Engineering Au single-atom sites embedded in TiO2 nanostructures for boosting photocatalytic methane oxidation†

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Nanoscale Advances Pub Date : 2025-01-13 DOI:10.1039/D4NA00947A
Qui Thanh Hoai Ta and Ly Tan Nhiem
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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.

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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。
在温和条件下使用单原子催化剂光催化氧化甲烷是一项先进的技术。在这项工作中,金单原子(Au SAs)通过一种简单的方法引入到TiO2纳米结构中。结果表明,在室温下,甲烷有效地转化为H2和C2产物。在优化条件下,Au SA/TiO2的产氢率高达2190 μmol g-1,选择性高达58%。研究了甲烷氧化机理,揭示了甲基自由基生成增值化学品的途径。本研究为单原子负载型光催化甲烷转化提供了一种策略。
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来源期刊
Nanoscale Advances
Nanoscale Advances Multiple-
CiteScore
8.00
自引率
2.10%
发文量
461
审稿时长
9 weeks
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