, this could result in the formation of two phases as parts of the cell react faster than others. The only indication that two-phase behavior was occurring was a reversible broadening of the 115 reflection (Figure 4A and B).
During cycling, the peak intensity of the 115 reflection reduced as more lithium was inserted into the structure and then increased as lithium was removed. Simultaneously, the peak width (full-width at half maximum, FWHM) varies in the opposite sense, resulting in the overall integrated peak intensity remaining constant during lithium insertion and extraction. The same trend occurred for all other observed and fitted reflections. Thus, there were no apparent structural components to the changes in peak intensity. While peak broadening can be associated with a loss of crystallinity or a reduction in particle size, the reversibility of the changes indicate the formation of several phases reacting at different rates. This phase segregation is then strongly enhanced below 1&#160;V with a second phase becoming distinct.
Preliminary electrochemical cycling experiments performed on Li0.18Sr0.66Ti0.5Nb0.5O3 have shown a flat potential output below 1&#160;V, leading to the anticipation that a second phase should appear within this region. It was also hypothesized that this second phase could be the cause of irreversible lithium insertion within this region. The regions where this second phase becomes most visually distinct are indicated with orange bars in Figure 4. Within the angular resolution provided by the Wombat diffractometer, the second phase seems to form at the same potential regardless of the discharge current used (2.5 mA g-1 for the second discharge, 3.8 mA g-1 for the third). As more lithium is inserted into the Li0.18Sr0.66Ti0.5Nb0.5O3 structure the diffusion of lithium into the bulk slows (from 10-7 to 10-8 cm2 sec-1).32 It appears as though the rate of diffusion into the bulk reduces enough to increase the rate of phase segregation during the course of discharge.
While a sequential refinement with a second perovskite phase was not possible due to the similarities of the two phases and resulting peak overlap, consideration of the topographical plot of the 115 reflection (Figure 4C) can still provide insight into the structural changes of the positive electrode. In a system at equilibrium, a two-phase region is marked by one phase disappearing at the same rate that a second phase appears as a function of composition (or as a function of any other order parameter, such as temperature), such that their phase fractions always sum to one. However, within the two-phase region observed below 1 V for Li0.18Sr0.66Ti0.5Nb0.5O3 the new phase varies continuously, while the first phase is unchanging. Thus, the in situ experiment was able to probe the non-equilibrium behavior of the positive electrode material as a function of state of charge. The second phase stops expanding before the end of discharge. This may signal a shift to an equilibrium two-phase conversion, however, no intensity changes were observed. Changes in the relative intensity of the two reflections were observed once the cell was allowed to relax (the region indicated by the red bar in Figure 4). During this time, the reflection at higher 2&#952; begins to lose intensity relative to the reflection at lower 2&#952;, indicating that phase equilibration occurs once the applied current has been switched off. A single phase was then rapidly reformed during charging, suggesting that the two-phase reaction is reversible. This prediction was confirmed by discharging below 1 V multiple times. Thus, it is still uncertain why cycling below 1 V results in irreversible lithium insertion. It appears as though the second phase forms as a result of inhibited lithium diffusion into the structure, possibly intrinsically or because of the low pressure applied to the battery stack. It should be noted that the unit cell does not return to its original size on each subsequent charge, implying that some lithium remains within the bulk structure. Cycling the cell below 1&#160;V will require a further experiment where polarization effects are greatly reduced or eliminated. Without polarization as a competing influence, the effect of the changing lithium diffusion within the material and its structural changes below 1&#160;V can be determined.
<img alt="Figure 1" src="/files/ftp_upload/52284/52284fig1highres.jpg" /> 
Figure 1: Photo of the positive electrode component on a strip of polyethylene-based separator following extraction from an in situ cell. The image demonstrates the relative sizes of positive electrode and separator required to prevent contact between the two electrodes. Also included in the photo are the copper wires which enable connection to an external circuit.
<img alt="Figure 2" src="/files/ftp_upload/52284/52284fig2highres.jpg" /> 
Figure 2: (A): Photo of the in situ NPD cell on the Wombat beamline at ANSTO. (B) Schematic of the in situ cell build, showing the layers that result from the &#8220;roll-over&#8221; design. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/52284/52284fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" src="/files/ftp_upload/52284/52284fig3highres.jpg" /> 
Figure 3: In situ NPD pattern of the constructed cell modeled using a multiphase refinement containing Li0.18Sr0.66Ti0.5Nb0.5O3 (LSTN), copper, and lithium. The upper curve corresponds to the model fitted to the data (black crosses) and the lower curve corresponds to the difference between them. Reflection markers are shown as vertical bars. The neutron wavelength (&#955;), goodness-of-fit (&#967;2), and Bragg-R factor (RB), are given inset.
<img alt="Figure 4" src="/files/ftp_upload/52284/52284fig4highres.jpg" /> 
Figure 4: Plots A-C relate to the Li0.18Sr0.66Ti0.5Nb0.5O3 (LSTN) 115 reflection specifically and show the evolution of its shape during cycling. The accuracy of these parameters decreases within the two-phase region as this reflection was modeled with a single pseudo-Voigt function. Plot D shows the variation of the lattice parameter as a function of discharge and plot E shows the battery potential that was collected simultaneously. The orange bars highlight regions where the discharge cycle was taken below 1 V, which also correlates with the onset of the two-phase region. The red bar highlights the region where the cell was allowed to relax and its potential to equilibrate.
<img alt="Figure 5" src="/files/ftp_upload/52284/52284fig5highres.jpg" /> 
Figure 5: (A) shows the Rietveld-derived lattice parameters and weight fraction of the LiFePO4/FePO4 cathode, selected 2&#952; region of the in situ NPD data (top) with scaled intensity highlighting the LiFePO4 and FePO4 221 and 202 reflections, and the current (red). Shaded regions indicate the coexistence of solid solution and two-phase reactions. This figure is reprinted with permission from the Journal of the American Chemical Society 134, 7867-7873, copyright 2012 American Chemical Society. (B) shows in situ NDP data of an uncycled cell (red) where, the calculated model for the Li(Co0.16Mn1.84)O4 cathode as a black solid line, the difference between the data and the model calculation as a purple line at the bottom, and vertical lines represent reflection markers for the modeled phases. This figure is reprinted with permission from the Journal of Physical Chemistry C 115, 21473-21480, copyright 2011 American Chemical Society. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/52284/52284fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="0" cellpadding="0" cellspacing="0">
	<tbody>
		<tr>
			<td class="xl63" colspan="7">Full-Cell Pre-discharge, Pm3m, a = 3.9368(5) &#197;</td>
		</tr>
		<tr>
			<td class="xl68" colspan="7">&#967;2 = 1.51, RB = 14.96%</td>
		</tr>
		<tr>
			<td class="xl64">Atom</td>
			<td class="xl65">Site</td>
			<td class="xl65">x</td>
			<td class="xl65">y</td>
			<td class="xl65">z</td>
			<td class="xl65">Occupancy</td>
			<td class="xl65">Uiso (&#197;2)</td>
		</tr>
		<tr>
			<td class="xl66">Sr</td>
			<td class="xl63">1b</td>
			<td class="xl63">0.5</td>
			<td class="xl63">0.5</td>
			<td class="xl63">0.5</td>
			<td class="xl63">0.66</td>
			<td class="xl63">0.0079</td>
		</tr>
		<tr>
			<td class="xl66">Ti</td>
			<td class="xl63">1a</td>
			<td class="xl63">0</td>
			<td class="xl63">0</td>
			<td class="xl63">0</td>
			<td class="xl63">0.5</td>
			<td class="xl63">0.0098</td>
		</tr>
		<tr>
			<td class="xl66">Nb</td>
			<td class="xl63">1a</td>
			<td class="xl63">0</td>
			<td class="xl63">0</td>
			<td class="xl63">0</td>
			<td class="xl63">0.5</td>
			<td class="xl63">0.0098</td>
		</tr>
		<tr>
			<td class="xl67">O</td>
			<td class="xl68">3d</td>
			<td class="xl68">0.5</td>
			<td class="xl68">0</td>
			<td class="xl68">0</td>
			<td class="xl68">1</td>
			<td class="xl68">0.006(2)</td>
		</tr>
	</tbody>
</table>
Table 1: Refined lattice parameter, space group, positional parameters and Debye-Waller factors for Li0.18Sr0.66Ti0.5Nb0.5O3 in the in situ cell prior to discharge.
<table border="0" cellpadding="0" cellspacing="0">
	<tbody>
		<tr>
			<td rowspan="2">Step</td>
			<td>Current&#160;</td>
			<td>Potential&#160;</td>
		</tr>
		<tr>
			<td>(mA g-1)</td>
			<td>(V)</td>
		</tr>
		<tr>
			<td>1</td>
			<td>-2.5</td>
			<td>1</td>
		</tr>
		<tr>
			<td>2</td>
			<td>5.0</td>
			<td>2</td>
		</tr>
		<tr>
			<td>3</td>
			<td>-2.5</td>
			<td>0.93</td>
		</tr>
		<tr>
			<td>4</td>
			<td>5.0</td>
			<td>1.73</td>
		</tr>
		<tr>
			<td>5</td>
			<td>12</td>
			<td>1.82</td>
		</tr>
		<tr>
			<td>6</td>
			<td>-3.8</td>
			<td>0.38</td>
		</tr>
		<tr>
			<td>7</td>
			<td colspan="2">Rest (300 min)</td>
		</tr>
		<tr>
			<td>8</td>
			<td>7.5</td>
			<td>2</td>
		</tr>
		<tr>
			<td>9</td>
			<td>-3.8</td>
			<td>1.04</td>
		</tr>
	</tbody>
</table>
Table 2: The electrochemical procedure followed during the in situ experiment performed on Li0.18Sr0.66Ti0.5Nb0.5O3.

Watch this Scientific Journal Video about In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries at JoVE.com

In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries

We describe the design and construction of an electrochemical cell for the examination of electrode materials using in situ neutron powder diffraction (NPD). We briefly comment on alternate in situ NPD cell designs and discuss methods for the analysis of the corresponding in situ NPD data produced using this cell.

In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries

Li-ion batteries are widely used in portable electronic devices and are considered as promising candidates for higher-energy applications such as electric ...

in-situ-neutron-powder-diffraction-using-custom-made-lithium-ion

Nanyang Technological University

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JoVE Journal

Engineering

15.7K Views.  University of Sydney.  We beschrijven het ontwerp en de bouw van een elektrochemische cel voor de behandeling van de elektrode materialen met behulp van in situ neutronen poeder diffractie (NPD). We kort ingaan op alternatieve in situ NPD celontwerpen en bespreken methoden voor de analyse van de overeenkomstige in situ NPD data geproduceerd met behulp van deze cel. 

Video: In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries

Construction and Testing of Coin Cells of Lithium Ion Batteries

Rechargeable lithium ion batteries have wide applications in electronics, where customers always demand more capacity and longer lifetime. Lithium ion batteries have also been considered to be used in electric and hybrid vehicles1 or even electrical grid stabilization systems2. All these applications simulate a dramatic increase in the research and development of battery materials3-7, including new materials3,8, doping9, nanostructuring10-13, coatings or surface modifications14-17 and novel binders18. Consequently, an increasing number of physicists, chemists and materials scientists have recently ventured into this area. Coin cells are widely used in research laboratories to test new battery materials; even for the research and development that target large-scale and high-power applications, small coin cells are often used to test the capacities and rate capabilities of new materials in the initial stage. 
 In 2010, we started a National Science Foundation (NSF) sponsored research project to investigate the surface adsorption and disordering in battery materials (grant no. DMR-1006515). In the initial stage of this project, we have struggled to learn the techniques of assembling and testing coin cells, which cannot be achieved without numerous help of other researchers in other universities (through frequent calls, email exchanges and two site visits). Thus, we feel that it is beneficial to document, by both text and video, a protocol of assembling and testing a coin cell, which will help other new researchers in this field. This effort represents the "Broader Impact" activities of our NSF project, and it will also help to educate and inspire students.
In this video article, we document a protocol to assemble a CR2032 coin cell with a LiCoO2 working electrode, a Li counter electrode, and (the mostly commonly used) polyvinylidene fluoride (PVDF) binder. To ensure new learners to readily repeat the protocol, we keep the protocol as specific and explicit as we can. However, it is important to note that in specific research and development work, many parameters adopted here can be varied. First, one can make coin cells of different sizes and test the working electrode against a counter electrode other than Li. Second, the amounts of C black and binder added into the working electrodes are often varied to suit the particular purpose of research; for example, large amounts of C black or even inert powder were added to the working electrode to test the "intrinsic" performance of cathode materials14. Third, better binders (other than PVDF) have also developed and used18. Finally, other types of electrolytes (instead of LiPF6) can also be used; in fact, certain high-voltage electrode materials will require the uses of special electrolytes7.

A protocol to construct and test coin cells of lithium ion batteries is described. The specific procedures of making a working electrode, preparing a counter electrode, assembling a cell inside a glovebox and testing the cell are presented.

Rechargeable lithium ion batteries have wide applications in electronics, where customers always demand more capacity and longer lifetime.  Lithium ion ...

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques

Intercalation compounds such as transition metal oxides or phosphates are the most commonly used electrode materials in Li-ion and Na-ion batteries. During insertion or removal of alkali metal ions, the redox states of transition metals in the compounds change and structural transformations such as phase transitions and/or lattice parameter increases or decreases occur. These behaviors in turn determine important characteristics of the batteries such as the potential profiles, rate capabilities, and cycle lives. The extremely bright and tunable x-rays produced by synchrotron radiation allow rapid acquisition of high-resolution data that provide information about these processes. Transformations in the bulk materials, such as phase transitions, can be directly observed using X-ray diffraction (XRD), while X-ray absorption spectroscopy (XAS) gives information about the local electronic and geometric structures (e.g.&#160;changes in redox states and bond lengths). In situ experiments carried out on operating cells are particularly useful because they allow direct correlation between the electrochemical and structural properties of the materials. These experiments are time-consuming and can be challenging to design due to the reactivity and air-sensitivity of the alkali metal anodes used in the half-cell configurations, and/or the possibility of signal interference from other cell components and hardware. For these reasons, it is appropriate to carry out ex situ experiments (e.g.&#160;on electrodes harvested from partially charged or cycled cells) in some cases. Here, we present detailed protocols for the preparation of both ex situ and in situ samples for experiments involving synchrotron radiation and demonstrate how these experiments are done.

We describe the use of synchrotron X-ray absorption spectroscopy (XAS) and X-ray diffraction (XRD) techniques to probe details of intercalation/deintercalation processes in electrode materials for Li-ion and Na-ion batteries. Both in situ and ex situ experiments are used to understand structural behavior relevant to the operation of devices

Intercalation compounds such as transition metal oxides or phosphates are the most commonly used electrode materials in Li-ion and Na-ion batteries. ...

Measuring Material Microstructure Under Flow Using 1-2 Plane Flow-Small Angle Neutron Scattering

A new small-angle neutron scattering (SANS) sample environment optimized for studying the microstructure of complex fluids under simple shear flow is presented. The SANS shear cell consists of a concentric cylinder Couette geometry that is sealed and rotating about a horizontal axis so that the vorticity direction of the flow field is aligned with the neutron beam enabling scattering from the 1-2 plane of shear (velocity-velocity gradient, respectively). This approach is an advance over previous shear cell sample environments as there is a strong coupling between the bulk rheology and microstructural features in the 1-2 plane of shear. Flow-instabilities, such as shear banding, can also be studied by spatially resolved measurements. This is accomplished in this sample environment by using a narrow aperture for the neutron beam and scanning along the velocity gradient direction. Time resolved experiments, such as flow start-ups and large amplitude oscillatory shear flow are also possible by synchronization of the shear motion and time-resolved detection of scattered neutrons. Representative results using the methods outlined here demonstrate the useful nature of spatial resolution for measuring the microstructure of a wormlike micelle solution that exhibits shear banding, a phenomenon that can only be investigated by resolving the structure along the velocity gradient direction. Finally, potential improvements to the current design are discussed along with suggestions for supplementary experiments as motivation for future experiments on a broad range of complex fluids in a variety of shear motions.

A shear cell is developed for small-angle neutron scattering measurements in the velocity-velocity gradient plane of shear and is used to characterize complex fluids. Spatially resolved measurements in the velocity gradient direction are possible for studying shear-banding materials. Applications include investigations of colloidal dispersions, polymer solutions, and self-assembled structures.

A new small-angle neutron scattering (SANS) sample environment optimized for studying the microstructure of complex fluids under simple shear flow is ...

Using Neutron Spin Echo Resolved Grazing Incidence Scattering to Investigate Organic Solar Cell Materials

The spin echo resolved grazing incidence scattering (SERGIS) technique has been used to probe the length-scales associated with irregularly shaped crystallites. Neutrons are passed through two well defined regions of magnetic field; one before and one after the sample. The two magnetic field regions have opposite polarity and are tuned such that neutrons travelling through both regions, without being perturbed, will undergo the same number of precessions in opposing directions. In this case the neutron precession in the second arm is said to &#34;echo&#34; the first, and the original polarization of the beam is preserved. If the neutron interacts with a sample and scatters elastically the path through the second arm is not the same as the first and the original polarization is not recovered. Depolarization of the neutron beam is a highly sensitive probe at very small angles (&#60;50&#160;&#956;rad) but still allows a high intensity, divergent beam to be used. The decrease in polarization of the beam reflected from the sample as compared to that from the reference sample can be directly related to structure within the sample.
In comparison to scattering observed in neutron reflection measurements the SERGIS signals are often weak and are unlikely to be observed if the in-plane structures within the sample under investigation are dilute, disordered, small in size and polydisperse or the neutron scattering contrast is low. Therefore, good results will most likely be obtained using the SERGIS technique if the sample being measured consist of thin films on a flat substrate and contain scattering features that contains a high density of moderately sized features (30 nm to 5 &#181;m) which scatter neutrons strongly or the features are arranged on a lattice. An advantage of the SERGIS technique is that it can probe structures in the plane of the sample.

Progress has been made in utilizing spin echo resolved grazing incidence scattering (SERGIS) as a neutron scattering technique to probe the length-scales in irregular samples. Crystallites of [6,6]-phenyl-C61-butyric acid methyl ester have been probed using the SERGIS technique and the results confirmed by optical and atomic force microscopy.

The spin echo resolved grazing incidence scattering (SERGIS) technique has been used to probe the length-scales associated with irregularly shaped ...

Failure Analysis of Batteries Using Synchrotron-based Hard X-ray Microtomography

Imaging morphological changes that occur during the lifetime of rechargeable batteries is necessary to understand how these devices fail. Since the advent of lithium-ion batteries, researchers have known that the lithium metal anode has the highest theoretical energy density of any anode material. However, rechargeable batteries containing a lithium metal anode are not widely used in consumer products because the growth of lithium dendrites from the anode upon charging of the battery causes premature cell failure by short circuit. Lithium dendrites can also form in commercial lithium-ion batteries with graphite anodes if they are improperly charged. We demonstrate that lithium dendrite growth can be studied using synchrotron-based hard X-ray microtomography. This non-destructive imaging technique allows researchers to study the growth of lithium dendrites, in addition to other morphological changes inside batteries, and subsequently develop methods to extend battery life.

Synchrotron-based hard X-ray microtomography is used to image the electrochemical growth of dendrites from a lithium metal electrode through a solid polymer electrolyte membrane.

Imaging morphological changes that occur during the lifetime of rechargeable batteries is necessary to understand how these devices fail. Since the advent ...

Non-aqueous Electrode Processing and Construction of Lithium-ion Coin Cells

Research into new and improved materials to be utilized in lithium-ion batteries (LIB) necessitates an experimental counterpart to any computational analysis. Testing of lithium-ion batteries in an academic setting has taken on several forms, but at the most basic level lies the coin cell construction. In traditional LIB electrode preparation, a multi-phase slurry composed of active material, binder, and conductive additive is cast out onto a substrate. An electrode disc can then be punched from the dried sheet and used in the construction of a coin cell for electrochemical evaluation. Utilization of the potential of the active material in a battery is critically dependent on the microstructure of the electrode, as an appropriate distribution of the primary components are crucial to ensuring optimal electrical conductivity, porosity, and tortuosity, such that electrochemical and transport interaction is optimized. Processing steps ranging from the combination of dry powder, wet mixing, and drying can all critically affect multi-phase interactions that influence the microstructure formation. Electrochemical probing necessitates the construction of electrodes and coin cells with the utmost care and precision. This paper aims at providing a step-by-step guide of non-aqueous electrode processing and coin cell construction for lithium-ion batteries within an academic setting and with emphasis on deciphering the influence of drying and calendaring.

Non-aqueous electrode processing is central to the construction of coin cells and the evaluation of new electrode chemistries for lithium-ion batteries. A step-by-step guide to the basic practices needed as an electrochemical engineer working with batteries in an academic experimental setting is furnished.

Research into new and improved materials to be utilized in lithium-ion batteries (LIB) necessitates an experimental counterpart to any computational ...

Measuring Spray Droplet Size from Agricultural Nozzles Using Laser Diffraction

When making an application of any crop protection material such as an herbicide or pesticide, the applicator uses a variety of skills and information to make an application so that the material reaches the target site (i.e., plant). Information critical in this process is the droplet size that a particular spray nozzle, spray pressure, and spray solution combination generates, as droplet size greatly influences product efficacy and how the spray moves through the environment. Researchers and product manufacturers commonly use laser diffraction equipment to measure the spray droplet size in laboratory wind tunnels. The work presented here describes methods used in making spray droplet size measurements with laser diffraction equipment for both ground and aerial application scenarios that can be used to ensure inter- and intra-laboratory precision while minimizing sampling bias associated with laser diffraction systems. Maintaining critical measurement distances and concurrent airflow throughout the testing process is key to this precision. Real time data quality analysis is also critical to preventing excess variation in the data or extraneous inclusion of erroneous data. Some limitations of this method include atypical spray nozzles, spray solutions or application conditions that result in spray streams that do not fully atomize within the measurement distances discussed. Successful adaption of this method can provide a highly efficient method for evaluation of the performance of agrochemical spray application nozzles under a variety of operational settings. Also discussed are potential experimental design considerations that can be included to enhance functionality of the data collected.

We present protocols to be used in the measurement of spray droplet size from agricultural nozzles used in both aerial and ground based agrochemical applications. These methods presented were developed to provide consistent and repeatable droplet size data both inter- and intra-laboratory, when using laser diffraction systems.

When making an application of any crop protection material such as an herbicide or pesticide, the applicator uses a variety of skills and information to ...

Focused Ion Beam Fabrication of LiPON-based Solid-state Lithium-ion Nanobatteries for In Situ Testing

Solid-state electrolytes are a promising replacement for current organic liquid electrolytes, enabling higher energy densities and improved safety of lithium-ion (Li-ion) batteries. However, a number of setbacks prevent their integration into commercial devices. The main limiting factor is due to nanoscale phenomena occurring at the electrode/electrolyte interfaces, ultimately leading to degradation of battery operation. These key problems are highly challenging to observe and characterize as these batteries contain multiple buried interfaces. One approach for direct observation of interfacial phenomena in thin film batteries is through the fabrication of electrochemically active nanobatteries by a focused ion beam (FIB). As such, a reliable technique to fabricate nanobatteries was developed and demonstrated in recent work. Herein, a detailed protocol with a step-by-step process is presented to enable the reproduction of this nanobattery fabrication process. In particular, this technique was applied to a thin film battery consisting of LiCoO2/LiPON/a-Si, and has further been previously demonstrated by in situ cycling within a transmission electron microscope.

Focused Ion Beam Fabrication of LiPON-based Solid-state Lithium-ion Nanobatteries for In Situ Testing

A protocol for the fabrication of electrochemically active LiPON-based solid-state lithium-ion nanobatteries using a focused ion beam is presented.

Solid-state electrolytes are a promising replacement for current organic liquid electrolytes, enabling higher energy densities and improved safety of ...

Elemental-sensitive Detection of the Chemistry in Batteries through Soft X-ray Absorption Spectroscopy and Resonant Inelastic X-ray Scattering

Energy storage has become more and more a limiting factor of today's sustainable energy applications, including electric vehicles and green electric grid based on volatile solar and wind sources. The pressing demand of developing high-performance electrochemical energy storage solutions, i.e., batteries, relies on both fundamental understanding and practical developments from both the academy and industry. The formidable challenge of developing successful battery technology stems from the different requirements for different energy-storage applications. Energy density, power, stability, safety, and cost parameters all have to be balanced in batteries to meet the requirements of different applications. Therefore, multiple battery technologies based on different materials and mechanisms need to be developed and optimized. Incisive tools that could directly probe the chemical reactions in various battery materials are becoming critical to advance the field beyond its conventional trial-and-error approach. Here, we present detailed protocols for soft X-ray absorption spectroscopy (sXAS), soft X-ray emission spectroscopy (sXES), and resonant inelastic X-ray scattering (RIXS) experiments, which are inherently elemental-sensitive probes of the transition-metal 3d and anion 2p states in battery compounds. We provide the details on the experimental techniques and demonstrations revealing the key chemical states in battery materials through these soft X-ray spectroscopy techniques.

Here, we present a protocol for typical experiments of soft X-ray absorption spectroscopy (sXAS) and resonant inelastic X-ray scattering (RIXS) with applications in battery material studies.

Energy storage has become more and more a limiting factor of today's sustainable energy applications, including electric vehicles and green electric grid ...

Chemistry

Identification and Quantification of Decomposition Mechanisms in Lithium-Ion Batteries; Input to Heat Flow Simulation for Modeling Thermal Runaway

The risks and possible accidents related to the normal use of lithium-ion batteries remain a serious concern. In order to get a better understanding of thermal runaway (TR), the exothermic decomposition reactions in anode and cathode were studied, using a Simultaneous Thermal Analysis (STA)/Gas Chromatography-Mass Spectrometry (GC-MS)/Fourier Transform Infrared (FTIR) spectrometer system. These techniques allowed the identification of the reaction mechanisms in each electrode, owing to the analysis of evolved gaseous species, the amount of heat released and mass loss. These results provided insight into the thermal events happening within a broader temperature range than covered in previously published models. This allowed the formulation of an improved thermal model to depict TR. The heat of reaction, activation energy, and frequency factor (thermal triplets) for each major exothermic process at material level were investigated in a Lithium Nickel-Manganese-Cobalt-Oxide (NMC (111))-Graphite battery cell. The results were analyzed, and their kinetics were derived. These data can be used to successfully simulate the experimental heat flow.

This work aims at determining the reaction kinetics of Li-ion battery cathode and anode materials undergoing thermal runaway (TR). Simultaneous Thermal Analysis (STA)/Fourier Transform Infrared (FTIR) spectrometer/Gas Chromatography Mass Spectrometry (GC-MS) were used to reveal thermal events and to detect evolved gases.

The risks and possible accidents related to the normal use of lithium-ion batteries remain a serious concern. In order to get a better understanding of ...

In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries

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