材料科学
导电体
金属有机骨架
吸附
分子
导线
纳米技术
氢键
金属
无机化学
化学工程
电导率
物理化学
有机化学
化学
复合材料
工程类
冶金
作者
Yun‐Xiang Ma,Bin Gao,Yongxin Li,Wei Wei,Yanli Zhao,Jian‐Fang Ma
标识
DOI:10.1021/acsami.1c05481
摘要
Conductive metal-organic frameworks (MOFs) have a wide range of applications in supercapacitors, electrocatalysts, and fuel cells, while gas-driven conductive MOFs have not yet been synthesized so far. Herein, we report a gas-driven conductive MOF (A) constructed from calix[4]resorcinarene macrocycle and Co(II) cations, which shows the conductivity enhancement by about eight orders of magnitude through NO2 adsorption. The conductivities of MOF A before and after the adsorption of NO2 were calculated to be about 1.3 × 10-11 and 8.4 × 10-4 S/cm, respectively. MOF A realizes the conversion from an insulator to a conductor by adsorbing NO2. When NO2 is evacuated, MOF A quickly changes from a conductor back to an insulator in 42 s. In the crystal structure of NO2-adsorbed MOF (termed as A-NO2), NO2 molecule connects Co(II) and uncoordinated carboxylate groups through hydrogen-bonding interactions to form a conductive pathway, greatly reducing the electron transmission distance between each two metal clusters. In addition, NO2 molecule and H3O+ may also form a conductive pathway by hydrogen-bonding interactions. This work presents an interesting macrocycle-based MOF with a NO2-driven on/off conductivity switch, proving the possibility for designing advanced gas-driven conductive systems.
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