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Facile Fabrication of Robust Hydrogen Evolution Electrodes under High Current Densities via Pt@Cu Interactions.

Authors :
Tan, Yeshu
Xie, Ruikuan
Zhao, Siyu
Lu, Xuekun
Liu, Longxiang
Zhao, Fangjia
Li, Chunzhong
Jiang, Hao
Chai, Guoliang
Brett, Dan J. L.
Shearing, Paul R.
He, Guanjie
Parkin, Ivan P.
Source :
Advanced Functional Materials. 11/3/2021, Vol. 31 Issue 45, p1-12. 12p.
Publication Year :
2021

Abstract

Durable and efficient hydrogen evolution reaction (HER) electrocatalysts that can satisfy industrial requirements need to be developed. Platinum (Pt)‐based catalysts represent the benchmark performance but are less studied for HER under high current densities in neutral electrolytes due to their high cost, poor stability, and extra water dissociation step. Here a facile and low‐temperature synthesis for constructing "blackberry‐shaped" Pt nanocrystals on copper (Cu) foams with low loading as self‐standing electrodes for HER in neutral media is proposed. Optimized hydrogen adsorption free energy and robust interaction induced by charge density exchange between Pt and Cu ensure the efficient and robust HER, especially under high current densities, which are demonstrated from both experimental and theoretical approaches. The electrode exhibits small overpotentials of 35 and 438 mV to reach current densities of ‐10 and ‐1000 mA cm−2, respectively. Meanwhile the electrode illustrates outstanding stability during chronoamperometry measurement under high current densities (‐100 to ‐400 mA cm−2) and 1000 cycles linear sweep voltammetry tests reaching ‐1000 mA cm−2. This study provides new design strategies for self‐standing electrocatalysts by fabricating robust metal–metal interactions between active materials and current collectors, thus facilitating the stable function of electrodes for HER under technologically relevant high current densities. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1616301X
Volume :
31
Issue :
45
Database :
Academic Search Index
Journal :
Advanced Functional Materials
Publication Type :
Academic Journal
Accession number :
153314354
Full Text :
https://doi.org/10.1002/adfm.202105579