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dc.contributor.authorLee, Jeongjae
dc.contributor.authorMonserrat, Bartomeu
dc.contributor.authorSeymour, Ieuan
dc.contributor.authorLiu, Zigeng
dc.contributor.authorDutton, Sian
dc.contributor.authorGrey, Clare
dc.date.accessioned2018-09-11T17:32:39Z
dc.date.available2018-09-11T17:32:39Z
dc.date.issued2018
dc.identifier.issn2050-7496
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/280205
dc.description.abstractWe present a comprehensive ab initio investigation on Mg3Bi2, a promising Mg-ion battery anode material with high rate capacity. Through combined DFT (PBE, HSE06) and G0W0 electronic structure calculations, we find that Mg3Bi2 is likely to be a small band gap semiconductor. DFT-based defect formation energies indicate that Mg vacancies are likely to form in this material, with relativistic spin-orbit coupling significantly lowering the defect formation energies. We show that a transition state searching methodology based on the hybrid eigenvector-following approach can be used effectively to search for the transition states in cases where full spin-orbit coupling is included. Mg migration barriers found through this hybrid eigenvector-following approach indicate that spin-orbit coupling also lowers the migration barrier, decreasing it to a value of 0.34 eV with spin-orbit coupling. Finally, recent experimental results on Mg diffusion are compared to the DFT results and show good agreement. This work demonstrates that vacancy defects and the inclusion of relativistic spin-orbit coupling in the calculations have a profound effect in Mg diffusion in this material. It also sheds light on the importance of relativistic spin-orbit coupling in studying similar battery systems where heavy elements play a crucial role.
dc.description.sponsorshipVia our membership of the UK’s HEC Materials Chemistry Consortium, which is funded by EPSRC (EP/L000202), this work used the ARCHER UK National Supercomputing Service (http://www.archer.ac.uk). Research was also carried out at the Center for Functional Nanomaterials, Brookhaven National Laboratory, which is supported by the U.S. Department of Energy, Office of Basic Energy Sciences, under Contract No. DE-AC02-98CH10886. J.L. acknowledges Trinity College Cambridge for the graduate studentship. B.M. acknowledges support from the Winton Programme for the Physics of Sustainability, and from Robinson College, Cambridge, and the Cambridge Philosophical Society for a Henslow Research Fellowship.
dc.publisherRoyal Society of Chemistry
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleAn Ab Initio Investigation on the Electronic Structure, Defect Energetics, and Magnesium Kinetics in Mg₃Bi₂
dc.typeArticle
prism.endingPage16991
prism.publicationNameJournal of Materials Chemistry A
prism.startingPage16983
prism.volume6
dc.identifier.doi10.17863/CAM.27572
dcterms.dateAccepted2018-07-25
rioxxterms.versionofrecord10.1039/C7TA11181A
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2018-07-25
dc.contributor.orcidLee, Jeongjae [0000-0003-4294-4993]
dc.contributor.orcidMonserrat Sanchez, Bartomeu [0000-0002-4233-4071]
dc.contributor.orcidLiu, Zigeng [0000-0002-2955-5080]
dc.contributor.orcidDutton, Sian [0000-0003-0984-5504]
dc.contributor.orcidGrey, Clare [0000-0001-5572-192X]
dc.identifier.eissn2050-7496
rioxxterms.typeJournal Article/Review
cam.issuedOnline2018-07-28
cam.orpheus.successThu Jan 30 10:54:25 GMT 2020 - The item has an open VoR version.
rioxxterms.freetoread.startdate2100-01-01


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International