极化子辅助表面水分子质子化TiO2的非绝热动力学

Zhongfei Xu , Chuanjia Tong , Rutong Si , Gilberto Teobaldi , Limin Liu
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引用次数: 0

摘要

我们研究了质子化TiO2中极化子辅助的非绝热动力学,以及极化子-水耦合及其对光生电子弛豫的影响。我们观察到,不同的极化子跳跃机制会导致不同的非绝热耦合和激发电子从导带最小到质子化TiO2的间隙态的弛豫,并且对极化子的实际捕获位置依赖性较弱。表面吸附的H2O分子可以将极化子吸引到被吸附的Ti位点上,并且H2O与极化子之间的耦合与它们的距离成反比。我们的研究结果表明,光生电荷载流子的寿命可以通过减少极化子与水的距离来延长,这对光催化应用中还原后的TiO2样品的效率有预期的好处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Polaron-assisted nonadiabatic dynamics in protonated TiO2 with surface water molecule

Polaron-assisted nonadiabatic dynamics in protonated TiO2 with surface water molecule

We investigated the polaron-assisted nonadiabatic dynamics in protonated TiO2, as well as the polaron-H2O coupling and its effects on the relaxation of photogenerated electrons. We observed that different polaron hopping regimes result in varied nonadiabatic couplings and relaxations of excited electrons from the conduction band minimum to the gap states of protonated TiO2, with a weak dependence on the actual trapping site of the polaron. Surface-adsorbed H2O molecules can attract polarons toward the adsorbed Ti sites, with the coupling between H2O and the polaron being inversely proportional to their distance. Our findings suggest that the lifetime of the photogenerated charge carriers can be extended by reducing the polaron-H2O distances, with expected benefits to the efficiency of the reduced TiO2 samples for photocatalytic applications.

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