Remarkably fast low-temperature hydrogen storage into aromatic benzyltoluenes over MgO-supported Ru nanoparticles with homolytic and heterolytic H-2 adsorption
- Authors
- Kim, Tae Wan; Kim, Minseok; Kim, Seok Ki; Choi, Yong Nam; Jung, Minji; Oh, Hyunchul; Suh, Young-Woong
- Issue Date
- Jun-2021
- Publisher
- ELSEVIER
- Keywords
- Liquid organic hydrogen carrier; Hydrogen storage; Supported Ru catalysts; MgO; Heterolytic hydrogen adsorption
- Citation
- APPLIED CATALYSIS B-ENVIRONMENTAL, v.286
- Indexed
- SCIE
SCOPUS
- Journal Title
- APPLIED CATALYSIS B-ENVIRONMENTAL
- Volume
- 286
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/72928
- DOI
- 10.1016/j.apcatb.2021.119889
- ISSN
- 0926-3373
1873-3883
- Abstract
- Hydrogen storage into aromatic compounds under mild conditions is a stringent issue in liquid organic hydrogen carrier (LOHC) systems. Herein, we report a highly active Ru/MgO catalyst in the hydrogenation of monobenzyltoluene and dibenzyltoluene at low temperatures. When MgO with basic surface oxygen was employed as a support, Ru/MgO showed a faster H-2 storage rate and superior kinetic parameters than the other supported Ru catalysts. The better catalytic performance of Ru/MgO was explained by the results of characterization and control experiments. Ru/MgO could adsorb the large amounts of monobenzyltoluene and hydrogen with higher strength. Particularly, homolytic and heterolytic hydrogen adsorption modes were identified in Ru/MgO, unlike Ru/Al2O3 showing homolytic H-2 adsorption. Density functional theory calculations confirmed heterolytic H-2 dissociation near the Ru-MgO interface, which assured the hydrogenation efficiency of Ru/MgO. Consequently, Ru/MgO is highly recommended for fast hydrogen storage into aromatic LOHC compounds at low temperatures.
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