Synthesis of Nickel and Cobalt Ferrite-Doped Graphene as Efficient Catalysts for Improving the Hydrogen Storage Kinetics of Lithium Borohydride.

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Title: Synthesis of Nickel and Cobalt Ferrite-Doped Graphene as Efficient Catalysts for Improving the Hydrogen Storage Kinetics of Lithium Borohydride.
Authors: Palade, Petru1 (AUTHOR), Comanescu, Cezar1,2 (AUTHOR) cezar.comanescu@infim.ro, Radu, Cristian1 (AUTHOR)
Source: Materials (1996-1944). Jan2023, Vol. 16 Issue 1, p427. 12p.
Subjects: Hydrogen storage, Lithium borohydride, Graphene oxide, Melt infiltration, Graphene, Cobalt
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. [ABSTRACT FROM AUTHOR]
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  Label: Title
  Group: Ti
  Data: Synthesis of Nickel and Cobalt Ferrite-Doped Graphene as Efficient Catalysts for Improving the Hydrogen Storage Kinetics of Lithium Borohydride.
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  Data: <searchLink fieldCode="AR" term="%22Palade%2C+Petru%22">Palade, Petru</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Comanescu%2C+Cezar%22">Comanescu, Cezar</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> cezar.comanescu@infim.ro</i><br /><searchLink fieldCode="AR" term="%22Radu%2C+Cristian%22">Radu, Cristian</searchLink><relatesTo>1</relatesTo> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Materials+%281996-1944%29%22">Materials (1996-1944)</searchLink>. Jan2023, Vol. 16 Issue 1, p427. 12p.
– Name: Subject
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  Data: <searchLink fieldCode="DE" term="%22Hydrogen+storage%22">Hydrogen storage</searchLink><br /><searchLink fieldCode="DE" term="%22Lithium+borohydride%22">Lithium borohydride</searchLink><br /><searchLink fieldCode="DE" term="%22Graphene+oxide%22">Graphene oxide</searchLink><br /><searchLink fieldCode="DE" term="%22Melt+infiltration%22">Melt infiltration</searchLink><br /><searchLink fieldCode="DE" term="%22Graphene%22">Graphene</searchLink><br /><searchLink fieldCode="DE" term="%22Cobalt%22">Cobalt</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: 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. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Materials (1996-1944) is the property of MDPI and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.3390/ma16010427
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      – Code: eng
        Text: English
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        PageCount: 12
        StartPage: 427
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      – SubjectFull: Hydrogen storage
        Type: general
      – SubjectFull: Lithium borohydride
        Type: general
      – SubjectFull: Graphene oxide
        Type: general
      – SubjectFull: Melt infiltration
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      – SubjectFull: Graphene
        Type: general
      – SubjectFull: Cobalt
        Type: general
    Titles:
      – TitleFull: Synthesis of Nickel and Cobalt Ferrite-Doped Graphene as Efficient Catalysts for Improving the Hydrogen Storage Kinetics of Lithium Borohydride.
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            NameFull: Palade, Petru
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            NameFull: Comanescu, Cezar
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            NameFull: Radu, Cristian
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            – D: 01
              M: 01
              Text: Jan2023
              Type: published
              Y: 2023
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