Li Neng, Zhang Zhongyong, Wang Zheng, Liu Bin, Zhou Deyong, Zhou Xing, Zhang Peng, Zhao Xiujian
State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology, Wuhan 430070, China.
Shenzhen Research Institute of Wuhan University of Technology, Shenzhen 518000, China.
Mater Horiz. 2024 Apr 2;11(7):1769-1778. doi: 10.1039/d3mh01945d.
Ammonia (NH) plays important roles in chemistry, the environment, and energy; however, the synthesis of NH relies heavily on the Haber-Bosch process, causing serious environmental pollution and energy consumption. A clean and effective strategy for the synthesis of NH involves nitrogen (N) being transformed to ammonia (NH) using electrocatalysis. Adjusting the magnetism of electrocatalysts may improve their performance, and therefore, four magnetic states, nonmagnetic (NM), ferromagnetic (FM), interlayer antiferromagnetic (Inter-AFM), and intra-layer antiferromagnetic (Intra-AFM) CrCO-MXene were designed to explore magnetoelectrocatalysis performance using well-defined density functional theory (DFT) calculations in this study. Upon comparing the nitrogen reduction limiting potentials of N molecules on the surface of the four different magnetic states in CrCO-MXene, and the selectivity calculations of the hydrogen evolution reaction (HER) and nitrogen reduction reaction (NRR), the Inter-AFM CrCO-MXene is shown to be a better NRR electrocatalyst than the other three cases. This study paves way to unravel the mystery of the spin-catalytic mechanism and will lay a solid foundation for eNRR electrocatalysts with magnetic materials for environmental and energy applications.
氨(NH₃)在化学、环境和能源领域发挥着重要作用;然而,氨的合成严重依赖哈伯-博施法,这会造成严重的环境污染和能源消耗。一种清洁有效的氨合成策略是利用电催化将氮(N₂)转化为氨(NH₃)。调整电催化剂的磁性可能会提高其性能,因此,本研究设计了四种磁性状态,即非磁性(NM)、铁磁性(FM)、层间反铁磁性(Inter-AFM)和层内反铁磁性(Intra-AFM)的CrCO-MXene,以使用精确的密度泛函理论(DFT)计算来探索磁电催化性能。通过比较CrCO-MXene中四种不同磁性状态表面上N₂分子的氮还原极限电位,以及析氢反应(HER)和氮还原反应(NRR)的选择性计算,结果表明层间反铁磁性CrCO-MXene是比其他三种情况更好的NRR电催化剂。本研究为揭开自旋催化机制之谜铺平了道路,并将为用于环境和能源应用的含磁性材料的电催化氮还原(eNRR)电催化剂奠定坚实基础。