Bifunctional Composite Catalysts Using Co3O4 Nanofibers Immobilized on Nonoxidized Graphene Nanoflakes for High-Capacity and Long-Cycle Li-O2 Batteries

被引:327
作者
Ryu, Won-Hee [1 ]
Yoon, Taek-Han [2 ]
Song, Sung Ho [1 ,3 ]
Jeon, Seokwoo [1 ,3 ]
Park, Yong-Joon [2 ]
Kim, Il-Doo [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, Taejon 305701, South Korea
[2] Kyonggi Univ, Dept Adv Mat Engn, Suwon 443760, Gyeonggi Do, South Korea
[3] Korea Adv Inst Sci & Technol, KAIST Inst NanoCentury, Graphene Res Ctr, Taejon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
Lithium-oxygen batteries; graphene nanoflake; electrospinning; composite catalyst; nanofiber; LITHIUM-OXYGEN BATTERIES; LI-AIR BATTERIES; TRANSMISSION ELECTRON-MICROSCOPY; ELECTROCATALYTIC ACTIVITY; THERMAL-CONDUCTIVITY; REDUCTION REACTION; LI/AIR BATTERIES; IN-SITU; PERFORMANCE; NANOSHEETS;
D O I
10.1021/nl401868q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Designing a highly efficient catalyst is essential to improve the electrochemical performance of Li-O-2 batteries for long-term cycling. Furthermore, these batteries often show significant capacity fading due to the irreversible reaction characteristics of the Li2O2 product. To overcome these limitations, we propose a bifunctional composite catalyst composed of electrospun one-dimensional (ID) Co3O4 nanofibers (NFs) immobilized on both sides of the 2D nonoxidized graphene nanoflakes (GNFs) for an oxygen electrode in Li-O-2 batteries. Highly conductive GNFs with noncovalent functionalization can facilitate a homogeneous dispersion in solution, thereby enabling simple and uniform attachment of ID Co3O4 NFs on GNFs without restacicing. High first discharge capacity of 10 500 mAh/g and superior cyclability for 80 cycles with a limited capacity of 1000 mAh/g were achieved by (i) improved catalytic activity of ID Co3O4 NFs with large surface area, (ii) facile electron transport via interconnected GNFs functionalized by Co3O4 NFs, and (iii) fast O-2 diffusion through the ultrathin GNF layer and porous Co3O4 NF networks.
引用
收藏
页码:4190 / 4197
页数:8
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