甲烷氧化偶联
光催化
甲烷
材料科学
吸附
化学工程
催化作用
光化学
营业额
氧化磷酸化
纳米技术
化学
有机化学
生物化学
工程类
作者
Xiyi Li,Chao Wang,Jianlong Yang,Youxun Xu,Yi Yang,Jiaguo Yu,Juan J. Delgado,Natalia Martsinovich,Xiaofeng Sun,Xusheng Zheng,Weixin Huang,Junwang Tang
标识
DOI:10.1038/s41467-023-41996-y
摘要
Abstract Methane activation by photocatalysis is one of the promising sustainable technologies for chemical synthesis. However, the current efficiency and stability of the process are moderate. Herein, a PdCu nanoalloy (~2.3 nm) was decorated on TiO 2 , which works for the efficient, stable, and selective photocatalytic oxidative coupling of methane at room temperature. A high methane conversion rate of 2480 μmol g −1 h −1 to C 2 with an apparent quantum efficiency of ~8.4% has been achieved. More importantly, the photocatalyst exhibits the turnover frequency and turnover number of 116 h −1 and 12,642 with respect to PdCu, representing a record among all the photocatalytic processes (λ > 300 nm) operated at room temperature, together with a long stability of over 112 hours. The nanoalloy works as a hole acceptor, in which Pd softens and weakens C-H bond in methane and Cu decreases the adsorption energy of C 2 products, leading to the high efficiency and long-time stability.
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