甲烷化
X射线光电子能谱
纳米颗粒
催化作用
钌
材料科学
电子转移
氧气
化学工程
纳米技术
分析化学(期刊)
结晶学
光化学
化学
有机化学
工程类
生物化学
色谱法
作者
Ruimin Jiang,Xuanyu Yue,Ke Wang,Yang Zhou,Wenxin Dai,Xianzhi Fu
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2022-05-18
卷期号:36 (19): 11636-11646
被引量:33
标识
DOI:10.1021/acs.energyfuels.2c00560
摘要
The Ru/CeO 2 samples were prepared with loading Ru nanoparticles onto three different shapes (nanocubes, rods, and polyhedrons) of the CeO 2 surface and evaluated for catalytic performances in CO 2 methanation under visible light or not. It was found that the cube-like Ru/CeO 2 sample (Ru/CeO 2 -c) exhibited a visible light-enhanced catalytic performance, but an insignificant photopromoted activity occurred on rod- or polyhedron-like Ru/CeO 2 samples (Ru/CeO 2 -r or Ru/CeO 2 -p). The detailed catalytic mechanism was monitored by temperature-programmed reduction, X-ray photoelectron spectroscopy, and electron paramagnetic resonance. It was proposed that the different photoassist activities of Ru/CeO 2 under illumination were caused by the different metal–support interaction forces. The strong interaction formed in Ru/CeO 2 -c could promote the photoexcited electrons from cube-like CeO 2 to transfer onto the Ru surface, which accelerated the generation of oxygen vacancies in Ru/CeO 2 -c. On the contrary, a weak interaction occurred on Ru/CeO 2 -r and Ru/CeO 2 -p samples. In this case, the photoexcited electrons would hardly transfer onto the Ru surface, and no more oxygen vacancies were generated on Ru/CeO 2 -r and Ru/CeO 2 -p, resulting in a negligible photopromoted activity.
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