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氨分解催化剂研究进展

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氢能作为清洁环保的可再生能源受到全世界的关注.但氢极低的体积能量密度及易燃易爆的特点,给氢气的大规模储运带来困难和危险.氨是一种无碳的氢载体,不仅具有较高的体积和质量能量密度,还有较成熟的储存和运输技术.氨的现场制氢可以解决氢气储存和运输问题,所以氨气储氢正受到人们的广泛关注.氨分解最高效的催化剂是Ru基催化剂,但由于其高昂的价格无法实现大规模应用.在非贵金属基催化剂中,Ni基催化剂的活性最高,且其成本相对较低,被认为十分具有应用潜力.然而,Ru基和Ni基催化体系在活性和稳定性等方面仍存在一些挑战.本文综述了氨分解催化剂的最新研究进展,包括Ru基催化剂、非贵金属Fe基和Ni基催化剂及双金属催化剂等,并对目前文献中的反应机理进行了梳理.
PROGRESS ON CATALYSTS FOR AMMONIA DECOMPOSITION
Hydrogen energy,as a clean and environmentally friendly renewable energy source,is attracting worldwide attention.However,the extremely low volume energy density and the flammable and explosive characteristics of hydrogen bring difficulties and dangers to large-scale storage and transportation of hydrogen.Ammonia is a kind of carbon-free hydrogen carrier,which not only has high volume and mass energy density,but also has mature storage and transportation technology.On-site hydrogen production from ammonia can solve the problems of hydrogen storage and transport,so ammonia hydrogen storage from ammonia is attracting a lot of attention.Currently,the most efficient catalyst for ammonia decomposition is ruthenium-based catalysts,but it can not be used in large scale because of its high price.Among the non-precious metal-based catalysts,Ni-based catalysts have the highest activity and relatively low cost,which are considered to have great application potential.However,Ru-based and Ni-based catalytic systems still have some challenges in terms of activity and stability.In this paper,the latest research progress of ammonia decomposition catalysts,including catalysts based on Ru,catalysts based on non-precious metals Fe and Ni,and bimetallic catalysts,and the reaction mechanism of ammonia decomposition in recent literature were reviewed.

hydrogen energyammonia decompositionruthenium catalystnon-precious metal catalystsmechanism

李世刚、李冰、刘晓晖、郭勇、王艳芹

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华东理工大学绿色化工与工业催化全国重点实验室,上海 200237

上海市质量监督检验技术研究院

储氢 氨分解 Ru基催化剂 非贵金属催化剂 反应机理

国家自然科学基金项目国家自然科学基金项目

2207204121832002

2024

石油炼制与化工
中国石油化工股份有限公司石油化工科学研究院

石油炼制与化工

CSTPCD北大核心
影响因子:0.825
ISSN:1005-2399
年,卷(期):2024.55(2)
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