NiO electrode for methanol electro-oxidation: Mesoporous vs. nanoparticulate

被引:81
作者
Gu, C. D. [1 ,2 ]
Huang, M. L. [1 ,2 ]
Ge, X. [1 ,2 ]
Zheng, H. [1 ,2 ]
Wang, X. L. [1 ,2 ]
Tu, J. P. [1 ,2 ]
机构
[1] Zhejiang Univ, State Key Lab Silicon Mat, Dept Mat Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] Key Lab Adv Mat & Applicat Batteries Zhejiang Pro, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Homogeneous precipitation; Deep eutectic solvent; Nickel oxide; Electrocatalyst; Direct methanol fuel cell; ENHANCED ELECTROCATALYTIC ACTIVITY; WALLED CARBON NANOTUBES; ANION-EXCHANGE MEMBRANE; REDUCED GRAPHENE OXIDE; DEEP EUTECTIC SOLVENTS; CHOLINE CHLORIDE; HYDROTHERMAL SYNTHESIS; SURFACE-AREA; IONIC-LIQUID; FUEL-CELLS;
D O I
10.1016/j.ijhydene.2014.05.028
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
Two NiO products with different microstructures have been obtained using a traditional NaOH-induced aqueous-phase precipitation and a homogeneous precipitation in choline chloride/urea mixture-based deep eutectic solvent (DES), respectively. The synthesis processes play a key role in the structure construction of NiO precursors as well as the final NiO products, and possible formation mechanisms are proposed. The DES-based homogeneous precipitation method provides plentiful nucleation sites, moderate crystal growth process and possible template effect, which could conduce to the production of flower-like NiO with continuously self-supporting mesoporous structure assembled by tiny grains. The flower-like NiO electrode exhibits higher current density, faster charge-transfer process, better electrode accessibility, and improved stability for methanol electro-oxidation in an electrolyte of 0.1 M CH3OH + 0.005 M KOH than the disorderly aggregated NiO nanoparticles. We believe that the DES-based homogeneous precipitation method can provide an effective approach to fabricate advanced electrocatalyst materials with homogeneous and well-assembled microstructure. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:10892 / 10901
页数:10
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