Spectroscopic analysis of the sum-frequency response of the carbon-hydrogen stretching modes in collagen type I.

We studied the origin of the vibrational signatures in the sum-frequency generation (SFG) spectrum of fibrillar collagen type I in the carbon-hydrogen stretching regime. For this purpose, we developed an all-reflective, laser-scanning SFG microscope with minimum chromatic aberrations and excellent retention of the polarization state of the incident beams. We performed detailed SFG measurements of aligned collagen fibers obtained from rat tail tendon, enabling the characterization of the magnitude and polarization-orientation dependence of individual tensor elements Xijk2 of collagen's nonlinear susceptibility.

Enhancement of Molecular Coherent Anti-Stokes Raman Scattering with Silicon Nanoantennas.

Surface-enhanced coherent anti-Stokes Raman scattering (SE-CARS) takes advantage of surface plasmon resonances supported on metallic nanostructures to amplify the coherent Raman response of target molecules. While these metallic antennas have found significant success in SE-CARS studies, photoinduced morphological changes to the nanoantenna under ultrafast excitation introduce significant hurdles in terms of stability and reproducilibty. These hurdles need to be overcome in order to establish SE-CARS as a reliable tool for rapid biomolecular sensing.

Surface-enhanced coherent anti-Stokes Raman scattering of molecules near metal-dielectric nanojunctions.

We discuss an experimental configuration consisting of {Au film}-molecule-{Au particle} or {Au film}-molecule-{Si particle} nanojunctions for performing wide-field surface-enhanced CARS (SE-CARS) measurements in a reproducible and controllable manner. While the allowable illumination dosage in the {Au film}-molecule-{Au particle} case is limited by the strong two-photon background from the gold, we successfully generate a detectable coherent Raman response from a molecular monolayer using the lowest reported average power densities to-date. With a vision to minimize the two-photon background and the intrinsic losses observed in all-metal plasmonic systems, we examine the possibility of using high-index dielectric particles on top of a thin metal film to generate strong nanoscopic hotspots.

Understanding phase transition and vibrational mode coupling in ammonium nitrate using 2D correlation Raman spectroscopy.

Ammonium nitrate (AN) is an important component of the chemical industry such as an active ingredient in fertilizers, as an oxidizer in explosive compositions and propellants, and as a blasting agent in civil explosives. Numerous accidents have been reported in the past which concerns its thermal instability and poses a big threat to its processing, transportation, and storage. Despite much literature being reported to understand its thermal instability, a mechanistic view remains unclear.

Probing the effect of solvation on photoexcited 2-(2'-hydroxyphenyl)benzothiazole via ultrafast Raman loss spectroscopic studies.

2-(2'-Hydroxyphenyl)benzothiazole (HBT) molecule is known to exhibit efficient excited state intramolecular proton transfer. As a consequence, it shows fluorescence with a large Stokes shift (∼10 000 cm) in non-polar solvents. However, fluorescence in polar solvents has a dual-band which corresponds to the emission from both the enol and the keto forms.

Ultrafast Raman Loss Spectroscopy Unravels the Dynamics in Entangled Singlet and Triplet States in Thioxanthone.

Thioxanthone (TX), an aromatic ketone, exhibits significant solvent-dependent photophysical properties. Herein, we employed time-resolved ultrafast Raman loss spectroscopy (URLS) to decipher the solvent-dependent structural dynamics in entangled singlet and triplet states of photoexcited TX. The evolution of the vibrational spectrum reveals structural changes that occur during the intersystem-crossing (ISC) process and the subsequent energy dissipation to the surrounding solvent.

Femtosecond coherent nuclear dynamics of excited tetraphenylethylene: Ultrafast transient absorption and ultrafast Raman loss spectroscopic studies.

Ultrafast torsional dynamics plays an important role in the photoinduced excited state dynamics. Tetraphenylethylene (TPE), a model system for the molecular motor, executes interesting torsional dynamics upon photoexcitation. The photoreaction of TPE involves ultrafast internal conversion via a nearly planar intermediate state (relaxed state) that further leads to a twisted zwitterionic state.

Understanding Ultrafast Dynamics of Conformation Specific Photo-Excitation: A Femtosecond Transient Absorption and Ultrafast Raman Loss Study.

Excited state ultrafast conformational reorganization is recognized as an important phenomenon that facilitates light-induced functions of many molecular systems. This report describes the femtosecond and picosecond conformational relaxation dynamics of middle-ring and terminal ring twisted conformers of the acetylene π-conjugated system bis(phenylethynyl)benzene, a model system for molecular wires. Through excitation wavelength dependent, femtosecond-transient absorption measurements, we found that the middle-ring and terminal ring twisted conformers relax at femtosecond (400-600 fs) and picosecond (20-24 ps) time scales, respectively.

Mode specific excited state dynamics study of bis(phenylethynyl)benzene from ultrafast Raman loss spectroscopy.

Femtosecond transient absorption (fs-TA) and Ultrafast Raman Loss Spectroscopy (URLS) have been applied to reveal the excited state dynamics of bis(phenylethynyl)benzene (BPEB), a model system for one-dimensional molecular wires that have numerous applications in opto-electronics. It is known from the literature that in the ground state BPEB has a low torsional barrier, resulting in a mixed population of rotamers in solution at room temperature. For the excited state this torsional barrier had been calculated to be much higher.