Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7330
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dc.contributor.authorSAHOO, SUPRIYAen_US
dc.contributor.authorDEKA, NILOTPALen_US
dc.contributor.authorBOOMISHANKAR, RAMAMOORTHYen_US
dc.date.accessioned2022-08-26T11:53:42Z
dc.date.available2022-08-26T11:53:42Z
dc.date.issued2022-09en_US
dc.identifier.citationCrystEngComm, 24(35), 6172-6177.en_US
dc.identifier.issn1466-8033en_US
dc.identifier.urihttps://doi.org/10.1039/D2CE00866Aen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7330
dc.description.abstractLead-free hybrid perovskite piezoelectrics have gained enormous attention due to their nontoxic metal content and notable physical properties. In this work, we report a bismuth-bromide-based perovskite-structured material stabilized by chiral ammonium cations. The enantiopure hybrid 1D-network of composition {[sCH(MePh)(Me)NH3][BiBr5]}n (1-S) is crystallized in the piezoelectrically active orthorhombic space group P212121. The piezoelectric measurements on the compacted pellet of 1-S gave a piezoelectric coefficient (d33) value of 2.6 pC/N. The dielectric permittivity measurements yielded the real part of the complex dielectric constant (ε′) value of 6.68 at room temperature and 1 kHz frequency. Furthermore, the piezoelectric energy harvesting applications were performed on the composite films of 1-S with polylactic acid (PLA) polymer. A considerable output voltage of 10.4 V was obtained for the 15 wt% 1-S-PLA composite film. Energy storage application was studied by charging a 100 μF capacitor by using the best performing 15 wt% 1-S-PLA device that reaches its maximum charging point in 60 seconds.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectLead-freeen_US
dc.subjectPolarizationen_US
dc.subjectFilmsen_US
dc.subject2022-AUG-WEEK4en_US
dc.subjectTOC-AUG-2022en_US
dc.subject2022en_US
dc.titlePiezoelectric energy harvesting of a bismuth halide perovskite stabilised by chiral ammonium cationsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleCrystEngCommen_US
dc.publication.originofpublisherForeignen_US
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