Yan-Ling Li , Yue Xu , Chen-Hong Wang , Rui Wang , Shuang-Quan Zang
{"title":"染料稳定原子精确铜簇增强光催化析氢","authors":"Yan-Ling Li , Yue Xu , Chen-Hong Wang , Rui Wang , Shuang-Quan Zang","doi":"10.1016/j.cclet.2025.111256","DOIUrl":null,"url":null,"abstract":"<div><div>Metal nanoclusters with well-defined atomic structures offer significant promise in the field of catalysis due to their sub-nanometer size and tunable organic-inorganic hybrid structural features. Herein, we successfully synthesized an 11-core copper(I)-alkynyl nanocluster (Cu<sub>11</sub>), which is stabilized by alkynyl ligands derived from a photosensitive rhodamine dye molecule. Notably, this Cu<sub>11</sub> cluster exhibited excellent photocatalytic hydrogen evolution activity (8.13 mmol g<sup>−1</sup>h<sup>−1</sup>) even in the absence of a mediator and noble metal co-catalyst. Furthermore, when Cu<sub>11</sub> clusters were loaded onto the surface of TiO<sub>2</sub> nanosheets, the resultant Cu<sub>11</sub>@TiO<sub>2</sub> nanocomposites exhibited a significant enhancement in hydrogen evolution efficiency, which is 60 times higher than that of pure TiO<sub>2</sub> nanosheets. The incorporation of Cu<sub>11</sub> clusters within the Cu<sub>11</sub>@TiO<sub>2</sub> effectively inhibits the recombination of photogenerated electrons and holes, thereby accelerating the charge separation and migration in the composite material. This work introduces a novel perspective for designing highly active copper cluster-based photocatalysts.</div></div>","PeriodicalId":10088,"journal":{"name":"Chinese Chemical Letters","volume":"36 10","pages":"Article 111256"},"PeriodicalIF":8.9000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dye-stabilized atomically precise copper clusters for enhanced photocatalytic hydrogen evolution\",\"authors\":\"Yan-Ling Li , Yue Xu , Chen-Hong Wang , Rui Wang , Shuang-Quan Zang\",\"doi\":\"10.1016/j.cclet.2025.111256\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Metal nanoclusters with well-defined atomic structures offer significant promise in the field of catalysis due to their sub-nanometer size and tunable organic-inorganic hybrid structural features. Herein, we successfully synthesized an 11-core copper(I)-alkynyl nanocluster (Cu<sub>11</sub>), which is stabilized by alkynyl ligands derived from a photosensitive rhodamine dye molecule. Notably, this Cu<sub>11</sub> cluster exhibited excellent photocatalytic hydrogen evolution activity (8.13 mmol g<sup>−1</sup>h<sup>−1</sup>) even in the absence of a mediator and noble metal co-catalyst. Furthermore, when Cu<sub>11</sub> clusters were loaded onto the surface of TiO<sub>2</sub> nanosheets, the resultant Cu<sub>11</sub>@TiO<sub>2</sub> nanocomposites exhibited a significant enhancement in hydrogen evolution efficiency, which is 60 times higher than that of pure TiO<sub>2</sub> nanosheets. The incorporation of Cu<sub>11</sub> clusters within the Cu<sub>11</sub>@TiO<sub>2</sub> effectively inhibits the recombination of photogenerated electrons and holes, thereby accelerating the charge separation and migration in the composite material. This work introduces a novel perspective for designing highly active copper cluster-based photocatalysts.</div></div>\",\"PeriodicalId\":10088,\"journal\":{\"name\":\"Chinese Chemical Letters\",\"volume\":\"36 10\",\"pages\":\"Article 111256\"},\"PeriodicalIF\":8.9000,\"publicationDate\":\"2025-04-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Chemical Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1001841725004413\",\"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":"Chinese Chemical Letters","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1001841725004413","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Dye-stabilized atomically precise copper clusters for enhanced photocatalytic hydrogen evolution
Metal nanoclusters with well-defined atomic structures offer significant promise in the field of catalysis due to their sub-nanometer size and tunable organic-inorganic hybrid structural features. Herein, we successfully synthesized an 11-core copper(I)-alkynyl nanocluster (Cu11), which is stabilized by alkynyl ligands derived from a photosensitive rhodamine dye molecule. Notably, this Cu11 cluster exhibited excellent photocatalytic hydrogen evolution activity (8.13 mmol g−1h−1) even in the absence of a mediator and noble metal co-catalyst. Furthermore, when Cu11 clusters were loaded onto the surface of TiO2 nanosheets, the resultant Cu11@TiO2 nanocomposites exhibited a significant enhancement in hydrogen evolution efficiency, which is 60 times higher than that of pure TiO2 nanosheets. The incorporation of Cu11 clusters within the Cu11@TiO2 effectively inhibits the recombination of photogenerated electrons and holes, thereby accelerating the charge separation and migration in the composite material. This work introduces a novel perspective for designing highly active copper cluster-based photocatalysts.
期刊介绍:
Chinese Chemical Letters (CCL) (ISSN 1001-8417) was founded in July 1990. The journal publishes preliminary accounts in the whole field of chemistry, including inorganic chemistry, organic chemistry, analytical chemistry, physical chemistry, polymer chemistry, applied chemistry, etc.Chinese Chemical Letters does not accept articles previously published or scheduled to be published. To verify originality, your article may be checked by the originality detection service CrossCheck.