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Amorphous-Carbon-Supported Ultrasmall TiB(2) Nanoparticles With High Catalytic Activity for Reversible Hydrogen Storage in NaAlH(4)

In this paper, we report amorphous-carbon-supported TiB(2) nanoparticles having sizes of 2–4 nm (nano-TiB(2)@C) as highly active catalysts for hydrogen storage in NaAlH(4). Nano-TiB(2)@C was synthesized by a simple calcination at 550°C with Cp(2)TiCl(2) and MgB(2) (molar ratio of 1:1) as precursors....

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Detalles Bibliográficos
Autores principales: Zhang, Xin, Zhang, Xuelian, Ren, Zhuanghe, Hu, Jianjiang, Gao, Mingxia, Pan, Hongge, Liu, Yongfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243354/
https://www.ncbi.nlm.nih.gov/pubmed/32500061
http://dx.doi.org/10.3389/fchem.2020.00419
Descripción
Sumario:In this paper, we report amorphous-carbon-supported TiB(2) nanoparticles having sizes of 2–4 nm (nano-TiB(2)@C) as highly active catalysts for hydrogen storage in NaAlH(4). Nano-TiB(2)@C was synthesized by a simple calcination at 550°C with Cp(2)TiCl(2) and MgB(2) (molar ratio of 1:1) as precursors. The addition of 7 wt% nano-TiB(2)@C reduced the onset dehydrogenation temperature of NaAlH(4) by 100 to 75°C. A practically available hydrogen capacity of 5.04 wt% could be desorbed at 140°C within 60 min, and completely hydrogenated at 100°C within 25 min under a hydrogen pressure of 100 bar. Notably, the hydrogen capacity was almost unchanged after 20 cycles, which shows the stable cyclability, considerably higher than those of structures catalyzed by Ti halides or TiO(2). The stable catalytic function was closely related to the in-situ-formed Ti–Al alloy, which considerably facilitated the dissociation and recombination of H–H and Al–H bondings.