Jahril Nur Fauzan, Ahsan Ali, M. A. Shadab Siddiqui, Md. Delowar Hossain, Md. Abdul Aziz, Md. Hasan Zahir, Fahad Alam, M. Nasiruzzaman Shaikh
{"title":"Ammonia as a Hydrogen Carrier: Advances in Storage, Catalytic Decomposition, Kinetics, and Techno-Economic Analysis","authors":"Jahril Nur Fauzan, Ahsan Ali, M. A. Shadab Siddiqui, Md. Delowar Hossain, Md. Abdul Aziz, Md. Hasan Zahir, Fahad Alam, M. Nasiruzzaman Shaikh","doi":"10.1002/tcr.70200","DOIUrl":null,"url":null,"abstract":"<p>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 CO<sub>2</sub>-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, Al<sub>2</sub>O<sub>3</sub>, 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 Al<sub>2</sub>O<sub>3</sub> 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.</p>","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":"26 9","pages":""},"PeriodicalIF":8.9000,"publicationDate":"2026-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical record","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/tcr.70200","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/29 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
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.
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.