Liuyang Zhang, Jianjun Zhang, Jiaguo Yu, Hermenegildo García
{"title":"Charge-transfer dynamics in S-scheme photocatalyst","authors":"Liuyang Zhang, Jianjun Zhang, Jiaguo Yu, Hermenegildo García","doi":"10.1038/s41570-025-00698-3","DOIUrl":null,"url":null,"abstract":"<p>Natural photosynthesis represents the pinnacle that green chemistry aims to achieve. Photocatalysis, inspired by natural photosynthesis and dating back to 1911, has been revitalized, offering promising solutions to critical energy and environmental challenges facing society today. As such, it represents an important research avenue in contemporary chemical science. However, single photocatalytic materials often suffer from the rapid recombination of photogenerated electrons and holes, resulting in poor performance. S-scheme heterojunctions have emerged as a general method to enhance charge transfer and separation, thereby greatly improving photocatalytic efficiencies. This Perspective delves into the electron transfer dynamics in S-scheme heterojunctions, providing a comprehensive overview of their development and key characterization techniques, such as femtosecond transient absorption spectroscopy, in situ irradiated X-ray photoelectron spectroscopy and Kelvin probe force microscopy. By addressing a critical research gap, this work aims to trigger further understanding and advances in photo-induced charge-transfer processes, thereby contributing to green chemistry and the United Nations sustainable development goals.</p><figure></figure>","PeriodicalId":18849,"journal":{"name":"Nature reviews. Chemistry","volume":"27 1","pages":""},"PeriodicalIF":38.1000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature reviews. Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1038/s41570-025-00698-3","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Natural photosynthesis represents the pinnacle that green chemistry aims to achieve. Photocatalysis, inspired by natural photosynthesis and dating back to 1911, has been revitalized, offering promising solutions to critical energy and environmental challenges facing society today. As such, it represents an important research avenue in contemporary chemical science. However, single photocatalytic materials often suffer from the rapid recombination of photogenerated electrons and holes, resulting in poor performance. S-scheme heterojunctions have emerged as a general method to enhance charge transfer and separation, thereby greatly improving photocatalytic efficiencies. This Perspective delves into the electron transfer dynamics in S-scheme heterojunctions, providing a comprehensive overview of their development and key characterization techniques, such as femtosecond transient absorption spectroscopy, in situ irradiated X-ray photoelectron spectroscopy and Kelvin probe force microscopy. By addressing a critical research gap, this work aims to trigger further understanding and advances in photo-induced charge-transfer processes, thereby contributing to green chemistry and the United Nations sustainable development goals.
期刊介绍:
Nature Reviews Chemistry is an online-only journal that publishes Reviews, Perspectives, and Comments on various disciplines within chemistry. The Reviews aim to offer balanced and objective analyses of selected topics, providing clear descriptions of relevant scientific literature. The content is designed to be accessible to recent graduates in any chemistry-related discipline while also offering insights for principal investigators and industry-based research scientists. Additionally, Reviews should provide the authors' perspectives on future directions and opinions regarding the major challenges faced by researchers in the field.