Related Experiment Video
Updated: Sep 13, 2026

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
Catalytic Advances in Naphthalene-Decalin Liquid Organic Hydrogen Carriers: A Comprehensive Review
Yi-Chen Huang1, Xiang-Yang Liu1, Yue Pan1
1College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan, Shanxi, P. R. China.
Abstract:
Liquid organic hydrogen carriers (LOHCs) provide an established framework for the safe, high-density storage, and transportation of hydrogen. Among current LOHC candidates, the naphthalene-decalin system distinguishes itself with a theoretical hydrogen storage capacity of 7.3 wt.%. However, the practical deployment of this cycle is fundamentally restricted by sluggish kinetics during deep hydrogenation, the high endothermicity of dehydrogenation, and phase transition challenges under ambient conditions. This review critically assesses the current state of catalyst and engineering development for the naphthalene and decalin platform. Specifically, it systematically synthesizes four core mechanistic pathways governing catalytic performance, including H2 activation and dissociation, PAH adsorption and activation, H2 spillover and subsurface hydrogen transport, alongside comprehensive evaluations of both hydrogenation and dehydrogenation catalysts. The core discussion links empirical catalytic performance to physical and chemical descriptors, examining how active site dispersion, electronic structure regulation, support microenvironment engineering, and bimetallic synergy dictate the activity, selectivity, and stability of noble and low-cost base metal systems. Furthermore, the review addresses the physical handling of reaction intermediates through current engineering strategies. By synthesizing these catalytic mechanisms, engineering strategies, and future perspectives, this review establishes a concrete, data-driven baseline for scaling up the naphthalene-decalin system toward practical industrial implementation.
More Related Videos
12:08Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
08:40Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
Related Concept Videos
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.
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 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 surface of...
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
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...