Zhang Yangyu, Li Jiaxin, Zhou Yanliang, Au Chak-Tong, Wang Xiuyun, Jiang Lilong
National Engineering Research Center of Chemical Fertilizer Catalyst, Fuzhou University, Fuzhou 350002, China.
Fundam Res. 2024 Jan 22;5(4):1464-1477. doi: 10.1016/j.fmre.2023.11.016. eCollection 2025 Jul.
Ammonia is an important chemical and a carrier of hydrogen. Artificial nitrogen fixation mainly relies on the Haber-Bosch process driven by thermo-catalysis, where the activation of N usually follows a dissociative route. Nonetheless, an associative route is common in electrocatalytic or biological nitrogen fixation under ambient conditions. Recently, it was reported that N can be activated via an associative mechanism in thermocatalytic ammonia synthesis over some special catalytic materials or active sites, which exhibits enormous potential to realize efficient ammonia synthesis under relatively mild conditions (≤ 400 °C and ≤ 1 MPa). In this review, we focus on the recent progress of ammonia synthesis that follows an associative mechanism. Besides the hydride and nitride materials, the catalysts with highly dispersed active sites are included. We discuss the key factors that drive N activation via an associative route and examine their correlation with catalytic performance. Finally, we delve into the perspectives of catalyst design tailored to facilitate an associative mechanism.
氨是一种重要的化学物质,也是氢的载体。人工固氮主要依赖于热催化驱动的哈伯-博施法,其中氮的活化通常遵循解离途径。然而,在环境条件下的电催化或生物固氮中,缔合途径很常见。最近,有报道称,在一些特殊的催化材料或活性位点上,通过缔合机制在热催化氨合成中可以活化氮,这在相对温和的条件下(≤400°C和≤1MPa)实现高效氨合成具有巨大潜力。在这篇综述中,我们重点关注遵循缔合机制的氨合成的最新进展。除了氢化物和氮化物材料外,还包括具有高度分散活性位点的催化剂。我们讨论了通过缔合途径驱动氮活化的关键因素,并研究了它们与催化性能的相关性。最后,我们深入探讨了为促进缔合机制而量身定制的催化剂设计前景。