Engineering high-entropy alloy nanowires network for alcohol electrooxidation

被引:40
|
作者
Fan, Dongping [1 ]
Guo, Ke [1 ]
Zhang, Yan [1 ]
Hao, Qiaoqiao [1 ]
Han, Min [2 ]
Xu, Dongdong [1 ]
机构
[1] Nanjing Normal Univ, Jiangsu Collaborat Innovat Ctr Biomed Funct Mat, Sch Chem & Mat Sci, Jiangsu Key Lab New Power Batteries, Nanjing 210023, Peoples R China
[2] Fujian Normal Univ, Fujian Cross Strait Inst Flexible Elect Future Tec, Fuzhou 350117, Peoples R China
关键词
High-entropy alloys; Nanowires; Alcohol electrooxidation; Surfactant assembly; Noble metal; ELECTROCATALYTIC ACTIVITY; ETHANOL OXIDATION; ULTRATHIN; NANOSTRUCTURES; CATALYSIS; PROGRESS;
D O I
10.1016/j.jcis.2022.06.105
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
High-entropy noble metals have attracted significant attention owning to their unique physicochemical characteristics. Here we report a simple method for the preparation of high-entropy PdPtCuAgAu nanowire networks using carboxyl-functionalized surfactants as soft templates. This PdPtCuAgAu alloy electrocatalysts possess synergetic compositional (e.g., high-entropy effect, sluggish diffusion effect, and lattice distortion effect) and structural (anisotropic and thin nanowires) advantages. The PdPtCuAgAu alloy electrocatalysts exhibit significantly enhanced electrocatalytic performance toward ethanol oxidation reaction, including high mass activity (7.7 A mg(Pd+Pt)(-1)), superior stability/durability, anti-poisoning ability, and fine electrocatalytic kinetics. Similar improvements in electrocatalytic performance are also seen in reactions involving other alcohols such as ethylene glycol and methanol. The high-entropy characteristics synergistically attributed to the enhanced electrocatalytic ability for different reaction process. This approach for the synthesis of high-entropy alloys will provide a new route to rationally design other high-entropy nanocatalysts with desired morphologies/structure and functions for a wide range of (electro)catalytic applications. (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:1012 / 1021
页数:10
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