氨生产
X射线光电子能谱
催化作用
氨
化学工程
多孔性
材料科学
组合化学
纳米技术
拉曼光谱
化学
扫描电子显微镜
金属
有机化学
物理
光学
工程类
复合材料
作者
Luis Sandoval‐Diaz,Raoul Blume,Kassiogé Dembélé,Jan Folke,Maxime Boniface,Frank Girgsdies,Adnan Hammud,Zahra Gheisari,Danail Ivanov,René Eckert,Stephan J. Reitmeier,Andreas Reitzmann,Robert Schloegl,Beatriz Roldán Cuenya,Holger Ruland,Axel Knop‐Gericke,Thomas Lunkenbein
标识
DOI:10.1038/s41467-025-63061-6
摘要
Ammonia is industrially produced by the Haber-Bosch process over a fused, multi-promoted iron-based catalyst. Current knowledge about the reaction has been derived from model systems of reduced structural complexity, impeding any clear-cut structure-activity correlation relevant for the industrial counterpart. Here, we unveil the structural evolution of complex, technical, multi-promoted ammonia synthesis catalysts by operando scanning electron microscopy and near-ambient pressure X-ray photoelectron spectroscopy. We highlight that the activation is the critical step in which the catalyst is formed and decode the pivotal role of the promoters. We discover that the active structure consists of a nanodispersion of Fe covered by mobile K-containing adsorbates, so called "ammonia K". The porous catalyst is stabilized by mineral cementitious phases containing oxides of Al, Si, Ca, and Fe. The synergism between the different promoters contributes simultaneously to the structural stability, hierarchical architecture, catalytic activity, and poisoning resistance. The confluence of these aspects is the key for the superior performance of technical catalyst formulations.
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