催化作用
贵金属
分解
氨生产
材料科学
氨
Atom(片上系统)
钡
金属
色散(光学)
无机化学
化学
有机化学
冶金
物理
嵌入式系统
光学
计算机科学
作者
Kai Xu,Y. Zhang,Weiwei Wang,Mi Peng,Jincheng Liu,Chao Ma,Yawen Zhang,Chun‐Jiang Jia,Ding Ma,Chun‐Hua Yan
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-11-05
卷期号:64 (4): e202416195-e202416195
被引量:24
标识
DOI:10.1002/anie.202416195
摘要
As a well-established topic, single-atom catalyst has drawn growing interest for its high utilization of metal. However, researchers prefer to develop various active metals with single-atom form, the intrinsic roles of single-atom promoters are usually underrated, which are significant in boosting reaction activity. In this work, Ba single atoms were in situ prepared in the Co-Ba/Y2O3 catalyst with crystallized BaCO3 as the precursor under the ammonia decomposition reaction condition. The optimized Co-Ba/Y2O3 catalyst achieves extremely high H2 production rate of 138.3 mmolH2 ⋅ gcat -1 ⋅ min-1 at very low temperature (500 °C, GHSV=840,000 mL ⋅ g-1 ⋅ h-1) and Co-Ba/Y2O3 exhibits excellent durability during the 350 h test, which realizes the highest activity among all non-noble catalysts, and reaches or even exceeds numerous reported Ru-based catalysts. Both Y2O3 and Co demonstrate positive interactions with Ba, which significantly facilitates the dispersion of Ba species at high temperatures (≥600 °C). Ba single atoms significantly enhance the charge density of Co and form additionally active Co-O-Ba-Y2O3 interfacial sites, which alleviates hydrogen poisoning and decreases the reaction barrier of the N-H bond activation of *NH. The exploration of atomically dispersed promoters is groundbreaking in heterogeneous catalysis, which opens up a whole new domain of catalytic material.
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