{"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}
引用次数: 0
Abstract
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.