Abstract
UV Raman spectra were measured using a novel experimental configuration. This configuration allows many of the difficulties associated with UV excitation and high-power pulsed laser sources to be mitigated. Large sample areas are imaged into the detection system allowing high power excitation sources to be used while simultaneously avoiding sample degradation and multi-photon absorption effects. Such large detection areas allow large numbers of molecular scatters to be probed even with minimal penetration depth. Alignment issues between sample and collection optics are also simplified. Several common solvents were studied using 213 nm light and their spectra reported.
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