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Plasma-Engraved Co3O4 Nanosheets with Oxygen Vacancies and High Surface Area for the Oxygen Evolution Reaction.

Authors :
Xu, Lei
Jiang, Qianqian
Xiao, Zhaohui
Li, Xingyue
Huo, Jia
Wang, Shuangyin
Dai, Liming
Source :
Angewandte Chemie International Edition; Apr2016, Vol. 55 Issue 17, p5277-5281, 5p
Publication Year :
2016

Abstract

Co<subscript>3</subscript>O<subscript>4</subscript>, which is of mixed valences Co<superscript>2+</superscript> and Co<superscript>3+</superscript>, has been extensively investigated as an efficient electrocatalyst for the oxygen evolution reaction (OER). The proper control of Co<superscript>2+</superscript>/Co<superscript>3+</superscript> ratio in Co<subscript>3</subscript>O<subscript>4</subscript> could lead to modifications on its electronic and thus catalytic properties. Herein, we designed an efficient Co<subscript>3</subscript>O<subscript>4</subscript>-based OER electrocatalyst by a plasma-engraving strategy, which not only produced higher surface area, but also generated oxygen vacancies on Co<subscript>3</subscript>O<subscript>4</subscript> surface with more Co<superscript>2+</superscript> formed. The increased surface area ensures the Co<subscript>3</subscript>O<subscript>4</subscript> has more sites for OER, and generated oxygen vacancies on Co<subscript>3</subscript>O<subscript>4</subscript> surface improve the electronic conductivity and create more active defects for OER. Compared to pristine Co<subscript>3</subscript>O<subscript>4</subscript>, the engraved Co<subscript>3</subscript>O<subscript>4</subscript> exhibits a much higher current density and a lower onset potential. The specific activity of the plasma-engraved Co<subscript>3</subscript>O<subscript>4</subscript> nanosheets (0.055 mA cm<superscript>−2</superscript><subscript>BET</subscript> at 1.6 V) is 10 times higher than that of pristine Co<subscript>3</subscript>O<subscript>4</subscript>, which is contributed by the surface oxygen vacancies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14337851
Volume :
55
Issue :
17
Database :
Complementary Index
Journal :
Angewandte Chemie International Edition
Publication Type :
Academic Journal
Accession number :
114490391
Full Text :
https://doi.org/10.1002/anie.201600687