Singular Temperatures Connected to Charge Transport Mechanism Transitions in Perylene Bisimides from Steady-State Photocurrent Measurements

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10045/47801
Registro completo de metadatos
Registro completo de metadatos
Campo DCValorIdioma
dc.contributorFísica de la Materia Condensadaes
dc.contributor.authorQuintana, José A.-
dc.contributor.authorVillalvilla, José M.-
dc.contributor.authorPeña, Alejandro de la-
dc.contributor.authorSegura, José L.-
dc.contributor.authorDíaz-García, María A.-
dc.contributor.otherUniversidad de Alicante. Departamento de Física Aplicadaes
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Materialeses
dc.date.accessioned2015-06-25T10:32:43Z-
dc.date.available2015-06-25T10:32:43Z-
dc.date.issued2015-05-29-
dc.identifier.citationThe Journal of Physical Chemistry C. 2015, 119(25): 14023–14028. doi:10.1021/acs.jpcc.5b03152es
dc.identifier.issn1932-7447 (Print)-
dc.identifier.issn1932-7455 (Online)-
dc.identifier.urihttp://hdl.handle.net/10045/47801-
dc.description.abstractPerylene bisimides (PBIs) are n-type semiconducting and photogenerating materials widely used in a variety of optoelectronic devices. Particularly interesting are PBIs that are simultaneously water-soluble and liquid-crystalline (PBI-W+LC) and, thus, attractive for the development of high-performing easily processable applications in biology and “green” organic electronics. In this work, singular temperatures connected to charge transport mechanism transitions in a PBI-W+LC derivative are determined with high accuracy by means of temperature-dependent photocurrent studies. These singular temperatures include not only the ones observed at 60 and 110 °C, corresponding to phase transition temperatures from crystalline to liquid-crystalline (LC) and from LC to the isotropic phase, respectively, as confirmed by differential scanning calorimetry (DSC), but also a transition at 45 °C, not observed by DSC. By analyzing the photocurrent dependence simultaneously on temperature and on light intensity, this transition is interpreted as a change from monomolecular to bimolecular recombination. These results might be useful for other semiconducting photogenerating materials, not necessarily PBIs or even organic semiconductors, which also show transport behavior changes at singular temperatures not connected with structural or phase transitions.es
dc.description.sponsorshipWe appreciate support from the Spanish government (MINECO) and the European Community (FEDER) through Grant MAT-2011-28167-C02-01, as well as the University of Alicante. We gratefully acknowledge financial support from MINECO (MAT2014-52305-P) and the UCM-BSCH joint project (GR3/14-910759). A. de la Peña thanks Universidad Complutense for a predoctoral fellowship.es
dc.languageenges
dc.publisherAmerican Chemical Societyes
dc.rights© 2015 American Chemical Societyes
dc.subjectPerylene bisimideses
dc.subjectSingular temperatureses
dc.subjectCharge transport mechanism transitionses
dc.subjectTemperature-dependent photocurrentes
dc.subject.otherFísica Aplicadaes
dc.subject.otherFísica de la Materia Condensadaes
dc.titleSingular Temperatures Connected to Charge Transport Mechanism Transitions in Perylene Bisimides from Steady-State Photocurrent Measurementses
dc.typeinfo:eu-repo/semantics/articlees
dc.peerreviewedsies
dc.identifier.doi10.1021/acs.jpcc.5b03152-
dc.relation.publisherversionhttp://dx.doi.org/10.1021/acs.jpcc.5b03152es
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
Aparece en las colecciones:INV - Física de la Materia Condensada - Artículos de Revistas

Archivos en este ítem:
Archivos en este ítem:
Archivo Descripción TamañoFormato 
Thumbnail2015_Quintana_etal_JPCC_final.pdfVersión final (acceso restringido)625 kBAdobe PDFAbrir    Solicitar una copia
Thumbnail2015_Quintana_etal_JPCC_accepted.pdfAccepted Manuscript (acceso abierto)308,71 kBAdobe PDFAbrir Vista previa


Todos los documentos en RUA están protegidos por derechos de autor. Algunos derechos reservados.