Electrochemical reduction of SnO2 to Sn from the Bottom: In-Situ formation of SnO2/Sn heterostructure for highly efficient electrochemical reduction of carbon dioxide to formate

被引:39
|
作者
Ning, Shunlian [1 ]
Wang, Jigang [1 ]
Xiang, Dong [1 ]
Huang, Shaobin [1 ]
Chen, Wei [2 ]
Chen, Shaowei [3 ]
Kang, Xiongwu [1 ]
机构
[1] South China Univ Technol, Sch Environm & Energy, Higher Educ Mega Ctr, 382 East Waihuan Rd, Guangzhou 510006, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
[3] Univ Calif Santa Cruz, 1156 High St, Santa Cruz, CA 95064 USA
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
electrochemical CO2 reduction; In-situ reconstruction; operando Raman spectroscopy; SnO2/Sn heterostructures; Formate; DFT calculations; ELECTROCATALYTIC CO2 REDUCTION; HYDROGEN EVOLUTION; FORMIC-ACID; TIN OXIDE; NANOSHEETS; PRINCIPLES; ELECTRODES; CATALYSTS;
D O I
10.1016/j.jcat.2021.04.028
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Design and engineering of low-cost, high-performance catalysts is a critical step in electrochemical CO2 reduction (CO2R) to value-added chemicals and fuels. Herein, SnO2 nanoparticles were grown onto carbon cloth (SnO2/CF) by a facile hydrothermal procedure and exhibited excellent electrocatalytic activity towards CO2R due to reconstruction into SnO2/Sn Mott-Schottky heterojunctions during CO2R electrolysis, as manifested in X-ray diffraction, X-ray photoelectron spectroscopy, and operando Raman spectroscopy measurements. The heterostructured SnO2/Sn electrode delivered a high faradaic efficiency of 93 +/- 1% and a partial current density of 28.7 mA cm(-2) for formate production at - 1.0 V vs. reversible hydrogen electrode in an H-type cell (which remained stable for 9 h), and 174.86 mA cm(-2) at - 1.18 V on a gas-diffusion electrode in a flow cell. Density functional theory calculations show that the SnO2/Sn heterostructures in situ formed under CO2R conditions helped decrease the energy barrier to form formate as compared to pristine SnO2 and Sn, and were responsible for the high activity and selectivity of formate production. Results from this study unravels the evolution dynamics of SnO2 catalysts under CO2R condition and provides a further understanding of the active component of SnO2 catalyst in CO2R. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:67 / 74
页数:8
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