Ammonia as a Hydrogen Carrier: Advances in Storage, Catalytic Decomposition, Kinetics, and Techno-Economic Analysis

IF 8.9 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Chemical record Pub Date : 2026-09-22 Epub Date: 2026-06-29 DOI:10.1002/tcr.70200
Jahril Nur Fauzan, Ahsan Ali, M. A. Shadab Siddiqui, Md. Delowar Hossain, Md. Abdul Aziz, Md. Hasan Zahir, Fahad Alam, M. Nasiruzzaman Shaikh
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引用次数: 0

Abstract

A carbon-free energy system might use ammonia as a hydrogen carrier owing to its high hydrogen concentration, good liquefaction, and worldwide production and transportation infrastructure. Catalytic ammonia breakdown provides a CO2-free hydrogen-generating method, but high temperatures, catalyst deactivation, and expense restrict its practicality. This study covers important aspects of ammonia decomposition catalysts, including Ru-, Ni-, and Co-based systems supported by carbon, Al2O3, and perovskite oxides. To develop structure–activity connections and identify rate-limiting stages under various operating regimes, thermodynamic, kinetic, and fundamental reaction processes are examined. Ru-based catalysts, especially those supported on conductive carbons and tailored perovskites, are standards for low-temperature activity, but their high cost and stability prevent large-scale application. Combining Ni-based catalysts with Al2O3 or basic perovskite supports offers a good balance between activity, cost, and commercial practicality, making them the dominant non-noble alternatives. Due to strong metal–support interactions and alternate reaction routes, Co-based catalysts in perovskite formulations seem promising despite being inherently less active. Support chemistry, promoters, metal dispersion, and oxygen vacancies are discussed, along with low-temperature operation and scale-up problems and research prospects.

氨作为氢载体:储存、催化分解、动力学和技术经济分析的进展。
由于氨的氢浓度高,液化性好,且生产和运输基础设施遍布全球,因此无碳能源系统可能会使用氨作为氢载体。催化氨分解提供了一种无co2的制氢方法,但高温、催化剂失活和费用限制了其实用性。本研究涵盖了氨分解催化剂的重要方面,包括碳、Al2O3和钙钛矿氧化物支持的Ru、Ni和co基体系。为了发展结构-活性联系,并确定在各种操作制度下的限速阶段,研究了热力学,动力学和基本反应过程。钌基催化剂,特别是那些在导电碳和定制钙钛矿上支撑的催化剂,是低温活性的标准,但它们的高成本和稳定性阻碍了大规模应用。将镍基催化剂与Al2O3或碱性钙钛矿载体结合,在活性、成本和商业实用性之间取得了很好的平衡,使其成为主要的非贵金属替代品。由于强大的金属支撑相互作用和交替的反应途径,钙钛矿配方中的co基催化剂尽管本身活性较低,但似乎很有希望。讨论了支持化学、促进剂、金属分散和氧空位,以及低温操作和放大问题和研究前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical record
Chemical record 化学-化学综合
CiteScore
11.00
自引率
3.00%
发文量
188
审稿时长
>12 weeks
期刊介绍: The Chemical Record (TCR) is a "highlights" journal publishing timely and critical overviews of new developments at the cutting edge of chemistry of interest to a wide audience of chemists (2013 journal impact factor: 5.577). The scope of published reviews includes all areas related to physical chemistry, analytical chemistry, inorganic chemistry, organic chemistry, polymer chemistry, materials chemistry, bioorganic chemistry, biochemistry, biotechnology and medicinal chemistry as well as interdisciplinary fields. TCR provides carefully selected highlight papers by leading researchers that introduce the author''s own experimental and theoretical results in a framework designed to establish perspectives with earlier and contemporary work and provide a critical review of the present state of the subject. The articles are intended to present concise evaluations of current trends in chemistry research to help chemists gain useful insights into fields outside their specialization and provide experts with summaries of recent key developments.
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