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Composition- and size-engineering of porous PdAg alloy for high-performance ethanol electrooxidation.

Authors :
Fang, Caihong
Xu, Xiaoxiao
Zhao, Jian
Cui, Zhiqing
Yu, Nan
Bi, Ting
Hu, Jinwu
Jiang, Xiaomin
Source :
Journal of Alloys & Compounds. Oct2019, Vol. 806, p239-245. 7p.
Publication Year :
2019

Abstract

Control over the architecture, elemental distribution, composition and size of metal bimetallic nanocrystals can effectively manipulate and improve their catalytic performances. Herein, we construct the PdAg bimetallic nanostructures with Pd and Ag overlapped distribution to form an alloy feature via an easy operation method at ambient conditions. The prepared PdAg alloy nanocrystals are porous that composed of numerous branches on their surfaces with a composition of Pd 100 Ag 0 to Pd 61 Ag 39 and a size ranging from 16.4 ± 1.8 to 45.0 ± 1.5 nm. Impressively, after detail size- and composition-dependent electrocatalytic evaluations toward ethanol oxidation in alkaline, the Pd 67 Ag 33 nanocrystals with a size of 27.0 ± 1.2 nm exhibit the highest mass activity (1394.49 mA mg−1), which is 4.77 and 5.46 times of porous Pd NCs and commercial Pd/C, respectively. Besides, the durability during electrocatalytic tests were also highly improved. The excellent electrocatalytic property is ascribed to the synergistic effect between Pd and Ag, the high surface area brought by the porous and branched morphology, as well as the proper size the alloy electrocatalysts provided. Image 1 • Porous PdAg nanoalloy with tuneable composition and size were successfully synthesized using an easy-operation process. • The alloy feature and porous architecture provide synergistic effect and high active area. • The prepared PdAg alloy exhibits higher catalytic activity and durability toward ethanol electrooxidation in alkaline. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
806
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
138545600
Full Text :
https://doi.org/10.1016/j.jallcom.2019.07.174