4.5 Article

Layered bismuth oxide/bismuth sulfide supported on carrageenan derived carbon for efficient carbon dioxide electroreduction to formate

期刊

CHINESE JOURNAL OF CHEMICAL ENGINEERING
卷 43, 期 -, 页码 116-123

出版社

CHEMICAL INDUSTRY PRESS CO LTD
DOI: 10.1016/j.cjche.2022.02.009

关键词

Nanomaterials; Catalyst; Selectivity; Bi2S3/Bi2O3; CO2 electroreduction; Formate

资金

  1. National Natural Science Foundation of China [21922811, 21878270, 22178308, 21961160742]
  2. Jiangxi Province double thousand plan project [205201000020]
  3. Zhejiang Provincial Natural Science Founda-tion of China [LR19B060002]
  4. Leading Innovative and Entrepre-neur Team Introduction Program of Zhejiang [2019R01006]
  5. Zhejiang Key Laboratory of Marine Materials and Protective Technologies [2020K10]
  6. Key Laboratory of Marine Materials and Related Technologies, CAS
  7. Startup Foundation for Hundred-Talent Program of Zhejiang University

向作者/读者索取更多资源

This study reports a novel hybrid CO2ER electrocatalyst that achieves efficient formate production and stable catalytic performance by supporting layered Bi2O3 and Bi2S3 on nanocarbon. The strong interfacial interactions between nanocarbon and Bi2O3/Bi2S3 are identified as the key factor for the enhanced CO2ER performance.
Electrochemical reduction of carbon dioxide (CO2ER) into formate plays a crucial role in CO2 conversion and utilization. However, it still faces the problems of high overpotential and poor catalytic stability. Herein, we report a hybrid CO2ER electrocatalyst composed of layered bismuth sulfide (Bi2S3) and bismuth oxide (Bi2O3) supported on carrageenan derived carbon (Bi-CDC) prepared by a combined pyrolysis with hydrothermal treatment. In such 3D hybrid, layered Bi2O3 and Bi2S3 are uniformly grown on nanocarbon supports. Benefiting from strong synergistic effect between Bi2O3/Bi2S3 and nanocarbon, Bi-CDC-1:2 displays a high Faradic efficiency (FE) of >80% for formate production in the range of -0.9 V to -1.1 V with the maximum formate FE of 85.6% and current density of 14.1 mA.cm(-2) at -1.0 V. Further, a positive onset potential of -0.5 V, a low Tafel slope of 112.38 mV.dec(-1), and a slight performance loss during long-term CO2ER tests are observed on Bi-CDC-1:2. Experimental results shows that the better CO2ER performance of Bi-CDC-1:2 than that of Bi2O3 can be attributed to the strong interfacial interactions between nanocarbons and Bi2O3/Bi2S3. In situ ATR-FTIR measurements reveal that the rate-determining step in the CO2ER is the formation of HCOO* intermediated. Compared with carbon support, Bi-CDC-1:2 can promote the production of HCOO* intermediate and thus promoting CO2ER kinetic. (C) 2022 The Chemical Industry and Engineering Society of China, and Chemical Industry Press Co., Ltd.

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