X-ray Transient Absorption Studies of Exciton Self-Trapping

被引:0
作者
Turner, Nathan A. [1 ]
Mance, Jason G. [1 ]
Attenkofer, Klaus [2 ,3 ]
Adams, Bernhard W. [2 ,4 ]
Zhang, Xiaoyi [2 ]
Dexheimer, Susan L. [1 ]
机构
[1] Washington State Univ, Dept Phys & Astron, Pullman, WA 99164 USA
[2] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[3] ALBA Synchrotron Light Source, Barcelona 08290, Spain
[4] IIT, Chicago, IL 60616 USA
基金
美国国家科学基金会;
关键词
LINEAR-CHAIN; SPECTROSCOPY; COMPLEXES; PLATINUM; SPECTRA; STATE;
D O I
10.1021/acs.jpcc.1c07270
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present optical pump/X-ray absorption probe studies to probe changes in electronic distribution and local structure upon formation of a self-trapped exciton. The experiments were carried out on the mixed-valence halide-bridged transition metal linear chain charge density wave material [Pt(en(2))][Pt(en(2))Cl-2]center dot(ClO4)(4). Photoinduced changes in the Pt L-m XANES spectrum were measured on a picosecond time scale following generation of excitons via optical excitation of the intervalence charge transfer transition. Ab initio FEFF9 modeling of the spectra and the associated angular momentum projected density of states was used to interpret the response. We find photoinduced changes reflecting electronic redistribution and local lattice distortions that correspond to strong localization of the self-trapped state.
引用
收藏
页码:349 / 355
页数:7
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