TY - JOUR
T1 - Novel Fe3O4@SiO2/Co-Mo-B core-shell magnetic nanocatalyst
T2 - A reusable system for high-performance hydrogen evolution in borohydride hydrolysis
AU - Lakhali, Houssem
AU - Ceyhan, Ayhan Abdullah
AU - Şahin, Ömer
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/7
Y1 - 2025/7
N2 - The present study focuses on the synthesis of a Fe3O4@SiO2/Co-Mo-B core–shell nanocatalyst, designed as a high-performance and reusable system optimized for hydrogen evolution in borohydride hydrolysis reactions. The catalytic activity and hydrogen generation rate were evaluated by varying the catalyst amount, temperature, reusability, and MOH/MBH4 wt% (M = Na, K). A range of characterization techniques, including FE-SEM, EDX, XRD, BET, XRF, TEM, XPS, and FTIR, were used to analyze the structure and composition of the samples. The Fe3O4@SiO2/Co-Mo-B nanocatalyst demonstrated exceptional catalytic performance, achieving a hydrogen generation rate of 22.6 L gmetal−1 min−1 with an activation energy of 23.72 kJ mol-1 for KBH4 hydrolysis at 50 °C. For NaBH4 hydrolysis, the HGR was 27.5 L gmetal−1 min−1, with an activation energy of 32.18 kJ mol−1, demonstrating its high catalytic efficiency. Reusability studies over six successive cycles confirmed the stability of the catalyst, maintaining high hydrogen yields of 99.84 %–97.29 % for NaBH4 and 95.25 %–99.09 % for KBH4 across varying concentrations, further supporting its strong potential for industrial hydrogen storage and on-demand hydrogen generation. FE-SEM analysis revealed a grape-like morphology, while TEM confirmed a uniform Co-Mo-B coating (18–20 nm) on the SiO2 shell, forming a robust core–shell structure that enhanced stability and durability. Additionally, the successful silica coating of Fe3O4 and effective adsorption of Co-Mo-B were validated, both of which contributed to the sustained catalytic activity of the catalyst. The remarkable performance of Fe3O4@SiO2/Co-Mo-B in NaBH4 and KBH4 hydrolysis, combined with its low activation energy and high reusability, make it as a promising candidate for sustainable and scalable hydrogen generation.
AB - The present study focuses on the synthesis of a Fe3O4@SiO2/Co-Mo-B core–shell nanocatalyst, designed as a high-performance and reusable system optimized for hydrogen evolution in borohydride hydrolysis reactions. The catalytic activity and hydrogen generation rate were evaluated by varying the catalyst amount, temperature, reusability, and MOH/MBH4 wt% (M = Na, K). A range of characterization techniques, including FE-SEM, EDX, XRD, BET, XRF, TEM, XPS, and FTIR, were used to analyze the structure and composition of the samples. The Fe3O4@SiO2/Co-Mo-B nanocatalyst demonstrated exceptional catalytic performance, achieving a hydrogen generation rate of 22.6 L gmetal−1 min−1 with an activation energy of 23.72 kJ mol-1 for KBH4 hydrolysis at 50 °C. For NaBH4 hydrolysis, the HGR was 27.5 L gmetal−1 min−1, with an activation energy of 32.18 kJ mol−1, demonstrating its high catalytic efficiency. Reusability studies over six successive cycles confirmed the stability of the catalyst, maintaining high hydrogen yields of 99.84 %–97.29 % for NaBH4 and 95.25 %–99.09 % for KBH4 across varying concentrations, further supporting its strong potential for industrial hydrogen storage and on-demand hydrogen generation. FE-SEM analysis revealed a grape-like morphology, while TEM confirmed a uniform Co-Mo-B coating (18–20 nm) on the SiO2 shell, forming a robust core–shell structure that enhanced stability and durability. Additionally, the successful silica coating of Fe3O4 and effective adsorption of Co-Mo-B were validated, both of which contributed to the sustained catalytic activity of the catalyst. The remarkable performance of Fe3O4@SiO2/Co-Mo-B in NaBH4 and KBH4 hydrolysis, combined with its low activation energy and high reusability, make it as a promising candidate for sustainable and scalable hydrogen generation.
KW - Core-shell
KW - Hydrogen generation
KW - Hydrothermal method
KW - KBH
KW - Magnetic catalyst
KW - NaBH
UR - http://www.scopus.com/inward/record.url?scp=105000866310&partnerID=8YFLogxK
U2 - 10.1016/j.inoche.2025.114406
DO - 10.1016/j.inoche.2025.114406
M3 - Article
AN - SCOPUS:105000866310
SN - 1387-7003
VL - 177
JO - Inorganic Chemistry Communications
JF - Inorganic Chemistry Communications
M1 - 114406
ER -