TY - JOUR
T1 - Metal Ni anchored to highly dispersed island-like CeO2 on the TS-1 for catalyzing methane dry reforming by regulating Ni–O–Ce species
AU - Yang, Zhuwei
AU - Li, Linsen
AU - Yang, Xiao
AU - Lin, Yijie
AU - Ma, Ming
AU - Zhang, Riguang
AU - Jiang, Zhao
N1 - Publisher Copyright:
© 2025 Hydrogen Energy Publications LLC
PY - 2025/5/9
Y1 - 2025/5/9
N2 - Metal Ni was deposited on the different island-like rare earth metal oxide/silica matrix composites. Among the rare earth metal oxides, CeO2 was favorable for the metal Ni dispersion, leading to small-size Ni nanoparticle. For the silica matrices, they could affect the CeO2 size, positively regulating the size of Ni nanoparticle. Among them, TS-1 (Titanium Silicalite-1) was beneficial to decrease the CeO2 size, as well as the Ni nanoparticle size. The 10 wt %Ni-10 wt %CeO2/TS-1 (NCT) catalyst consisting of CeO2 and TS-1, exhibited the optimal catalytic performance, achieving 92 % CH4 and 94 % CO2 conversions, along with 0.98H2/CO ratio within 50 h under 750 °C. This is mainly because small Ni nanoparticle could strengthen Ni–O–Ce species, increasing the surface charge density of metal Ni, which was conducive to CH4 activation. Also, based on the similar Ni loading, small Ni particle could bring more Ni–O–Ce species, promoting the CO2 activation. Furthermore, NCT catalyst also showed the best stability with 4.1 % CH4 and 3.4 % CO2 activity loss after 100 h, which was caused by the superior anti-sintering and anti-coking properties, because of the significant island barrier effect, and many strengthened Ni–O–Ce species. In-situ DRIFTS was performed to investigate reaction mechanism, revealing that significant amounts of strengthened Ni–O–Ce species were beneficial for the reactant activation processes, facilitating the DRM reaction.
AB - Metal Ni was deposited on the different island-like rare earth metal oxide/silica matrix composites. Among the rare earth metal oxides, CeO2 was favorable for the metal Ni dispersion, leading to small-size Ni nanoparticle. For the silica matrices, they could affect the CeO2 size, positively regulating the size of Ni nanoparticle. Among them, TS-1 (Titanium Silicalite-1) was beneficial to decrease the CeO2 size, as well as the Ni nanoparticle size. The 10 wt %Ni-10 wt %CeO2/TS-1 (NCT) catalyst consisting of CeO2 and TS-1, exhibited the optimal catalytic performance, achieving 92 % CH4 and 94 % CO2 conversions, along with 0.98H2/CO ratio within 50 h under 750 °C. This is mainly because small Ni nanoparticle could strengthen Ni–O–Ce species, increasing the surface charge density of metal Ni, which was conducive to CH4 activation. Also, based on the similar Ni loading, small Ni particle could bring more Ni–O–Ce species, promoting the CO2 activation. Furthermore, NCT catalyst also showed the best stability with 4.1 % CH4 and 3.4 % CO2 activity loss after 100 h, which was caused by the superior anti-sintering and anti-coking properties, because of the significant island barrier effect, and many strengthened Ni–O–Ce species. In-situ DRIFTS was performed to investigate reaction mechanism, revealing that significant amounts of strengthened Ni–O–Ce species were beneficial for the reactant activation processes, facilitating the DRM reaction.
KW - Metal nickel
KW - Methane dry reforming
KW - Rare earth metal oxide
KW - Silica matrix
KW - TS-1
UR - https://www.scopus.com/pages/publications/105002130409
U2 - 10.1016/j.ijhydene.2025.04.121
DO - 10.1016/j.ijhydene.2025.04.121
M3 - 文章
AN - SCOPUS:105002130409
SN - 0360-3199
VL - 126
SP - 396
EP - 412
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
ER -