氧化还原
电导率
电化学
催化作用
金属有机骨架
瓶颈
材料科学
导电体
纳米技术
金属
电催化剂
电极
化学工程
化学
无机化学
计算机科学
有机化学
物理化学
复合材料
吸附
嵌入式系统
冶金
工程类
作者
Ran Shimoni,Wenhui He,Itamar Liberman,Idan Hod
标识
DOI:10.1021/acs.jpcc.8b12392
摘要
Redox-active Metal–Organic Frameworks (MOFs) are considered as promising platforms for assembling high quantities of solution-accessible molecular catalysts on conductive surfaces, toward their utilization in electrochemical solar fuel related reactions. Nevertheless, slow redox hopping-based conductivity often constitutes a kinetic bottleneck hindering the overall electrocatalytic performance of these systems. In this work, we show that, by a systematic control of MOF defect site density, one can modulate the spatial distribution of post synthetically installed molecular catalyst and hence accelerate charge transport rates by an order of magnitude. Moreover, the improved MOF conductivity also yields an enhancement in its intrinsic electrocatalytic activity. Consequently, these results offer new possibilities for designing efficient MOF-based electrocatalytic systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI