催化作用
氨
金属
碳纤维
热解
氨生产
材料科学
大气压力
兴奋剂
Atom(片上系统)
无机化学
化学工程
化学
冶金
复合材料
复合数
有机化学
计算机科学
嵌入式系统
海洋学
光电子学
工程类
地质学
作者
Yuting Jiang,Ziquan Chen,Tao Peng,Long Jiao,Xiulian Pan,Xinhe Bao,Hai‐Long Jiang
标识
DOI:10.1002/anie.202501190
摘要
Ammonia synthesis is a cornerstone in the chemical industry. Given 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 wt% to 2.39 wt%. This effectively suppresses the migration and agglomeration of Fe, yielding Fe‐N‐C with high metal loading (FeHL‐N‐C). Notably, the FeHL‐N‐C catalyst exhibits a catalytic rate of 558 μmol·gcat‐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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