Unique CO 2 methanation catalysts comprising bimetallic Ni–Rh nanoalloy/3DOM LaAlO 3 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 LaAlO 3 [13.9 mol/(mol h)] compared to Rh/3DOM LaNi 0.08 Al 0.92 O 3 [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 CO 2 methanation. The hierarchically porous structure of the perovskite support provides a high dispersion of bimetallic Ni–Rh NPs.
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Arandiyan et al. (2018) studied this question.
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