详细信息
Nitrogen doped graphene anchored cobalt oxides efficiently bi-functionally catalyze both oxygen reduction reaction and oxygen revolution reaction ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Nitrogen doped graphene anchored cobalt oxides efficiently bi-functionally catalyze both oxygen reduction reaction and oxygen revolution reaction
作者:Wang, Qing[1];Hu, Wenhui[1];Huang, Yongmin[1]
机构:[1]East China Univ Sci & Technol, Sch Chem & Mol Engn, Key Lab Specially Funct Polymer Mat & Related Tec, Minist Educ, Shanghai 200237, Peoples R China
年份:2017
卷号:42
期号:9
起止页码:5899
外文期刊名:INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
收录:;EI(收录号:20171003408780);WOS:【SCI-EXPANDED(收录号:WOS:000399507100027)】;
基金:This work was funded by the National Natural Science Foundation of China (No. 21476071), Shanghai Leading Academic Discipline Project (B502).
语种:英文
外文关键词:Nitrogen doped graphene; Cobalt oxides; Oxygen reduction reaction; Oxygen evolution reaction; Synergistic effect
摘要:A series of efficient bifunctional electrocatalyst composed of nitrogen-doped graphene-cobalt oxide nanoparticles nano-hybrids (Co-N/G) are fabricated by one-pot hydrothermal synthesis, which involves in-situ growth of cobalt oxides nanocrystals and nitrogen doping into graphene. 2, 4, 6-Triaminopyrimidine used as nitrogen precursor could anchor cobalt oxides nanoparticles on graphene oxide as active centers for oxygen electrode reactions. The TEM, Raman, XRD and XPS confirm the germination of nitrogen doped graphene and nano-sized cobalt oxides. The optimized Co-N/G catalyst consists of the highest contents of pyridinic nitrogen and CoO, which efficiently catalyze both ORR and OER. The strong coupling between cobalt oxides and N-graphene endows Co-N/G 600 with a low reversible overvoltage of 0.96 V between ORR and OER in alkaline medium, which is superior to novel catalysts such as Pt/C (1.24 V), IrO2 (1.43 V) and RuO2 (1.35 V), rendering it bi-catalyst efficient and economical for reversible oxygen electrode reactions. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
参考文献:
正在载入数据...
