Enlarging the Three-Phase Boundary to Raise CO2/CH4 Conversions on Exsolved Ni-Fe Alloy Perovskite Catalysts by Minimal Rh Doping

被引:8
作者
Yao, Xueli [1 ]
Cheng, Qingpeng [1 ]
Bai, Xueqin [1 ]
Davaasuren, Bambar [2 ]
Melinte, Georgian [2 ]
Morlanes, Natalia [1 ]
Cerrillo, Jose Luis [1 ]
Velisoju, Vijay Kumar [1 ]
Mohamed, Hend Omar [1 ]
Kolubah, Pewee Datoo [1 ]
Zheng, Lirong [3 ]
Han, Yu [1 ]
Bakr, Osman M. [1 ]
Gascon, Jorge [1 ,4 ]
Castano, Pedro [1 ,4 ]
机构
[1] King Abdullah Univ Sci & Technol KAUST, KAUST Catalysis Ctr KCC, Thuwal 239556900, Saudi Arabia
[2] KAUST, Core Labs, Thuwal 239556900, Saudi Arabia
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
[4] King Abdullah Univ Sci & Technol KAUST, Chem Engn Program, Phys Sci & Engn PSE Div, Thuwal 239556900, Saudi Arabia
来源
ACS CATALYSIS | 2024年 / 14卷 / 08期
关键词
exsolved perovskite; CO2 reforming of CH4; nickel-ironalloy; three-phaseboundary; catalyst deactivation; METAL-SUPPORT INTERACTIONS; IN-SITU EXSOLUTION; CARBON DEPOSITION; ACTIVE CATALYST; ANODE MATERIAL; CO2; REDUCTION; NANOPARTICLES; METHANE; OXIDE; PERFORMANCE;
D O I
10.1021/acscatal.4c00151
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Exsolved Ni-Fe alloy perovskite catalysts exhibit remarkable coking resistance during C-H and C-O activation. However, metallic utilization is typically incomplete, resulting in relatively low catalytic activity. Herein, we investigated minimal doping with Rh to boost the catalytic activity in the dry reforming of methane by promoting exsolution and enlargement of the three-phase boundary between the alloy, support, and reactants. The Rh influences the formation of the Ni-Fe alloy, as revealed by X-ray diffraction, and promotes the individual and collective CH4 and CO2 conversions, as revealed by packed bed reactor runs, temperature-programmed surface reactions, and in situ infrared spectroscopy. A minimal 0.21 wt % Rh addition enlarges the three-phase boundary while improving oxygen mobility and storage. The oxygen mobility is responsible for promoting CH4 dissociation and dynamic removal of carbon-containing intermediates, such that the catalyst remains stable for over 100 h under both 1 and 14 bar.
引用
收藏
页码:5639 / 5653
页数:15
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