Luis Velarde

Quantitative Sum-Frequency Generation Vibrational Spectroscopy of Molecular Surfaces and Interfaces: Lineshape, Polarization and Orientation

Sum-frequency generation vibrational spectroscopy (SFG-VS) can provide detailed information and understanding of the molecular composition, interactions, and orientational and conformational structure of surfaces and interfaces through quantitative measurement and analysis. In this review, we present the current status of and discuss important recent developments in the measurement of intrinsic SFG spectral lineshapes and formulations for polarization measurements and orientational analysis of SFG-VS spectra. The focus of this review is to present a coherent description of SFG-VS and discuss the main concepts and issues that can help advance this technique as a quantitative analytical research tool for revealing the chemistry and physics of complex molecular surfaces and interfaces.

Communication: Spectroscopic phase and lineshapes in high-resolution broadband sum frequency vibrational spectroscopy: Resolving interfacial inhomogeneities of “identical” molecular groups

The ability to achieve sub-wavenumber resolution (0.6 cm(-1)) and a large signal-to-noise ratio in high-resolution broadband sum-frequency generation vibrational spectroscopy (HR-BB-SFG-VS) allows for the detailed SFG spectral lineshapes to be used in the unambiguous determination of fine spectral features. Changes in the structural spectroscopic phase in SFG-VS as a function of beam polarization and experimental geometry proved to be instrumental in the identification of an unexpected 2.78 ± 0.07 cm(-1) spectral splitting for the two methyl groups at the vapor/dimethyl sulfoxide (DMSO, (CH(3))(2)SO) liquid interface as well as in the determination of their orientational angles.

Consistency in the Sum Frequency Generation Intensity and Phase Vibrational Spectra of the Air/Neat Water Interface

Substantial progress has been made in the quantitative understanding and interpretation of the hydrogen bonding and ordering structure of the air/water interface since the first sum-frequency generation vibrational spectroscopy (SFG-VS) measurement by Q. Du et al. in 1993 (Phys. Rev. Lett. 1993, 70, 2312-2316). However, there are still disagreements and controversies on the consistency between the different experimental measurements, as well as in the theoretical and computational results. One critical problem lies in the lack of consistency between the SFG-VS intensity measurements and the recently developed SFG-VS phase spectra measurements of the neat air/water interface, which has inspired various theoretical efforts. In this report, the reliability of the SFG-VS intensity spectra of the air/neat water interface is to be quantitatively examined, and possible sources of inaccuracies in the SFG-VS phase spectral measurement are to be discussed based on the nonresonant SHG phase measurements. Solid evidence is shown indicating that the SFG-VS intensity spectra from different laboratories are now quantitatively converging and in agreement with each other. However, the possible inaccuracies and inconsistencies in the SFG-VS phase spectra measurements need to be carefully examined against a properly corrected phase standard to take full advantage of this powerful experimental tool.

Capturing inhomogeneous broadening of the –CN stretch vibration in a Langmuir monolayer with high-resolution spectra and ultrafast vibrational dynamics in sum-frequency generation vibrational spectroscopy (SFG-VS)

While in principle the frequency-domain and time-domain spectroscopic measurements should generate identical information for a given molecular system, the inhomogeneous character of surface vibrations in sum-frequency generation vibrational spectroscopy (SFG-VS) studies has only been studied with time-domain SFG-VS by mapping the decay of the vibrational polarization using ultrafast lasers, this due to the lack of SFG vibrational spectra with high enough spectral resolution and accurate enough lineshape. Here, with the recently developed high-resolution broadband SFG-VS (HR-BB-SFG-VS) technique, we show that the inhomogeneous lineshape can be obtained in the frequency-domain for the anchoring CN stretch of the 4-n-octyl-4-cyanobiphenyl (8CB) Langmuir monolayer at the air-water interface, and that an excellent agreement with the time-domain SFG free-induction-decay can be established. We found that the 8CB CN stretch spectrum consists of a single peak centered at 2234.00 ± 0.01 cm(-1) with a total linewidth of 10.9 ± 0.3 cm(-1) at half maximum. The Lorentzian contribution accounts only for 4.7 ± 0.4 cm(-1) to this width and the Gaussian (inhomogeneous) broadening for as much as 8.1 ± 0.2 cm(-1). Polarization analysis of the -CN spectra showed that the -CN group is tilted 57° ± 2° from the surface normal. The large heterogeneity in the -CN spectrum is tentatively attributed to the -CN group interactions with the interfacial water molecules penetrated/accommodated into the 8CB monolayer, a unique phenomenon for the nCB Langmuir monolayers reported previously.

Accurate line shapes from sub-1 cm(-1) resolution sum frequency generation vibrational spectroscopy of α-pinene at room temperature.

Despite the importance of terpenes in biology, the environment, and catalysis, their vibrational spectra remain unassigned. Here, we present subwavenumber high-resolution broad-band sum frequency generation (HR-BB-SFG) spectra of the common terpene (+)-α-pinene that reveal 10 peaks in the C-H stretching region at room temperature. The high spectral resolution resulted in spectra with more and better resolved spectral features than those of the Fourier transform infrared, femtosecond stimulated Raman spectra in the bulk condensed phase and those of the conventional BB-SFG and scanning SFG spectroscopy of the same molecule on a surface. Experiment and simulation show the spectral line shapes with HR-BB-SFG to be accurate. Homogeneous vibrational decoherence lifetimes of up to 1.7 ps are assigned to specific oscillators and compare favorably to lifetimes computed from density functional tight binding molecular dynamics calculations. Phase-resolved spectra provided their orientational information. We propose the new spectroscopy as an attractive alternative to time domain vibrational spectroscopy or heterodyne detection schemes for studying vibrational energy relaxation and vibrational coherences in molecules at molecular surfaces or interfaces.

Interfacial Surfactant Ordering in Thin Films of SDS-Encapsulated Single-Walled Carbon Nanotubes.

The molecular self-assembly of surfactants on the surface of single-walled carbon nanotubes (SWCNT) is currently a common strategy for the tuning of nanotube properties and the stabilization of carbon nanotube dispersions. Here, we report direct measurements of the degree of interfacial ordering for sodium dodecyl sulfate (SDS) surfactants adsorbed on colloidal, single-chirality enriched, SWCNTs within a solid film and investigate the dependence of surface alkyl chain order on the surfactant concentration in the precursor solution. The degree of order for the SWCNT-bound SDS molecules, is probed by vibrational sum frequency generation (VSFG) spectroscopy. We find concrete evidence for the presence of highly ordered surface structures at sufficiently high SDS concentrations, attributed here to cylindrical-like micelle assemblies with the SWCNT at the core. As the SDS concentration decreases, the interfacial order is found to decrease as well, generating a more disordered or random adsorption of surfactants on the nanotube surfaces.

Vibrational spectral signatures of crystalline cellulose using high resolution broadband sum frequency generation vibrational spectroscopy (HR-BB-SFG-VS)

Both the C–H and O–H region spectra of crystalline cellulose were studied using the sub-wavenumber high-resolution broadband sum frequency generation vibrational spectroscopy (HR-BB-SFG-VS) for the first time. The resolution of HR-BB-SFG-VS is about 10-times better than conventional scanning SFG-VS and has the capability of measuring the intrinsic spectral lineshape and revealing many more spectral details. With HR-BB-SFG-VS, we found that in cellulose samples from different sources, including Avicel and cellulose crystals isolated from algae Valonia (Iα) and tunicates (Iβ), the spectral signatures in the O–H region were unique for the two allomorphs, i.e. Iα and Iβ, while the spectral signatures in the C–H regions varied in all samples examined. Even though the origin of the different spectral signatures of the crystalline cellulose in the O–H and C–H vibrational frequency regions are yet to be correlated to the structure of cellulose, these results lead to new spectroscopic methods and opportunities to classify and to understand the basic crystalline structures, as well as variations in polymorphism of the crystalline cellulose.

Coherent Vibrational Dynamics and High-resolution Nonlinear Spectroscopy： A Comparison with the Air/DMSO Liquid Interface

We present a comparative study on the C—H stretching vibrations at air/DMSO (dimethyl sulfoxide) interface with both the free‐induction decay (FID) coherent vibrational dynamics and the sub‐wavenumber high resolution sum‐frequency generation vibrational spectroscopy measurements. In principle the frequency‐domain and time‐domain spectroscopic measurements should generate identical information for a given molecular system. However, when the molecular systems are with several coupled or overlapping vibrational modes, obtaining detailed spectroscopic and coherent dynamics information is not as straightforward and rather difficult from either the time‐domain or the frequency domain measurements. For the case of air/DMSO interface that is with moderately complex vibrational spectra, we show that the frequency‐domain measurement with sub‐wavenumber high‐resolution sum‐ frequency generation vibrational spectroscopy is probably more advantageous than the time‐ domain measurement in obtaining quantitative understa...

Tuning the Surface Ordering of Self-Assembled Ionic Surfactants on Semiconducting Single-Walled Carbon Nanotubes: Concentration, Tube Diameter and Counterions

We report direct spectroscopic measurements of the macromolecular organization of ionic surfactants on the surface of semiconducting single-walled carbon nanotubes (SWCNTs) within solution-processed thin films. By using vibrational sum frequency generation (VSFG) spectroscopy, sensitive measurements of interfacial surfactant ordering were obtained as a function of surfactant concentration for sodium dodecyl sulfate (SDS)-encapsulated (6,5) and (7,6) SWCNTs with and without excess electrolytes. Anionic surfactants are known to effectively stabilize SWCNTs. The current models suggest a strong influence of the dispersion conditions on the surfactant interfacial macromolecular organization and self-assembly. Direct experimental probes of such an organization using nanotubes of specific chirality are needed to validate the existing models. We found that as the bulk SDS concentration increases near the surfactant critical micelle concentration, the interfacial ordering increased, approaching the formation of cylindrical-like micelles with the nanotube at the core. At the higher surfactant concentrations measured here, the (6,5) SWCNTs produced more ordered structures relative to those with the (7,6) SWCNTs. The relatively larger-diameter (7,6) chiral tubes support enhanced van der Waals (vdW) interactions between the tube carbon surface and the surfactant methylene chain groups that likely increase the density of gauche defects. A new effect arises when the precursor solution is exposed to a small concentration of divalent Ca2+ counterions. We postulate that a salt-bridging configuration on such highly curved surfaces decreases the ordering of interfacial surfactant molecules, resulting in compact, disordered structures. However, this phenomenon was not observed with excess Na+ ions at the same ionic strength. Instead, a modest increase in surfactant ordering was observed with the excess monovalent electrolyte. These results provide new insights for thin film solution processing of vdW nanomaterials and demonstrate that VSFG is a sensitive probe of surfactant organization on nanostructures.

Elucidation of the bonding of a near infrared dye to hollow gold nanospheres-a chalcogen tripod

Determining how Raman labels orientate on the surface of HGNs to aid in future advancements of designing NIR nanosensors.