Affiliation:
1. Institut de Chimie Moléculaire de l'Université de Bourgogne UMR CNRS 6302 Université Bourgogne Dijon France
2. Institute of Energy and Climate Research Fundamental Electrochemistry (IEK-9) Forschungszentrum Jülich GmbH 52425 Jülich Germany
3. CNRS Université de Bordeaux Institut de Chimie de la Matière Condensée de Bordeaux (ICMCB) 87 Av. Dr. Schweitzer F-33608 Pessac Cedex France
4. Institute of Physical Chemistry RWTH Aachen University 52074 Aachen Germany
Abstract
AbstractThe adoption of green hydrogen economy is an indispensable necessity in the current global scenario of environment and energy security. In this endeavor, ammonia is poised to play a key vector of hydrogen to mitigate the challenges arising from transportation, storage and safety. Besides containing a high volumetric and gravimetric hydrogen density, NH3 decomposition into H2 for onsite utilization as a distributed energy source is devoid of greenhouse gases production. In this endeavor, significant technological advancements have been made for in situ production of H2 from NH3 decomposition and the use of NH3 in fuel cell devices to produce electricity. The ammonia decomposition methods to produce H2 mainly involve thermocatalytic, oxidative, electrocatalytic and photocatalytic, among which the catalyst assisted thermal cracking of NH3 has been widely investigated. The research progress in electrolysis of NH3 has been notable in the last couple of years and provides a low‐cost alternative to produce H2 at room temperature. In the area of device development, solid oxide fuel cells (SOFC) have witnessed rapid development in the performances and stability, as ammonia is completely decomposed into H2 and N2 at high operating temperature above ~700 °C.
Funder
Université de Bourgogne
Agence Nationale de la Recherche
Cited by
1 articles.
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