{"title":"铂负载的氧化铟锡催化剂在双电子水氧化反应中高效生产H2O2","authors":"Kiran Srinivasan Hamkins, Lauren Vallez, Xiaolin Zheng","doi":"10.1021/acscatal.5c02385","DOIUrl":null,"url":null,"abstract":"The two-electron water oxidation reaction (2e<sup>–</sup> WOR) has drawn growing attention as a potential method of producing hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) on-site through electrochemical water splitting. Nevertheless, despite ongoing efforts to identify more effective electrocatalysts for 2e<sup>–</sup> WOR, it remains a challenge to simultaneously achieve good activity, selectivity, and stability with a single catalyst material. In the field of thermocatalysis, metal oxide supports have been used to tune the catalytic properties of the supported metal catalysts. Inspired by this support effect, herein, we explore using the inverse structure─a metal-supported metal oxide bilayer─as the electrocatalyst for 2e<sup>–</sup> WOR. The metal underlayer modifies the top metal oxide catalytic properties by forming a Mott–Schottky junction, where the built-in potential influences the electron transport. We investigated several semiconducting metal oxide catalysts and different metal support materials and observed a strong metal substrate effect on the metal oxide catalytic activity. We found that a thin layer of indium tin oxide (ITO) supported by a layer of platinum (Pt) shows the best catalytic ability toward 2e<sup>–</sup> WOR, which is significantly more active and stable than the unsupported ITO catalyst, and its H<sub>2</sub>O<sub>2</sub> production rates are also greater than most reported single component electrocatalysts in the literature. The method of metal underlayer provides a pathway to create future catalysts for this electrochemical reaction.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"100 1","pages":""},"PeriodicalIF":11.3000,"publicationDate":"2025-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Platinum-Supported Indium Tin Oxide Catalyst for Efficient H2O2 Production via Two-Electron Water Oxidation Reaction\",\"authors\":\"Kiran Srinivasan Hamkins, Lauren Vallez, Xiaolin Zheng\",\"doi\":\"10.1021/acscatal.5c02385\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The two-electron water oxidation reaction (2e<sup>–</sup> WOR) has drawn growing attention as a potential method of producing hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) on-site through electrochemical water splitting. Nevertheless, despite ongoing efforts to identify more effective electrocatalysts for 2e<sup>–</sup> WOR, it remains a challenge to simultaneously achieve good activity, selectivity, and stability with a single catalyst material. In the field of thermocatalysis, metal oxide supports have been used to tune the catalytic properties of the supported metal catalysts. Inspired by this support effect, herein, we explore using the inverse structure─a metal-supported metal oxide bilayer─as the electrocatalyst for 2e<sup>–</sup> WOR. The metal underlayer modifies the top metal oxide catalytic properties by forming a Mott–Schottky junction, where the built-in potential influences the electron transport. We investigated several semiconducting metal oxide catalysts and different metal support materials and observed a strong metal substrate effect on the metal oxide catalytic activity. We found that a thin layer of indium tin oxide (ITO) supported by a layer of platinum (Pt) shows the best catalytic ability toward 2e<sup>–</sup> WOR, which is significantly more active and stable than the unsupported ITO catalyst, and its H<sub>2</sub>O<sub>2</sub> production rates are also greater than most reported single component electrocatalysts in the literature. The method of metal underlayer provides a pathway to create future catalysts for this electrochemical reaction.\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"100 1\",\"pages\":\"\"},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2025-06-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acscatal.5c02385\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.5c02385","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Platinum-Supported Indium Tin Oxide Catalyst for Efficient H2O2 Production via Two-Electron Water Oxidation Reaction
The two-electron water oxidation reaction (2e– WOR) has drawn growing attention as a potential method of producing hydrogen peroxide (H2O2) on-site through electrochemical water splitting. Nevertheless, despite ongoing efforts to identify more effective electrocatalysts for 2e– WOR, it remains a challenge to simultaneously achieve good activity, selectivity, and stability with a single catalyst material. In the field of thermocatalysis, metal oxide supports have been used to tune the catalytic properties of the supported metal catalysts. Inspired by this support effect, herein, we explore using the inverse structure─a metal-supported metal oxide bilayer─as the electrocatalyst for 2e– WOR. The metal underlayer modifies the top metal oxide catalytic properties by forming a Mott–Schottky junction, where the built-in potential influences the electron transport. We investigated several semiconducting metal oxide catalysts and different metal support materials and observed a strong metal substrate effect on the metal oxide catalytic activity. We found that a thin layer of indium tin oxide (ITO) supported by a layer of platinum (Pt) shows the best catalytic ability toward 2e– WOR, which is significantly more active and stable than the unsupported ITO catalyst, and its H2O2 production rates are also greater than most reported single component electrocatalysts in the literature. The method of metal underlayer provides a pathway to create future catalysts for this electrochemical reaction.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.