Two-Dimensional Titanium and Molybdenum Carbide MXenes as Electrocatalysts for CO2 Reduction

被引:139
作者
Handoko, Albertus D. [1 ]
Chen, Hetian [2 ]
Lum, Yanwei [1 ]
Zhang, Qianfan [2 ]
Anasori, Babak [3 ,4 ,5 ]
Seh, Zhi Wei [1 ]
机构
[1] ASTAR, Inst Mat Res & Engn, 2 Fusionopolis Way, Singapore 138634, Singapore
[2] Beihang Univ, Sch Mat Sci & Engn, Beijing 100191, Peoples R China
[3] Indiana Univ Purdue Univ, Integrated Nanosyst Dev Inst, Dept Mech & Energy Engn, Indianapolis, IN 46202 USA
[4] Drexel Univ, AJ Drexel Nanomat Inst, Philadelphia, PA 19104 USA
[5] Drexel Univ, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
基金
新加坡国家研究基金会;
关键词
CARBON-DIOXIDE; ELECTROCHEMICAL REDUCTION; MECHANISTIC INSIGHTS; SCALING RELATIONS; ENHANCED ACTIVITY; CONVERSION; EVOLUTION; FUNCTIONALIZATION; ELECTROREDUCTION; ELECTRODES;
D O I
10.1016/j.isci.2020.101181
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Electrocatalytic CO2 reduction reaction (CO2RR) is an attractive way to produce renewable fuel and chemical feedstock, especially when coupled with efficient CO2 capture and clean energy sources. On the fundamental side, research on improving CO2RR activity still revolves around late transition metal-based catalysts, which are limited by unfavorable scaling relations despite intense investigation. Here, we report a combined experimental and theoretical investigation into electrocatalytic CO2RR on Ti- and Mo-based MXene catalysts. Formic acid is found as the main product on Ti2CTx and Mo2CTx MXenes, with peak Faradaic efficiency of over 56% on Ti2CTx and partial current density of up to -2.5 mA cm(-2) on Mo2CTx. Furthermore, simulations reveal the critical role of the T-x group: a smaller overpotential is found to occur at lower amounts of -F termination. This work represents an important step toward experimental demonstration of MXenes for more complex electrocatalytic reactions in the future.
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页数:39
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