Zhang Ke, Cao Ang, Wandall Lau Halkier, Vernieres Jerome, Kibsgaard Jakob, Nørskov Jens K, Chorkendorff Ib
Department of Physics, Technical University of Denmark, Kongens Lyngby, Denmark.
Science. 2024 Mar 22;383(6689):1357-1363. doi: 10.1126/science.adn0558. Epub 2024 Mar 21.
Over the past two decades, there has been growing interest in developing catalysts to enable Haber-Bosch ammonia synthesis under milder conditions than currently pertain. Rational catalyst design requires theoretical guidance and clear mechanistic understanding. Recently, a spin-mediated promotion mechanism was proposed to activate traditionally unreactive magnetic materials such as cobalt (Co) for ammonia synthesis by introducing hetero metal atoms bound to the active site of the catalyst surface. We combined theory and experiment to validate this promotion mechanism on a lanthanum (La)/Co system. By conducting model catalyst studies on Co single crystals and mass-selected Co nanoparticles at ambient pressure, we identified the active site for ammonia synthesis as the B site of Co steps with La adsorption. The turnover frequency of 0.47 ± 0.03 per second achieved on the La/Co system at 350°C and 1 bar surpasses those of other model catalysts tested under identical conditions.
在过去二十年中,人们对开发能够在比当前条件更温和的条件下实现哈伯-博施法合成氨的催化剂的兴趣与日俱增。合理的催化剂设计需要理论指导和清晰的机理理解。最近,有人提出了一种自旋介导的促进机制,通过引入与催化剂表面活性位点结合的杂金属原子来激活传统上无反应性的磁性材料,如钴(Co)用于氨合成。我们结合理论和实验来验证镧(La)/Co体系上的这种促进机制。通过在环境压力下对Co单晶和质量选择的Co纳米颗粒进行模型催化剂研究,我们确定氨合成的活性位点是La吸附的Co台阶的B位。在350°C和1巴下,La/Co体系实现的每秒0.47±0.03的周转频率超过了在相同条件下测试的其他模型催化剂的周转频率。