Zhu Yao, Chen Shaoqin, Fang Siyuan, Li Zhangyang, Wang Chunling, Hu Yun Hang
School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Department of Materials Science and Engineering, Michigan Technological University, Houghton, Michigan 49931, United States.
J Phys Chem Lett. 2021 Aug 12;12(31):7459-7465. doi: 10.1021/acs.jpclett.1c02053. Epub 2021 Aug 2.
The utilization of visible light for direct photocatalytic methane conversion remains a huge challenge. Here, we developed a thermo-photo catalytic process with a visible-light-responsive Pt/WO catalyst and realized highly efficient visible-light driven methane conversion for the first time. The conversion efficiency was enhanced by 4.6 and 14.7 times compared to room-temperature photocatalysis and thermal catalysis at 150 °C, respectively. Furthermore, the production of liquid oxygenates (mainly CHOH) was found to proceed via photocatalysis with high apparent quantum efficiencies of 5.9%, 4.5%, and 1.9% at 350, 420, and 450 nm, respectively, while CO evolution was contributed by photoassisted thermal catalysis. Solid isotope evidence further confirmed that CHOH, HCHO, and CO were produced via parallel rather than sequential reactions. These observations provide a valuable guide for designing a visible-light driven system for methane conversion with high efficiency and controllable selectivity.
利用可见光进行直接光催化甲烷转化仍然是一个巨大的挑战。在此,我们开发了一种使用可见光响应型Pt/WO催化剂的热光催化过程,并首次实现了高效的可见光驱动甲烷转化。与室温光催化和150°C的热催化相比,转化效率分别提高了4.6倍和14.7倍。此外,发现液态含氧化合物(主要是CHOH)的生成通过光催化进行,在350、420和450nm处的表观量子效率分别高达5.9%、4.5%和1.9%,而CO的生成则由光辅助热催化贡献。固体同位素证据进一步证实,CHOH、HCHO和CO是通过平行反应而非顺序反应生成的。这些观察结果为设计高效且选择性可控的可见光驱动甲烷转化系统提供了有价值的指导。