双金属片
甲烷化
材料科学
催化作用
化学工程
纳米颗粒
钙钛矿(结构)
金属
无机化学
纳米技术
冶金
有机化学
化学
工程类
作者
Hamidreza Arandiyan,Yuan Wang,Jason Scott,Sara Mesgari,Hongxing Dai,Rose Amal
标识
DOI:10.1021/acsami.8b00889
摘要
Unique CO2 methanation catalysts comprising bimetallic Ni-Rh nanoalloy/3DOM LaAlO3 have been successfully prepared via a poly(methyl methacrylate) microsphere colloidal crystal-templating route, followed by the in situ growth of Ni nanoparticles (NPs). Here, we show that unlike traditional Ni particles deposited on a perovskite support, the exsolution of Ni occurs on both the external and internal surface of the porous perovskite substrate, leading to a strong metal-support interaction. Owing to the exsolution of Ni and the formation of Ni-Rh nanoalloys, a 52% enhancement in the methanation turnover frequency was obtained over the Ni-Rh/3DOM LaAlO3 [13.9 mol/(mol h)] compared to Rh/3DOM LaNi0.08Al0.92O3 [9.16 mol/(mol h)] before reduction treatment. The results show that the low-temperature reducibility, rich surface adsorbed oxygen species, and basic sites of the catalyst greatly improve its activity toward CO2 methanation. The hierarchically porous structure of the perovskite support provides a high dispersion of bimetallic Ni-Rh NPs.
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