Clean Electrochemical Synthesis of Pd-Pt Bimetallic Dendrites with High Electrocatalytic Performance for the Oxidation of Formic Acid

被引:3
|
作者
Liu, Jie [1 ]
Li, Fangchao [1 ]
Zhong, Cheng [1 ,2 ,3 ,4 ]
Hu, Wenbin [1 ,2 ,3 ,4 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Minist Educ, Key Lab Adv Ceram & Machining Technol, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Mat Sci & Engn, Tianjin Key Lab Composite & Funct Mat, Tianjin 300072, Peoples R China
[3] Joint Sch Natl Univ Singapore, Fuzhou 350207, Peoples R China
[4] Int Campus Tianjin Univ, Tianjin Univ, Fuzhou 350207, Peoples R China
基金
中国国家自然科学基金;
关键词
electrochemical synthesis; Pd-Pt dendrites; formic acid oxidation; high electrocatalytic performance; REDUCED GRAPHENE OXIDE; CARBON NANOTUBES; METHANOL ELECTROOXIDATION; CATALYTIC PERFORMANCE; ALLOY NANOPARTICLES; FACILE SYNTHESIS; ETHANOL; NANOCRYSTALS; CO; NANOCOMPOSITE;
D O I
10.3390/ma15041554
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
Pd-Pt bimetallic catalysts with a dendritic morphology were in situ synthesized on the surface of a carbon paper via the facile and surfactant-free two step electrochemical method. The effects of the frequency and modification time of the periodic square-wave potential (PSWP) on the morphology of the Pd-Pt bimetallic catalysts were investigated. The obtained Pd-Pt bimetallic catalysts with a dendritic morphology displayed an enhanced catalytic activity of 0.77 A mg(-1), almost 2.5 times that of the commercial Pd/C catalyst reported in the literature (0.31 A mg(-1)) in acidic media. The enhanced catalytic activity of the Pd-Pt bimetallic catalysts with a dendritic morphology towards formic acid oxidation reaction (FAOR) was not only attributed to the large number of atomic defects at the edges of dendrites, but also ascribed to the high utilization of active sites resulting from the "clean" electrochemical preparation method. Besides, during chronoamperometric testing, the current density of the dendritic Pd-Pt bimetallic catalysts for a period of 3000 s was 0.08 A mg(-1), even four times that of the commercial Pd/C catalyst reported in the literature (about 0.02 A mg(-1)).
引用
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页数:13
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