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Solvent Triggered Change of the Electron Excitation Route of KI in Supercritical NH_3

机译:溶剂触发的超临界NH_3中KI的电子激发途径的变化

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摘要

The UV-spectroscopic behavior of KI contact ion pairs (CIPs) dissolved in supercritical NH3 was studied combining classical molecular dynamics simulations with electronic structure calculations,and the results show that an abrupt change of the photoexcitation route of KI CIPs occurs at very low solvent densities.Few NH_3 solvating molecules are required to hamper the well-known photoinduced intramolecular electron (e~-) transfer observed in isolated ion pairs of alkali metal halides in the vapor drawing the e~- to solvent cavities leading to a charge-transfer-to-solvent process.
机译:结合经典的分子动力学模拟和电子结构计算,研究了超临界NH3中KI接触离子对(CIPs)的紫外光谱行为,结果表明,在极低的溶剂密度下,KICIPs的光激发途径发生突变。几乎不需要NH_3溶剂化分子来阻止在蒸气中碱金属卤化物的分离离子对中观察到的众所周知的光诱导分子内电子(e〜-)转移,从而将e〜-吸引到溶剂腔中,从而导致电荷转移到-溶剂过程。

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