Synthesis of core/shell structured Pd3Au@Pt/C with enhanced electrocatalytic activity by regioselective atomic layer deposition combined with a wet chemical method

被引:14
作者
Liu, Huiyuan [1 ,2 ,3 ]
Song, Yujiang [2 ]
Li, Shushuang [1 ]
Li, Jia [2 ]
Liu, Yuan [1 ,4 ]
Jiang, Ying-Bing [5 ]
Guo, Xinwen [2 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Labs Clean Energy, Dalian 116023, Liaoning, Peoples R China
[2] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Liaoning, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
[4] Chinese Acad Sci, CIGIT, Chongqing 400714, Peoples R China
[5] Univ New Mexico, Dept Earth & Planetary Sci, Albuquerque, NM 87131 USA
来源
RSC ADVANCES | 2016年 / 6卷 / 71期
基金
中国国家自然科学基金;
关键词
OXYGEN REDUCTION REACTION; CORE-SHELL NANOPARTICLES; PLATINUM-MONOLAYER SHELL; FUEL-CELLS; PERFORMANCE; CATALYSTS; NANOCATALYSTS; STABILITY; HYDROGEN; DESIGN;
D O I
10.1039/c6ra04990g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the synthesis of Pd3Au@Pt/C by atomic layer deposition (ALD) combined with a wet chemical method. Initially, nearly uniform Pd3Au nanoparticles (NPs) (similar to 4.7 nm) supported on carbon with a loading of similar to 20 wt% were prepared by reducing metal complexes confined in reverse micelles adsorbed on carbon. Next, a Pt thin layer (less than 1 nm) was selectively deposited on purified Pd3Au particles instead of on carbon by regioselective ALD that likely arises from the coverage of nucleation sites on carbon by surfactant molecules in conjunction with catalytic decomposition of the Pt precursor on Pd3Au. The resulting core-shell structured material was subject to TEM, HAADF-STEM/EDX, XRD, XPS and electrochemical measurements. Interestingly, Pd3Au@Pt/C demonstrates a significantly improved electrocatalytic activity toward both formic acid oxidation reaction (FAOR) and oxygen reduction reaction (ORR) compared with Pd3Au/C and state-of-the art Pt/C. This study opens up a unique avenue for the synthesis core/shell structured materials with potential applications in catalysis, electrocatalysis, and so on.
引用
收藏
页码:66712 / 66720
页数:9
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