In-situ reaction-growth of PtNiX nanocrystals on supports for enhanced electrochemical catalytic oxidation of ethanol via continuous flow microfluidic process

被引:11
作者
Wang, Junmei
Ye, Huanyu
Song, Yujun [1 ]
机构
[1] Univ Sci & Technol Beijing, Sch Math & Phys, Ctr Modern Phys Technol, Beijing 100083, Peoples R China
关键词
Pt-based electrocatalysts; Ethanol electro-oxidation; Microfluidic; In-situ reaction; Ultra-small nanocrystal; OXYGEN REDUCTION REACTION; HIGH-PERFORMANCE; ELECTROCATALYTIC ACTIVITY; PLATINUM; NANOPARTICLES; ELECTROOXIDATION; METAL; CARBON; NANOCATALYSTS; CONSEQUENCES;
D O I
10.1016/j.electacta.2018.05.013
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
An in-situ composite methodology was first proposed to prepare carbon supported PtNix (X = 1, 3, 1/3) via online reaction, nucleation and growth of nanocrystals (NCs) on carbon support along the microfluidic channel. Uniform dispersed ultra-small PtNiX NCs (1 nm(-3) nm) with high surface exposed Pt atoms and enhanced nanocrystal-carbon interface interaction can be constructed. The annealed nanocomposites with a Pt/Ni ratio of 1/3 exhibit a mass catalytic activity of 7.6 times higher than the commercial Pt/C nanocatalysts in the ethanol oxidation reaction. The chronoamperometry measurement indicates that their mass activity still retains 3.6 times of the commercial Pt/C nanocatalysts at 4000 s. Moreover, PtNi3/C nanocatalysts have the highest tolerance to CO poisoning according to CO stripping measurements. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:149 / 155
页数:7
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