Accelerating oxygen evolution reaction via sodium extraction of Na0.71CoO2

被引:8
作者
Wang, Guopeng [1 ]
Yang, He [1 ]
Guan, Jian [1 ]
Huan, Daoming [1 ]
Liu, Yu [1 ]
Cai, Honglei [1 ]
Peng, Ranran [1 ,2 ,3 ,4 ]
Lu, Yalin [1 ,2 ,3 ,4 ]
机构
[1] Univ Sci & Technol China, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
[3] Univ Sci & Technol China, Synerget Innovat Ctr Quantum Informat & Quantum P, Hefei 230026, Anhui, Peoples R China
[4] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230026, Anhui, Peoples R China
关键词
OER; Structure engineering; Na-based; Electrocatalysts; WATER OXIDATION; ELECTROCATALYTIC ACTIVITY; PEROVSKITE; OXIDE;
D O I
10.1016/j.electacta.2018.02.095
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Developing efficient and cost-effective electroctalysts to accelerate the sluggish kinetics of the oxygen evolution reaction (OER) is of great importance to emerging renewable energy technologies. In this work, a chemical sodium extraction of Na from low-cost Na0.71CoO2 electrocatalyst was demonstrated as an effective way to enhance its catalytic activity and durability toward enhancing OER. By continuously extracting sodium ions out of Na0.71CoO2 for 2 days, a low overpotential eta (0.44 V) at 10 mA cm(-2), a good mass activity (65.93 mA mg(-1)) and a small Tafel slope (55 mV dec(-1)) were achieved, which are superior to those of using precious metal oxide IrO2. XPS measurements and BET surface areas investigations suggest that the dramatic improved OER performance should be ascribed to several major factors, including formed Co4+ ions oxidized from Co3+, increased surface oxygen vacancies and enlarged specific surface areas occurred during the Na extraction process. The research here highlights the importance of tuning cation deficiency in Na-based oxides for further designing advanced OER electrocatalysts. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:316 / 322
页数:7
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