Electrochemical tuning of layered lithium transition metal oxides for improvement of oxygen evolution reaction

被引:524
作者
Lu, Zhiyi [1 ,2 ]
Wang, Haotian [3 ]
Kong, Desheng [1 ]
Yan, Kai [1 ]
Hsu, Po-Chun [1 ]
Zheng, Guangyuan [4 ]
Yao, Hongbin [1 ]
Liang, Zheng [1 ]
Sun, Xiaoming [2 ]
Cui, Yi [1 ,5 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[2] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[3] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[5] Stanford Inst Mat & Energy Sci, SLAC Natl Accelerator Lab, Menlo Pk, CA 94025 USA
关键词
WATER OXIDATION; COBALT OXIDE; NI; CATALYSIS; IRON; ELECTROCATALYSTS; INTERCALATION; PHOSPHATE;
D O I
10.1038/ncomms5345
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Searching for low-cost and efficient catalysts for the oxygen evolution reaction has been actively pursued owing to its importance in clean energy generation and storage. While developing new catalysts is important, tuning the electronic structure of existing catalysts over a wide electrochemical potential range can also offer a new direction. Here we demonstrate a method for electrochemical lithium tuning of catalytic materials in organic electrolyte for subsequent enhancement of the catalytic activity in aqueous solution. By continuously extracting lithium ions out of LiCoO2, a popular cathode material in lithium ion batteries, to Li0.5CoO2 in organic electrolyte, the catalytic activity is significantly improved. This enhancement is ascribed to the unique electronic structure after the delithiation process. The general efficacy of this methodology is demonstrated in several mixed metal oxides with similar improvements. The electrochemically delithiated LiCo0.33Ni0.33Fe0.33O2 exhibits a notable performance, better than the benchmark iridium/carbon catalyst.
引用
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页数:7
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