首页|金属催化剂催化水合肼分解制氢的研究进展

金属催化剂催化水合肼分解制氢的研究进展

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氢能是一种高效、清洁的新能源,有望在未来的能源领域占据重要地位。开发安全、高效的储氢材料是实现氢能大规模实际应用的关键。水合肼(N2H4·H2O)的储氢含量高(8%)且便于运输和储存,是一种具有良好应用前景的储氢材料。研究表明,使用合适的催化剂可以有效降低水合肼分解制氢反应能垒,显著提高水合肼脱氢速率。因此,开发温和条件下高效脱氢催化剂已成为水合肼作为储氢材料规模化应用的研究热点。简要介绍水合肼分解脱氢机制,并阐述水合肼脱氢催化剂体系近年的研究进展,并对提高催化剂的催化性能的策略进行分析。归纳总结改善水合肼脱氢催化剂的催化活性和制氢选择性的方法(如构筑合金结构等),添加助剂创造适宜的外部化学环境,调控金属-载体强相互作用,优化合成方法增加金属催化剂表面积和活性位点等,并对该领域未来的发展进行了展望。
Research Progress of Hydrogen Production from Hydrous Hydrazine Decompo-sition Catalyzed by Metal Catalysts
Hydrogen is an efficient and clean new energy,and it is expected to occupy an important position in the future energy field.Developing safe and efficient hydrogen storage materials is the key to realize large-scale practical application of hydrogen energy.Hydrous hydrazine(N2H4·H2O)is a promising hydrogen storage material because of its high hydrogen storage content(8%)and conve-nient transportation and storage.The research show that the appropriate metal catalyst can effectively reduce the reaction energy barrier of hydrous hydrazine decomposition and hydrogen production,and significantly increase the dehydrogenation rate of hydrous hydra-zine.Therefore,the development of efficient dehydrogenation catalyst under mild conditions has become a research hotspot of hydrous hydrazine as a hydrogen storage material.In this paper,the decomposition and dehydrogenation mechanism of hydrous hydrazine were briefly introduced,and the research progress of hydrous hydrazine dehydrogenation catalyst system in recent years was systematically expounded,and the strategies to improve the catalytic performance of the catalyst were analyzed.Essentially,the catalytic decomposi-tion reaction path of N2H4 mainly depended on the cleavage sequence of N-N bond and N-H bond.The purpose of the prepared cata-lyst was to promote the cleavage of N-H bond.In recent years,the research on dehydrogenation catalysts of hydrous hydrazine had ex-perienced metal nanoparticles,composite oxides and metal-supported catalysts.Metal nanoparticles were usually synthesized by co-re-duction method,some of which could selectively decompose hydrous hydrazine,but the overall catalytic performance was poor.This was because the free metal nanoparticles were easy to agglomerate,which reduced the specific surface area and active sites of the cata-lyst,resulting in the decline of catalytic performance.Although the addition of surfactant could avoid the aggregation of metal nanopar-ticles,it would cover the active sites on the surface of the particles,which could not fundamentally improve the catalytic performance.Relatively speaking,as a catalyst in strong alkaline environment,composite oxide could achieve 100%selectivity of hydrogen produc-tion,and its catalytic performance was considerable,but there were some problems such as low strength and easy change of metal va-lence.Supported catalyst was to load metal nanoparticles on the carrier/carrier surface,which not only ensured the good dispersion of active metal nanoparticles,but also provided excellent catalytic performance stability for nano-catalyst.In addition,the carrier would have a synergistic effect with metal nanoparticles,and sometimes the carrier could provide a suitable chemical environment for the re-action,which was conducive to improving the catalytic activity and hydrogen production selectivity of the catalyst.With the deepening of scholars'research and understanding on the mechanism of hydrogen production by catalytic decomposition,the nano-catalyst devel-oped showed extremely high catalytic activity for hydrogen production by catalytic decomposition of hydrous hydrazine.After continu-ous exploration,the researchers summarized the following design strategies that affect the catalytic performance of the catalyst:build-ing alloy structure,create a suitable chemical environment for nano-catalyst,introducing strong metal-carrier interaction(SMSI)and optimizing the synthesis method to increase the surface area and active sites.

hydrogen energyhydrogen storage materialshydrous hydrazinemetal catalysts

孔军、李蓉、刘勇、许立信、叶明富、万超

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安徽工业大学化学与化工学院,工程研究院,安徽马鞍山 243000

南开大学先进能源材料化学教育部重点实验室,天津 300071

安庆师范大学光电磁功能材料安徽省重点实验室,光电磁功能配合物和纳米配合物安徽省重点实验室,安徽安庆 246011

九江学院江西省生态化工工程技术研究中心,江西九江 332005

浙江大学化学工程与生物工程学院,浙江杭州 310027

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氢能 储氢材料 水合肼 金属催化剂

国家自然科学基金青年项目联合项目安徽省自然科学基金青年项目安徽省科技重大专项中国博士后面上项目派出项目特别资助站中项目安徽省光电磁性功能材料重点实验室开放基金项目江西省生态化工工程研究中心开放基金项目

22108238U22A204081908085QB68201903a050200552019M662060PC20220462020T130580ZD2021007STKF2109

2024

稀有金属
北京有色金属研究总院

稀有金属

CSTPCD北大核心
影响因子:1.483
ISSN:0258-7076
年,卷(期):2024.48(8)