In situexsolved Co nanoparticles coupled on LiCoO2nanofibers to induce oxygen electrocatalysis for rechargeable Zn-air batteries

被引:38
作者
Gui, Liangqi [1 ]
Liu, Yuzhou [1 ]
Zhang, Jing [1 ]
He, Beibei [1 ,2 ]
Wang, Qing [3 ]
Zhao, Ling [1 ,2 ]
机构
[1] China Univ Geosci, Dept Mat Sci & Chem, Wuhan 430074, Peoples R China
[2] China Univ Geosci Wuhan, Zhejiang Inst, Hangzhou 311305, Peoples R China
[3] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
基金
中国国家自然科学基金;
关键词
DOPED CARBON NANOSHEETS; IN-SITU EXSOLUTION; BIFUNCTIONAL ELECTROCATALYSTS; EVOLUTION REACTION; METALLIC NANOPARTICLES; HIGH-EFFICIENCY; REDUCTION; HYDROGEN; PERFORMANCE; NANOFIBERS;
D O I
10.1039/d0ta07362h
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
Layered lithium cobalt oxide, LiCoO2(LCO), is a promising catalyst for oxygen evolution reaction (OER) and oxygen reduction reaction (ORR); however, its bifunctional activity is still far from desirable. Here, a novel heterointerface of Co@LCO nanofibers (Co@LCO-NFs) is developedviaan elegantin situexsolution approach to promote bifunctionality. Thisin situexsolution promises improved electrical conductivity, rich oxygen vacancies, and in particular a modulated electronic structure, thereby demonstrating a substantially enhanced bifunctional activity. Density functional theory calculations further reveal that the synergistic coupling of LCO and Co results in strengthened covalency of Co-O and facilitated OER/ORR kinetics. As a result, an assembled Zn-air battery using the Co@LCO-NFs electrode delivers high peak power density with competitive cycling stability, favorably outperforming the benchmark Pt/C-IrO(2)based batteries. This protocol provides new insights into designing heterostructured bifunctional catalysts for related energy conversion and storage devices.
引用
收藏
页码:19946 / 19953
页数:8
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