材料科学
导电体
结晶度
导电的
等结构
电阻率和电导率
水分
纳米技术
法拉第效率
微晶
吸附
电接点
电导率
电荷(物理)
光电子学
电容感应
俘获
载流子
合理设计
机制(生物学)
电流
生理适应
流线、条纹线和路径线
化学
作者
Yingchao Wang,Xiaohe Miao,Paul A. Kempler,Jin‐Hu Dou,Carl K. Brozek,Lei Sun
标识
DOI:10.26434/chemrxiv-2025-gj0k1-v2
摘要
Electrically conductive metal–organic frameworks (MOFs) combine high crystallinity and large surface area with guest-tunable electrical conductivity, making them ideal for chemiresistive gas sensing. Whereas many sensitive and selective MOF-based chemiresistive sensors have been fabricated, their underlying sensing mechanisms often remain elusive, primarily due to the reliance on polycrystalline films. Herein, we overcome this limitation by investigating chemiresistive moisture sensing using single crystals of a series of isostructural MOFs, M₂(TTFTB) (M2+ = Mn2+, Co2+, Zn2+, Cd2+; TTFTB4− = tetrathiafulvalene tetrabenzoate). We reveal that electrical conductivity in these materials is strongly affected by Coulombic interactions between TTF·+ radical defects and charge-balancing anions. In dry conditions, these interactions induce charge trapping. The adsorption of water vapor screens the hole-anion interactions, mitigating charge trapping and thereby significantly enhancing electrical conductivity. This mechanism is particularly pronounced in Zn₂(TTFTB) owing to the high Coulombic potential of Zn²⁺. This study establishes a general methodology for understanding charge transport in MOFs and provides critical guidelines for the rational design of high-performance chemiresistive sensors.
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