Porous and single-crystalline-like molybdenum nitride nanobelts as a non-noble electrocatalyst for alkaline fuel cells and electrode materials for supercapacitors

被引:59
|
作者
Liu, J. [1 ,2 ]
Huang, K. [3 ,4 ]
Tang, H. L. [5 ]
Lei, M. [3 ,4 ]
机构
[1] Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2522, Australia
[2] Cent South Univ, Sch Mat Sci & Engn, Changsha 410083, Hunan, Peoples R China
[3] Beijing Univ Posts & Telecommun, State Key Lab Informat Photon & Opt Commun, Beijing 100876, Peoples R China
[4] Beijing Univ Posts & Telecommun, Sch Sci, Beijing 100876, Peoples R China
[5] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
Porous Mo2N nanobelts; Oxygen reduction reactions; AFCs; Supercapacitors; OXYGEN REDUCTION; TRANSFORMATION; CATALYST; GRAPHENE; GAS;
D O I
10.1016/j.ijhydene.2015.11.086
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
Replacing precious and nondurable Pt catalysts with cheap materials is a key issue for commercialization of fuel cells. Intriguing transition metal nitrides (TMNs) have attracted great attentions as promising economic alternatives to Pt catalysts due to their noble metal-like properties. However, most of as-synthesized TMNs are nanoparticles until now. Clearly, the practical catalytic activities of such materials have hitherto been intrinsically restricted by the relatively small surface area and poor crystallinity of nanoparticles. Here, highly porous and "single-crystal-like" Mo2N nanobelts with high density of nanopores have been synthesized on gram-scale. These novel Mo2N nanobelts exhibited high electrocatalytic activity in alkaline electrolyte even better than that of other non-Pt materials and appear to be promising Pt-free cathodic electrocatalysts in alkaline fuel cells. This discovery reveals a new type of metal nitride ORR catalyst and appear to be promising Pt-free cathodic electrocatalysts in alkaline fuel cells. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:996 / 1001
页数:6
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