拉曼光谱
金属有机骨架
分子
电子受体
四氰基对醌二甲烷
兴奋剂
接受者
共振拉曼光谱
拉曼散射
共振(粒子物理)
材料科学
光化学
光谱学
化学
化学物理
物理化学
有机化学
光电子学
光学
物理
粒子物理学
吸附
量子力学
凝聚态物理
作者
Michal Bláha,Václav Valeš,Zdeněk Bastl,Martin Kalbáč,Hidetsugu Shiozawa
标识
DOI:10.1021/acs.jpcc.0c07473
摘要
Metal-organic frameworks (MOFs) represent a class of porous materials whose properties can be altered by doping with redox-active molecules. Despite advanced properties such as enhanced electrical conduction that doped MOFs exhibit, understanding physical mechanisms remains challenging because of their heterogeneous nature hindering experimental observations of host-guest interactions. Here, we show a study of charge transfer between Mn-MOF-74 and electron acceptors, 7,7,8,8-tetracyanoquinodimethane (TCNQ) and XeF2, employing selective enhancement of Raman scattering of different moieties under various optical-resonance conditions. We identify Raman modes of molecular components and elucidate that TCNQ gets oxidized into dicyano-p-toluoyl cyanide (DCTC-) while XeF2 fluorinates the MOF upon infiltration. The framework's linker in both cases acts as an electron donor as deduced from blue shifts of the C-O stretching mode accompanied by the emergence of a quinone-like mode. This work demonstrates a generally applicable methodology for investigating charge transfer in various donor-acceptor systems by means of resonance Raman spectroscopy.
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