Jingguo Li*, Hang Chen, Siqin Liu, Yu Wang, Wenchao Wan, Yonggui Zhao, Carlos A. Triana, Zihao Xu and Greta R. Patzke*,
{"title":"光阳极表面FeIV=O积累加速复合反应","authors":"Jingguo Li*, Hang Chen, Siqin Liu, Yu Wang, Wenchao Wan, Yonggui Zhao, Carlos A. Triana, Zihao Xu and Greta R. Patzke*, ","doi":"10.1021/jacs.5c02231","DOIUrl":null,"url":null,"abstract":"<p >The observation of third-order water oxidation kinetics by <i>Fe</i><sup><i>IV</i></sup><i>=O</i> accumulation at the semiconductor–electrolyte interface is a milestone for understanding the four-electron transfer reaction mechanism. However, the consequences of such <i>Fe</i><sup><i>IV</i></sup><i>=O</i> accumulation for the associated recombination reaction kinetics at the interface have not been fully explored so far. Here, we observe fast second-order recombination reaction kinetics for <i>Fe</i><sup><i>IV</i></sup><i>=O</i> as the result of its accumulation at the model hematite–electrolyte interface, compared to the first-order recombination reaction kinetics for a lesser amount of available <i>Fe</i><sup><i>IV</i></sup><i>=O</i>. We refer to this phenomenon as “accumulation-accelerated recombination (AAR)” and highlight the adverse role of <i>Fe</i><sup><i>IV</i></sup><i>=O</i> accumulation at the interface. Further, we demonstrate that this fast second-order <i>AAR</i> could be slowed down to first-order kinetics by (i) deprotonation of the metal oxide surface; (ii) evacuating the conduction band electrons; and (iii) partial substitution of <i>Fe</i><sup><i>IV</i></sup><i>=O</i> with less active <i>Co</i><sup><i>IV</i></sup><i>=O</i> species. Such an insight is vital not only for understanding the efficiency loss mechanisms at the semiconductor–electrolyte interface but also for interpreting the interfacial behavior of photovoltaic systems and photocatalysts.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"147 25","pages":"21492–21500"},"PeriodicalIF":15.6000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Accelerated Recombination Reaction through Interfacial FeIV=O Accumulation on Photoanode Surfaces\",\"authors\":\"Jingguo Li*, Hang Chen, Siqin Liu, Yu Wang, Wenchao Wan, Yonggui Zhao, Carlos A. Triana, Zihao Xu and Greta R. Patzke*, \",\"doi\":\"10.1021/jacs.5c02231\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The observation of third-order water oxidation kinetics by <i>Fe</i><sup><i>IV</i></sup><i>=O</i> accumulation at the semiconductor–electrolyte interface is a milestone for understanding the four-electron transfer reaction mechanism. However, the consequences of such <i>Fe</i><sup><i>IV</i></sup><i>=O</i> accumulation for the associated recombination reaction kinetics at the interface have not been fully explored so far. Here, we observe fast second-order recombination reaction kinetics for <i>Fe</i><sup><i>IV</i></sup><i>=O</i> as the result of its accumulation at the model hematite–electrolyte interface, compared to the first-order recombination reaction kinetics for a lesser amount of available <i>Fe</i><sup><i>IV</i></sup><i>=O</i>. We refer to this phenomenon as “accumulation-accelerated recombination (AAR)” and highlight the adverse role of <i>Fe</i><sup><i>IV</i></sup><i>=O</i> accumulation at the interface. Further, we demonstrate that this fast second-order <i>AAR</i> could be slowed down to first-order kinetics by (i) deprotonation of the metal oxide surface; (ii) evacuating the conduction band electrons; and (iii) partial substitution of <i>Fe</i><sup><i>IV</i></sup><i>=O</i> with less active <i>Co</i><sup><i>IV</i></sup><i>=O</i> species. Such an insight is vital not only for understanding the efficiency loss mechanisms at the semiconductor–electrolyte interface but also for interpreting the interfacial behavior of photovoltaic systems and photocatalysts.</p>\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\"147 25\",\"pages\":\"21492–21500\"},\"PeriodicalIF\":15.6000,\"publicationDate\":\"2025-06-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/jacs.5c02231\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacs.5c02231","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Accelerated Recombination Reaction through Interfacial FeIV=O Accumulation on Photoanode Surfaces
The observation of third-order water oxidation kinetics by FeIV=O accumulation at the semiconductor–electrolyte interface is a milestone for understanding the four-electron transfer reaction mechanism. However, the consequences of such FeIV=O accumulation for the associated recombination reaction kinetics at the interface have not been fully explored so far. Here, we observe fast second-order recombination reaction kinetics for FeIV=O as the result of its accumulation at the model hematite–electrolyte interface, compared to the first-order recombination reaction kinetics for a lesser amount of available FeIV=O. We refer to this phenomenon as “accumulation-accelerated recombination (AAR)” and highlight the adverse role of FeIV=O accumulation at the interface. Further, we demonstrate that this fast second-order AAR could be slowed down to first-order kinetics by (i) deprotonation of the metal oxide surface; (ii) evacuating the conduction band electrons; and (iii) partial substitution of FeIV=O with less active CoIV=O species. Such an insight is vital not only for understanding the efficiency loss mechanisms at the semiconductor–electrolyte interface but also for interpreting the interfacial behavior of photovoltaic systems and photocatalysts.
期刊介绍:
The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.