Oxygen Reduction Electrocatalyst of Pt on Au Nanoparticles through Spontaneous Deposition

被引:47
作者
Dai, Yu [1 ,2 ]
Chen, Shengli [2 ]
机构
[1] China Univ Geosci, Fac Mat Sci & Chem, Wuhan 430074, Peoples R China
[2] Wuhan Univ, Dept Chem, Hubei Electrochem Power Sources Key Lab, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
core-shell structure; gold; low-platinum electrocatalyst; oxygen reduction reaction; spontaneous deposition; CARBON-MONOXIDE OXIDATION; SINGLE-CRYSTAL; RU SURFACES; ELECTRODES; HYDROGEN; COVERAGE; AU(111); GROWTH; BARE;
D O I
10.1021/am5073029
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A straightforward one-step spontaneous deposition approach for growth of Pt atomic shell on Au nanoparticles and the superior activity and durability of the resulted Pt-on-Au nanoparticles for the oxygen reduction reaction (ORR) are reported. Transmission electron microscopy, X-ray photoelectron spectroscopy, energy-dispersive spectrometry, and electrochemical measurements indicate that Pt can be spontaneously deposited on Au surface upon simply dispersing carbon-supported Au nanoparticles in PtCl42- Containing solution, without introducing any extraneous reducing agents or any pre/post-treatments. The deposited Pt atoms are uniformly distributed on the surface of Au nanoparticles, with coverage tunable by the concentration of PtCl42 and temperatures. An approximate monolayer of Pt forms at temperature of ca. 80 degrees C and PtCl42- concentrations of above 10(-4) mol/L. The obtained Pt-on-Au coreshell nanoparticles catalyze the ORR with specific and mass activities of Pt that are 3.5 times higher than that of pure Pt nanoparticles. Moreover, they exhibit no visible activity degradation after undergoing long-term oxidization/reduction cycling in O-2-saturated acid media, therefore showing great prospect as durable cathode electrocatalysts in proton-exchange membrane fuel cells.
引用
收藏
页码:823 / 829
页数:7
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