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Bimetallic palladium-copper nanoplates with optimized d-band center simultaneously boost oxygen reduction activity and methanol tolerance.

Authors :
Huang, Shaoda
Wang, Jinyan
Hu, Hongyin
Li, Yang
Xu, Fangping
Duan, Fang
Zhu, Han
Lu, Shuanglong
Du, Mingliang
Source :
Journal of Colloid & Interface Science. Jan2023:Part B, Vol. 630, p375-384. 10p.
Publication Year :
2023

Abstract

A simple strategy is developed for synthesis of PdCu nanoplates as efficient ORR electrocatalysts with simultaneously highly methanol tolerance. [Display omitted] The methanol-poisoning of electrocatalysts at the cathodic part of direct methanol fuel cells (DMFCs) can severely degrade the overall efficiency. Therefore, engineering cathodic catalysts with outstanding oxygen reduction activity, and simultaneously, superior methanol tolerance is greatly desired. Herein, bimetallic palladium-copper (PdCu) nanoplates with the optimized d-band center are designed as promising cathodic catalysts for DMFCs. It shows outstanding oxygen reduction activity with a mass activity (MA) of 0.522 A mg Pd −1 in alkaline electrolyte, overwhelming the benchmarked commercial Pt/C and Pd/C. Meanwhile, it has prominent stability with only 4.0 % loss in MA after continuous 20 K cycles. More importantly, the PdCu nanoplates are almost inert toward methanol oxidation and show excellent anti-methanol capability. The theoretical calculations reveal that the downshift of d-band center in PdCu nanoplates and the electronic interaction between Pd and Cu atoms could effectively lower the methanol adsorption energy, thus leading to enhanced methanol tolerance. This work highlights the important role of tuning the electronic structure and optimized geometry of electrocatalysts to simultaneously boost their oxygen reduction activity, stability, and methanol tolerance for their future application in DMFCs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219797
Volume :
630
Database :
Academic Search Index
Journal :
Journal of Colloid & Interface Science
Publication Type :
Academic Journal
Accession number :
160332502
Full Text :
https://doi.org/10.1016/j.jcis.2022.09.139