双金属片
催化作用
甲烷化
贵金属
离解(化学)
镍
金属
铑
无机化学
材料科学
纳米颗粒
铱
选择性
吸附
化学
化学工程
物理化学
纳米技术
冶金
有机化学
工程类
作者
Anastasios I. Tsiotsias,Nikolaos D. Charisiou,Cristina Italiano,Giovanni Drago Ferrante,L. Pino,Antonio Vita,Víctor Sebastián,Steven J. Hinder,Mark Baker,Abhishek Sharan,Nirpendra Singh,Kyriaki Polychronopoulou,Maria A. Goula
标识
DOI:10.1016/j.apsusc.2023.158945
摘要
Bimetallic nickel-noble metal catalysts with a low noble metal loading (1 wt% of Ru, Pt, Rh, Pd, or Ir) supported on Pr-doped CeO2 were comparatively evaluated regarding their CO2 methanation catalytic performance. Ru was the sole noble metal phase that could dramatically promote the catalytic activity of the corresponding monometallic catalyst, whereas the incorporation of the other noble metals either retained (Pt and Ir) or worsened (Rh and Pd) the catalytic performance. The best–performing RuNi bimetallic catalyst maintained around 80 % CO2 conversion and 99.5 % CH4 selectivity at 325 °C during 50 h of operation. Ru was found to be well dispersed along the support (as single atoms or small clusters), while a small part of it was also dispersed atop the medium-sized Ni nanoparticles. Its promoting ability was attributed to the improved metal dispersion, catalyst reducibility, moderate basicity and provision of additional active sites for CO2 and H2 dissociation, while DFT analysis evidenced that a Ru single atom atop a Ni cluster/ small particle is the structure that is most favorable towards the initial CO2 adsorption and dissociation.
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