Highly efficient cobalt catalysts promoted by CeO2-Al2O3 for ammonia decomposition

被引:2
作者
Xu, Kai [1 ,2 ]
Jiang, Na [2 ]
Wang, Peng [1 ]
Wang, Wei-Wei [2 ]
Jia, Chun-Jiang [2 ]
机构
[1] Shandong Univ, State Key Lab Crystal Mat, Jinan 250100, Peoples R China
[2] Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, Key Lab Special Aggregated Mat, Jinan 250100, Peoples R China
基金
美国国家科学基金会;
关键词
NH3;
D O I
10.1039/d4cy00835a
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
Hydrogen production by ammonia decomposition reveals great advantages in the utilization of hydrogen. Low-cost, efficient and stable transition metal catalysts are the key for the ammonia decomposition reaction. Using multi-component promoters adjust the electronic and geometric structures of bulk catalysts, which might be an effective approach for obtaining non-noble metal catalysts with excellent performance. In this work, CeO2-Al2O3 bi-promoters were used and significantly improved the catalytic performance of bulk cobalt catalysts. The optimized CoCeAlOx catalyst achieved 94.3% and 65.3% NH3 conversion at 550 degrees C and 500 degrees C (GHSV = 30 000 mL g(cat)(-1) h(-1)), respectively, and exhibited strong stability within 200 h. It was found that the interaction between Co-CeO2-Al2O3 effectively inhibited the aggregation of the Co-0 active species, which enormously promoted the catalytic activity and stability of CoCeAlOx. CeO2-Al2O3 bi-promoters adjusted the surface properties of catalysts, bringing suitable NH3 adsorption and N-2 desorption, and suppressing the hydrogen poisoning significantly. This work provided a reliable strategy for the construction of high-efficiency catalysts working under the harsh conditions for ammonia decomposition.
引用
收藏
页码:5678 / 5686
页数:9
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