Zhu Siyuan, Wu Qian, Dai Chencheng, Yu Anke, Wu Tianze, Ren Xiao, Li Xiaoning, Tadich Anton, Deng Dengfu, Liu Tao, Wu Qiong, Yue Ming, Xu Zhichuan J
School of Energy Storage Science and Engineering, North China University of Technology, Beijing, China.
School of Materials Science and Engineering, Nanyang Technological University, Singapore, Singapore.
Nat Chem. 2025 Aug 14. doi: 10.1038/s41557-025-01900-1.
Ammonia has recently attracted growing attention as a promising hydrogen carrier because it can be liquefied and stored in bulk under mild conditions. To fully harness its potential, more efforts are needed to elucidate and control the mechanisms of its decomposition. Here we show that intermediate dimerization processes proceed through a cooperative spin alignment effect between intermediates and can be promoted by the magnetic ordering rearrangement of magnetic substrates. We explored a series of Co/Pt magnetic thin-film catalysts as model materials to investigate spin-sensitive NH dimerization and eventual enhancement on catalytic activity. Through in situ spectroscopic analysis and theoretical verification, we demonstrate that coupling of N-NH with aligned net magnetic moments is the most favourable with the lowest energy barriers. This provides a precedent for understanding spin kinetics to help improve the catalytic efficiency of electrochemical ammonia decomposition.
氨作为一种有前景的氢载体最近受到了越来越多的关注,因为它可以在温和条件下液化并大量储存。为了充分发挥其潜力,需要付出更多努力来阐明和控制其分解机制。在这里,我们表明中间二聚化过程通过中间体之间的协同自旋排列效应进行,并且可以通过磁性基底的磁有序重排来促进。我们探索了一系列Co/Pt磁性薄膜催化剂作为模型材料,以研究自旋敏感的NH二聚化以及最终对催化活性的增强作用。通过原位光谱分析和理论验证,我们证明N-NH与排列的净磁矩的耦合是最有利的,且能量垒最低。这为理解自旋动力学以帮助提高电化学氨分解的催化效率提供了一个先例。