In Situ Exsolution of Bimetallic Rh-Ni Nanoalloys: a Highly Efficient Catalyst for CO2 Methanation

被引:104
作者
Arandiyan, Hamidreza [1 ]
Wang, Yuan [1 ]
Scott, Jason [1 ]
Mesgari, Sara [2 ]
Dai, Hongxing [3 ,4 ]
Amal, Rose [1 ]
机构
[1] Univ New South Wales, Particles & Catalysis Res Grp, Sch Chem Engn, Sydney, NSW 2052, Australia
[2] Univ New South Wales, Sch Mech & Mfg Engn, Sydney, NSW 2052, Australia
[3] Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Beijing 100124, Peoples R China
[4] Beijing Univ Technol, Lab Catalysis Chem & Nanosci, Beijing 100124, Peoples R China
关键词
in situ exsolution; bimetallic Rh-Ni; perovskite catalyst; three-dimensionally ordered macropore; CO2; methanation; PEROVSKITE CATALYST; CARBON-DIOXIDE; COMBUSTION; PERFORMANCE; HYDROGENOLYSIS; PARTICLES; ALLOY; SIZE;
D O I
10.1021/acsami.8b00889
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Unique CO2 methanation catalysts comprising bimetallic Ni-Rh nano-alloy/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.
引用
收藏
页码:16352 / 16357
页数:6
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