Accelerating CO2 Electroreduction to Multicarbon Products via Synergistic Electric–Thermal Field on Copper Nanoneedles

化学 催化作用 电催化剂 电解质 电场 选择性 化学工程 电化学 法拉第效率 电极 物理化学 有机化学 量子力学 物理 工程类
作者
Baopeng Yang,Kang Liu,Huangjingwei Li,Changxu Liu,Junwei Fu,Hongmei Li,Jianan Erick Huang,Pengfei Ou,Tartela Alkayyali,Chao Cai,Yuxia Duan,Hui Liu,Pengda An,Ning Zhang,Wenzhang Li,Xiaoqing Qiu,Chuankun Jia,Junhua Hu,Liyuan Chai,Zhang Lin
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:144 (7): 3039-3049 被引量:247
标识
DOI:10.1021/jacs.1c11253
摘要

Electrochemical CO2 reduction is a promising way to mitigate CO2 emissions and close the anthropogenic carbon cycle. Among products from CO2RR, multicarbon chemicals, such as ethylene and ethanol with high energy density, are more valuable. However, the selectivity and reaction rate of C2 production are unsatisfactory due to the sluggish thermodynamics and kinetics of C-C coupling. The electric field and thermal field have been studied and utilized to promote catalytic reactions, as they can regulate the thermodynamic and kinetic barriers of reactions. Either raising the potential or heating the electrolyte can enhance C-C coupling, but these come at the cost of increasing side reactions, such as the hydrogen evolution reaction. Here, we present a generic strategy to enhance the local electric field and temperature simultaneously and dramatically improve the electric-thermal synergy desired in electrocatalysis. A conformal coating of ∼5 nm of polytetrafluoroethylene significantly improves the catalytic ability of copper nanoneedles (∼7-fold electric field and ∼40 K temperature enhancement at the tips compared with bare copper nanoneedles experimentally), resulting in an improved C2 Faradaic efficiency of over 86% at a partial current density of more than 250 mA cm-2 and a record-high C2 turnover frequency of 11.5 ± 0.3 s-1 Cu site-1. Combined with its low cost and scalability, the electric-thermal strategy for a state-of-the-art catalyst not only offers new insight into improving activity and selectivity of value-added C2 products as we demonstrated but also inspires advances in efficiency and/or selectivity of other valuable electro-/photocatalysis such as hydrogen evolution, nitrogen reduction, and hydrogen peroxide electrosynthesis.
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