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Synthesis of Nickel and Cobalt Ferrite-Doped Graphene as Efficient Catalysts for Improving the Hydrogen Storage Kinetics of Lithium Borohydride.
Palade, Petru; Comanescu, Cezar; Radu, Cristian.
Afiliação
  • Palade P; National Institute of Materials Physics, Atomistilor 405A, 077125 Magurele, Romania.
  • Comanescu C; National Institute of Materials Physics, Atomistilor 405A, 077125 Magurele, Romania.
  • Radu C; Faculty of Physics, University of Bucharest, Atomiștilor 405, 77125 Magurele, Romania.
Materials (Basel) ; 16(1)2023 Jan 02.
Article em En | MEDLINE | ID: mdl-36614768
ABSTRACT
Featuring a high hydrogen storage content of up to 20 wt%, complex metal borohydrides remain promising solid state hydrogen storage materials, with the real prospect of reversible behavior for a zero-emission economy. However, the thermodynamic barriers and sluggish kinetics are still barriers to overcome. In this context, nanoconfinement has provided a reliable method to improve the behavior of hydrogen storage materials. The present work describes the thermodynamic and kinetic enhancements of LiBH4 nanoconfined in MFe2O4 (M=Co, Ni) ferrite-catalyzed graphene host. Composites of LiBH4-catalysts were prepared by melt infiltration and investigated by X-ray diffraction, TEM, STEM-EDS and TPD. The role of ferrite additives, metal precursor treatment (Ar, Ar/H2) and the effect on hydrogen storage parameters are discussed. The thermodynamic parameters for the most promising composite LiBH4-graphene-NiFe2O4 (Ar) were investigated by Kissinger plot method, revealing an EA = 127 kJ/mol, significantly lower than that of neat LiBH4 (170 kJ/mol). The reversible H2 content of LiBH4-graphene-NiFe2O4 (Ar) after 5 a/d cycles was ~6.14 wt%, in line with DOE's target of 5.5 wt% storage capacity, while exhibiting the lowest desorption temperature peak of 349 °C. The composites with catalysts treated in Ar have lower desorption temperature due to better catalyst dispersion than using H2/Ar.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article