Surface-Modified Porous Carbon Nitride Composites as Highly Efficient Electrocatalyst for Zn-Air Batteries

被引:162
|
作者
Niu, Wenhan [1 ]
Li, Zhao [2 ]
Marcus, Kyle [1 ,2 ]
Zhou, Le [1 ]
Li, Yilun [3 ]
Ye, Ruquan [3 ]
Liang, Kun [1 ]
Yang, Yang [1 ,2 ]
机构
[1] Univ Cent Florida, NanoSci Technol Ctr, Orlando, FL 32826 USA
[2] Univ Cent Florida, Dept Mat Sci & Engn, Orlando, FL 32826 USA
[3] Rice Univ, Dept Chem, 6100 Main St, Houston, TX 77005 USA
关键词
carbon nitride; oxygen evolution reaction; oxygen reduction reaction; porous materials; Zn-air batteries; OXYGEN REDUCTION REACTION; METAL-FREE ELECTROCATALYSTS; EVOLUTION REACTIONS; IN-SITU; PERFORMANCE; NANOSHEETS; GRAPHENE; COBALT; NANOTUBES; CATALYST;
D O I
10.1002/aenm.201701642
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
Porous carbon nitride (PCN) composites are fabricated using a top-down strategy, followed by additions of graphene and CoSx nanoparticles. This subsequently enhances conductivity and catalytic activity of PCN (abbreviated as CoSx@PCN/rGO) and is achieved by one-step sulfuration of PCN/graphene oxides (GO) composite materials. As a result, the as-prepared CoSx@PCN/rGO catalysts display excellent activity and stability toward both oxygen evolution and reduction reactions, surpassing electrocatalytic performance shown by state-of-the-art Pt, RuO2 and other carbon nitrides. Remarkably, the CoSx@PCN/rGO bifunctional activity allows for applications in zinc-air batteries, which show better rechargeability than Pt/C. The enhanced catalytic performance of CoSx@PCN/rGO can primarily be attributed to the highly porous morphology and sufficiently exposed active sites that are favorable for electrocatalytic reactions.
引用
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页数:8
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