4.4 Review

Recent progress in dehydrogenation catalysts for heterocyclic and homocyclic liquid organic hydrogen carriers

Journal

KOREAN JOURNAL OF CHEMICAL ENGINEERING
Volume 39, Issue 1, Pages 20-37

Publisher

KOREAN INSTITUTE CHEMICAL ENGINEERS
DOI: 10.1007/s11814-021-0947-5

Keywords

Liquid Organic Hydrogen Carriers; Dehydrogenation; Heterogeneous Catalysts

Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Science and ICT, Republic of Korea [NRF-2019M3E6A1064908]
  2. Ministry of Education, Republic of Korea [NRF-2016R1A6A1 A03013422]

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Liquid organic hydrogen carriers (LOHC) are promising for H-2 storage and transportation, with the most stringent limitation being high temperatures required for the dehydrogenation reaction. Pd-based catalysts are preferred in the conversion of heterocyclic LOHC due to preferential adsorption of heteroatoms, while Pt-based catalysts dominate in the cleavage of C-H bonds for homocyclic LOHC. Efforts are needed to inhibit the generation of byproducts and improve overall performance and stability.
Liquid organic hydrogen carriers (LOHC) are recently recognized as an attractive solution for H-2 storage and transportation. Among several challenging tasks for practical application, the most stringent limitations stem from the dehydrogenation reaction requiring high temperatures thermodynamically. Unlike previous reviews focusing on the LOHC concept, LOHC molecules, and process integration, this review highlights the state-of-the-art catalysts reported for the dehydrogenation of homocyclic and heterocyclic LOHC molecules. In the conversion of heterocyclic LOHC, Pd-based catalysts overnumbered Pt-based ones owing to preferential adsorption of heteroatoms onto the Pd surface. However, because of low stability of C-heteroatom bonds, catalyst development needs to concentrate on inhibiting the generation of byproducts while maintaining superior performance under mild conditions. In the case of homocyclic LOHC, Pt is overwhelmed in single metal and bimetallic catalysts owing to pronounced C-H bond cleavage. Nevertheless, the ability of Pt in C-C bond cleavage should be diminished for higher H-2 selectivity, better catalyst stability, and steady LOHC recyclability, which is possible by tuning electronic and geometric effects of main active metals, as well as adding metal promoters. Consequently, great efforts will be diversely devoted to achieving an active and stable dehydrogenation catalyst for future LOHC demonstration.

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