Strong Electron–Phonon Coupling and Lattice Dynamics in One-Dimensional [(CH3)2NH2]PbI3 Hybrid Perovskite

UDC.coleccionInvestigación
UDC.departamentoQuímica
UDC.endPage1026
UDC.grupoInvQuímica Molecular e de Materiais (QUIMOLMAT)
UDC.institutoCentroCICA - Centro Interdisciplinar de Química e Bioloxía
UDC.issue3
UDC.journalTitleChemistry of Materials
UDC.startPage1013
UDC.volume37
dc.contributor.authorSilva, Ariel Nonato Almeida de Abreu
dc.contributor.authorRodríguez Hernández, J. S.
dc.contributor.authorAbreu, Dieric S.
dc.contributor.authorSoares, C. C. S.
dc.contributor.authorGómez, Mayra A. P.
dc.contributor.authorGarcía-Fernández, Alberto
dc.contributor.authorSeñarís-Rodríguez, M. A.
dc.contributor.authorSánchez-Andújar, Manuel
dc.contributor.authorAyala, Alejandro Pedro
dc.contributor.authorSilva, Rosivaldo Xavier da
dc.contributor.authorPaschoal, Carlos William de Araujo
dc.date.accessioned2026-04-10T13:28:09Z
dc.date.available2026-04-10T13:28:09Z
dc.date.issued2025-01-17
dc.description.abstract[Abstract] Hybrid halide perovskites (HHPs) have attracted significant attention due to their remarkable optoelectronic properties that combine the advantages of low-cost, effective fabrication methods of organic–inorganic materials. Notably, low-dimensional hybrid halide perovskites including two-dimensional (2D) layers and one-dimensional (1D) chains are recognized for their superior stability and moisture resistance, making them highly appealing for practical applications. Particularly, DMAPbI3 has attracted attention due to other interesting behaviors and properties, such as thermally induced order–disorder processes, dielectric transition, and cooperative electric ordering of DMA dipole moments. In this paper, we investigated the interplay between the low-temperature structural phase transition (SPT) undergone by the low-dimensional (1D) hybrid halide perovskite-like DMAPbI3 and its optoelectronic properties. Our approach combines synchrotron X-ray powder diffraction, Raman spectroscopy, thermo-microscopy, differential scanning calorimetry (DSC), and photoluminescence (PL) techniques. Temperature-dependent synchrotron powder diffraction and Raman spectroscopy reveal that the modes associated with I–Pb–I and DMA+ ions play a crucial role in the order–disorder SPT in DMAPbI3. The reversible SPT modifies its optoelectronic properties, notably affecting its thermochromic behavior and PL emission. The origin of the PL phenomenon is associated with self-trapped excitons (STEs), which are allowed due to a strong electron–phonon coupling quantified by the Huang–Rhys factor (S = 97 ± 1). Notably, we identify the longitudinal optical (LO) phonon mode at 84 cm–1, which plays a significant role in the electron–phonon interaction. Our results show that these STEs not only intensify the PL spectra at lower temperatures but also induce a shift in the color emission, transforming it from a light orange-red to an intense bright strong red.
dc.description.sponsorshipThis investigation was financed in part by Fundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico (UNI-0210-00047.01.00/23, 07548003/2023), Conselho Nacional de Pesquisa e Desenvolvimento do Brasil (CNPq – Projetos 407956/2022-0, 407954/2022-8, 406322/2022-8, and 310353/2023-8), and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior do Brasil (CAPES) – Finance Code 001 (CAPES – Q6 Projeto 88887.669776/2022-00)
dc.description.sponsorshipBrasil. Fundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico; UNI-0210-00047.01.00/23
dc.description.sponsorshipBrasil. Fundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico; 07548003/2023
dc.description.sponsorshipBrasil. Conselho Nacional de Pesquisa e Desenvolvimento; 407956/2022-0
dc.description.sponsorshipBrasil. Conselho Nacional de Pesquisa e Desenvolvimento; 407954/2022-8
dc.description.sponsorshipBrasil. Conselho Nacional de Pesquisa e Desenvolvimento; 406322/2022-8
dc.description.sponsorshipBrasil. Conselho Nacional de Pesquisa e Desenvolvimento; 310353/2023-8
dc.description.sponsorshipBrasil. Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; 88887.669776/2022-00
dc.description.urihttp://hdl.handle.net/2183/23945
dc.identifier.citationNonato, A.; Rodríguez-Hernández, J. S.; Abreu, D. S.; Soares, C. C. S.; Gómez, M. A. P.; García-Fernández, A.; Señarís-Rodríguez, M. A.; Andújar, M. S.; Ayala, A. P.; Silva, R. X. da; Paschoal, C. W. A. Strong Electron–Phonon Coupling and Lattice Dynamics in One-Dimensional [(CH3)2NH2]PbI3 Hybrid Perovskite. Chem. Mater. 2025, 37 (3), 1013–1026. https://doi.org/10.1021/acs.chemmater.4c02670.
dc.identifier.doi10.1021/acs.chemmater.4c02670
dc.identifier.issn0897-4756
dc.identifier.issn1520-5002
dc.identifier.urihttps://hdl.handle.net/2183/47934
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleStrong Electron–Phonon Coupling and Lattice Dynamics in One-Dimensional [(CH3)2NH2]PbI3 Hybrid Perovskite
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
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relation.isAuthorOfPublication49f2ebe3-c964-4db9-8899-5da1fddbfa42
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relation.isAuthorOfPublication.latestForDiscoverycaf83c36-213b-4905-af41-e5da7aed80ed

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