Single‐Atom Fe Catalysts With Improved Metal Loading for Efficient Ammonia Synthesis Under Mild Conditions

Y Yuting Jiang Z Ziquan Chen T Tao Peng L Long Jiao X Xiulian Pan (State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, P. R. China) H Hai‐Long Jiang (Hefei National Research Center for Physical Sciences At the Microscale, Department of Chemistry University of Science and Technology of China Anhui P. R. China) X Xinhe Bao (State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) Dalian Institute of Chemical Physics)

Abstract

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.

Article Details

Volume / Issue Vol. 64, Issue 27
Published July 01, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (7)

Y

Yuting Jiang

Z

Ziquan Chen

T

Tao Peng

L

Long Jiao

X

Xiulian Pan

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, P. R. China

H

Hai‐Long Jiang

Hefei National Research Center for Physical Sciences At the Microscale, Department of Chemistry University of Science and Technology of China Anhui P. R. China

X

Xinhe Bao

State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) Dalian Institute of Chemical Physics