Thermal Stability of Organic Semiconductor Thin Film Glasses by Local Changes in Spontaneous Orientation Polarization

Vapor-deposited organic semiconductor glasses exhibit distinct molecular anisotropy and exceptional kinetic and thermodynamic stability, distinguishing them from the inherently isotropic and poorly stable glasses formed through liquid cooling. In this study, we exploit these unique properties to exa...

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Detalles Bibliográficos
Autores: Ruiz-Ruiz, Marta|||0009-0001-7462-6327, Villalobos-Martin, A., Bar, Tapas|||0000-0002-5947-074X, Rodríguez-Tinoco, Cristian|||0000-0003-2693-957X, Fraxedas, Jordi|||0000-0002-2821-4831, Capaccioli, S., Labardi, M., Gonzalez-Silveira, Marta|||0000-0003-1510-5262, Rodríguez-Viejo, Javier|||0000-0002-9735-263X
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:315704
Acceso en línea:https://ddd.uab.cat/record/315704
https://dx.doi.org/urn:doi:10.1021/acs.jpcb.5c01679
Access Level:acceso abierto
Palabra clave:Glass transition temperature Tg
Isotropics
Kinetics and thermodynamics
Liquid cooling
Molecular anisotropy
Organic semiconductor thin films
Organics
Property
Supercooled liquids
Thermal
Descripción
Sumario:Vapor-deposited organic semiconductor glasses exhibit distinct molecular anisotropy and exceptional kinetic and thermodynamic stability, distinguishing them from the inherently isotropic and poorly stable glasses formed through liquid cooling. In this study, we exploit these unique properties to examine local changes in surface potential as the stable glass transitions to a supercooled liquid upon heating above the glass transition temperature (T). Vapor deposited glasses of organic molecules with permanent dipole moments can generate a measurable surface potential due to their anisotropic molecular orientation. We use local electrostatic force microscopy and Kelvin probe force microscopy to provide insights into the dynamics of the phase transformation occurring above T. We demonstrate that changes in polarization upon conversion to the isotropic liquid serve as an effective proxy for tracking this transition and highlight their potential for evaluating the thermal stability of organic devices under diverse thermal conditions.