Publication:
Experimental and theoretical assessment of the enhanced hydrogen adsorption on polycyclic aromatic hydrocarbons upon decoration with alkali metals

dc.contributor.coauthorReider, Anna Maria
dc.contributor.coauthorKollotzek, Siegfried
dc.contributor.coauthorScheier, Paul
dc.contributor.coauthorCalvo, Florent
dc.contributor.coauthorPirani, Fernando
dc.contributor.coauthorBartolomei, Massimiliano
dc.contributor.coauthorHernandez, Marta I.
dc.contributor.coauthorGonzalez-Lezana, Tomas
dc.contributor.coauthorCampos-Martinez, Jose
dc.contributor.departmentDepartment of Chemistry
dc.contributor.kuauthorYurtsever, İsmail Ersin
dc.contributor.otherDepartment of Chemistry
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.date.accessioned2024-12-29T09:38:02Z
dc.date.issued2024
dc.description.abstractHydrogen storage by physisorption on carbon-based materials is limited by comparatively low adsorption energies. However, decoration of the carbon substrate with alkali, alkaline earth, or other metal atoms has been proposed as a means to enhance adsorption energies. The decoration affects also the stability of these materials since it makes them more stable and resilient in the repeated cycles of charge and discharge that would be required for a good material devoted to storage. We investigate hydrogen storage capacities of small polycyclic aromatic hydrocarbons (PAHs) cations grown in ultracold helium nanodroplets by analyzing the ion abundances and stabilities. The observations are assessed with quantum chemical calculations and atomistic simulations. It is experimentally shown that the addition of an alkali ion significantly enhances the hydrogen adsorption of the studied PAHs, up to 25% over the bare PAH in the experimental conditions studied here, and the simulations confirm this general trend except for some minor residual discrepancies in the special stabilities (magic numbers). Several approaches to study larger and different PAH compounds are also proposed, and for all cases it is found that alkali decoration increases energy stability by more than 100%.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.openaccesshybrid
dc.description.publisherscopeInternational
dc.description.sponsorsThis work was supported by the Austrian Science Fund, FWF (projects number W1259-N27 and P31149) and the Spanish MICINN with Grants PID2020-114654GB-I00/AEI/10.13039/501100011033, 2021-2024 (TGL,MB) and PID2020-114957GB-I00/AEI/10.13039/501100011033 (JCM, MIH) . FC gratefully acknowledges support from the PSMN (Pple Scientifique de Modelisation Numerique) of the ENS de Lyon for some of the computing resources. Collaboration has also been supported by the CSIC under i-Link+ program LINKB20041. Allocation of computing time by CESGA (Spain) is also acknowledged.
dc.description.volume58
dc.identifier.doi10.1016/j.ijhydene.2024.01.244
dc.identifier.eissn1879-3487
dc.identifier.issn0360-3199
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85183304400
dc.identifier.urihttps://doi.org/10.1016/j.ijhydene.2024.01.244
dc.identifier.urihttps://hdl.handle.net/20.500.14288/22562
dc.identifier.wos1171073900001
dc.keywordsPolycyclic aromatic hydrocarbons
dc.keywordsHelium nanodroplet experiments
dc.keywordsAlkali decoration
dc.keywordsEnhanced hydrogen storage
dc.languageen
dc.publisherElsevier
dc.relation.grantnoAustrian Science Fund,FWF [W1259-N27, P31149]
dc.relation.grantnoSpanish MICINN
dc.relation.grantnoCSIC under i-Link+ program
dc.relation.grantno[LINKB20041]
dc.relation.grantno[PID2020-114654GB-I00/AEI]
dc.relation.grantno[PID2020-114957GB-I00/AEI]
dc.sourceInternational Journal of Hydrogen Energy
dc.subjectChemistry, physical
dc.subjectElectrochemistry
dc.subjectEnergy and fuels
dc.titleExperimental and theoretical assessment of the enhanced hydrogen adsorption on polycyclic aromatic hydrocarbons upon decoration with alkali metals
dc.typeJournal article
dspace.entity.typePublication
local.contributor.kuauthorYurtsever, İsmail Ersin
relation.isOrgUnitOfPublication035d8150-86c9-4107-af16-a6f0a4d538eb
relation.isOrgUnitOfPublication.latestForDiscovery035d8150-86c9-4107-af16-a6f0a4d538eb

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