Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3748
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dc.contributor.authorPious, JK-
dc.contributor.authorBasavarajappa, MG-
dc.contributor.authorMuthu, C-
dc.contributor.authorNishikubo, R-
dc.contributor.authorSaeki, A-
dc.contributor.authorChakraborty, S-
dc.contributor.authorNair, VC-
dc.date.accessioned2021-05-12T09:12:53Z-
dc.date.available2021-05-12T09:12:53Z-
dc.date.issued2020-08-20-
dc.identifier.citationThe Journal of Physical Chemistry Letters;11(16): 6757-6762en_US
dc.identifier.urihttps://doi.org/10.1021/acs.jpclett.0c01772-
dc.identifier.urihttp://hdl.handle.net/123456789/3748-
dc.description.abstractBismuth-based perovskites are attracting intense scientific interest due to low toxicity and excellent moisture stability compared to lead-based analogues. However, high exciton binding energy, poor charge carrier separation, and transport efficiencies lower their optoelectronic performances. To address these issues, we have integrated an electronically active organic cation, naphthalimide ethylammonium, between the [BiI5 2−]n chains via crystal engineering to form a novel perovskite-like material (naphthalimide ethylammonium) 2BiI5 (NBI). Single crystal analysis revealed a one-dimensional quantum-well structure for NBI in which inter-inorganic well electronic coupling is screened by organic layers. It exhibited anisotropic photoconductivity and long-lived charge carriers with milliseconds lifetime, which is higher than that of CH3NH3PbI3. Density functional theory calculations confirmed type-IIa band alignment between organic cations and inorganic chains, allowing the former to electronically contribute to the overall charge transport properties of the material.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectperovskiteen_US
dc.subjecttype-IIa band alignmenten_US
dc.subjectbismuth-baseden_US
dc.titleAnisotropic Photoconductivity and Long-Lived Charge Carriers in Bismuth-Based One-Dimensional Perovskite with Type-IIa Band Alignmenten_US
dc.typeArticleen_US
Appears in Collections:2020



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