High ionic conduction and polarity-induced piezoresponse in layered bimetallic Rb4Ag2BiBr9 single crystals

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dc.contributor.author Singh, Manoj
dc.contributor.author Paul, Tufan
dc.contributor.author Pal, Pulak
dc.contributor.author Sahoo, Aditi
dc.contributor.author Tanwar, Lokesh Singh
dc.contributor.author Makani, Nisha Hiralal
dc.contributor.author Ghosh, Aswini
dc.contributor.author Banerjee, Rupak
dc.coverage.spatial United States of America
dc.date.accessioned 2022-12-30T07:51:11Z
dc.date.available 2022-12-30T07:51:11Z
dc.date.issued 2022-12
dc.identifier.citation Singh, Manoj; Paul, Tufan; Pal, Pulak; Sahoo, Aditi; Tanwar, Lokesh Singh; Makani, Nisha Hiralal; Ghosh, Aswini and Banerjee, Rupak, “High ionic conduction and polarity-induced piezoresponse in layered bimetallic Rb4Ag2BiBr9 single crystals”, The Journal of Physical Chemistry C, DOI: 10.1021/acs.jpcc.2c06844, vol. 126, no. 51, pp. 21810-21824, Dec. 2022. en_US
dc.identifier.issn 1932-7447
dc.identifier.issn 1932-7455
dc.identifier.uri https://doi.org/10.1021/acs.jpcc.2c06844
dc.identifier.uri https://repository.iitgn.ac.in/handle/123456789/8439
dc.description.abstract The emergence of lead-free metal-halide perovskites in modern-day energy research is primarily due to their competent semiconducting and optoelectronic properties, as well as their nontoxicity and improved stability in ambient operating conditions. However, a detailed understanding of ion transport dynamics and the relaxation behavior of these materials is still elusive. In this article, we report on the single-crystal (SC) growth of a bimetallic two-dimensional layered Rb4Ag2BiBr9 and explore its dielectric, piezoelectric, and ferroelectric properties. The dielectric attributes are investigated by studying the temperature-dependent complex impedance, complex electric modulus, and AC conductivity over an extensive frequency range from 4 Hz to 8 MHz. The role of grain and grain boundaries in the effective impedance is established using the Maxwell–Wagner equivalent circuit model from the Nyquist plots. The observed electric modulus spectra are studied using the Havriliak-Nigami and the Kohlrausch-Williams-Watts formalisms to understand the ionic transport and relaxation mechanisms in Rb4Ag2BiBr9. The DC conductivity and relaxation time show Arrhenius-like behavior with the inverse temperature validating the hopping motion of ions. The values of the activation energy required for ion hopping are calculated independently from the relaxation time, hopping frequency, and DC conductivity Arrhenius plots and are in good agreement with a value of 0.47 eV. The scaling of the temperature-dependent conductivity and electric modulus spectra into a single master curve demonstrates the congruence of the ionic conduction and the relaxation phenomena at different temperatures for Rb4Ag2BiBr9. This SC demonstrates decent thermal and ambient stability up to 500 °C and 12 months, respectively. The pristine orthorhombic Rb4Ag2BiBr9 SC shows a piezoelectric amplitude value of ∼564 pm at the maximum applied bias (±10 V), and a saturation polarization of ∼0.14 nC/cm2 estimated from the piezoelectric force microscopy and polarization hysteresis loop measurement, respectively. The ferroelectric and semiconducting attributes of this material can be harnessed for prospective applications as a thin film in designing mechanical energy harvesters as well as functional photoferroelectrics, such as optical switches and ferroelectric photovoltaics.
dc.description.statementofresponsibility by Manoj Singh, Tufan Paul, Pulak Pal, Aditi Sahoo, Lokesh Singh Tanwar, Nisha Hiralal Makani, Aswini Ghosh and Rupak Banerjee
dc.format.extent vol. 126, no. 51, pp. 21810-21824
dc.language.iso en_US en_US
dc.publisher American Chemical Society en_US
dc.subject Perovskites en_US
dc.subject SC growth en_US
dc.subject Nyquist plots en_US
dc.subject Ferroelectric photovoltaics en_US
dc.subject Piezoelectric en_US
dc.title High ionic conduction and polarity-induced piezoresponse in layered bimetallic Rb4Ag2BiBr9 single crystals en_US
dc.type Journal Paper en_US
dc.relation.journal The Journal of Physical Chemistry C


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