Tunable Cationic Vacancies of Cobalt Oxides for Efficient Electrocatalysis in Li-O2Batteries

被引:208
作者
Liu, Xiaomeng [1 ]
Zhao, Lanling [2 ]
Xu, Haoran [1 ]
Huang, Qishun [1 ]
Wang, Yueqing [3 ]
Hou, Chuanxin [4 ]
Hou, Yuyang [5 ]
Wang, Jun [1 ,3 ]
Dang, Feng [1 ]
Zhang, Jintao [3 ]
机构
[1] Shandong Univ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Minist Educ, Jinan 250061, Peoples R China
[2] Shandong Univ, Sch Phys, Jinan 250100, Peoples R China
[3] Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, Minist Educ, Jinan 250061, Peoples R China
[4] Yantai Univ, Sch Environm & Mat Engn, Yantai 264005, Peoples R China
[5] CSIRO Mineral Resources, Clayton, Vic 3168, Australia
关键词
cationic vacancies; density functional theory; electrocatalysis; Li-O(2)batteries; spinel Co3O4; LITHIUM-OXYGEN BATTERIES; LI-O-2; BATTERIES; CO3O4; NANOSHEETS; BIFUNCTIONAL CATALYST; CATHODE CATALYSTS; FACILE SYNTHESIS; FUEL-CELL; LI; PERFORMANCE; ZINC;
D O I
10.1002/aenm.202001415
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Vacancy engineering is one of the most effective strategies to introduce defects for improving electrocatalytic activities of cobalt oxides. Recent intensive research has been conducted to introduce oxygen vacancies for boosting Li-O(2)battery performance. However, it is difficult to examine the efficiency of cationic vacancies due to their complicated preparation. Herein, a feasible method is demonstrated to introduce cationic vacancies into cobalt oxides via the thermal treatment of glycerolatocobalt (GlyCo) nanostructure. The formation of GlyCo composed of the repeating Co-O-Co-O units provides the possibility to regulate the ratio between cobalt and oxygen, thus cobalt vacancies in cobalt oxides can be easily created by the thermal treatment. The presence of cobalt vacancies enables the regulation of electronic structure and charge-transport properties of cobalt oxides with abundant defects on the basis of the experimental results and theoretical calculations, thus improving electrocatalytic activities. Therefore, the Li-O(2)battery delivers superior electrochemical performance with large specific capacities of 13 331/12 040 mAh g(-1), low overpotentials for the oxygen evolution reaction/oxygen reduction reaction of 1.15/0.23 V and good cycling stability. This work provides a favorable method to create metal vacancies for improving catalytic efficiency of advanced energy materials.
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页数:10
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