非阻塞I/O
分解
制氢
催化作用
氨
铈
氨生产
无机化学
氢
氢气储存
材料科学
化学工程
贵金属
化学
有机化学
工程类
作者
Zhaohua Wang,Xuan Tang,Maolin Wang,Yao Xu,Xuetao Qin,Lihui Zhou,Mi Peng,Sheng Dai,Ding Ma
出处
期刊:Chem catalysis
[Elsevier]
日期:2024-05-01
卷期号:4 (5): 101000-101000
标识
DOI:10.1016/j.checat.2024.101000
摘要
Ammonia is recognized for its potential in hydrogen storage and transportation. Among methods for hydrogen production from ammonia, catalytic decomposition stands out, and developing economical alternatives to noble metal catalysts like ruthenium (Ru) is crucial. Here, we report an exsolution strategy to obtain a size-constrained Ni0-NiO small ensemble on MgO that outperforms bare Ni single atoms and particles in ammonia decomposition. Adding Ce to the NiMg catalyst significantly enhances activity, doubling the hydrogen production rate to 92 mmolH2 gcat−1 min−1 at 550°C, surpassing most Ni-based catalysts. Characterization reveals the role of cerium in forming active Ni0-NiO ensembles by occupying specific sites on MgO. Cerium (Ce) also affects hydrogen and ammonia adsorption and alters reaction pathways. Our work highlights the structure control of transition metal sites and the promotion mechanism of rare-earth elements for ammonia conversion and hydrogen production reaction.
科研通智能强力驱动
Strongly Powered by AbleSci AI