Site-specific reactivity of stepped Pt surfaces driven by stress release

Guangdong Liu, Arthur J. Shih, Huiqiu Deng, Kasinath Ojha, Xiaoting Chen, Mingchuan Luo, Ian T. McCrum, Marc T. M. Koper, Jeffrey Greeley () and Zhenhua Zeng ()
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Guangdong Liu: Hunan University
Arthur J. Shih: Leiden University
Huiqiu Deng: Hunan University
Kasinath Ojha: Leiden University
Xiaoting Chen: Leiden University
Mingchuan Luo: Leiden University
Ian T. McCrum: Clarkson University
Marc T. M. Koper: Leiden University
Jeffrey Greeley: Purdue University
Zhenhua Zeng: Purdue University

Nature, 2024, vol. 626, issue 8001, 1005-1010

Abstract: Abstract Heterogeneous catalysts are widely used to promote chemical reactions. Although it is known that chemical reactions usually happen on catalyst surfaces, only specific surface sites have high catalytic activity. Thus, identifying active sites and maximizing their presence lies at the heart of catalysis research1–4, in which the classic model is to categorize active sites in terms of distinct surface motifs, such as terraces and steps1,5–10. However, such a simple categorization often leads to orders of magnitude errors in catalyst activity predictions and qualitative uncertainties of active sites7,8,11,12, thus limiting opportunities for catalyst design. Here, using stepped Pt(111) surfaces and the electrochemical oxygen reduction reaction (ORR) as examples, we demonstrate that the root cause of larger errors and uncertainties is a simplified categorization that overlooks atomic site-specific reactivity driven by surface stress release. Specifically, surface stress release at steps introduces inhomogeneous strain fields, with up to 5.5% compression, leading to distinct electronic structures and reactivity for terrace atoms with identical local coordination, and resulting in atomic site-specific enhancement of ORR activity. For the terrace atoms flanking both sides of the step edge, the enhancement is up to 50 times higher than that of the atoms in the middle of the terrace, which permits control of ORR reactivity by either varying terrace widths or controlling external stress. Thus, the discovery of the above synergy provides a new perspective for both fundamental understanding of catalytically active atomic sites and design principles of heterogeneous catalysts.

Date: 2024
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DOI: 10.1038/s41586-024-07090-z

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