乙烯
催化作用
化学
脱氢
氧化磷酸化
量子产额
光化学
氧气
光催化
选择性
化学工程
多相催化
组合化学
产量(工程)
活性氧
反应机理
材料科学
作者
Yachao Wang,Yanqing Jiao,Shufen Ma,Yaxiong Wei,Weixin Huang,Cong Fu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-12-06
卷期号:15 (24): 20939-20946
被引量:1
标识
DOI:10.1021/acscatal.5c06445
摘要
Photocatalytic oxidative dehydrogenation of ethane (ODHE) offers a promising strategy for ethylene production under mild conditions. However, achieving a high ethylene yield and selectivity remains challenging due to the high activation barrier of ethane C–H bonds and the propensity for overoxidation to CO2. Herein, we demonstrate that Pd/TiO2-6, a palladium-decorated, 6 nm-sized TiO2 support, functions as a selective photocatalyst for ODHE using O2 under continuous-flow conditions. The optimized Pd/TiO2-6 catalyst exhibits an ethylene production rate of 69.9 mmol g–1 h–1 with 78.9% selectivity and a high apparent quantum efficiency of 17.9%. It also demonstrates robust stability over 45 h of continuous operation, outperforming most reported photo- and thermocatalysts. In situ and time-resolved characterizations revealed that the highly dispersed, oxidized Pd species serve as essential mediators in promoting charge separation and enabling moderate oxygen activation. This synergistic effect enables the selective activation of C2H6 to form key *C2H4 intermediates, ultimately leading to a high ethylene formation rate. This work reveals key insights into preparing highly efficient ODHE photocatalysts by harnessing the support size effect.
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