Bláha Michal, Valeš Václav, Bastl Zdeněk, Kalbáč Martin, Shiozawa Hidetsugu
J. Heyrovský Institute of Physical Chemistry, Czech Academy of Sciences, Dolejškova 2155/3, CZ-182 23 Prague 8, Czech Republic.
Faculty of Physics, University of Vienna, Boltzmanngasse 5, 1090 Vienna, Austria.
J Phys Chem C Nanomater Interfaces. 2020 Nov 5;124(44):24245-24250. doi: 10.1021/acs.jpcc.0c07473. Epub 2020 Oct 21.
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 XeF, 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--toluoyl cyanide (DCTC) while XeF 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.
金属有机框架材料(MOFs)是一类多孔材料,其性质可通过掺杂氧化还原活性分子来改变。尽管掺杂的MOFs具有诸如增强导电性等先进特性,但由于其异质性阻碍了对主客体相互作用的实验观察,理解其物理机制仍然具有挑战性。在这里,我们展示了一项关于Mn-MOF-74与电子受体7,7,8,8-四氰基对苯二甲烷(TCNQ)和XeF之间电荷转移的研究,该研究利用了在各种光学共振条件下不同部分拉曼散射的选择性增强。我们识别了分子成分的拉曼模式,并阐明了TCNQ被氧化为二氰基-对甲苯酰氰(DCTC),而XeF在渗透时使MOF氟化。从C-O伸缩模式的蓝移以及醌类模式的出现推断,在这两种情况下框架的连接体都充当电子供体。这项工作展示了一种通过共振拉曼光谱研究各种供体-受体系统中电荷转移的普遍适用方法。