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dc.contributor.authorSiriwardane, Edirisuriya M. D.
dc.contributor.authorDemiroğlu, İlker
dc.contributor.authorSevik, Cem
dc.contributor.authorÇakır, Deniz
dc.date.accessioned2019-10-21T21:12:25Z
dc.date.available2019-10-21T21:12:25Z
dc.date.issued2019
dc.identifier.issn2574-0962
dc.identifier.urihttps://dx.doi.org/10.1021/acsaem.8b01801
dc.identifier.urihttps://hdl.handle.net/11421/21370
dc.descriptionWOS: 000459948900037en_US
dc.description.abstractUsing first-principles calculations, we demonstrated that high lithium storage capacity and fast kinetics are achieved for Ti3C2O2 by preintercalating organic molecules. As a proof-of-concept, two different quinone molecules, namely 1,4-benzoquinone (C6H4O2) and tetrafluoro-1,4-benzoquinone (C6F4O2) were selected as the molecular linkers to demonstrate the feasibility of this interlayer engineering strategy for energy storage. As compared to Ti3C2O2 bilayer without linker molecules, our pillared structures facilitate a much faster ion transport, promising a higher charge/discharge rate for Li. For example, while the diffusion barrier of a single Li ion within pristine Ti3C2O2 bilayer is at least 1.0 eV, it becomes 0.3 eV in pillared structures, which is comparable and even lower than that of commercial materials. At high Li concentrations, the calculated diffusion barriers are as low as 0.4 eV. Out-of-plane migration of Li ions is hindered due to large barrier energy with a value of around 1-1.35 eV. Concerning storage capacity, we can only intercalate one monolayer of Li within pristine Ti3C2O2 bilayer. In contrast, pillared structures offer significantly higher storage capacity. Our calculations showed that at least two layers of Li can be intercalated between Ti3C2O2 layers without forming bulk Li and losing the pillared structure upon Li loading/unloading. A small change in the in-plane lattice parameters (<0.5%) and volume (<1.0%) and ab initio molecular dynamics simulations prove the stability of the pillared structures against Li intercalation and thermal effects. Intercalated molecules avoid the large contraction/expansion of the whole structure, which is one of the key problems in electrochemical energy storage. Pillared structures allow us to realize electrodes with high capacity and fast kinetics. Our results open new research paths for improving the performance of not only MXenes but also other layered materials for supercapacitor and battery applications.en_US
dc.description.sponsorshipUniversity of North Dakota Early Career Award [20622-4000-02624]; ND EPSCoR through NSF Grant [OIA-1355466]; U.S. Department of Energy, Office of Science [DE-AC02-06CH11357]en_US
dc.description.sponsorshipComputer resources used in this work is provided by Computational Research Center (HPC-Linux cluster) at University of North Dakota. A part of this work was supported by University of North Dakota Early Career Award (Grant 20622-4000-02624). We also acknowledge financial support from ND EPSCoR through NSF Grant OIA-1355466. This work was performed in part at the Center for Nanoscale Materials, a U.S. Department of Energy Office of Science User Facility, and supported by the U.S. Department of Energy, Office of Science, under contract no. DE-AC02-06CH11357.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionof10.1021/acsaem.8b01801en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMxenesen_US
dc.subjectTi3C2O2en_US
dc.subjectLi-Ion Batteriesen_US
dc.subjectFirst-Principles Calculationsen_US
dc.subjectPillared Structuresen_US
dc.subjectQuinone Moleculesen_US
dc.subjectInterlayer Engineeringen_US
dc.titleAchieving Fast Kinetics and Enhanced Li Storage Capacity for Ti3C2O2 by Intercalation of Quinone Moleculesen_US
dc.typearticleen_US
dc.relation.journalAcs Applied Energy Materialsen_US
dc.contributor.departmentAnadolu Üniversitesi, Mühendislik Fakültesi, Makine Mühendisliği Bölümüen_US
dc.identifier.volume2en_US
dc.identifier.issue2en_US
dc.identifier.startpage1251en_US
dc.identifier.endpage1258en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorSevik, Cem


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