催化作用
氨生产
氨
金属
化学
Atom(片上系统)
无机化学
有机化学
嵌入式系统
计算机科学
作者
Yuting Jiang,Ziquan Chen,Tao Peng,Long Jiao,Xiulian Pan,Hai‐Long Jiang,Xinhe Bao
标识
DOI:10.1002/ange.202501190
摘要
Abstract Ammonia synthesis is a cornerstone in the chemical industry. Given that the traditional Haber–Bosch (H‐B) process requires very high temperature and pressure, it is imperative to develop catalysts capable of facilitating ammonia synthesis under mild conditions. In this work, a post‐metal replacement strategy is developed to improve the Fe loading in single‐atom Fe‐implanted N‐doped carbon catalysts. Starting from the Zn–Fe–N–C material with single‐atom Zn and Fe sites coexisting in N‐doped porous carbon pyrolyzed from porphyrinic metal–organic frameworks (MOFs), the replacement of single‐atom Zn with Fe sites is performed, which significantly increases the Fe loading from 1.33 to 2.39 wt%. This effectively suppresses the migration and agglomeration of Fe, yielding Fe–N–C with high metal loading (Fe HL –N–C). Notably, the Fe HL –N–C catalyst exhibits a catalytic rate of 558 µmol·g cat −1 ·h −1 at 300 °C for ammonia synthesis at atmospheric pressure, far surpassing the performance of the traditional dominant fused iron and even Ru‐based precious metal catalysts.
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