The research is supported by the Office of Naval Research (ONR) (Award N00014-16-1-2578 and N00014-16-1-3054), Robert A. Welch Foundation (Grant No. A-1547, No. A-1261), Air Force Office of&#160;Scientific&#160;Research (Award No. FA9550-18-1-0141), SMART Fellowship and a grant from King Abdulaziz City for Science and Technology (KACST).

1. Creation of the Femtosecond Laser Filament
<ol>
	<li>As femtosecond filaments require the output of a Class 4 laser, wear appropriate eye protection rated for the particular laser system in use and establish a clear and well-defined beam line with an appropriate beam dump. Follow all standard laser safety procedures.</li>
	<li>Begin with the output of a pulsed, amplified femtosecond laser whose instantaneous output power is greater than or equal to the critical power for self-focusing in air, about 3.2 GW for a Ti:Sapphire laser at 800 nm wavelength. Generate the amplified pulse in a commercial femtosecond laser amplifier system using manufacturer&#8217;s protocol. In practice, pulse energy of about 1 mJ for an approximately 35 fs pulse is sufficient. Good results are obtained with pulse energy of 2-4 mJ.</li>
	<li>Pass the laser beam through an iris that slightly clips the outer edges. It is observed to promote filament formation, since filament formation is known to be seeded by sharp gradients and inhomogeneity in the spatial intensity profile of the laser.</li>
	<li>Pass the beam through the converging lens that has a focal length of approximately 200 cm or greater, so that the geometric focusing is not so great that self-focusing is overwhelmed by optical breakdown or diffraction. Slightly tilt the lens with respect to the direction of propagation, since additional anisotropy is known to help seed the self-focusing process.</li>
	<li>Observe a filament at a location near the geometric focus of the lens. Diagnose filamentation by a diffuse (several-mm-sized) halo surrounding a bright (approximately 100-&#181;m-sized) core. The halo could be seen on a white paper and the bright cores usually flicker.
	<ol>
		<li>Additionally, observe a characteristic self-phase modulation process in the air, which produces bright, multi-colored conical emission rings that are visible beyond the filament. For lasers with energies which are several times the threshold for filamentation, multiple filaments are observed. These are visible as multiple bright spots in the conical emission pattern, and can be eliminated by attenuation before the iris.</li>
	</ol>
	</li>
</ol>
2. Remote Scanning of the Target Surface
<ol>
	<li>Put a two-axis motorized translation stage capable of moving the sample in the direction transverse to the propagation of the laser beam on the table. Ensure that the laser beam is incident on the center of the stage. Bolt the stage on the table with screws. For laboratory purposes, it is generally easier to keep the laser beam fixed in space while scanning the target under the beam.</li>
	<li>Place sand in a container (5 mm x 25.4 mm x 25.4 mm). The thickness of sand is around 2 mm.
	<ol>
		<li>Put the metals (copper, stainless steel, aluminum) on the top of sand (Figure 3a). Cover the metals with another 2 mm layer of sand (Figure 3b).</li>
		<li>With the laser off, put the container in the center of the translation stage. Make sure that the center of container is at the location where filamentation is observed for step 1.1-1.5.</li>
	</ol>
	</li>
	<li>Set up the laser&#8217;s computer control to fire a single shot when electronically commanded. Write a LabVIEW or a similar computer language to perform the control. For automated single-shot pulses, an external trigger is required.
	<ol>
		<li>Connect a trigger TTL pulse to the External Trigger port on the back of the laser control module with a BNC cable. Enable the external trigger option on the laser control module. The TTL pulse will now trigger the laser to fire a single shot.</li>
	</ol>
	</li>
	<li>Set up the appropriate sensor apparatus. Set up the entrance of the spectrometer pointing to the impact point.
	<ol>
		<li>Use a lens to couple the light from filamentation impact point into a spectrometer. Make sure that the distance between the lens and filamentation is about the focal length.</li>
		<li>Connect the spectrometer with computer using USB cable. Use software to monitor the spectrum. Open the software and the spectrum, and then click the Run button.</li>
		<li>Use the mouse to zoom in the range that is recorded in the experiment. Optimize the spectrometer position after seeing the signal on the screen.</li>
		<li>For imaging measurements, replace the spectrometer with a photomultiplier tube or a CCD camera.</li>
	</ol>
	</li>
	<li>Write a program in LabVIEW or a similar computer language to perform a loop over the following steps: Fire a single shot from the laser; collect and save the resulting data; move the translation stage to the next coordinate point.</li>
</ol>

<ol>
	<li>Kocharocsky, V., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Gain-swept+superrandiance+applied+to+the+stand-off+detection+of+trace+impurities+in+the+atmosphere.">Gain-swept superrandiance applied to the stand-off detection of trace impurities in the atmosphere.</a> Proceedings of the National Academy of Sciences of the United States of America. 102 (22), 7806-7811 (2005).</li><li>Hemmer\, P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Standoff+spectroscopy+via+remote+generation+of+a+backward-propagation+laser+beam.">Standoff spectroscopy via remote generation of a backward-propagation laser beam.</a> Proceedings of the National Academy of Sciences of the United States of America. 108 (8), 3130-3134 (2011).</li><li>Zuber, M. T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+Mars+Observer+laser+altimeter+investigation.">The Mars Observer laser altimeter investigation.</a> Journal of Geophysical Research. 97, 7781 (1992).</li><li>Mejean, G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Remote+detection+and+identification+of+biological+aerosols+using+a+femtosecond+terawatt+lidar+system.">Remote detection and identification of biological aerosols using a femtosecond terawatt lidar system.</a> Applied Physics B: Lasers and Optics. 78 (5), 535-537 (2004).</li><li>Boyd, R. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Nonlinear Optics. , (2008).</li><li>Gattass, R. R., Mazur, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Femtosecond+laser+micromachining+in+transparent+materials.">Femtosecond laser micromachining in transparent materials.</a> Nature Photonics. 2, 219-225 (2008).</li><li>Tognoni, E., Palleschi, V., Corsi, M., Christoforetti, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantitative+micro-analysis+by+laser-induced+breakdown+spectroscopy:+a+review+of+the+experimental+approaches.">Quantitative micro-analysis by laser-induced breakdown spectroscopy: a review of the experimental approaches.</a> Spectrochimica Acta Part B: Atomic Spectroscopy. 57 (7), 1115-1130 (2002).</li><li>Beadie, G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Toward+a+FAST+CARS+anthrax+detector:+coherence+preparation+using+simultaneous+femtosecond+laser+pulses.">Toward a FAST CARS anthrax detector: coherence preparation using simultaneous femtosecond laser pulses.</a> Optics Communications. 244, 423-430 (2005).</li><li>Scully, M. O., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=FAST+CARS:+Engineering+of+a+laser+spectroscopic+technique+for+rapid+identification+of+bacterial+spores.">FAST CARS: Engineering of a laser spectroscopic technique for rapid identification of bacterial spores.</a> Proceedings of the National Academy of Sciences of the United States of America. 99 (17), 10994-11001 (2002).</li><li>Pestov, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optimizing+the+laser-pulse+configuration+for+coherent+Raman+spectroscopy.">Optimizing the laser-pulse configuration for coherent Raman spectroscopy.</a> Science. 316 (5822), 265-268 (2007).</li><li>Braun, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Self-channeling+of+high-peak-power+femtosecond+laser+pulses+in+air.">Self-channeling of high-peak-power femtosecond laser pulses in air.</a> Optics Letters. 20 (1), 73-75 (1995).</li><li>Couairon, A., Mysyrowicz, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Femtosecond+filamentation+in+transparent+media.">Femtosecond filamentation in transparent media.</a> Physics Reports. 441, 47-189 (2007).</li><li>Wang, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Remote+sub-diffraction+imaging+with+femtosecond+laser+filaments.">Remote sub-diffraction imaging with femtosecond laser filaments.</a> Optics Letters. 37 (8), 1343-1345 (2012).</li><li>Strycker, B. D., Wang, K., Springer, M. D., Sokolov, A. V. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Chemical-specific+imaging+of+shallowly+buried+objects+using+femtosecond+laser+pulses.">Chemical-specific imaging of shallowly buried objects using femtosecond laser pulses.</a> Applied Optics. 52 (20), 4792-4796 (2013).</li><li>Heck, G., Sloss, J., Levis, R. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Adaptive+control+of+the+spatial+position+of+white+light+filaments+in+an+aqueous+solution.">Adaptive control of the spatial position of white light filaments in an aqueous solution.</a> Optics Communications. 259 (1), 216-222 (2006).</li><li>Li, H. 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No conflicts of interest declared.

The method presented above is a laboratory protocol for the use of high-intensity laser light delivered at classically intractable distances. Of the numerous possible applications of such light &#8211; CARS, FIBS, THz radiation, photoacoustics, superradiance, etc. &#8211; many applications can deliver point information about surface material properties. Femtosecond laser filaments with sub-classical-diffraction-limited spot size allows use of these techniques while scanning the surface on a point-by-point basis. This protocol is an ideal test bed for the development of such techniques.
The most critical aspect of the protocol is to generate the laser filamentation. To generate the stable laser filamentation, the critical laser intensity is a few 1013 W/cm2 and the clamped intensity is around 1.4x1014 W/cm2 measured in experiment16. There is no laser filamentation when the intensity is either high or low. If the intensity is too high, the medium might be ionized strongly at the focal point and a laser induced break-down will happen. A bright spark instead of a laser filamentation will be observed. In that case, attenuate the power or use a lens with a longer focal length. Conversely, if the power is low (no plasma generation is observed), increase the power or use a lens with short focal length. Moreover, in either case, it is worthwhile to adjust the chirp to help to form a laser filamentation.
This scanning technique is generally better suited for laboratory use and proof-of-concept rather than field deployment since remote sensing in the field generally does not allow fine translation-stage control of the target under investigation. In those scenarios the same lab-developed laser techniques can be used, but the laser itself will have to be scanned through more traditional beam steering methods such as changing the orientation of the laser apparatus itself.
The protocol could be relatively easily extended to involve experiments with multiple filaments, filament bundles, pump-probe experiments, standoff spectroscopy, waveguide, or numerous other possibilities. In each case, one of the major experimental hurdles is the alignment of the intersecting focal spots, but with this protocol, this need only be done once. The optical elements are fixed in place and the sample itself is the only object required to move. This can be done very precisely with a translation stage. Further modification of this protocol to achieve further control over the location of the filament formation distance, including filament formation at hundreds of meters from the laser, is possible in principle by careful control of the output laser pulse. Multi-filamentation will also form a waveguide during the propagation, which could help to deliver a light in free space.
Remote sensing is a broad subject that spans disciplines such as physics, chemistry, engineering, environmental science, etc. In the supplementary material, we propose additional remote sensing schemes including stand-off spectroscopy and superradiance in addition to filamentation.

The spatial coherence and corresponding small divergence angle of laser beams have led to numerous applications in remote sensing, including chemically-sensitive measurements of the atmosphere1,2, range-finding3, and remote spectroscopy4. The same coherence properties allow very tight focusing of laser light that can deliver continuous focused intensities of billions of watts per square centimeter and pulsed intensities of 1013 watts per square centimeter over a period of a few femtoseconds. Such extreme intensities are useful for numerous applications including examining the nonlinear optical properties of matter5, precision optical micromachining6, materials characterization through laser-induced-breakdown spectroscopy7, stimulated Raman spectroscopy8,9,10, and trace chemical detection11.
However, the physical limitations of Gaussian beams set limits on the ability to apply these properties of extreme intensity and small divergence angle simultaneously. A laser beam focused to a small spot size will necessarily diverge with a greater angle. Classically, the beam divergence angle is given by , where &#955; is the wavelength and w0 is the radius of the beam waist. Since the divergence angle is set by the diameter of the laser beam and the focal length f of the focusing lens, , and tight focusing is not possible at distances of many meters as f becomes large compared to d.
Workers in the field of amplified femtosecond pulses noticed that this limitation on intensity vs. range was violated for high-intensity femtosecond pulses, with burn marks smaller than the diffraction limit appearing on targets at large distance from the originating laser12. This was found to be due to Kerr-effect self-focusing. The refractive index of the air is modified in proportion to the intensity of the laser field, and when the laser has a Gaussian intensity profile, the resulting refractive intensity profile becomes functionally a lens5. The beam self-focuses as it propagates, resulting in a narrow and intense filament of less than 100 &#181;m radius whose small size is maintained by a dynamic balance among classical diffraction, Kerr self-focusing, and defocusing due to plasma generation13.
With femtosecond laser filaments, intensities on the order of 1013 W/cm2 can be delivered to targets at distances of many meters with commercially-available femtosecond chirped-pulse amplifiers. Thus, many experiments which previously required tight focusing conditions and targets very close to a lens of high numerical aperture can now be done at distance more typical of remote sensing applications. However, intensities much higher than this threshold are not easily possible with filamentation, as the beam tends to break up into multiple filaments where each individual filament is near the critical power for self-focusing13.
Numerous applications are possible. We present a protocol primarily applicable to imaging and spectroscopy of remote targets using a femtosecond laser filament scanned over the target surface. The experimental setup is shown in Figure 1.

<table>
	<tbody>
		<tr>
			<td>Femtosecond laser system</td>
			<td>Coherent Co</td>
			<td>Legend Elite System</td>
			<td>1 kHz system, fs system pulse energy 4 mJ</td>
		</tr>
		<tr>
			<td>IRIS</td>
			<td>Thorlabs</td>
			<td>id25</td>
			<td>Mounted Standard Iris, &#216;25.0 mm Max Aperture, TR3 Post</td>
		</tr>
		<tr>
			<td>Lens</td>
			<td>Thorlabs</td>
			<td>LA1908-C</td>
			<td>L=50 cm, Plano-Convex Lenses (AR Coating: 1050 - 1700 nm)</td>
		</tr>
		<tr>
			<td>Mirrors</td>
			<td>Thorlabs</td>
			<td>PF10-03-P01</td>
			<td>Plano metallic mirror</td>
		</tr>
		<tr>
			<td>Photodetector</td>
			<td>Hamamatsu</td>
			<td>H12694</td>
			<td>Thermoelectric cooled NIR-PMT unit</td>
		</tr>
		<tr>
			<td>Spectrometer</td>
			<td>Ocean Optics</td>
			<td>OCEAN_HDX_VIS_NIR</td>
			<td>Spectrometer, high dynamic range, 350-950</td>
		</tr>
		<tr>
			<td>Translation Stage</td>
			<td>Thorlabs</td>
			<td>PT3-Z8</td>
			<td>25 mm (0.98&#34;) Three-Axis Motorized Translation Stage, 1/4&#34;-20 Taps</td>
		</tr>
	</tbody>
</table>

femtosecond laser filaments for use in sub-diffraction-limited imaging and remote sensing

Probing remote matter with laser light is a ubiquitous technique used in circumstances as diverse as laser-induced breakdown spectroscopy and barcode scanners. In classical optics, the intensity that can be brought to bear on a remote target is limited by the spot size of the laser at the distance of the target. This spot size has a lower bound determined by the diffraction limit of classical optics. However, amplified femtosecond laser pulses generate intensity sufficient to modify the refractive index of the ambient air and undergo self-focusing. This self-focusing effect leads to the generation of highly intense laser filaments which maintain their intensity and small sub-millimeter diameter size at distances well beyond the classical Rayleigh length. Such intensity provides the capability of remote scanning, imaging, sensing, and spectroscopy with enhanced spatial resolution. We describe a technique for generating filaments with a femtosecond regenerative chirped-pulse amplifier, and for using the resulting filament to conduct imaging and spectroscopic measurements at remote distances of at least several meters.

The resolution of the scanned images is limited optically only by the ~100 &#181;m. Therefore, the translation stage motion should be of this order of magnitude or smaller for maximum resolution. However, this level of resolution is not necessary for all measurements. This protocol has been used for both imaging14&#160;and spectroscopic15&#160;measurements. Figure 1 shows the experimental setup. The pulse is generated in an amplifier system. The pulse is 1 kHz, 50 fs, and centered at 800 nm. Figure 2 compares a scan of a small Texas A&#38;M logo target taken with a laser at the diffraction limit compared to a scan taken with a filament-forming beam. This experiment was performed using filaments in liquid water, but the results may be rescaled for air in remote sensing13. Figure 3 shows spatially-resolved filament-induced breakdown spectroscopy scans of metal objects of different composition buried approximately two millimeters below a layer of sand. The shapes and compositions of the metal objects are apparent. In general, filamentation provides a number of mechanisms for target effects. The initial pulse can provide information on the surface layer, while subsequent pulses can provide information on deeper portions of the material through ablation or mechanical removal of surface layers.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/58207/58207fig1.jpg" /> 
Figure 1. The experimental setup. The laser is 1 kHz, 50 fs, and centered at 800 nm. It is focused with a lens to reach the intensity (~1013 W/cm2) to form laser filaments. The object is under sand and put on a translation stage. The scattered light is collected with a spectrometer. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/58207/58207fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/58207/58207fig2.jpg" /> 
Figure 2. Sub-diffraction-limited Imaging. Remote images generated by scanning a laser beam across a printed Texas A&#38;M logo at a distance of several meters. a) Logo imaged with non-filamented beam. b) Logo imaged with filamented beam. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/58207/58207fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/58207/58207fig3.jpg" /> 
Figure 3. The chemical map. Spectrally and spatially resolved image of metal objects buried under sand. a) Objects above sand. b) Objects below 2.3 &#177; 0.3 mm of sand. c) Image with material composition color-coded to metal spectral features. Composite image of the buried objects with aluminum (Al), copper (Cu), and stainless steel (SS) corresponding to the red, green, and cyan color components, respectively <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/58207/58207fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Femtosecond Laser Filaments for Use in Sub-Diffraction-Limited Imaging and Remote Sensing at JoVE.com

Femtosecond Laser Filaments for Use in Sub-Diffraction-Limited Imaging and Remote Sensing

High-intensity femtosecond pulses of laser light can undergo cycles of Kerr self-focusing and plasma defocusing, propagating an intense sub-millimeter-diameter beam over long distances. We describe a technique for generating and using these filaments to perform remote imaging and sensing beyond the classical diffraction limits of linear optics.

Probing remote matter with laser light is a ubiquitous technique used in circumstances as diverse as laser-induced breakdown spectroscopy and barcode ...

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7.4K Views.  Texas A&M University. High-intensity femtosecond pulses of laser light can undergo cycles of Kerr self-focusing and plasma defocusing, propagating an intense sub-millimeter-diameter beam over long distances. We describe a technique for generating and using these filaments to perform remote imaging and sensing beyond the classical diffraction limits of linear optics.

Video: Femtosecond Laser Filaments for Use in Sub-Diffraction-Limited Imaging and Remote Sensing

Synthesis and Operation of Fluorescent-core Microcavities for Refractometric Sensing

This paper discusses fluorescent core microcavity-based sensors that can operate in a microfluidic analysis setup. These structures are based on the formation of a fluorescent quantum-dot (QD) coating on the channel surface of a conventional microcapillary. Silicon QDs are especially attractive for this application, owing in part to their negligible toxicity compared to the II-VI and II-VI compound QDs, which are legislatively controlled substances in many countries. While the ensemble emission spectrum is broad and featureless, an Si-QD film on the channel wall of a capillary features a set of sharp, narrow peaks in the fluorescence spectrum, corresponding to the electromagnetic resonances for light trapped within the film. The peak wavelength of these resonances is sensitive to the external medium, thus permitting the device to function as a refractometric sensor in which the QDs never come into physical contact with the analyte. The experimental methods associated with the fabrication of the fluorescent-core microcapillaries are discussed in detail, as well as the analysis methods. Finally, a comparison is made between these structures and the more widely investigated liquid-core optical ring resonators, in terms of microfluidic sensing capabilities.

Fluorescent-core microcavity sensors employ a high-index quantum-dot coating in the channel of silica microcapillaries. Changes in the refractive index of fluids pumped into the capillary channel cause shifts in the microcavity fluorescence spectrum that can be used to analyze the channel medium.

This paper discusses  fluorescent core microcavity-based sensors that can operate in a microfluidic  analysis setup. These structures are based on the ...

Measurement of Coherence Decay in GaMnAs Using Femtosecond Four-wave Mixing

The application of femtosecond four-wave mixing to the study of fundamental properties of diluted magnetic semiconductors ((s,p)-d hybridization, spin-flip scattering) is described, using experiments on GaMnAs as a prototype III-Mn-V system.&#160; Spectrally-resolved and time-resolved experimental configurations are described, including the use of zero-background autocorrelation techniques for pulse optimization.&#160; The etching process used to prepare GaMnAs samples for four-wave mixing experiments is also highlighted.&#160; The high temporal resolution of this technique, afforded by the use of short (20 fsec) optical pulses, permits the rapid spin-flip scattering process in this system to be studied directly in the time domain, providing new insight into the strong exchange coupling responsible for carrier-mediated ferromagnetism.&#160; We also show that spectral resolution of the four-wave mixing signal allows one to extract clear signatures of (s,p)-d hybridization in this system, unlike linear spectroscopy techniques.&#160;&#160; This increased sensitivity is due to the nonlinearity of the technique, which suppresses defect-related contributions to the optical response. This method may be used to measure the time scale for coherence decay (tied to the fastest scattering processes) in a wide variety of semiconductor systems of interest for next generation electronics and optoelectronics.

The technique of femtosecond four-wave mixing is described, including spectrally-resolved and time-resolved configurations. We illustrate the utility of this technique for the investigation of crucial physical properties in the III-V diluted magnetic semiconductors, afforded by its nonlinearity and high temporal resolution.

The application of femtosecond four-wave mixing to the study of fundamental properties of diluted magnetic semiconductors ((s,p)-d hybridization, ...

Spatial Separation of Molecular Conformers and Clusters

Gas-phase molecular physics and physical chemistry experiments commonly use supersonic expansions through pulsed valves for the production of cold molecular beams. However, these beams often contain multiple conformers and clusters, even at low rotational temperatures. We present an experimental methodology that allows the spatial separation of these constituent parts of a molecular beam expansion. Using an electric deflector the beam is separated by its mass-to-dipole moment ratio, analogous to a bender or an electric sector mass spectrometer spatially dispersing charged molecules on the basis of their mass-to-charge ratio. This deflector exploits the Stark effect in an inhomogeneous electric field and allows the separation of individual species of polar neutral molecules and clusters. It furthermore allows the selection of the coldest part of a molecular beam, as low-energy rotational quantum states generally experience the largest deflection. Different structural isomers (conformers) of a species can be separated due to the different arrangement of functional groups, which leads to distinct dipole moments. These are exploited by the electrostatic deflector for the production of a conformationally pure sample from a molecular beam. Similarly, specific cluster stoichiometries can be selected, as the mass and dipole moment of a given cluster depends on the degree of solvation around the parent molecule. This allows experiments on specific cluster sizes and structures, enabling the systematic study of solvation of neutral molecules.

We present a technique that allows the spatial separation of different conformers or clusters present in a molecular beam. An electrostatic deflector is used to separate species by their mass-to-dipole moment ratio, leading to the production of gas-phase ensembles of a single conformer or cluster stoichiometry.

Gas-phase molecular physics and physical chemistry experiments commonly use supersonic expansions through pulsed valves for the production of cold ...

Use of a Multi-compartment Dynamic Single Enzyme Phantom for Studies of Hyperpolarized Magnetic Resonance Agents

Imaging of hyperpolarized substrates by magnetic resonance shows great clinical promise for assessment of critical biochemical processes in real time. Due to fundamental constraints imposed by the hyperpolarized state, exotic imaging and reconstruction techniques are commonly used. A practical system for characterization of dynamic, multi-spectral imaging methods is critically needed. Such a system must reproducibly recapitulate the relevant chemical dynamics of normal and pathological tissues. The most widely utilized substrate to date is hyperpolarized [1-13C]-pyruvate for assessment of cancer metabolism. We describe an enzyme-based phantom system that mediates the conversion of pyruvate to lactate. The reaction is initiated by injection of the hyperpolarized agent into multiple chambers within the phantom, each of which contains varying concentrations of reagents that control the reaction rate. Multiple compartments are necessary to ensure that imaging sequences faithfully capture the spatial and metabolic heterogeneity of tissue. This system will aid the development and validation of advanced imaging strategies by providing chemical dynamics that are not available from conventional phantoms, as well as control and reproducibility that is not possible in vivo.

A multi-compartment dynamic phantom is used to simulate some biology of interest for metabolic studies using hyperpolarized magnet resonance agents.

Imaging of hyperpolarized substrates by magnetic resonance shows great clinical promise for assessment of critical biochemical processes in real time. Due ...

Compact Lens-less Digital Holographic Microscope for MEMS Inspection and Characterization

A micro-electro-mechanical-system (MEMS) is a widely used component in many industries, including energy, biotechnology, medical, communications, and automotive. However, effective inspection and characterization metrology systems are needed to ensure the functional reliability of MEMS. This study presents a system based on digital holography as a tool for MEMS metrology. Digital holography has gained increasing attention in the past 20 years. With the fast development and decreasing cost of sensor arrays, resolution of such systems has increased broadening potential applications. Thus, it has attracted attention from both research and industry sides as a potential reliable tool for industrial metrology. Indeed, by recording the interference pattern between an object beam (which contains sample height information) and a reference beam on a CCD camera, one can retrieve the quantitative phase information of an object. However, most of digital holographic systems are bulky and thus not easy to implement on industry production lines. The novelty of the system presented is that it is lens-less and thus very compact. In this study, it is shown that the Compact Digital Holographic Microscope (CDHM) can be used to evaluate several characteristics typically consider as criteria in MEMS inspections. The surface profiles of MEMS in both static and dynamic conditions are presented. Comparison with AFM is investigated to validate the accuracy of the CDHM.

We present a compact reflection digital holographic system (CDHM) for inspection and characterization of MEMS devices. A lens-less design using a diverging input wave providing natural geometrical magnification is demonstrated. Both static and dynamic studies are presented.

A micro-electro-mechanical-system (MEMS) is a widely used component in many industries, including energy, biotechnology, medical, communications, and ...

Automation of Mode Locking in a Nonlinear Polarization Rotation Fiber Laser through Output Polarization Measurements

When a laser is mode-locked, it emits a train of ultra-short pulses at a repetition rate determined by the laser cavity length. This article outlines a new and inexpensive procedure to force mode locking in a pre-adjusted nonlinear polarization rotation fiber laser. This procedure is based on the detection of a sudden change in the output polarization state when mode locking occurs. This change is used to command the alignment of the intra-cavity polarization controller in order to find mode-locking conditions. More specifically, the value of the first Stokes parameter varies when the angle of the polarization controller is swept and, moreover, it undergoes an abrupt variation when the laser enters the mode-locked state. Monitoring this abrupt variation provides a practical easy-to-detect signal that can be used to command the alignment of the polarization controller and drive the laser towards mode locking. This monitoring is achieved by feeding a small portion of the signal to a polarization analyzer measuring the first Stokes parameter. A sudden change in the read out of this parameter from the analyzer will occur when the laser enters the mode-locked state. At this moment, the required angle of the polarization controller is kept fixed. The alignment is completed. This procedure provides an alternate way to existing automating procedures that use equipment such as an optical spectrum analyzer, an RF spectrum analyzer, a photodiode connected to an electronic pulse-counter or a nonlinear detecting scheme based on two-photon absorption or second harmonic generation. It is suitable for lasers mode locked by nonlinear polarization rotation. It is relatively easy to implement, it requires inexpensive means, especially at a wavelength of 1550 nm, and it lowers the production and operation costs incurred in comparison to the above-mentioned techniques.

A protocol to detect and automate mode locking in a pre-adjusted nonlinear polarization rotation fiber laser is presented. The detection of a sudden change in the output polarization state when mode locking occurs is used to command the alignment of an intra-cavity polarization controller in order to find mode-locking conditions.

When a laser is mode-locked, it emits a train of ultra-short pulses at a repetition rate determined by the laser cavity length. This article outlines a ...

Applying X-ray Imaging Crystal Spectroscopy for Use as a High Temperature Plasma Diagnostic

X-ray spectra provide a wealth of information on high temperature plasmas; for example electron temperature and density can be inferred from line intensity ratios. By using a Johann spectrometer viewing the plasma, it is possible to construct profiles of plasma parameters such as density, temperature, and velocity with good spatial and time resolution. However, benchmarking atomic code modeling of X-ray spectra obtained from well-diagnosed laboratory plasmas is important to justify use of such spectra to determine plasma parameters when other independent diagnostics are not available. This manuscript presents the operation of the High Resolution X-ray Crystal Imaging Spectrometer with Spatial Resolution (HIREXSR), a high wavelength resolution spatially imaging X-ray spectrometer used to view hydrogen- and helium-like ions of medium atomic number elements in a tokamak plasma. In addition, this manuscript covers a laser blow-off system that can introduce such ions to the plasma with precise timing to allow for perturbative studies of transport in the plasma.

X-ray spectra provide a wealth of information on high temperature plasmas. This manuscript presents the operation of a high wavelength resolution spatially imaging X-ray spectrometer used to view hydrogen- and helium-like ions of medium atomic number elements in a tokamak plasma.

X-ray spectra provide a wealth of information on high temperature plasmas; for example electron temperature and density can be inferred from line ...

Fabrication of 1-D Photonic Crystal Cavity on a Nanofiber Using Femtosecond Laser-induced Ablation

We present a protocol for fabricating 1-D Photonic Crystal (PhC) cavities on subwavelength-diameter tapered optical fibers, optical nanofibers, using femtosecond laser-induced ablation. We show that thousands of periodic nano-craters are fabricated on an optical nanofiber by irradiating with just a single femtosecond laser pulse. For a typical sample, periodic nano-craters with a period of 350 nm and with diameter gradually varying from 50 - 250 nm over a length of 1 mm are fabricated on a nanofiber with diameter around 450 - 550 nm. A key aspect of such a nanofabrication is that the nanofiber itself acts as a cylindrical lens and focuses the femtosecond laser beam on its shadow surface. Moreover, the single-shot fabrication makes it immune to mechanical instabilities and other fabrication imperfections. Such periodic nano-craters on nanofiber, act as a 1-D PhC and enable strong and broadband reflection while maintaining the high transmission out of the stopband. We also present a method to control the profile of the nano-crater array to fabricate apodized and defect-induced PhC cavities on the nanofiber. The strong confinement of the field, both transverse and longitudinal, in the nanofiber-based PhC cavities and the efficient integration to the fiber networks, may open new possibilities for nanophotonic applications and quantum information science.

We present a protocol for fabricating 1-D photonic crystal cavities on subwavelength diameter silica fibers (optical nanofibers) using femtosecond laser-induced ablation.

We present a protocol for fabricating 1-D Photonic Crystal (PhC) cavities on subwavelength-diameter tapered optical fibers, optical nanofibers, using ...

Fabrication of Polymer Microspheres for Optical Resonator and Laser Applications

This paper describes three methods of preparing fluorescent microspheres comprising &#960;-conjugated or non-conjugated polymers: vapor diffusion, interface precipitation, and mini-emulsion. In all methods, well-defined, micrometer-sized spheres are obtained from a self-assembling process in solution. The vapor diffusion method can result in spheres with the highest sphericity and surface smoothness, yet the types of the polymers able to form these spheres are limited. On the other hand, in the mini-emulsion method, microspheres can be made from various types of polymers, even from highly crystalline polymers with coplanar, &#960;-conjugated backbones. The photoluminescent (PL) properties from single isolated microspheres are unusual: the PL is confined inside the spheres, propagates at the circumference of the spheres via the total internal reflection at the polymer/air interface, and self-interferes to show sharp and periodic resonant PL lines. These resonating modes are so-called "whispering gallery modes" (WGMs). This work demonstrates how to measure WGM PL from single isolated spheres using the micro-photoluminescence (&#181;-PL) technique. In this technique, a focused laser beam irradiates a single microsphere, and the luminescence is detected by a spectrometer. A micromanipulation technique is then used to connect the microspheres one by one and to demonstrate the intersphere PL propagation and color conversion from coupled microspheres upon excitation at the perimeter of one sphere and detection of PL from the other microsphere. These techniques, &#181;-PL and micromanipulation, are useful for experiments on micro-optic application using polymer materials.

Protocols for the synthesis of microspheres from polymers, the manipulation of microspheres, and micro-photoluminescence measurements are presented.

This paper describes three methods of preparing fluorescent microspheres comprising &#960;-conjugated or non-conjugated polymers: vapor diffusion, ...

Drawing and Hydrophobicity-patterning Long Polydimethylsiloxane Silicone Filaments

Polydimethylsiloxane (PDMS) silicone is a versatile polymer that cannot readily be formed into long filaments. Traditional spinning methods fail because PDMS does not exhibit long-range fluidity at melting. We introduce an improved method to produce filaments of PDMS by a stepped temperature profile of the polymer as it cross-links from a fluid to an elastomer. By monitoring its warm-temperature viscosity, we estimate a window of time when its material properties are amendable to drawing into long filaments. The filaments pass through a high-temperature tube oven, curing them sufficiently to be harvested. These filaments are on the order of hundreds of micrometers in diameter and tens of centimeters in length, and even longer and thinner filaments are possible. These filaments retain many of the material properties of bulk PDMS, including switchable hydrophobicity. We demonstrate this capability with an automated corona-discharge patterning method. These patternable PDMS silicone filaments have applications in silicone weavings, gas-permeable sensor components, and model microscale foldamers.

Here, we present a protocol to produce long filaments of polydimethylsiloxane (PDMS) silicone by gravity-drawing through a furnace. Filaments are on the order of hundreds of micrometers in diameter and tens of centimeters in length and are hydrophobically patternable via an Arduino-controlled corona discharge system.

Polydimethylsiloxane (PDMS) silicone is a versatile polymer that cannot readily be formed into long filaments. Traditional spinning methods fail because ...