Ziyang Wu, Fengting Xie, Wenping Sun, Dingsheng Wang, Jianping Yang
{"title":"Metal–Support Interactions in Heterogeneous Electrocatalysis","authors":"Ziyang Wu, Fengting Xie, Wenping Sun, Dingsheng Wang, Jianping Yang","doi":"10.1021/acs.chemrev.6c00356","DOIUrl":null,"url":null,"abstract":"<p>Electrochemical energy conversion underpins the sustainable\r\nproduction\r\nof fuels and chemicals, with efficiency and selectivity governed by\r\nreactions at electrified solid–liquid interfaces. In supported\r\nelectrocatalysts, metal–support interactions (MSIs) shape how\r\ncatalytic states form and persist under polarization. Yet a predictive\r\ndescription of MSI remains elusive. The as-prepared contact may reconstruct\r\nunder operating conditions. Activity shifts, morphology, and charge\r\nredistribution do not uniquely identify the current-carrying ensemble.\r\nThese limitations motivate this review, which separates interfacial\r\nstructure, chemical bonding, and collective adhesion before relating\r\nthem to catalytic function. The framework spans single atoms, clusters,\r\nnanoparticles, core–shell architectures, and reconstructed\r\ninterphases. We assess how atomic-resolution imaging, <em>operando</em> characterization, and potential-aware calculations constrain models\r\nof the working interface and relate them to electrocatalytic performance.\r\nTogether, these analyses show that MSI effects depend on the working\r\ninterfacial state and its reaction environment. Predictive design\r\ntherefore requires balancing interfacial stabilization with the active-site\r\naccessibility and structural adaptability needed for turnover.</p>","PeriodicalId":32,"journal":{"name":"Chemical Reviews","volume":"126 19","pages":"10804–10945"},"PeriodicalIF":64.2000,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Reviews","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.chemrev.6c00356","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/29 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Electrochemical energy conversion underpins the sustainable
production
of fuels and chemicals, with efficiency and selectivity governed by
reactions at electrified solid–liquid interfaces. In supported
electrocatalysts, metal–support interactions (MSIs) shape how
catalytic states form and persist under polarization. Yet a predictive
description of MSI remains elusive. The as-prepared contact may reconstruct
under operating conditions. Activity shifts, morphology, and charge
redistribution do not uniquely identify the current-carrying ensemble.
These limitations motivate this review, which separates interfacial
structure, chemical bonding, and collective adhesion before relating
them to catalytic function. The framework spans single atoms, clusters,
nanoparticles, core–shell architectures, and reconstructed
interphases. We assess how atomic-resolution imaging, operando characterization, and potential-aware calculations constrain models
of the working interface and relate them to electrocatalytic performance.
Together, these analyses show that MSI effects depend on the working
interfacial state and its reaction environment. Predictive design
therefore requires balancing interfacial stabilization with the active-site
accessibility and structural adaptability needed for turnover.
期刊介绍:
Chemical Reviews is a highly regarded and highest-ranked journal covering the general topic of chemistry. Its mission is to provide comprehensive, authoritative, critical, and readable reviews of important recent research in organic, inorganic, physical, analytical, theoretical, and biological chemistry.
Since 1985, Chemical Reviews has also published periodic thematic issues that focus on a single theme or direction of emerging research.