Interrogation of the Plasma-Catalyst Interface via In Situ/Operando Transmission Infrared Spectroscopy
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Understanding the structural dynamics of covalent organic frameworks (COFs) in response to external temperature change is necessary for these materials' application at cryogenic temperatures.
Preparation techniques for producing films of individualized solution-dispersed nanoparticles (NPs) for optical spectroscopy are frequently technically challenging and tailored for a specific NP system. In this work, we present a rapid, easy, and economical technique for producing polyvinyl acetate (PVAc)-based NP-polymer films on the order of 100’s of micrometers thick that exhibit high uniformity, low aggregation, excellent optical transparency, and low terahertz absorption. In addition, we find that these films are robust at cryogenic temperatures and have a high laser damage threshold of 0.3 TW cm –2 , which make them suitable for pulsed laser measurements. We show that free-standing, flexible, PVAc films can incorporate both one-dimensional single-wall carbon nanotubes (SWCNTs) and zero-dimensional Au NPs. Using absorbance, Raman scattering, and photoluminescence excitation spectroscopy, we observe that SWCNT individualization is maintained, and minimized polymer strain imposed, when the nanotubes are transitioned from the solution to the polymer host. This PVAc-based polymer host presents researchers with a straightforward method for producing free-standing and flexible NP films with low aggregation.
An IR–vacuum ultraviolet (VUV) ion-dip spectroscopy method is utilized to examine the IR spectrum of acetaldehyde oxide (CH3CHOO) in the overtone CH stretch (2νCH) spectral region. IR activation creates a depletion of the ground state population that reduces the VUV photoionization signal on the parent mass channel. IR activation of the more stable and populated syn-CH3CHOO conformer results in rapid unimolecular decay to OH + vinoxy products and makes the most significant contribution to the observed spectrum. The resultant IR–VUV ion-dip spectrum of CH3CHOO is similar to that obtained previously for syn-CH3CHOO using IR action spectroscopy with UV laser-induced fluorescence detection of OH products. The prominent IR features at 5984 and 6081 cm−1 are also observed using UV + VUV photoionization of OH products. Complementary theoretical calculations utilizing a general implementation of second-order vibrational perturbation theory provide new insights on the vibrational transitions that give rise to the experimental spectrum in the overtone CH stretch region. The introduction of physically motivated small shifts of the harmonic frequencies yields remarkably improved agreement between experiment and theory in the overtone CH stretch region. The prominent features are assigned as highly mixed states with contributions from two quanta of CH stretch and/or a combination of CH stretch with an overtone in mode 4. The generality of this approach is demonstrated by applying it to three different levels of electronic structure theory/basis sets, all of which provide spectra that are virtually indistinguishable despite showing large deviations prior to introducing the shifts to the harmonic frequencies.
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IR spectrography applied to Mars biological studies, discussing organic IR radiation absorption and emission mechanisms
IR spectroscopy applications to high temperature molecules
Biaxially drawn polyethylene terephthalate films structural changes, noting alignment and crystallinity using polarized IR spectroscopy
IR Michelson interferometer for Mariner Mars 1971 mission, investigating atmospheric and surface temperatures and atmospheric water vapor content
Mars IR spectra with Connes-type interferometer, noting atmospheric absorption and albedo drop due to surface water
Measurements obtained during and after the planet-wide dust storm indicate that large diurnal variations in atmospheric temperature existed up to at least 30 km; winds inferred from the temperature fields show a strong tidal component and significant ageostrophic behavior. With the dissipation of the dust, the daily maximum in the atmospheric temperature field moved from approximately latitude -60 and late afternoon local time to near the subsolar point in latitude and time. Analysis of spectral features due to the atmospheric dust indicates as SIO2 content of 60 ? 10%, implying that substantial geochemical differentiation has occurred. Water vapor estimates indicate abundances of 10 to 20 precipitable micrometers. Between November 1971 and April 1972 no gross latitudinal or temporal dependence in the water vapor distribution was detected from the south polar region to the equator. Water vapor was not detected over the north polar regions. Surface pressure mapping was carried out from which topographic relief of nearly two pressure scale heights is inferred. Extensive regions were found where the surface pressure exceeds the triple point pressure of water.