纳米颗粒
电催化剂
材料科学
催化作用
铂金
双金属片
化学工程
氧还原反应
铂纳米粒子
壳体(结构)
金属
纳米材料基催化剂
贵金属
钯
纳米技术
单层
过渡金属
胶体金
作者
Xiaokun Li,Youlin Zhang,Xiaowen Wang,Wei Chen
出处
期刊:Zhongguo kexue
[Science in China Press]
日期:2017-04-17
卷期号:47 (5): 655-662
被引量:1
标识
DOI:10.1360/n032016-00211
摘要
We have developed for the first time an Au-catalytic-reduction strategy to synthesize the core-shell structured Au@Pt nanoparticles (NPs). In the synthesized Au@Pt NPs, only monolayer Pt shell can be formed by the catalytic reduction of Pt2+in the presence of 15 nm Au NPs in HEPES buffer at room temperature. The structure and morphology of the as-prepared Au@Pt NPs were characterized by UV-visible absorption spectrum (UV-Vis), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and inductively coupled plasma-atomic emission spectrum (ICP-AES). Electrochemical measurements displayed that the core-shell structured Au@Pt NPs with a monolayer Pt shell have good electrocatalytic performance for oxygen reduction reaction (ORR). The specific electrochemical surface area (ECSA, 183.40 cm2/mgPt) and mass activity (573.20 mA/mgPt at −0.075 V) of Au@Pt NPs were found to be 1.72 and 5.06 times higher than those of commercial Pt/C catalyst (102 cm2/mgPt, 113.39 mA/mgPt), respectively.
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