化学
吸附
脱质子化
电阻率和电导率
氧化还原
电导率
金属
电荷(物理)
碘
金属有机骨架
同步加速器
结晶学
化学物理
无机化学
物理化学
有机化学
离子
工程类
核物理学
物理
电气工程
量子力学
作者
Xinran Zhang,Iván da Silva,Rodrigo Boni Fazzi,Alena M. Sheveleva,Xue Han,Ben F. Spencer,Sergey A. Sapchenko,Floriana Tuna,Eric J. L. McInnes,Ming Li,Sihai Yang⧫,Martin Schröder
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2019-09-30
卷期号:58 (20): 14145-14150
被引量:97
标识
DOI:10.1021/acs.inorgchem.9b02176
摘要
We report a comparative study of the binding of I2 (iodine) in a pair of redox-active metal-organic framework (MOF) materials, MFM-300(VIII) and its oxidized, deprotonated analogue, MFM-300(VIV). Adsorption of I2 in MFM-300(VIII) triggers a host-to-guest charge-transfer, accompanied by a partial (∼30%) oxidation of the VIII centers in the host framework and formation of I3- species residing in the MOF channels. Importantly, this charge-transfer induces a significant enhancement in the electrical conductivity (Δσ = 700000) of I2@MFM-300(VIII/IV) in comparison to MFM-300(VIII). In contrast, no host-guest charge-transfer or apparent change in the conductivity was observed upon adsorption of I2 in MFM-300(VIV). High-resolution synchrotron X-ray diffraction of I2@MFM-300(VIII/IV) confirms the first example of self-aggregation of adsorbed iodine species (I2 and I3-) into infinite helical chains within a MOF.
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