Related Experiment Video
Updated: Sep 25, 2025

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
Published on: August 17, 2016
A comprehensive study on lithium-based reactive hydride composite (Li-RHC) as a reversible solid-state hydrogen
Fahim Karimi1, Philipp Klaus Pranzas1, Julián Atillio Puszkiel1,2
1Department of Nanotechnology, Institute of Materials Research, Helmholtz-Zentrum HEREON Max-Planck-Straße 1 21502 Geesthacht Germany fahim.karimi2017hh@gmail.com.
Adding niobium pentafluoride (NbF5) significantly enhances the hydrogen storage kinetics of lithium borohydride-magnesium hydride (LiBH4-MgH2) composites. This breakthrough improves hydrogen release and uptake speeds by approximately 96% for sustainable energy applications.
Area of Science:
- Materials Science
- Solid-State Chemistry
- Sustainable Energy Technologies
Background:
- Reversible solid-state hydrogen storage is crucial for clean energy solutions.
- The LiBH4-MgH2 composite offers high gravimetric capacity but suffers from slow kinetics.
- Sluggish dehydrogenation/hydrogenation rates (approx. 40 hours) limit practical applications.
Purpose of the Study:
- To significantly enhance the hydrogen storage kinetics of the LiBH4-MgH2 composite system.
- To investigate the catalytic mechanism of NbF5 in the dehydrogenation/hydrogenation process.
- To develop a model explaining NbF5's catalytic function.
Main Methods:
- Addition of a small amount of NbF5 to the LiBH4-MgH2 composite.
- Systematic investigation using advanced characterization techniques.
- In situ synchrotron radiation X-ray powder diffraction (SR-XPD), X-ray absorption spectroscopy (XAS), anomalous small angle X-ray scattering (ASAXS), and ultra/small-angle neutron scattering (USANS/SANS).
Main Results:
- Achieved a significant enhancement (approx. 96%) in the dehydrogenation/hydrogenation kinetics.
- Demonstrated the catalytic role of NbF5 in accelerating hydrogen release and uptake.
- Collected comprehensive data to support a mechanistic model.
Conclusions:
- NbF5 acts as an effective catalyst to overcome the kinetic limitations of LiBH4-MgH2.
- The study provides a pathway for developing practical solid-state hydrogen storage materials.
- Understanding the catalytic mechanism is key to optimizing hydrogen storage performance.
Related Concept Videos
Batteries and Fuel Cells
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Esters to Alcohols: Hydride Reductions
Lithium aluminum hydride is a source of hydride ions and functions as a nucleophile. The mechanism proceeds in three steps. Firstly, the nucleophilic hydride ion attacks the carbonyl carbon of the ester to form a tetrahedral intermediate. Subsequently, the carbonyl group re-forms,...
Amides to Amines: LiAlH4 Reduction
Amide reduction requires two equivalents of the reducing agent, acting as a source of hydride ions. As shown in the figure, the reaction is initiated with a nucleophilic attack by the hydride ion at the carbonyl carbon to form a tetrahedral intermediate.
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...

