The instrument development is supported by Grant NSF CHE-1828666. ZW, JCW and WX are supported by the National Institutes of Health, National Institute of General Medical Sciences, Grant 1R35GM138092-01. BY is supported by the Youth Innovation Promotion Association, Chinese Academy of Sciences (CAS, 2021183).

1. Hyperspectral line-scanning VSFG microscope
<ol>
	<li>Laser system
	<ol>
		<li>Use a pulsed laser system (see Table of Materials) centered at 1025 nm &#177; 5 nm. The laser is set at 40 W, 200 kHz (200 &#181;J/pulse) with a pulse width of ~290 fs. 
		NOTE: The exact repetition rate can vary, and a high repetition rate laser generally works better for this VSFG microscope.</li>
		<li>Guide the output of the seed laser into a commercial optical parametric amplifier (OPA) to generate a mid-infrared (MIR) beam (see Table of Materials). Tune the MIR to the frequency of interests (Figure 1A). 
		NOTE: In the present study, the MIR is centered at 3450 nm &#177; 85 nm (~2900&#160;&#177; 72 cm-1) with a pulse duration of ~290 fs and pulse energy of ~6 &#181;J, which encompasses part of the -CHx functional group region.</li>
	</ol>
	</li>
	<li>Up-conversion beam
	<ol>
		<li>Pass the residual 1025 nm beam from OPA through a Fabry-Perot etalon (see Table of Materials) to produce a spectrally narrowed up-conversion beam with an FWHM of ~4.75 cm-1.</li>
		<li>Spatially filter the narrowed 1025 nm beam with an 8 &#181;m sapphire pinhole. 
		NOTE: The 1025 nm beam can be visualized using a NIR card.</li>
		<li>Control the polarization of the 1025 nm pulse with a &#955;/2 waveplate (see Table of Materials).</li>
	</ol>
	</li>
	<li>MIR beam
	<ol>
		<li>Guide the MIR beam through a delay stage for fine control of the temporal overlap.</li>
		<li>Control the polarization of the MIR with a &#955;/2 waveplate.</li>
	</ol>
	</li>
	<li>VSFG microscope
	<ol>
		<li>Spatially overlap both up-conversion, and MIR beams at a customized dichroic mirror (DM,&#160;Figure 1B) that is transmissive to MIR and reflective to NIR (see Table of Materials). Use two irises to guide the alignment: one right after the DM, and one at the far end. Use a power meter after the iris to determine whether MIR is centered, and use a NIR card to locate NIR positions. 
		NOTE: After the overlap, the NIR beam can be used to guide both beams.</li>
		<li>Direct the overlapped beams into an inverted microscope with an integrated 325 Hz single-axis resonant beam scanner (mounted to an integrated two-position scanner (I2PS), Figure 1B) (see Table of Materials). 
		NOTE: The resonant scanner projects a line of the two overlapped beams onto the back aperture of the condenser objective. It is mounted to a slider which enables the seamless reconfiguration between VSFG/SHG and brightfield modalities.</li>
		<li>Focus the two spatially overlapped beams onto the sample with a purely reflective Schwarzschild objective (SO, Figure 1B,D) (see Table of Materials).</li>
		<li>Collect the VSFG signal generated by the sample with an infinity-corrected refractive objective (RO, Figure 1B,D) (see Table of Materials).</li>
		<li>Guide the collimated output VSFG signal through a linear polarizer and then through a telecentric tube lens system composed of two f = 60 mm focal lenses (TL1 and TL2, Figure 1B,C) (see Table of Materials). 
		NOTE: The magnified image from the tube lenses is formed at the entrance slit of the monochromator (MC, Figure 1B,C), and the spatially/frequency resolved data is detected on a two-dimensional CCD detector (CCD, Figure 1B).</li>
	</ol>
	</li>
	<li>SHG mode
	<ol>
		<li>To switch to SHG imaging, block the IR beam and rotate the grating of the spectrograph to 501.5 nm to image the SHG signal.</li>
	</ol>
	</li>
	<li>Brightfield mode
	<ol>
		<li>To switch to brightfield optical imaging, turn on the whitelight source (see Table of Materials). Move the integrated slider (I2PS, Figure 1B) to collect brightfield images in the counter-propagating direction, with the imaging objective (RO) acting as the condenser and the condenser objective (SO) acting as the imaging objective.</li>
		<li>Form an image of the collimated output of the refractive objective at the sensor plane of an RGB brightfield camera using a commercially available tube-lens system (see Table of Materials).</li>
	</ol>
	</li>
</ol>
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/65388/65388fig01.jpg" /> 
Figure 1:&#160;Multimodal hyperspectral VSFG microscope. (A) Top view of the core setup. A 1025 nm pump laser was sent to an OPA to generate a tunable mid-IR pulse. The residual 1025 nm was frequently narrowed by an etalon (E) and spatially filtered into a Gaussian beam by a spatial filter (SFG). Mid-IR and 1025 nm beams are spatially overlapped at a customized dichroic mirror (DM) and guided through the inverted microscope (boxed region in A). (B) The two beams are sent to a 325 Hz resonant beam scanner mounted to an integrated 2-position slider (I2PS), enabling seamless switching between brightfield and nonlinear optical modalities.&#160;The microscope platform is equipped with a reflective-based infinity-corrected Schwarzschild objective (SO) acting as a condenser and a refractive-based infinity-corrected imaging objective (RO) mounted to a vertical nanopositioning (VNP) z-axis stage. The SO focuses the line of incoming beams that the resonant beam scanner reflects onto the sample while the RO collects the VSFG line section of signals. It is important to fine-control the z-axis position of the RO at 1 &#181;m precision to ensure the sample is at the best focal condition for high-quality imaging. The collimated line of the VSFG signal is then directed to a tube lens system composed of 2 tub lenses (TL1 and TL2), forming a magnified image at the entrance slit of the monochromator (MC). The frequency-resolved line of spectra is then hyperspectrally imaged on a charge-coupled device (CCD). After collecting each hyperspectral line, the sample is scanned in the axis perpendicular to the resonant beam scanner scanning axis using the NP. To collect bright field images of the sample, the I2PS is moved to the brightfield position, and a mirror intercepting the white light source (WLS) is installed. Light is then focused by the RO and imaged by the SO. An image is then formed at the sensor plane of the brightfield camera (BC) at the top of the inverted microscope. (C) Detailed view of the optical path through the tube-lens area into the MC and CCD. (D) Detailed view of the sample area between the SO and RO. <a href="https://www.jove.com/files/ftp_upload/65388/65388fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
2. Hyperspectral microscope alignment and vertical CCD axis spatial calibration
<ol>
	<li>Roughly optimize the position of the sample plane (nano positioner z-axis) using a standard sample of ZnO (1 &#181;m thick) pattern sputter coated 15 mm x 15 mm x 0.170 mm &#177; 0.005 mm coverslip and bringing it into brightfield focus using the brightfield imaging modality. 
	NOTE: The z-position of the RO as well as the alignment of the white light, may need to be adjusted as necessary. A representative image of the ZnO on the glass pattern used for alignment calibration is shown in Figure 2.</li>
	<li>Move the I2PS back to the nonlinear illumination arm and optimize the sample height for the maximum nonresonant VSFG intensity generated by the ZnO regions observed on the CCD camera. 
	NOTE: The z-position of the RO must be adjusted for maximum intensity. One may have to iterate steps 2.1 and 2.2 a few times before the optimal height of the sample, and RO are reached.</li>
	<li>Turn the resonant beam scanner on and collect a line of the images.</li>
	<li>Collect nonresonant intensity images by scanning the sample perpendicularly to the beam scanner direction. Take vertical slices of the image data and establish the pixel:micron ratio. (refer to Figure 3 and its legend). 
	&#8203;NOTE: The derivative of these line sections is analyzed to produce the vertical CCD axis pixel:micron ratio that will be used for future images.</li>
</ol>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/65388/65388fig02.jpg" /> 
Figure 2: Representative image quality for rough alignment of brightfield imaging modality of a ZnO pattern. <a href="https://www.jove.com/files/ftp_upload/65388/65388fig02large.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/65388/65388fig03.jpg" /> 
Figure 3: Vertical axis calibration workflow. This figure illustrates how to convert the CCD pixels to vertical spatial dimensions in the unit of &#181;m. (A) An image is collected and reconstructed of the ZnO patterned coverslip. Then, the pixel distance from one to the other edges of the pattern (small vertical bar in A). Because the ZnO pattern cross is designed to have a 25 &#181;m width, one can use the ratio of physical width to pixel width here to calculate the physical/pixel dimension ratio. A representative, vertical axis calibrated image is shown in (B). (C) Lastly, a vertical slice is taken as indicated by the red line. (D) The derivative of the vertical slice is taken to obtain the spatial resolution. The derivative of the vertical slice is used to obtain the spatial resolution. <a href="https://www.jove.com/files/ftp_upload/65388/65388fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
3. Hyperspectral data collection
<ol>
	<li>Collect the spectra of a vertical line of the VSFG signals on the CCD, whose spectra are dispersed along the horizontal axis and spatial positions are recorded on the vertical axis of the CCD. 
	NOTE: This results in a two-dimensional data set for a single-line section.</li>
	<li>After the line section of the sample is hyperspectrally imaged, scan the sample in the axis perpendicular to the line scanning axis using the three-dimensional nano-positioner (NP, Figure 1). 
	NOTE: The 3D nano positioner is important for high precision and reproducibility in locating sample regions (x-y plane) as well as bringing the sample into focus (z-axis).</li>
	<li>Iterate between step 3.1 and step 3.2 to collect a VSFG hyperspectral image.</li>
</ol>
4. Hyperspectral data analysis
<ol>
	<li>Spectrally unmix the data using the MatLab imaging toolbox hyperspectral imaging library workflow41. 
	NOTE: Spectral unmixing correlates spatial locations to unique spectra. Matlab code for hyperspectral data analysis is provided in Supplementary File 1.
	<ol>
		<li>Create a 4-dimensional hypercube (x = spatial, y = spatial, z = frequency-dependent intensity, &#969; = frequency) using the hypercube function in the Matlab image processing toolbox hyperspectral imaging library41.</li>
		<li>Identify the number of unique spectra with the countEndmembersHFC&#160;function with a probability of false alarm (PFA) value of 10-7.</li>
		<li>Identify unique spectra using the nfindr spectral unmixing function.</li>
		<li>Finally, using the sid function, associate each pixel with one of the unique spectra identified in the previous step. 
		NOTE: Additional spectral unmixing and matching methods can be done with alternative functions/algorithms offered in the MatLab Hyperspectral Imaging Library41.</li>
	</ol>
	</li>
	<li>Fit the sum data for each isolated sheet to the Voigt function42 (Supplementary File 1). 
	NOTE: Lorentzian function represents the pure homogeneous lineshape limit, whereas the Gaussian function originates from inhomogeneous limits. In reality, the systems could be in a combination of homogeneous and inhomogeneous limits, which requires a Voigt function - a common practice for condensed phase spectroscopy, including VSFG.</li>
</ol>
5. Geometric analysis of the sample
<ol>
	<li>Determine the geometry of the samples following the procedure mentioned in step 5.2-5.3. In this study, SDS@2&#946;-CD is used as an example. Derive the symmetry-allowed tensor elements of &#967;(2) based on the C7 symmetry of the molecular subunit of the SDS@2&#946;-CD meso-sheets sample. 
	NOTE: The symmetry allowed &#967;(2) depends on symmetry. To calculate the allowed nonlinear susceptibility of any symmetry, refer to reference43.</li>
	<li>Apply the Euler rotation27 to relate the lab frame measurements to the molecular frame. 
	NOTE: In the case of SDS@2&#946;-CD, its C7 symmetry leads to eight independent equations relating 8 output (lab frame &#967;(2)) to 8 input (6 independent hyperpolarizability &#946;(2), and two angles: &#1012;, the tilt angle relative to the sample plane of all sheets, and &#966;, the in-plane rotation of the sheet (Figure 4)). Two sheets are used to extract the common molecular alignments of the two sheets. The relationships between &#966;1 and &#966;2 (in-plane rotation angle of the two sheets) can be extracted from the brightfield images. In the current example, &#966;2 = &#966;1 + 60&#176;. It is assumed that all molecular unit tile at the same angle, so &#1012;1 = &#1012;2. This results in 11 unknowns (9 independent ones, including 6 independent hyperpolarizability &#946;(2), &#1012;1 and &#966;1, and the relative coverage ratio between sheets N, and the two dependent angles, that are &#966;2, and &#1012;2) for 16 knowns (8 lab frame polarizations per sheet, and two sheets).</li>
	<li>Relate the polarization-resolved lab frame &#967;(2) and molecular frame hyperpolarizability &#946;(2) with a neural network function solver. 
	NOTE: A detailed summary of this approach can be found in reference27.
	<ol>
		<li>Create a layered neural network model in Python44using Keras comprised of 200-100-50 node structure and a hyperbolic tangent activation function.</li>
		<li>Create a randomly generated 100000 x 11 matrix of values of &#946;(2), &#1012;1, &#1012;2, &#966;1, &#966;2&#160;and N. Calculate the corresponding lab frame 16 &#967;(2), using the equation determined in 5.2 by Euler rotations.</li>
		<li>Use the calculated &#967;(2) values (a total of 100,000 by 16 values) as the input, and learn to predict 11 values (&#946;(2), &#1012;1, &#1012;2, &#966;1, &#966;2and N) when supplied 16 &#967;(2) values.</li>
		<li>Once trained, use another set of 1000 entries with both the inputs and outputs to test the trained model. The predicted output and the true output should show a linear relationship with a slope of 1.</li>
		<li>Lastly, supply the experimentally measured &#967;(2) from two sheets (each sheet have 8 &#967;(2) measured), and use the trained model to predict the tilt angle &#1012;, along with other properties.</li>
	</ol>
	</li>
</ol>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/65388/65388fig04.jpg" /> 
Figure 4: Illustration of Euler transformation. (A) Illustration of the Euler transformation between the laboratory coordinates (XYZ) second-order susceptibility &#967;(2) and the molecular coordinates (xyz) hyperpolarizability &#946;ijk. z-y&#39;-z&#39;&#39; Euler rotation is performed on the molecular coordinates, with &#966; as the in-plane rotation angle, &#952; as the tilt angle, and &#968; as the twist angle. &#968; is integrated out for arbitrary twist angles about the molecular axis. &#966; is not integrated out because all molecules rotate to a specific angle relative to the lab frame to form the self-assembled sheets. N is the relative surface coverage of the two sheets. (B) Visualization of the tilted subunits forming a sheet determined by the neural network results. This figure has been modified from Wagner et al.27. <a href="https://www.jove.com/files/ftp_upload/65388/65388fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Using a VSFG Microscope for Multimodal, Rapid, Hyperspectral Chemical Analysis

The authors have nothing to disclose.

The most critical steps are from 1.42 to 1.44. It is critical to align the objective lens well for an optical spatial resolution. It is also important to collect the emitted signal, relay, and project the scanning beam as a line at the entrance slits. Proper alignments would guarantee the best resolution and signal-to-noise ratio. For a typical sample, like&#160;SDS@2&#946;-CD 100 &#181;m by 100 &#181;m sheets, a good resolution image (~1 &#181;m resolution) with a high signal-to-noise ratio would take 20 min. This is al...

Vibrational sum-frequency generation (VSFG), a second-order nonlinear optical technique1,2, has been used extensively as a spectroscopy tool to chemically profile symmetry-allowed samples3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22. Traditionally, VSFG has been applied to interfacial systems8,9,10,11 (i.e., gas-liquid, liquid-liquid, gas-solid, solid-liquid), which lack inversion symmetry - a requirement for VSFG activity. This application of VSFG has provided a wealth of molecular details of buried interfaces12,13, configurations of water molecules at interfaces14,15,16,17,18, and chemical species at interfaces19,20,21,22.
Although VSFG has been powerful in determining molecular species and configurations at interfaces, its potential in measuring molecular structures of materials lacking inversion centers has not been fulfilled. This is partly because the materials could be heterogeneous in their chemical environment, compositions, and geometric arrangement, and a traditional VSFG spectrometer has a large illumination area on the order of 100 &#181;m2. Thus, traditional VSFG spectroscopy reports on ensemble-averaged information of the sample over a typical 100 &#181;m2 illumination area. This ensemble averaging may lead to signal cancellations between well-ordered domains with opposite orientations and mischaracterization of local heterogeneities15,20,23,24.
With advances in high numerical aperture (NA), reflective-based microscope objectives (Schwarzschild and Cassegrain geometries), which are nearly free of chromatic aberrations, the focus size of the two beams in VSFG experiments can be decreased from 100 &#181;m2 to 1-2 &#181;m2 and in some cases submicron25. Including this technological advancement, our group and others have developed VSFG into a microscopy platform20,23,26,27,28,29,30,31,32,33,34,35,36. Recently, we have implemented an inverted optical layout and broadband detection scheme37, which enables a seamless collection of multimodal images (VSFG, second harmonic generation (SHG), and brightfield optical). The multi-modality imaging allows quick inspection of samples using optical imaging, correlating various types of images together, and locating signal positions on the sample images. With the achromatic illumination optics and choice of pulsed laser illumination source, this optical platform allows for future seamless integration of additional techniques such as Fluorescence microscopy38 and Raman microscopy, among others.
In this new arrangement, samples such as hierarchical organizations and a class of molecular self-assemblies (MSAs) have been studied. These materials include collagen and biomimetics, where both the chemical composition and geometric organization are important to the ultimate function of the material. Because VSFG is a second-order nonlinear optical signal, it is specifically sensitive to intermolecular arrangements39,40, such as intermolecular distance or twisting angles, making it an ideal tool for revealing both chemical compositions and molecular arrangements. This work describes the VSFG, SHG, and brightfield modalities of the core instrument consisting of a ytterbium-doped cavity solid-state laser that pumps an optical parametric amplifier (OPA), a home-built multimodal inverted microscope and monochromator frequency analyzer coupled to a two-dimensional charged coupled device (CCD) detector27. A step-by-step construction and alignment procedures, and a complete part list of the setup, are provided. An in-depth analysis of an MSA, whose fundamental molecular subunit is comprised of one molecule of sodium-dodecyl sulfate (SDS), a common surfactant, and two molecules of &#946;-cyclodextrin (&#946;-CD), known as SDS@2&#946;-CD herein, are also provided as an example to show how VSFG can reveal molecule-specific geometric details of organized matter. It has also been demonstrated that chemical-specific geometric details of the MSA can be determined with a neural network function solver approach.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>1x Camera Por</td>
			<td>Thorlabs</td>
			<td>WFA4100</td>
			<td>connect a camera to a microscope or optical system</td>
		</tr>
		<tr>
			<td>25.0 mm Right-Angle Prism Mirror, Protected Gold</td>
			<td>Thorlabs</td>
			<td>MRA25-M01</td>
			<td>reflect light and produce retroreflection, redirecting light back along its original path</td>
		</tr>
		<tr>
			<td>3&#8221; Universal Post Holder-5 Pack</td>
			<td>Thorlabs</td>
			<td>UPH3-P5</td>
			<td>hold and support posts of various sizes and configurations</td>
		</tr>
		<tr>
			<td>30 mm to 60 mm Cage Plate, 4 mm Thick</td>
			<td>Thorlabs</td>
			<td>LCP4S</td>
			<td>convert between a 30 mm cage system and a 60 mm cage system</td>
		</tr>
		<tr>
			<td>500 mm Tall Cerna Body with Epi Arm</td>
			<td>Thorlabs</td>
			<td>CEA1500</td>
			<td>provide the function of enabling top illumination techniques in microscopy</td>
		</tr>
		<tr>
			<td>60 mm Cage Mounted &#216;50.0 mm Iris</td>
			<td>Thorlabs</td>
			<td>LCP50S</td>
			<td>control the amount of light passing through an optical system</td>
		</tr>
		<tr>
			<td>60 mm Cage Mounting Bracket</td>
			<td>Thorlabs</td>
			<td>LCP01B</td>
			<td>mount and position a 60 mm cage system in optical setups</td>
		</tr>
		<tr>
			<td>Air spaced Etalon</td>
			<td>SLS Optics Ltd.</td>
			<td>Customized</td>
			<td>generate narrow-band 1030 nm light&#160;</td>
		</tr>
		<tr>
			<td>Cage Plate Mounting Bracket</td>
			<td>Thorlabs</td>
			<td>KCB2</td>
			<td>hold and adjust mirrors at a precise angle</td>
		</tr>
		<tr>
			<td>CCD</td>
			<td>Andor Technologies</td>
			<td>Newton&#160;</td>
			<td>2D CCD for frequency and spatial resolution</td>
		</tr>
		<tr>
			<td>Collinear Optical Parametric Amplifier</td>
			<td>Light Conversion</td>
			<td>Orpheus-One-HP</td>
			<td>Tunable MID light generator</td>
		</tr>
		<tr>
			<td>Copper Chloride</td>
			<td>Thermo Fischer Scientific</td>
			<td>A16064.30</td>
			<td>Self-assembly component</td>
		</tr>
		<tr>
			<td>Customized Dichroic Mirror</td>
			<td>Newport</td>
			<td>Customized</td>
			<td>selectively reflects or transmits light based on its wavelength or polarization</td>
		</tr>
		<tr>
			<td>Ext to M32 Int Adapter</td>
			<td>Thorlabs</td>
			<td>SM1A34</td>
			<td>provide compatibility and facilitating the connection between components with different thread types</td>
		</tr>
		<tr>
			<td>Infinity Corrected Refractive Objective</td>
			<td>Zeiss</td>
			<td>420150-9900-000</td>
			<td>Refractive Objective</td>
		</tr>
		<tr>
			<td>Infinity Corrected Schwarzschild Objective</td>
			<td>Pike Technologies Inc.</td>
			<td>891-0007</td>
			<td>Reflective objective</td>
		</tr>
		<tr>
			<td>Laser</td>
			<td>Carbide, Light-Conversion</td>
			<td>C18212</td>
			<td>Laser source</td>
		</tr>
		<tr>
			<td>M32x0.75 External to Internal RMS</td>
			<td>Thorlabs</td>
			<td>M32RMSS</td>
			<td>adapt or convert the threading size or type of microscope objectives&#160;</td>
		</tr>
		<tr>
			<td>M32x0.75 External to M27x0.75 Internal Engraving</td>
			<td>Thorlabs</td>
			<td>M32M27S</td>
			<td>adapt or convert the threading size or type of microscope objectives&#160;</td>
		</tr>
		<tr>
			<td>Manual Mid-Height Condenser Focus Module</td>
			<td>Thorlabs</td>
			<td>ZFM1030</td>
			<td>adjust the focus of an optical element</td>
		</tr>
		<tr>
			<td>Monochromator</td>
			<td>Andor Technologies</td>
			<td>Shamrock 500i</td>
			<td>Provides frequency resolution for each line scan</td>
		</tr>
		<tr>
			<td>Motorized module with 1&#34; Travel for Edge-Mounted Arms</td>
			<td>Thorlabs</td>
			<td>ZFM2020</td>
			<td>control the vertical positon of the imaging objective</td>
		</tr>
		<tr>
			<td>Nanopositioner</td>
			<td>Mad City Labs Inc.</td>
			<td>MMP3</td>
			<td>3D sample stage</td>
		</tr>
		<tr>
			<td>Resonant Scanner</td>
			<td>EOPC</td>
			<td>SC-25</td>
			<td>325Hz resonant beam scanner</td>
		</tr>
		<tr>
			<td>RGB Color CCD Camera</td>
			<td>Thorlabs</td>
			<td>DCU224C</td>
			<td>Brightfield camera, discontinued but other cameras will work just as well</td>
		</tr>
		<tr>
			<td>RGB tube lens</td>
			<td>Thorlabs</td>
			<td>ITL200</td>
			<td>white light collection</td>
		</tr>
		<tr>
			<td>Right Angle Kinematic Breadboard</td>
			<td>Thorlabs</td>
			<td>OPX2400</td>
			<td>incorporate a sliding mechanism with two fixed positions</td>
		</tr>
		<tr>
			<td>Right Angle Kinematic Mirror Mount, 30 mm</td>
			<td>Thorlabs</td>
			<td>KCB1</td>
			<td>hold and adjust mirrors at a precise angle</td>
		</tr>
		<tr>
			<td>Right Angle Kinematic Mirror Mount, 60 mm</td>
			<td>Thorlabs</td>
			<td>KCB2</td>
			<td>hold and adjust mirrors at a precise angle</td>
		</tr>
		<tr>
			<td>SM2, 60 mm Cage Arm for Cerna Focusing Stage</td>
			<td>Thorlabs</td>
			<td>CSA2100</td>
			<td>securely mount and position condensers</td>
		</tr>
		<tr>
			<td>Snap on Cage Cover for 60 mm Cage, 24 in Long,</td>
			<td>Thorlabs</td>
			<td>C60L24</td>
			<td>enclose and protect the components inside the cage</td>
		</tr>
		<tr>
			<td>Sodium dodecyl sulfate</td>
			<td>Thermo Fischer Scientific</td>
			<td>J63394.AK</td>
			<td>Self-assembly component</td>
		</tr>
		<tr>
			<td>Three-Chnnale Controller and Knob Box for 1&#34; Cerna Travel Stages</td>
			<td>Thorlabs</td>
			<td>MCM3001</td>
			<td>control ZFM2020</td>
		</tr>
		<tr>
			<td>Tube lens</td>
			<td>Thorlabs</td>
			<td>LA1380-AB - N-BK7</td>
			<td>SFG signal collection</td>
		</tr>
		<tr>
			<td>Visible LED Set</td>
			<td>Thorlabs</td>
			<td>WFA1010</td>
			<td>provide illumination in imaging setup</td>
		</tr>
		<tr>
			<td>Whitelight Source</td>
			<td>Thorlabs</td>
			<td>WFA1010</td>
			<td>Whitelight illumination source for brightfield imaging</td>
		</tr>
		<tr>
			<td>WPH05M-1030 - &#216;1/2&#34; Zero-Order Half-Wave Plate, &#216;1&#34; Mount, 1030 nm&#160;</td>
			<td>Thorlabs</td>
			<td>WPH05M-1030</td>
			<td>alter the polarization state of light passing through it</td>
		</tr>
		<tr>
			<td>WPLQ05M-3500 - &#216;1/2&#34; Mounted Low-Order Quarter-Wave Plate, 3.5 &#181;m&#160;</td>
			<td>Thorlabs</td>
			<td>WPLQ05M-3500</td>
			<td>alter the polarization state of light passing through it</td>
		</tr>
		<tr>
			<td>X axis Long Travel Steel Extended Contact Slide Stages</td>
			<td>Optosigma</td>
			<td>TSD-65122CUU</td>
			<td>positioning stages that offer extended travel in the horizontal (X) direction</td>
		</tr>
		<tr>
			<td>XT95 4in Rail Carrier</td>
			<td>Thorlabs</td>
			<td>XT95RC4</td>
			<td>mount and position optical components</td>
		</tr>
		<tr>
			<td>X-Y Axis Translation Stage w/ 360 deg. Rotation</td>
			<td>Thorlabs</td>
			<td>XYR1</td>
			<td>precise movement and positioning of objects in two dimensions, along with the ability to rotate the platform</td>
		</tr>
		<tr>
			<td>XY(1/2&#34;) Linear Translator with Central SM1 Thru Hole</td>
			<td>Thorlabs</td>
			<td>XYT1</td>
			<td>provide precise movement and positioning in two dimensions</td>
		</tr>
		<tr>
			<td>Yb doped Solid State Laser</td>
			<td>Light Conversion</td>
			<td>CB3-40W</td>
			<td>Seed laser</td>
		</tr>
		<tr>
			<td>&#946;-Cyclodextrin</td>
			<td>Thermo Fischer Scientific</td>
			<td>J63161.22</td>
			<td>Self-assembly component</td>
		</tr>
	</tbody>
</table>

multimodal nonlinear hyperspectral chemical imaging using line-scanning vibrational sum-frequency generation microscopy

Vibrational sum-frequency generation (VSFG), a second-order nonlinear optical signal, has traditionally been used to study molecules at interfaces as a spectroscopy technique with a spatial resolution of ~100 &#181;m. However, the spectroscopy is not sensitive to the heterogeneity of a sample. To study mesoscopically heterogeneous samples, we, along with others, pushed the resolution limit of VSFG spectroscopy down to ~1 &#181;m level and constructed the VSFG microscope. This imaging technique not only can resolve sample morphologies through imaging, but also record a broadband VSFG spectrum at every pixel of the images. Being a second-order nonlinear optical technique, its selection rule enables the visualization of non-centrosymmetric or chiral self-assembled structures commonly found in biology, materials science, and bioengineering, among others. In this article, the audience will be guided through an inverted transmission design that allows for imaging unfixed samples. This work also showcases that VSFG microscopy can resolve chemical-specific geometric information of individual self-assembled sheets by combining it with a neural network function solver. Lastly, the images obtained under brightfield, SHG, and VSFG configurations of various samples briefly discuss the unique information revealed by VSFG imaging.

Author Spotlight: Unveiling the Potential of VSFG Microscopy in Studying Mesoscopically Heterogeneous Self-Assembled Structures 

Multimodal Nonlinear Hyperspectral Chemical Imaging Using Line-Scanning Vibrational Sum-Frequency Generation Microscopy

We aim to study mesoscopically heterogeneous self-assembled samples, such as biological tissues, to reveal their chemical composition and molecular arrangements. We are exploring how the microscopic arrangement and mesoscopic morphology of these self materials relate to their microscopic properties. With advances in high numerical aperture and reflective-based microscope objectives, we as well as others have demonstrated vibrational sum-frequency generation microscope with one square micron resolution, which can simultaneously record images of soft materials and also spatially resolve the spectral, forming the so-called hyperspectral images.Hyperspectral imaging records experimental data in multiple dimensions, two in spaces, one in frequency and possibly one in time. However, quick collection, storage, and analysis of such big data to maximize information remains a challenge. Sampling the image only to collect useful data points is also challenging.By developing a faster line-scanning technology, we could accelerate the data acquisition time by 100-fold. Furthermore, the microscope is compatible with sum-frequency generation or SFG, second harmonic generation or SHG, as well as broad-field imaging. Multimodality imaging allows quick inspection of samples using optical imaging and correlating various image modalities.SHG imaging assists the optical technique of our technique, but without the spectral resolving power, is widely used in biophysics. Our SFG microscope will now be able to provide powerful molecular level insights currently missing in biophysical studies of soft tissues.

<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/65388/65388fig05.jpg" /> 
Figure 5: Molecular structure, morphology and potential orientation of SDS@&#946;-CD. (A) Top-view and (B)&#160;side-view chemical structure of SDS@&#946;-CD. (C) Representative heterogeneous sample distribution of the mesoscale sheets on the sample plane. The molecular subunit could have diffe...

Watch this Scientific Journal Video about Unveiling the Potential of VSFG Microscopy in Studying Mesoscopically Heterogeneous Self-Assembled Structures at JoVE.com

A multimodal, rapid hyperspectral imaging framework was developed to obtain broadband vibrational sum-frequency generation (VSFG) images, along with brightfield, second harmonic generation (SHG) imaging modalities. Due to the infrared frequency being resonant with molecular vibrations, microscopic structural and mesoscopic morphology knowledge is revealed of symmetry-allowed samples.

Vibrational sum-frequency generation (VSFG), a second-order nonlinear optical signal, has traditionally been used to study molecules at interfaces as a ...

multimodal-nonlinear-hyperspectral-chemical-imaging-using-line

Research

JoVE Journal

Chemistry

Hyperspectral Line-Scanning VSFG Microscope Setup, Alignment, and Calibration

Begin by setting up the pulsed laser system, centered at 1025 nanometers. Guide the output of the seed laser into a commercial Optical Parametric Amplifier, or OPA, to generate a mid-infrared or mid-IR beam. Tune the mid-IR beam to the frequency of interest.Pass the residual 1025 nanometer beam from OPA through a Fabry-Perot etalon to produce a spectrally-narrowed up-conversion beam. Spatially filter the narrowed beam with an eight-micron sapphire pinhole. Control the polarization of the 1025 nanometer pulse with a lambda by two wave plate.Next, guide the mid-IR beam through a delay stage for fine control of the temporal overlap. Control the polarization of the mid-IR with a lambda by two wave plate. Spatially overlap both the up-conversion and mid-IR beams at a customized Dichroic Mirror, or DM, that is transmissive to mid-IR and reflective to near-IR.Use two irises to guide the alignment, one right after the DM and one at the far end. Use a power meter after the iris to determine whether mid-IR is centered, and use a near-IR card to locate near-IR positions. Direct the overlapped beams into an inverted microscope with an integrated 325 hertz, single-axis, resonant beam scanner that is mounted to an integrated two-position scanner, or I2PS.Focus the two spatially-overlapped beams onto the sample with a purely reflective Schwarzschild Objective, SO.Collect the Vibrational Sum Frequency Generation, or VSFG, signal generated by the sample with an infinity-corrected Refractive Objective, RO.Guide the collimated output VSFG signal through a linear polarizer and then through a telecentric tube lens system composed of two focal lenses, TL1 and TL2, each having a 60 millimeter focal length. To switch to the Second Harmonic Generation, or SHG mode, block the IR beam and rotate the grading of the spectrograph to 501.5 nanometers. To switch to bright-field optical imaging.Turn on the white light source. Move the integrated slider, I2PS, to collect bright-field images in the counterpropagating direction. With the imaging objective, RO, acting as the condenser and the condenser objective, SO, acting as the imaging objective.Then use a commercially available two-blends system to form an image of the collimated output of the RO at the sensor plane of an RGB bright-field camera. Use a standard one-micron-thick sample of zinc oxide pattern sputter coated on a coverslip to roughly optimize the position of the sample plane or the nanopositioner z-axis by bringing it into bright-field focus, using the bright-field imaging modality. Turn on the resonant beam scanner to collect a line of images.After the line section of the sample is hyperspectrally imaged, scan the sample in the axis perpendicular to the line scanning axis using the three-dimensional nano positioner. Take vertical slices of the image data and establish the pixel-to-micron ratio.

Hyperspectral Line-Scanning VSFG Microscope Data Collection and Analysis

Begin by collecting the spectra of a vertical line of the VS-FG signals on the charged coupled device or CCD. Collect non-resonant intensity images by scanning the sample perpendicularly to the beam scanner direction. To spectrally unmix the data using the MATLAB imaging toolbox hyperspectral imaging library workflow.Use the hypercube function in the library to create a four-dimensional hypercube where X and Y are spatial, Z corresponds to the frequency dependent intensity, and omega is the frequency. Identify the number of unique spectra with the count end members HFC function, with a probability of false alarm or PFA value of 10 to the negative seven. Then identify unique spectra using the N-finder spectral unmixing function.Using the SID function, associate each pixel with one of the previously identified unique spectra. Finally, fit the sum data for each isolated sheet to the Voit function. VS-FG images of self-assembled sheets dispersed on a cover slip were captured.And through spectral identification, it was found that all sheets could be categorized into two types, one with higher VS-FG intensity and the other with lower intensity. By inspecting and comparing with the optical image, the large sheet at the center of the images appeared to have stacked double sheets, thereby attributing the smaller VS-FG intensity to destructive interference. Two of the sheets were measured by various VS-FG polarizations and the spectra were fitted using the Voit functions.

902 Views.  UC San Diego.  A multimodal, rapid hyperspectral imaging framework was developed to obtain broadband vibrational sum-frequency generation (VSFG) images, along with brightfield, second harmonic generation (SHG) imaging modalities. Due to the infrared frequency being resonant with molecular vibrations, microscopic structural and mesoscopic morphology knowledge is revealed of symmetry-allowed samples. 

Using a VSFG Microscope for Multimodal, Rapid, Hyperspectral Chemical Analysis

概要