Ordered mesoporous carbons (OMCs) as supports of electrocatalysts for direct methanol fuel cells (DMFCs): Effect of the pore characteristics of OMCs on DMFCs

被引:25
作者
Sun, Zhi-Peng [1 ]
Zhang, Xiao-Gang [1 ]
Liang, Yan-Yu [1 ,2 ]
Tong, Hao [1 ]
Xue, Rui Li [1 ]
Yang, Su Dong [1 ]
Li, Hu-Lin [1 ,3 ]
机构
[1] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Engn, Nanjing 210016, Peoples R China
[2] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[3] Lanzhou Univ, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
Ordered mesoporous carbons; Soft template methods; Pore characteristics; Pt nanoparticles; Electrocatalytic activities; PLATINUM NANOPARTICLES; CATALYST SUPPORTS; OXIDATION; SILICA; MESOSTRUCTURE; NANOFIBERS; NANOTUBES;
D O I
10.1016/j.jelechem.2009.04.013
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Two types of ordered mesoporous carbons (OMCs-FT and OMCs-F) with different hexagonal pore frameworks were synthesized via two soft template routes. Structural characterizations revealed that OMCs-FT possessed broader mesopore range, more enhanced mesoporosity and higher surface area, compared with the counterpart of OMCs-F. In order to systematically investigate the relationship between the pore characteristics and electrochemical performances, two catalysts of OMCs-FT/Pt and OMCs-F/Pt were achieved by ethylene glycol-assisted reduction procedure. X-ray diffraction (XRD) and transmission electron microscopy (TEM) measurements indicated that face-centered cubic Pt nanoparticles with an average size of 5.3 nm were homogeneously deposited on OMCs-FT while the mean size of 5.5 nm Pt nanoparticles had a relatively ransom dispersion on OMCs-F supports with some aggregations. The electrochemical results disclosed that OMCs-FT/Pt catalyst exhibited higher electrocatalytic activity and better stability than OMCs-F/Pt and commercially available E-TEK/Pt catalysts for methanol electro-oxidation. The broad mesopore range, enhanced mesoporosity and high surface area of OMCs-FT supports were considered to be the main reasons for its enhanced catalytic activity. (C) 2009 Published by Elsevier B.V.
引用
收藏
页码:1 / 6
页数:6
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