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首页> 外文期刊>The Journal of Chemical Physics >Quantum-state resolved reaction dynamics at the gas-liquid interface:Direct absorption detection of HF(v,J) product from F(~2P)+squalane
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Quantum-state resolved reaction dynamics at the gas-liquid interface:Direct absorption detection of HF(v,J) product from F(~2P)+squalane

机译:气液界面处的量子态解析反应动力学:直接吸收检测F(〜2P)+角鲨烷中的HF(v,J)产物

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摘要

Exothermic reactive scattering of F atoms at the gas-liquid interface of a liquid hydrocarbon (squalane) surface has been studied under single collision conditions by shot noise limited high-resolution infrared absorption on the nascent HF(v,J) product.The nascent HF(v,J) vibrational distributions are inverted,indicating insufficient time for complete vibrational energy transfer into the surface liquid.The HF(v=2,J) rotational distributions are well fit with a two temperature Boltzmann analysis,with a near room temperature component (T_(TD) approx = 290 K) and a second much hotter scattering component (T_(HDS) approx = 1040 K).These data provide quantum state level support for microscopic branching in the atom abstraction dynamics corresponding to escape of nascent HF from the liquid surface on time scales both slow and fast with respect to rotational relaxation.
机译:通过在新生的HF(v,J)产物中受散粒噪声限制的高分辨率红外吸收,研究了在单次碰撞条件下液态碳氢化合物(角鲨烷)表面的气-液界面处F原子的放热反应性散射。 (v,J)的振动分布反转,表明没有足够的时间将完整的振动能量转移到表面液体中.HF(v = 2,J)的旋转分布与两个温度的Boltzmann分析很好地拟合,并且具有接近室温的成分(T_(TD)大约= 290 K)和第二个更热的散射分量(T_(HDS)大约= 1040 K)。这些数据为原子抽象动力学中的微观分支提供了量子态水平的支持,这与新生HF从中逃逸相对应。液体表面在时间上相对于旋转弛豫既缓慢又迅速。

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