Related Experiment Video
Updated: Sep 13, 2025

Hydrogen Production and Utilization in a Membrane Reactor
Published on: March 10, 2023
Accelerating lithium-mediated nitrogen reduction through an integrated palladium membrane hydrogenation reactor
Hossein Bemana1, Hendrik Schumann1, Morgan McKee1
1Institute of Inorganic Chemistry, University of Bonn, Bonn, Germany.
This study introduces a novel dual-reactor system for ammonia synthesis using lithium-mediated nitrogen reduction. It utilizes a palladium membrane to supply hydrogen from water, enhancing efficiency in electrified ammonia production.
Area of Science:
- Electrochemistry
- Materials Science
- Chemical Engineering
Background:
- Electrified ammonia synthesis via lithium-mediated N2 reduction (LiNRR) is promising but hindered by hydrogen impurities.
- Existing methods often suffer from low efficiency due to unwanted hydrogen sources in the reaction system.
Purpose of the Study:
- To develop an alternative hydrogen source for LiNRR to improve ammonia synthesis efficiency.
- To demonstrate a novel dual-reactor setup integrating a palladium membrane reactor (PMR) with a LiNRR reactor.
Main Methods:
- A palladium membrane was used to extract hydrogen atoms directly from water (H2O).
- These hydrogen atoms were transferred to an electrodeposited lithium layer under non-aqueous conditions.
- The system was operated under nitrogen (N2) to synthesize ammonia (NH3).
Main Results:
- Successfully utilized water-derived hydrogen atoms for ammonia synthesis in the LiNRR process.
- Demonstrated orthogonal reaction pathways within the metal-mediated nitrogen reduction concept.
- Overcame limitations associated with traditional hydrogen sources in LiNRR.
Conclusions:
- The integrated PMR-LiNRR system provides a viable alternative hydrogen source for efficient electrified ammonia synthesis.
- This approach opens new avenues for metal-mediated nitrogen reduction by controlling hydrogen supply.
- The findings contribute to the advancement of sustainable ammonia production technologies.
More Related Videos
Related Concept Videos
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
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.
Preparation of Amines: Reduction of Amides and Nitriles
Amides can be reduced to primary, secondary, and tertiary amines using catalytic hydrogenation, active metals like Fe,...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.

