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Research Article

Sm2+ ions boost ammonia electrooxidation reaction on samarium oxide anode for hydrogen generation in non-aqueous electrolyte

Xingyu Liu, Xue Yang, Han Sun( ), Zekai Yang, Haijun Chen( )
Tianjin Key Laboratory of Optoelectronic Thin Film Devices and Technology, College of Electronic Information and Optical Engineering, Nankai University, Tianjin 300350, China
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Abstract

Ammonia has garnered recognition as a zero-carbon fuel due to its high-density hydrogen storage capacity and its convenience for storage and transportation. To address the challenges associated with the direct usage of ammonia, the development of NH3-to-H2 conversion technologies has emerged as a promising and effective approach. Herein, we present for the first time that crystallized Sm2O3−x electrodes demonstrate high and stable electrocatalytic activities, including N2 evolution rate and Faradaic efficiency, for ammonia electrolysis in a non-aqueous electrolyte. It was observed that Sm2+ ions in samarium oxide play an indispensable role in the ammonia electrooxidation reaction on the anodes. Furthermore, the mechanism of ammonia electrooxidation has also been elucidated, laying the foundation for a better understanding of the relationship between local structure and electrochemical properties in order to facilitate research on Pt-free electrocatalysts for the electrolysis of ammonia into H2.

Graphical Abstract

The concentration of Sm2+ ions in samarium oxide (Sm2O3−x) was controlled by a simple pyrolysis method. Sm2+ ions present in Sm2O3−x were found to be favorable for NH3 adsorption and contribute to the dehydrogenation of NH3, leading to enhanced electrocatalytic activities for ammonia electrolysis in a non-aqueous electrolyte.

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Nano Research
Pages 5856-5862

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Cite this article:
Liu X, Yang X, Sun H, et al. Sm2+ ions boost ammonia electrooxidation reaction on samarium oxide anode for hydrogen generation in non-aqueous electrolyte. Nano Research, 2024, 17(7): 5856-5862. https://doi.org/10.1007/s12274-024-6553-1
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Received: 28 November 2023
Revised: 09 January 2024
Accepted: 05 February 2024
Published: 13 March 2024
© Tsinghua University Press 2024