RESUMEN
Wavelength conversion afforded by stimulated Raman scattering within a hollow core fiber is potentially useful for multispectral light detection and ranging (LiDAR). Herein, we make use of the ideal 1550 cm-1 vibrational Raman shift of an antiresonant fiber filled with gaseous oxygen so that the first and second Raman orders as well as the transmitted pump are all located in separate atmospheric transmission windows. To the best of our knowledge, this is the first report of stimulated Raman scattering in an oxygen-filled fiber. The host of closely spaced rotational stimulated Raman scattering (SRS) lines (12 cm-1) accompanying the transmitted pump and vibrational Raman orders form continuum bands allowing for much greater spectral coverage of the atmospheric transmission windows. The temporal profiles of the Raman orders can be separated without the use of a grating to potentially achieve a multi-band LiDAR.
RESUMEN
Although χ(2) nonlinear optical processes, such as difference frequency generation (DFG), are often used in conjunction with fiber lasers for wavelength conversion and photon-pair generation, the monolithic fiber architecture is broken by the use of bulk crystals to access χ(2). We propose a novel solution by employing quasi-phase matching (QPM) in molecular-engineered hydrogen-free, polar-liquid core fiber (LCF). Hydrogen-free molecules offer attractive transmission in certain NIR-MIR regions and polar molecules tend to align with an externally applied electrostatic field creating a macroscopic χ e f f(2). To further increase χ e f f(2) we investigate charge transfer (CT) molecules in solution. Using numerical modeling we investigate two bromotrichloromethane based mixtures and show that the LCF has reasonably high NIR-MIR transmission and large QPM DFG electrode period. The inclusion of CT molecules has the potential to yield χ e f f(2) at least as large as has been measured in silica fiber core. Numerical modeling for the degenerate DFG case indicates that signal amplification and generation through QPM DFG can achieve nearly 90% efficiency.
RESUMEN
Doubly resonant infrared-visible sum-frequency generation (DR-IVSFG) spectroscopy, encompassing coupled vibrational and electronic transitions, provides a powerful method to gain a deep understanding of nuclear motion in photoresponsive surface adsorbates and interfaces. Here, we use DR-IVSFG to elucidate the role of vibronic coupling in a surface-confined donor-acceptor substituted azobenzene. Our study reveals some unique features of DR-IVSFG that have not been previously reported. In particular, vibronic coupling resulted in prominent SFG signal enhancement of selective stretching modes that reveal electronic properties of coexisting photochromic isomers. Our analysis explores two concepts: (1) In partially isomerized azobenzene at the surface, coupling of the fundamental vibrations to the S0 â S1 transition is more prominent for the cis isomer due to symmetry breaking, whereas coupling to the S0 â S2 transition was dominant in the trans isomer. (2) A strong coupling between the fundamental vibrations and the valence π-electron density, promoted by the initial absorption of an infrared photon, may result in suppression of the intensity of the hot band vibronic transition. This may translate into a suppressed sum-frequency generation signal at sum frequency wavelengths resonant with the S0 â S2 transition of the trans isomer. The weaker coupling of the fundamental vibrations to the non-bonding electron density localized on the azo group can therefore produce detectable sum-frequency generation at the resonance wavelength of the weaker S0 â S1 transition in the cis form. These results are explained in the framework of a linear coupling model, involving both Franck-Condon and Herzberg-Teller coupling terms. Our theoretical analysis reveals the important role played by molecular conformation, orientation, and vibronic interference in DR-SFG spectroscopy.
RESUMEN
Rare-earth doped multi-shell nanoparticles slated for theranostic applications produce a variety of emission bands upon near-infrared (NIR) excitation. Their downshifting emission is useful for high-contrast NIR imaging, while the upconversion light can induce photodynamic therapy (PDT). Unfortunately, integration of imaging and therapy is challenging. These modalities are better to be controlled independently so that, with the help of imaging, selective delivery of a theranostic agent at the site of interest could be ensured prior to on-demand PDT initiation. We introduce here multi-shell rare-earth doped nanoparticles (RENPs) arranged in a manner to produce only downshifting emission for NIR imaging when excited at one NIR wavelength and upconversion emission for therapeutic action by using a different excitation wavelength. In this work, multi-shell RENPs with a surface-bound sensitizer have been synthesized for decoupled 1550 nm downshifting emission upon 800 nm excitation and 550 nm upconversion emission caused by 980 nm irradiation. The independently controlled emission bands allow for high-contrast NIR imaging in NIR-IIb of optical transparency that gives high-contrast images due to significantly reduced light scattering. This can be conducted prior to PDT using 980 nm to produce upconverted light at 550 nm that excites the RENP surface-bound photosensitizer, Rose Bengal (RB), to effect photodynamic therapy with high specificity and safer theranostics.
RESUMEN
Emission bands from thermally coupled states in lanthanide-doped nanoparticles have been studied for ratiometric nanothermometry in biological applications. Unfortunately certain factors such as water absorption distort the intensity, limiting the accuracy of ratiometric nanothermometry. However, the decay time of such states does not suffer from such distortions. We introduce the decay time of the 3H4 state in Yb3+, Tm3+-doped nanoparticles for improved nanothermometry. The strong 800 nm upconversion emission exists in the first biological transparency window. This is the first use of a single upconversion band for lifetime nanothermometry.