TY - JOUR
T1 - Nickel-doped La0.2Sr0.7Ti1-xNixO3-δ catalysts containing abundant oxygen vacancies as an optimized bifunctional catalyst for dry reforming of methane
AU - Xu, Yamei
AU - Li, Leyang
AU - Qiao, Jinshuo
AU - Sun, Wang
AU - Wang, Zhenhua
AU - Sun, Kening
N1 - Publisher Copyright:
© 2025 Hydrogen Energy Publications LLC
PY - 2026/1/23
Y1 - 2026/1/23
N2 - 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.
AB - 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.
KW - CO activation
KW - Dry reforming of methane
KW - Ni-based catalysts
KW - Oxygen vacancy
UR - https://www.scopus.com/pages/publications/105025190371
U2 - 10.1016/j.ijhydene.2025.152826
DO - 10.1016/j.ijhydene.2025.152826
M3 - Article
AN - SCOPUS:105025190371
SN - 0360-3199
VL - 203
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
M1 - 152826
ER -