| Literature DB >> 29522310 |
Hamidreza Arandiyan, Yuan Wang, Jason Scott, Sara Mesgari, Hongxing Dai1, Rose Amal.
Abstract
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.Entities:
Keywords: CO2 methanation; bimetallic Rh−Ni; in situ exsolution; perovskite catalyst; three-dimensionally ordered macropore
Year: 2018 PMID: 29522310 DOI: 10.1021/acsami.8b00889
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229