Kim Na Young, Lee Seok-Ho, Lee Seong Ho, Lee Kwan-Young
Department of Chemical and Biological Engineering, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, Republic of Korea.
Strategic Research Center for Clean Hydrogen Storage and Utilization Korea Institute of Science and Technology, Seoul 02792, Republic of Korea.
ACS Appl Mater Interfaces. 2025 Aug 6;17(31):44596-44607. doi: 10.1021/acsami.5c10234. Epub 2025 Jul 24.
Ammonia (NH) has great potential as a hydrogen carrier material and plays an important role in chemistry. NH is synthesized through a conventional Haber-Bosch process; however, this method requires considerable energy. Thus, it is important to develop NH synthesis catalysts that operate under mild conditions. This research revealed that Sm-doped Ru/LaCeO catalysts (Ru/LaCeSmO) increased the NH synthesis under mild conditions (400 °C, 0.1 MPa). Catalyst with an optimal Sm doping ratio ( = 0.75) showed the highest NH productivity of 4563 μmol h g. This result is mainly attributed to the transition from a fluorite to a C-type structure by introducing Sm to Ru/LaCeO, since the C-type structure possesses a higher abundance of oxygen vacancies compared to fluorite. This structural transition facilitated electron transfer to the active Ru metal and enhanced hydrogen spillover on the support, substantially improving the performance of the optimized catalysts. Nevertheless, the introduction of Sm dopants brought certain deactivation effects, including blocking active sites on Ru and promoting a high degree of ordering in the oxygen vacancy, which induced the degradation of electron mobility. As a result, it became evident that not just the concentration but also the arrangement of oxygen vacancies critically influences the catalytic performance. These results underscore the importance of precisely tuning the Sm doping level to achieve a balance between its beneficial and adverse effects on the structural and electronic properties, which is critical for maximizing ammonia synthesis activity.
氨(NH₃)作为一种氢载体材料具有巨大潜力,在化学领域发挥着重要作用。NH₃通过传统的哈伯-博施工艺合成;然而,这种方法需要大量能量。因此,开发在温和条件下运行的NH₃合成催化剂很重要。本研究表明,Sm掺杂的Ru/LaCeO催化剂(Ru/LaCeSmO)在温和条件(400℃,0.1MPa)下提高了NH₃的合成。具有最佳Sm掺杂比( = 0.75)的催化剂显示出最高的NH₃生产率,为4563 μmol h⁻¹ g⁻¹。这一结果主要归因于通过将Sm引入Ru/LaCeO,使其从萤石结构转变为C型结构,因为与萤石相比,C型结构具有更高丰度的氧空位。这种结构转变促进了电子向活性Ru金属的转移,并增强了载体上的氢溢流,显著提高了优化后催化剂的性能。然而,Sm掺杂剂的引入带来了一定的失活效应,包括阻塞Ru上的活性位点和促进氧空位的高度有序化,这导致了电子迁移率的下降。结果表明,不仅氧空位的浓度,而且其排列对催化性能都有至关重要的影响。这些结果强调了精确调节Sm掺杂水平以在其对结构和电子性质的有利和不利影响之间取得平衡的重要性,这对于最大化氨合成活性至关重要。