Improved ethanol electro-oxidation at Ni@Pd/C and Ni@PdRh/C core-shell catalysts

被引:40
|
作者
Almeida, Caio V. S. [1 ,2 ]
Tremiliosi-Filho, Germano [3 ]
Eguiluz, Katlin I. B. [1 ,2 ]
Salazar-Banda, Giancarlo R. [1 ,2 ]
机构
[1] Inst Technol & Res, Lab Electrochem & Nanotechnol, BR-49032490 Aracaju, Sergipe, Brazil
[2] Univ Tiradentes, Proc Engn Postgrad Program, BR-49032490 Aracaju, Sergipe, Brazil
[3] Univ Sao Paulo, Inst Chem Sao Carlos, POB 780, BR-13560970 Sao Paulo, Brazil
关键词
Fuel cells; Trimetallic catalyst; PdNiRh-based electrocatalyst; Core-shell nanostructure; Ethanol oxidation; Alkaline media; ALKALINE DIRECT ETHANOL; IN-SITU FTIR; CARBON-SUPPORTED PALLADIUM; OXYGEN REDUCTION REACTION; REDUCED GRAPHENE OXIDE; ONE-POT SYNTHESIS; FORMIC-ACID; METHANOL ELECTROOXIDATION; ELECTROCATALYTIC ACTIVITY; ALLOY NANOPARTICLES;
D O I
10.1016/j.jcat.2020.08.024
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
This paper describes the synthesis and catalytic activity of carbon-supported Pd/C, PdNi/C, and PdNiRh/C catalysts with core-shell morphologies towards the oxidation of ethanol in alkaline media. The catalysts are synthesised by a chemical reduction method using sodium borohydride as the reducing agent. Electrochemical characterisations show that the addition of Ni and Rh enhances remarkably the electrocatalytic activity of the materials due to the bifunctional and electronic effects in PdNi/C and PdNiRh/C catalysts, and the synergetic effect of the bifunctional and core-shell morphology on the Ni@Pd/C and Ni@PdRh/C catalysts. Electrochemical impedance spectra reveal lower values of charge transfer resistance for Pd60Ni20Rh20/C and Ni-20@Pd60Rh20/C. Chronoamperometric tests also reveal the Ni-20@Pd60Rh20/C catalyst displays current densities 9.3 times higher than the Pd/C catalyst. The superior catalytic performance of the trimetallic core-shell Ni-20@Pd60Rh20/C catalyst can result from the synergy between the metals and the presence of core-shell morphology. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:175 / 189
页数:15
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