Ligand-mediated bifunctional catalysis for enhanced oxygen reduction and methanol oxidation tolerance in fuel cells

被引:21
作者
Lu, Linfang [1 ]
Wang, Zhiqiang [2 ,3 ]
Zou, Shihui [1 ]
Zhou, Yuheng [1 ]
Hong, Wei [1 ]
Li, Renhong [4 ]
Xiao, Liping [1 ]
Liu, Juanjuan [5 ]
Gong, Xue-Qing [2 ,3 ]
Fan, Jie [1 ]
机构
[1] Zhejiang Univ, Dept Chem, Key Lab Appl Chem Zhejiang Prov, Hangzhou 310027, Zhejiang, Peoples R China
[2] East China Univ Sci & Technol, Ctr Computat Chem, Key Lab Adv Mat, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Res Inst Ind Catalysis, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China
[4] Zhejiang Sci Tech Univ, Minist Educ China, Key Lab Adv Text Mat & Mfg Technol, Hangzhou 310027, Zhejiang, Peoples R China
[5] Hangzhou Dianzi Univ, Coll Mat & Environm Engn, Hangzhou 310036, Zhejiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
ELECTROCATALYTIC ACTIVITY; NANOPOROUS NANOWIRES; TRANSITION-METALS; PT-NI; PLATINUM; SURFACE; NANOPARTICLES; PERFORMANCE; SELECTIVITY; ALLOY;
D O I
10.1039/c8ta06071a
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
Though it is widely accepted that both electronic and steric effects are important in ligand-regulated heterogeneous catalysis, no experimental method has visually distinguished these two effects. Herein, by controllably tuning the surface coverage of pyridine on Pt nanoparticles, we successfully achieve bifunctional catalysis in direct methanol fuel cells with simultaneously improved oxygen reduction and methanol oxidation tolerance. More importantly, by combining the experimental results and density functional theory calculations, we reveal that the variation of the activity with the surface coverage of pyridine in these two reactions is due to the competition or cooperation between the electronic and steric effects. Other ligand experiments further confirmed the above conjecture. The stability of the pyridine ligand on Pt was also systematically studied in this paper.
引用
收藏
页码:18884 / 18890
页数:7
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