期刊
JOURNAL OF ALLOYS AND COMPOUNDS
卷 856, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2020.157379
关键词
Electrocatalyst; Ag-Cu; Oxygen reduction reaction; SECM; DFT
资金
- General Research Fund of the Research Grants Council of Hong Kong Special Administrative Region, China [17204516, 17206518]
- Environment and Conservation Fund [ECF 49/2017]
- HKU-Zhejiang Institute of Research and Innovation (HKU-ZIRI)
The study successfully synthesized a bimetallic Ag-Cu nanostructure using the cyclic scanning electrodeposition method and systematically investigated its catalytic performance for the oxygen reduction reaction in alkaline media. The results showed that the Ag-Cu nanostructure exhibited competitive catalytic ability, with a close to four electrons transfer number, which was attributed to the widely distributed Ag-Cu steps formed by decorating Cu atoms on the Ag nanosheets.
Fabricating low-cost and Pt-free fuel cell catalysts towards highly active and durable oxygen-reduction reaction catalysis remains a great challenge. Herein, we synthesize a bimetallic Ag-Cu nanosheets assembled flower-like structure by our developed cyclic scanning electrodeposition (CSE) method. The formation mechanism of this structure is investigated systematically, where Cu2+ can affect oxidative etching during the formation process. The prepared bimetallic nanostructure is studied for kinetics towards oxygen reduction reaction (ORR) in alkaline media. The electrochemical test results indicate that the ORR catalytic ability of bimetallic Ag-Cu nanostructure is competitive with Pt/C-20%, better than Pt disk, and far superior to the pure Ag nanostructure. The electrons transfer number (n) is close to four, which is further proved by scanning electrochemical microscope (SECM) experiments. Density functional theory (DFT) calculations reveal that the high ORR activity is attributable to the widely distributed Ag-Cu steps, which is formed by decorating Cu atoms on the Ag nanosheets. (C) 2020 Elsevier B.V. All rights reserved.
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