Tan, Yuanlong, Zhao, Qiao, Liang, Chen, Zeng, Chaobin, Guo, Hongwen, Liu, Fengyuan, Pei, Guang Xian, Hayward, James, Ma, Jingyuan, Zhao, Han, Liu, Xiao Yan, Liu, Wei, Yang, Tao, Wang, Aiqin, Hutchings, Graham J. ORCID: https://orcid.org/0000-0001-8885-1560 and Zhang, Tao
2026.
In situ generation of active motifs on Ni/Al2O3 during partial oxidation of methane to syngas.
Nature Catalysis
9
, pp. 848-857.
10.1038/s41929-026-01580-1
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Abstract
The active phase for the partial oxidation of methane (POM) to syngas on Ni catalysts has been attributed to metallic nanoparticles, with high Ni loadings (~10 wt%) considered essential. Here we show, on NiO surfaces, that in situ-generated [Ni1O1Ni4] motifs, where one Ni atom sits on an oxygen atom that bridges four surrounding Ni atoms, drive POM with promising efficiency. A Ni/Al2O3-ME catalyst with Ni loading of 0.8 wt% fabricated via deposition of preformed Ni nanoparticles onto Al2O3 achieves 92.0% CH4 conversion and 87.0% CO/H2 selectivity at 650 °C for POM, maintaining a stable H2/CO ratio of 2.0. Operando spectroscopy and environmental microscopy confirm the oxidation of metallic Ni to NiO during POM. The results of operando high-resolution annular bright-field imaging, combined with density functional theory calculations, suggest that the [Ni1O1Ni4] structure formed on the NiO(100) surface reduces the C–H activation barrier to 12.5 kcal mol−1. Thus, metallic Ni nanoparticles with high metal loadings may not be strictly required for efficient POM.
| Item Type: | Article |
|---|---|
| Date Type: | Published Online |
| Status: | Published |
| Schools: | Schools > Chemistry Schools > Physical, Chemical & Environmental Sciences |
| Publisher: | Nature Research |
| ISSN: | 2520-1158 |
| Date of First Compliant Deposit: | 19 August 2026 |
| Date of Acceptance: | 19 June 2026 |
| Last Modified: | 19 Aug 2026 12:00 |
| URI: | https://orca.cardiff.ac.uk/id/eprint/189088 |
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