Palladium atomic layers coated on ultrafine gold nanowires boost oxygen reduction reaction

被引:6
|
作者
Wei, Di-Ye
Xing, A. Guan-Nan
Chen, A. Heng-Quan
Xie, Xiao-Qun [1 ]
Huang, Hui-Mei
Dong, Jin-Chao
Tian, Jing-Hua [2 ]
Zhang, Hua [1 ,2 ]
Li, Jian-Feng [1 ,2 ,3 ,4 ]
机构
[1] Xiamen Univ, MOE Key Lab Spectrochem Anal & Instrumentat, State Key Lab Phys Chem Solid Surfaces, iChEM,Coll Chem & Chem Engn,Coll Mat,Fujian Key La, Xiamen 361005, Peoples R China
[2] Innovat Lab Sci & Technol Energy Mat Fujian Prov I, Xiamen, Peoples R China
[3] Xiamen Univ, Shenzhen Res Inst, Shenzhen 518000, Peoples R China
[4] China Jiliang Univ, Coll Opt & Elect Technol, Hangzhou 310018, Peoples R China
关键词
Oxygen reduction reaction; Ultrafine nanowires; Pd -based catalysts; Core -shell nanostructures; Fuel cells; ELECTROCATALYSTS; NANOPARTICLES; CATALYSTS; SURFACE; RAMAN;
D O I
10.1016/j.jcis.2023.07.080
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
Palladium-based nanocatalysts play an important role in catalyzing the cathode oxygen reduction reaction (ORR) for fuel cells working under alkaline conditions, but the performance still needs to be improved to meet the requirements for large-scale applications. Herein, Au@Pd core-shell nanowires have been developed by coating Pd atomic layers on ultrafine gold nanowires and display outstanding electrocatalytic performance towards alkaline ORR. It is found that Pd overlayers with atomic thickness can be coated on 3 nm Au nanowires under CO atmosphere and completely cover the surfaces. The obtained ultrafine Au@Pd nanowires exhibit an electrochemical active area (ECSA) of 68.5 m(2)/g and a mass activity of 0.91 A/mg (at 0.9 V vs. RHE), which is around 3.1 and 15.2 times higher than that of commercial Pd/C. The activity loss of the ultrafine Au@Pd nanowire after 10,000 cycles of accelerated degradation tests is only similar to 20 %, demonstrating its much better stability compared to commercial Pd/C. Further characterizations combined with density functional theory (DFT) calculations
引用
收藏
页码:1518 / 1524
页数:7
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