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Probing photoinduced phase transition in a charge-transfer molecular crystal by 100 picosecond X-ray diffraction

机译:通过100皮秒X射线衍射探测电荷转移分子晶体中的光诱导相变

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摘要

Watching with an atomic resolution at structural changes as fast or ultra-fast photoinduced physical processes take place benefits from recent progresses in time-resolved X-ray diffraction. Molecular materials where electronic and structural changes are strongly coupled are model systems to perform such time-resolved crystallography studies. We report the structural investigation of photoinduced phase transformations between ionic and neutral states in an organic charge-transfer molecular material, using 100 picosecond (ps) synchrotron pulses. This light-induced phenomenon, triggered by an ultra-short optical pulse from a femtosecond laser, occurs by virtue of intrinsic cooperativity. Since electronic and structural changes are strongly coupled, it is of fundamental interest to perform time-resolved X-ray diffraction to obtain information at the atomic scale. We also discuss the problem of coexistence of phases and the interest of future investigations in faster timescale.
机译:随着时间分辨X射线衍射的最新进展,以原子分辨率观察快速或超快光诱导的物理过程发生时的结构变化。电子和结构变化紧密耦合的分子材料是进行此类时间分辨晶体学研究的模型系统。我们报告了使用100皮秒(ps)同步加速器脉冲对有机电荷转移分子材料中的离子态和中性态之间的光诱导相变进行结构研究。飞秒激光产生的超短光脉冲触发了这种光诱导现象,这是由于固有的协同作用而发生的。由于电子和结构的变化是紧密耦合的,因此进行时间分辨的X射线衍射以获得原子级的信息至关重要。我们还讨论了阶段共存的问题以及在更短的时间范围内进行未来研究的兴趣。

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