Abstract
The exsolution of metal nanoparticles from a perovskite oxide combined with concomitant oxygen vacancy creation can enhance the catalytic performance of the parent perovskite for the dry reforming of methane (DRM). Herein, a series of the Ni-substituted La0.2Sr0.7Ti1-xNixO3-δ (LSTNx, x = 0.1, 0.2, 0.3, 0.4, 0.5) perovskite oxides were synthesized and comparatively characterized for their application in DRM. The multiphase oxide Ni–La2NiO4/LSTNx was formed through the “doping-precipitation” strategy. The results showed that Ni nanoparticles and La2NiO4 nanoparticles were loaded on the surface of LSTNx perovskite, accompanied by the generation of oxygen vacancies. Among them, Ni sites promoted the adsorption and dissociation of CH4, while oxygen vacancies and La2NiO4 nanoparticles enhanced the activation of CO2 and the migration ability of oxygen species. The synergistic effect of these three components achieved a balance in the activation of CH4 and CO2. The LSTN0.4 catalyst maintained a stable CH4 conversion of 82 % after time-on-stream experiments at 750 °C for 100 h. The reaction mechanism was further studied in combination with CH4-TPSR and in-situ DRIFTS characterization.
| Original language | English |
|---|---|
| Article number | 152826 |
| Journal | International Journal of Hydrogen Energy |
| Volume | 203 |
| DOIs | |
| Publication status | Published - 23 Jan 2026 |
| Externally published | Yes |
Keywords
- CO activation
- Dry reforming of methane
- Ni-based catalysts
- Oxygen vacancy
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