Related Experiment Video
Updated: May 24, 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
Chemical Bonds Containing Hydrogen: Choices for Hydrogen Carriers and Catalysts
James Cashel1, Dai Yan1, Rui Han1
1School of Civil and Environmental Engineering, University of Technology Sydney, Broadway, Ultimo, New South Wales, 2007, Australia.
Abstract:
Compounds containing B─H, C─H, N─H, or O─H bonds with high hydrogen content have been extensively studied as potential hydrogen carriers. Their hydrogen storage performance is largely determined by the nature of these bonds, decomposition pathways, and the properties of the dehydrogenation products. Among these compounds, methanol, cyclohexane, and ammonia stand out due to their low costs and established infrastructure, making them promising hydrogen carriers for large-scale storage and transport. They offer viable pathways for decarbonizing society by enabling hydrogen to serve as a clean energy source. However, several challenges persist, including the high temperatures required for (de)hydrogenation, slow kinetics, and the reliance on costly catalysts. To address these issues, strategies such as chemical modification and catalyst development are being pursued to improve hydrogen cycling performance. This review highlights recent progress in hydrogen carriers with B─H, C─H, N─H, or O─H bonds. It examines the fundamental characteristics of these bonds and carriers, as well as advances in catalyst development. Our objective is to offer a comprehensive understanding of current state of hydrogen carriers and identify future research directions, such as molecular modification and system optimization. Innovations in these areas are crucial to advance hydrogen storage technologies for a large-scale hydrogen deployment.
Related Concept Videos
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 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...
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Catalysis
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.
Hydrogen Bonds

