Jianning Feng, Kezhou Fan, Qinxuan Cao, Wenfei Liang, Pui Ying Wong, Jie Xue, Kin Ting Chang, Kam Sing Wong, Haipeng Lu
{"title":"Hot Electron Photocatalysis Using Nontoxic Self-Doped Quantum Dots.","authors":"Jianning Feng, Kezhou Fan, Qinxuan Cao, Wenfei Liang, Pui Ying Wong, Jie Xue, Kin Ting Chang, Kam Sing Wong, Haipeng Lu","doi":"10.1002/anie.202508543","DOIUrl":null,"url":null,"abstract":"<p><p>Colloidal semiconductor quantum dots (QDs) have emerged as versatile photocatalysts for organic transformations. However, a significant drawback is their reliance on toxic metals like lead and cadmium, which limits their widespread application in solar-to-chemical conversion. Furthermore, current systems primarily utilize band-edge carriers for simpler photoredox reactions, while the potential for harvesting hot carriers in chemical transformations remains largely unexplored. To address these challenges, we developed nontoxic, cost-effective, and recyclable ternary CuInS<sub>2</sub> and quaternary Cu─In─Zn─S QDs as potent photocatalysts. Our findings demonstrate that hot electrons can be effectively generated through an ultrafast Auger process, enabling the photoreduction of aryl halides (with reduction potentials up to -2.90 V versus saturated calomel electrode (SCE)) and various cross-coupling (C─C, C─P, C─B, and C─S) transformations. Notably, quaternary Cu─In─Zn─S QDs exhibit significantly higher reactivity compared to CuInS<sub>2</sub> QDs, which is attributed to enhanced Auger-mediated hot electron generation. This work underscores the potential of directly utilizing Auger-generated hot electrons for extreme-potential organic transformations under mild conditions using nontoxic QDs.</p>","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202508543"},"PeriodicalIF":16.9000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie (International ed. in English)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/anie.202508543","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Colloidal semiconductor quantum dots (QDs) have emerged as versatile photocatalysts for organic transformations. However, a significant drawback is their reliance on toxic metals like lead and cadmium, which limits their widespread application in solar-to-chemical conversion. Furthermore, current systems primarily utilize band-edge carriers for simpler photoredox reactions, while the potential for harvesting hot carriers in chemical transformations remains largely unexplored. To address these challenges, we developed nontoxic, cost-effective, and recyclable ternary CuInS2 and quaternary Cu─In─Zn─S QDs as potent photocatalysts. Our findings demonstrate that hot electrons can be effectively generated through an ultrafast Auger process, enabling the photoreduction of aryl halides (with reduction potentials up to -2.90 V versus saturated calomel electrode (SCE)) and various cross-coupling (C─C, C─P, C─B, and C─S) transformations. Notably, quaternary Cu─In─Zn─S QDs exhibit significantly higher reactivity compared to CuInS2 QDs, which is attributed to enhanced Auger-mediated hot electron generation. This work underscores the potential of directly utilizing Auger-generated hot electrons for extreme-potential organic transformations under mild conditions using nontoxic QDs.