Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8079
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dc.contributor.authorChakraborty, Sudipen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:14:58Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:14:58Z-
dc.date.issued2019-
dc.identifier.citationBanerjee, A., Chakraborty, S., & Ahuja, R. (2019). Rashba triggered electronic and optical properties tuning in mixed cation-mixed halide hybrid perovskites. ACS Applied Energy Materials, 2(10), 6990-6997. doi:10.1021/acsaem.9b01479en_US
dc.identifier.issn2574-0962-
dc.identifier.otherEID(2-s2.0-85073110510)-
dc.identifier.urihttps://doi.org/10.1021/acsaem.9b01479-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/8079-
dc.description.abstractThe inherent spin-orbit coupling (SOC) effect in non-centrosymmetric crystal structure has laid the foundation of Rashba splitting phenomena. This Rashba splitting directly governs the charge carrier recombination, which eventually controls the carrier lifetime and diffusion length and therefore the solar cell efficiency for such hybrid perovskite materials. In this work, we have performed a rigorous structural search prediction of the mixed cation-mixed halide hybrid perovskites FA0.83MA0.17Pb(I0.83Br0.17)3 and FA0.875MA0.125Pb(I0.875Br0.125)3, which are the two nearest neighbor structures of record efficiency (22.1%) holder FA0.85MA0.15Pb(I0.85Br0.15)3 in the structural composition phase space. We have found the prediction routes for a structural search such as the mixed perovskite structure govern the Rashba splitting energy value, depending on whether it has been predicted from FPI (FAPbI3) or MPB (MAPbBr3) as parent structure, which are leading to the mixed phase FA0.83MA0.17Pb(I0.83Br0.17)3 and FA0.875MA0.125Pb(I0.875Br,0.125)3 respectively. The strong dependency of the splitting energy on the structural phase evolution along with the stoichiometry and space group is also observed, where in the mixed phase, 0.045 difference in concentration could lead to a remarkable difference in the splitting energy, which is more pronounced in the valence band as compared to the conduction band. We have also determined the Goldschmidt tolerance factor to envisage structural stability of the newly predicted crystal structures based on the corresponding chemical route in the composition phase space. Copyright © 2019 American Chemical Society.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.sourceACS Applied Energy Materialsen_US
dc.subjectBromine compoundsen_US
dc.subjectCarrier lifetimeen_US
dc.subjectChemical stabilityen_US
dc.subjectHybrid materialsen_US
dc.subjectLead compoundsen_US
dc.subjectOptical propertiesen_US
dc.subjectPerovskiteen_US
dc.subjectPerovskite solar cellsen_US
dc.subjectPhase space methodsen_US
dc.subjectPositive ionsen_US
dc.subjectTuningen_US
dc.subjectCharge carrier recombinationen_US
dc.subjectElectronic and optical propertiesen_US
dc.subjectHalide perovskitesen_US
dc.subjectNon-centrosymmetric crystalsen_US
dc.subjectRashba splittingen_US
dc.subjectSolar cell efficienciesen_US
dc.subjectStructural compositionen_US
dc.subjectStructural stabilitiesen_US
dc.subjectCrystal structureen_US
dc.titleRashba Triggered Electronic and Optical Properties Tuning in Mixed Cation-Mixed Halide Hybrid Perovskitesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Physics

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