Pd/CuO-Ni(OH)2/C as a highly efficient and stable catalyst for the electrocatalytic oxidation of ethanol

被引:68
|
作者
Zhang, Sifan [1 ]
Pei, An [1 ]
Li, Guang [2 ]
Zhu, Lihua [1 ,5 ,6 ]
Li, Guoda [1 ]
Wu, Fengshun [1 ]
Lin, Shuting [1 ]
Chen, Wenqi [1 ]
Chen, Bing Hui [2 ]
Luque, Rafael [3 ,4 ]
机构
[1] Jiangxi Univ Sci & Technol, Fac Mat Met & Chem, Coll Chem & Chem Engn, Jiangxi Prov Key Lab Funct Mol Mat Chem, Ganzhou 341000, Jiangxi, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Natl Engn Lab Green Prod Alcohols Ethers Esters, Xiamen 361005, Peoples R China
[3] Univ Cordoba, Dept Quim Organ, Campus Rabanales,Edificio Marie Curie C-3, E-14071 Cordoba, Spain
[4] Peoples Friendship Univ Russia, RUDN Univ, 6 Miklukho Maklaya Str, Moscow 117198, Russia
[5] South China Univ Nchnol, Key Lab Fuel Cell Technol Guangdong Prov, Guangzhou 510640, Peoples R China
[6] South China Univ Technol, Guangdong Prov Key Lab Green Chem Prod Technol, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
OXYGEN REDUCTION; ELECTROOXIDATION; PERFORMANCE; ALLOY; NANOPARTICLES; PALLADIUM; METHANOL; PT/C; NANOCATALYSTS; STABILITY;
D O I
10.1039/d1gc04799j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel-Pd/CuO-Ni(OH)(2)/C catalyst utilizing carbon black as a support was successfully synthesized using hydrazine hydrate reduction and galvanic replacement strategies and was subsequently tested for activity in the electrocatalytic oxidation of ethanol. The observed peak current density (3.74 A mg(Pd)(-1)) for Pd/CuO-Ni(OH)(2)/C was 19.68 times higher than that of commercial Pd/C (0.19 A mg(Pd)(-1)). The as-synthesized Pd/CuO-Ni(OH)(2)/C (hereafter denoted as PdCuNi/C) catalyst exhibited a significantly improved electrocatalytic activity and durability compared with Pd/C, PdNi/C, PdCu/C and the PdCuNi/C catalysts reduced in N-2/H-2 at different temperatures. The reason for this is that the high dispersion of Pd resulted in the exposure of more active sites on the surface of the catalyst. The excellent CO2 selectivity of Pd/CuO-Ni(OH)(2)/C (22.5%) for the ethanol electronic oxidation reaction (EOR) was observed using in situ Fourier transform infrared spectroscopy (FTIR) spectra and could be attributed to the synergistic effect of Pd, CuO and Ni(OH)(2) and the presence of the OHad adsorption at Ni(OH)(2) at a low potential.
引用
收藏
页码:2438 / 2450
页数:13
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