{"title":"在TiO2纳米结构中嵌入Au单原子位点以促进光催化甲烷氧化。","authors":"Qui Thanh Hoai Ta and Ly Tan Nhiem","doi":"10.1039/D4NA00947A","DOIUrl":null,"url":null,"abstract":"<p >Photocatalytic methane oxidation under mild conditions using single-atom catalysts remains an advanced technology. In this work, gold single atoms (Au SAs) were introduced onto TiO<small><sub>2</sub></small> nanostructures using a simple method. The resulting performance demonstrated effective conversion of methane into H<small><sub>2</sub></small> and C<small><sub>2</sub></small> products at room temperature. The as-synthesized Au SA/TiO<small><sub>2</sub></small> exhibited a high hydrogen production rate of 2190 μmol g<small><sup>−1</sup></small>, with selectivity reaching up to 58% under optimized conditions. The methane oxidation mechanism was investigated, revealing a methyl radical pathway for generating value-added chemicals. This research provides a strategy for photocatalytic methane conversion over single-atom-supported photocatalysts.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 6","pages":" 1543-1551"},"PeriodicalIF":4.6000,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770591/pdf/","citationCount":"0","resultStr":"{\"title\":\"Engineering Au single-atom sites embedded in TiO2 nanostructures for boosting photocatalytic methane oxidation†\",\"authors\":\"Qui Thanh Hoai Ta and Ly Tan Nhiem\",\"doi\":\"10.1039/D4NA00947A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Photocatalytic methane oxidation under mild conditions using single-atom catalysts remains an advanced technology. In this work, gold single atoms (Au SAs) were introduced onto TiO<small><sub>2</sub></small> nanostructures using a simple method. The resulting performance demonstrated effective conversion of methane into H<small><sub>2</sub></small> and C<small><sub>2</sub></small> products at room temperature. The as-synthesized Au SA/TiO<small><sub>2</sub></small> exhibited a high hydrogen production rate of 2190 μmol g<small><sup>−1</sup></small>, with selectivity reaching up to 58% under optimized conditions. The methane oxidation mechanism was investigated, revealing a methyl radical pathway for generating value-added chemicals. This research provides a strategy for photocatalytic methane conversion over single-atom-supported photocatalysts.</p>\",\"PeriodicalId\":18806,\"journal\":{\"name\":\"Nanoscale Advances\",\"volume\":\" 6\",\"pages\":\" 1543-1551\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-01-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770591/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nanoscale Advances\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/na/d4na00947a\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanoscale Advances","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/na/d4na00947a","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Engineering Au single-atom sites embedded in TiO2 nanostructures for boosting photocatalytic methane oxidation†
Photocatalytic methane oxidation under mild conditions using single-atom catalysts remains an advanced technology. In this work, gold single atoms (Au SAs) were introduced onto TiO2 nanostructures using a simple method. The resulting performance demonstrated effective conversion of methane into H2 and C2 products at room temperature. The as-synthesized Au SA/TiO2 exhibited a high hydrogen production rate of 2190 μmol g−1, with selectivity reaching up to 58% under optimized conditions. The methane oxidation mechanism was investigated, revealing a methyl radical pathway for generating value-added chemicals. This research provides a strategy for photocatalytic methane conversion over single-atom-supported photocatalysts.