Issue 33, 2025

LaMnO3 perovskite supported Co–Ni catalysts for efficient ammonia decomposition

Abstract

Ammonia is a promising hydrogen carrier, but its decomposition at low temperatures using cost-effective, non-noble metal catalysts remains a significant challenge. In this work, several catalysts with 50 wt% metal loading on an LaMnO3 perovskite support were synthesized using a dry mixing method. Various metal ratios were studied, such as 50%CoNi(1 : 1)/LaMnO3, 50%CoNi(0.5 : 1)/LaMnO3, 50%Co/LaMnO3, and their respective 0.5%Ru-incorporated samples. Different characterization techniques, such as XRD, SEM, TEM, and HRTEM, were conducted to evaluate their structural properties. The catalytic performance of these catalysts was investigated in a fixed-bed reactor within a temperature range of 200–700 °C. Initially, monometallic catalysts, 50% Co/LaMnO3, 50%Ni/LaMnO3, and 0.5%Ru/LaMnO3, were tested, and the results showed that 90% ammonia conversion was achieved at 555 °C, 590 °C, and 610 °C, respectively, when reduced at 350 °C. Among the catalysts, the 0.5%Ru–50%CoNi(1 : 1)/LaMnO3 catalyst showed better activity when reduced at 350 °C, whereas the optimal reduction temperature was 700 °C for the 0.5%Ru–50%Co/LaMnO3 catalyst. The pre-reduced catalyst 0.5%Ru–50%CoNi(1 : 1)/LaMnO3 at 350 °C decomposed 95% ammonia at 535 °C with the GHSV of 20 400 mL g−1 h−1. Catalysts 50%CoNi(1 : 1)/LaMnO3 and 0.5%Ru–50%CoNi(1 : 1)/LaMnO3 retained their stability over 48 h. The synergies between Co and Ni in the bimetallic system facilitate the transfer of electrons, thereby increasing the active site availability for ammonia molecules.

Graphical abstract: LaMnO3 perovskite supported Co–Ni catalysts for efficient ammonia decomposition

Supplementary files

Article information

Article type
Paper
Submitted
08 May 2025
Accepted
15 Jul 2025
First published
22 Jul 2025

New J. Chem., 2025,49, 14442-14457

LaMnO3 perovskite supported Co–Ni catalysts for efficient ammonia decomposition

A. Ali, A. M. Ajeebi, M. Usman, M. Aktary, M. M. Hossain, H. Alghamdi, Md. H. Zahir and M. N. Shaikh, New J. Chem., 2025, 49, 14442 DOI: 10.1039/D5NJ01949D

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