四硫富瓦烯
过电位
共价有机骨架
法拉第效率
卟啉
化学
电子转移
氧化还原
电流密度
金属有机骨架
共价键
电极
化学工程
光化学
材料科学
纳米技术
多孔性
分子
电化学
物理
有机化学
物理化学
吸附
复合材料
工程类
量子力学
冶金
作者
Qiao Wu,Ruikuan Xie,Min‐Jie Mao,Guoliang Chai,Jun‐Dong Yi,Shao–Shuai Zhao,Yuan‐Biao Huang,Rong Cao
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-02-18
卷期号:5 (3): 1005-1012
被引量:208
标识
DOI:10.1021/acsenergylett.9b02756
摘要
Electroreduction of CO2 (CO2RR) into value-added fuels is of significant importance but remains a big challenge because of poor selectivity, low current density, and large overpotential. Crystalline porous covalent organic frameworks (COFs) are promising alternative electrode materials for CO2RR owing to their tunable and accessible single active sites. However, the poor electron-transfer capability of COFs limits their application. Herein, a tetrathiafulvalene (TTF) strut was integrated into a two-dimensional cobalt porphyrin-based COF (TTF-Por(Co)-COF) to enhance its electron-transfer capability from the TTF to the porphyrin ring. Compared with COF-366-Co without TTF, TTF-Por(Co)-COF showed enhanced CO2RR performance in water with 95% Faradaic efficiency of the CO2-to-CO conversion at −0.7 V vs RHE and a partial current density of 6.88 mA cm–2 at −0.9 V vs RHE. This work provides a new insight for the rational design of porous organic framework materials for improving the activity of CO2RR.
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