Abstract

The development of highly active and cost-effective catalysts based on noble metal free oxygen electro-catalysis is critical to energy storage and conversion devices. Herein, we highlight a plasma-treated Bi0.1(Ba0.5Sr0.5)0.9Co0.8Fe0.2O3−δ perovskite (denoted as P-Bi0.1BSCF) as a promising catalyst for oxygen evolution reaction (OER) in alkaline media. H2/Ar plasma engraving could significantly increase electrochemically active O22−/O concentration and tune the electronic structure of Co ions efficiently, and consequently tailor the intrinsic electrocatalytic ability for OER. Of note, P-Bi0.1BSCF, with unique crystalline core/amorphous shell structure, exhibits an enhanced intrinsic OER activity and higher stability than the noble metal IrO2 catalyst, which outperforms most of the reported perovskite catalysts. The present work provides new insights into exploring efficient catalysts for OER, and it suggests that, in addition to the extensively applied for surface treatment of various catalysts such as carbons and metal oxides, the plasma engraved perovskite materials also exhibits great potential as precious metal-free catalysts.

Details

Title
Plasma engraved Bi0.1(Ba0.5Sr0.5)0.9Co0.8Fe0.2O3−δ perovskite for highly active and durable oxygen evolution
Author
Sun, Juan 1 ; Zhang Zonghuai 1 ; Gong Yansheng 1 ; Wang Huanwen 1 ; Wang, Rui 1 ; Zhao, Ling 1 ; He Beibei 1   VIAFID ORCID Logo 

 Engineering Research Center of Nano-Geomaterials of Ministry of Education, China University of Geosciences, Department of Material Science and Chemistry, Wuhan, China (GRID:grid.503241.1) (ISNI:0000 0004 1760 9015) 
Publication year
2019
Publication date
Dec 2019
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2190467983
Copyright
This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.