Platinum-decorated palladium-nanoflowers as high efficient low platinum catalyst towards oxygen reduction

被引:10
|
作者
Zhang, Bingqing [1 ,2 ,3 ,4 ]
Yu, Jinnan [1 ,2 ]
Tang, Haibo [1 ,2 ]
Du, Li [1 ,2 ]
Li, Can [3 ]
Liao, Shijun [1 ,2 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, Key Lab Fuel Cell Technol Guangdong Prov, Guangzhou 510641, Guangdong, Peoples R China
[2] South China Univ Technol, Sch Chem & Chem Engn, Key Lab New Energy Technol Guangdong Univ, Guangzhou 510641, Guangdong, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, State Key Lab Catalysis, Dalian 116023, Peoples R China
[4] Hubei Engn Univ, Fac Chem & Mat Sci, Xiaogan 432100, Hubei, Peoples R China
基金
美国国家科学基金会;
关键词
Palladium-nanoflowers; Platinum-decorated; Underpotential deposition; Oxygen reduction reaction; MONOLAYER ELECTROCATALYSTS; O-2; REDUCTION; FUEL-CELLS; SHELL; NANOPARTICLES; CO; PERFORMANCE; DEPOSITION; SURFACES; LAYERS;
D O I
10.1016/j.ijhydene.2017.07.135
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
A three-dimensional, low platinum (Pt) catalyst was prepared by decorating platinum on the palladium nanoflowers (Pd-NF) by an underpotential deposition (UPD) method. The Pd-NF was synthesized by a solvothermal approach, using oleic acid as the template and benzyl alcohol as the solvent-reducing agent. The obtained Pd with a morphology of uniform nanoflowers is composed of plentiful nanosheets. After decorating with platinum, the catalyst Pd-NF@Pt exhibits much higher activity for the oxygen reduction reaction (ORR) compared to commercial Pt/C (Pt 20 wt%). The interaction between deposited Pt and Pd-NF was revealed by XPS analysis, and the high performance of the Pd-NF@Pt catalyst was attributed to following two aspects: the increased of dispersion of platinum based on Pd-NF substrate, and the increased intrinsic activity of the active sites caused by the interaction of Pt and Pd NF. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:22909 / 22914
页数:6
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