甲烷化
催化作用
X射线光电子能谱
化学工程
粒径
甲烷
材料科学
替代天然气
镍
空间速度
电力转天然气
格式化
选择性
无机化学
化学
合成气
冶金
物理化学
有机化学
电解
工程类
电解质
电极
作者
Lili Lin,Clifford A. Gerlak,Chang Liu,Jordi Llorca,Siyu Yao,Ning Rui,Feng Zhang,Zongyuan Liu,Sen Zhang,Kaixi Deng,Christopher B. Murray,José A. Rodríguez,Sanjaya D. Senanayake
标识
DOI:10.1016/j.jechem.2021.02.021
摘要
Production of ‘renewable Methane’ has attracted renewed research interest as a fundamental probe reaction and process for CO2 utilization through potential use in C1 fuel production and even for future space exploration technologies. CO2 methanation is a structure sensitive reaction on Ni/CeO2 catalysts. To precisely elucidate the size effect of the Ni metal center on the CO2 methanation performance, we prepared 2%Ni/CeO2 catalysts with pre-synthesized uniform Ni particles (2, 4 and 8 nm) on a high surface area CeO2 support. Transmission electron microscopy (TEM) and ambient pressure X-ray photo spectroscopy (AP-XPS) characterization have confirmed that the catalyst structure and chemical state was uniform and stable under reaction conditions. The 8 nm sized catalyst showed superior methanation selectivity over the 4 and 2 nm counterparts, and the methanation activity in term of TOF is 10 times and 70 times higher than for the 4 and 2 nm counterparts, respectively. The DRIFTS studies revealed that the larger Ni (8 nm particles) over CeO2 efficiently facilitated the hydrogenation of the surface formate intermediates, which is proposed as the rate determining step accounting for the excellent CO2 methanation performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI