N,S dual-doped carbon nanosheet networks with hierarchical porosity derived from biomass of Allium cepa as efficient catalysts for oxygen reduction and Zn-air batteries

被引:33
作者
Zhang, Jimin [1 ]
He, Jing [1 ]
Zheng, Hongying [1 ]
Li, Rong [1 ]
Gou, Xinglong [1 ]
机构
[1] China West Normal Univ, Coll Chem & Chem Engn, Chem Synth & Pollut Control Key Lab Sichuan Prov, Nanchong, Peoples R China
基金
中国国家自然科学基金;
关键词
REDUCED GRAPHENE OXIDE; CODOPED POROUS CARBON; METAL-FREE CATALYST; BIFUNCTIONAL ELECTROCATALYSTS; MESOPOROUS CARBON; FACILE SYNTHESIS; NITROGEN; SULFUR; PERFORMANCE; ELECTRODE;
D O I
10.1007/s10853-020-04535-4
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Efficient metal-free electrocatalysts for oxygen reduction reactions (ORR) have been actively pursued in recent years to promote the application of fuel cells and metal-air batteries. In this work, hierarchically porous nitrogen and sulfur dual-doped carbon nanosheet networks (N,S-HPC) were facilely synthesized by pyrolysis of Allium cepa chips impregnated with thiourea and KOH. The as-prepared N,S-HPC featured high content of N and S dopants (5.32 at.% for N and 2.23 at.% for S, respectively), abundant catalytically active sites, unique hierarchically porous architecture, large surface area (1859 m(2) g(-1)) and exhibited remarkable electrocatalytic activity toward ORR with positive onset/half-wave potential and large limiting diffusion current. In addition, N,S-HPC showed much better long-time stability and resistance to methanol crossover than Pt/C did. When used as the cathodic catalysts of Zn-air battery, N,S-HPC outperformed Pt/C in terms of the open-circuit potential, discharge current density, peak power density, specific capacity and rate performance, showing promise as an alternative to Pt/C for application in fuel cells and metal-air batteries.
引用
收藏
页码:7464 / 7476
页数:13
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