Interface Engineering of Polymeric Carbon Nitride with Enhanced Charge Separation for Efficient Visible Light Photosynthesis of Hydrogen Peroxide from Oxygen and Water
{"title":"Interface Engineering of Polymeric Carbon Nitride with Enhanced Charge Separation for Efficient Visible Light Photosynthesis of Hydrogen Peroxide from Oxygen and Water","authors":"Zhenchun Yang, Kunlong Liu, Hangyu Zhuzhang, Wandong Xing, Masakazu Anpo, Guigang Zhang","doi":"10.1002/adfm.202510267","DOIUrl":null,"url":null,"abstract":"Photosynthesis of H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> from O<jats:sub>2</jats:sub> and H<jats:sub>2</jats:sub>O with inexhaustible sunlight as an energy source is a promising approach. However, the photocatalytic performance of pristine polymeric carbon nitride (PCN) is extremely restrained due to the rapid recombination of photo‐generated electrons and holes, and slow surface reaction processes. Herein, a new strategy is developed to rationally integrate N, S‐co‐doped carbon (C<jats:sub>NS</jats:sub>), and CoS<jats:sub>2</jats:sub> on cyano‐rich PCN (PCN‐Cy) for photosynthesis of H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> under ambient conditions. The engineering with cyano groups (electron‐withdrawing groups) promotes the bulk charge separation of PCN. Experimental results reveal that the CoS<jats:sub>2</jats:sub> co‐catalyst not only serves as an electron acceptor to extract charges from the bulk but also functions as an active site to promote the 2‐e<jats:sup>−</jats:sup> ORR process. Besides, the N, S‐co‐doped carbon performs as an electron channel to promote migration of charges at the interface of PCN‐Cy and CoS<jats:sub>2</jats:sub>. Accordingly, the as‐synthesized cyano‐rich PCN photocatalyst integrated with N, S‐co‐doped carbon and CoS<jats:sub>2</jats:sub> exhibits a remarkable activity of 321.9 µ<jats:sc>m</jats:sc> h<jats:sup>−1</jats:sup> for photocatalytic production of H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>, which is 44.9 times higher than that of the pristine PCN.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"44 1","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202510267","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Photosynthesis of H2O2 from O2 and H2O with inexhaustible sunlight as an energy source is a promising approach. However, the photocatalytic performance of pristine polymeric carbon nitride (PCN) is extremely restrained due to the rapid recombination of photo‐generated electrons and holes, and slow surface reaction processes. Herein, a new strategy is developed to rationally integrate N, S‐co‐doped carbon (CNS), and CoS2 on cyano‐rich PCN (PCN‐Cy) for photosynthesis of H2O2 under ambient conditions. The engineering with cyano groups (electron‐withdrawing groups) promotes the bulk charge separation of PCN. Experimental results reveal that the CoS2 co‐catalyst not only serves as an electron acceptor to extract charges from the bulk but also functions as an active site to promote the 2‐e− ORR process. Besides, the N, S‐co‐doped carbon performs as an electron channel to promote migration of charges at the interface of PCN‐Cy and CoS2. Accordingly, the as‐synthesized cyano‐rich PCN photocatalyst integrated with N, S‐co‐doped carbon and CoS2 exhibits a remarkable activity of 321.9 µm h−1 for photocatalytic production of H2O2, which is 44.9 times higher than that of the pristine PCN.
利用取之不尽的阳光作为能源,利用O2和H2O中的H2O2进行光合作用是一种很有前途的方法。然而,由于光产生的电子和空穴的快速重组以及表面反应过程缓慢,原始聚合物氮化碳(PCN)的光催化性能受到极大的限制。本文提出了一种新的策略,将N、S掺杂碳(CNS)和CoS2合理地集成在富氰PCN (PCN‐Cy)上,用于环境条件下H2O2的光合作用。氰基(吸电子基团)工程促进了PCN的体电荷分离。实验结果表明,co_2共催化剂不仅可以作为电子受体从体中提取电荷,还可以作为活性位点促进2‐e−ORR过程。此外,N, S - co掺杂的碳作为电子通道,促进电荷在PCN - Cy和CoS2界面的迁移。因此,合成的含N、S掺杂碳和CoS2的富氰PCN光催化剂的H2O2光催化活性为321.9 μ m h−1,是原始PCN光催化活性的44.9倍。
期刊介绍:
Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week.
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