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Friction-induced electrochemical activation of platinum group metals via electromechanical coupling

Chenxu Liu, Zhaoran Zhu, Wengen Ouyang, Haoran Pan, Zhijun Shi, Xingxing Chen, James Ewen, Jie Zhang, Daniele Dini, Ming Ma, Hongbo Zeng, Yu Tian, Yonggang Meng

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Abstract

Platinum group metals (PGMs), long considered chemically inert, exhibit unexpected reactivity at the metal-water interface when subjected to simultaneous friction and electric fields. This tribo-electrochemical coupling unveils a reaction regime fundamentally different from conventional electrochemical or mechanical activation. Here, we demonstrate that friction, coupled with a positive surface potential, drives the rapid formation of submicron oxide layers on platinum surfaces. We propose that friction lowers activation energy barriers and enhances mass transport, thereby accelerating anodic oxidation through a stress-augmented thermally activated mechanism. The resulting nanostructured oxides apparently exhibit higher electrocatalytic activity than that of metallic platinum, offering promising potential for microscale sensors and catalytic microreactors. Notably, this localized oxidation also occurs in other PGMs, indicating a broadly applicable strategy for activating inert metals via electromechanical coupling.
Original languageEnglish
Article number103323
JournalMaterials Today
Volume96
Early online date11 Apr 2026
DOIs
Publication statusE-pub ahead of print - 11 Apr 2026

Data Availability Statement

Data will be made available on request.

Funding

This work was financially supported by National Natural Science Foundation of China (Grant Nos. 52105193), China Postdoctoral Science Foundation (Grant No. 2021TQ0175) and the starting-up fund of Wuhan University. Z.Z. thanks the UK Department of Science, Innovation, and Technology (DSIT) and the Engineering and Physical Sciences Research Council (EPSRC) through an iCASE studentship (EP/X524773/1). J.P.E. was supported by the DSIT and the Royal Academy of Engineering (RAEng) through the Research Fellowships scheme. C.L. and H.Z. acknowledge the support from Natural Sciences and Engineering Research Council of Canada and the Canada Research Chairs Program. D.D. was supported by the DSIT, RAEng, and Shell via a Research Chair in Complex Engineering Interfaces. We acknowledge the use of Imperial College London Research Computing Service (https://doi.org/10.14469/hpc/2232) and the UK Materials and Molecular Modelling Hub, which is partially funded by the EPSRC (EP/T022213/1, EP/W032260/1, and EP/P020194/1).

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