Singlet fission is usually the only reaction channel for excited states in rubrene-based organic light-emitting diodes (OLEDs) at ambient temperature. Intriguingly, we discover that triplet fusion (TF) and intersystem crossing (ISC) within rubrene-based devices begin at moderate and high current densities (j), respectively. Both processes enhance with decreasing temperature. This behavior is discovered by analyzing the magneto-electroluminescence curves of the devices. The j-dependent magneto-conductance, measured at ambient temperature indicates that spin mixing within polaron pairs that are generated by triplet-charge annihilation (TQA) causes the occurrence of ISC, while the high concentrations of triplets are responsible for generating TF. Additionally, the reduction in exciton formation and the elevated TQA with decreasing temperature may contribute to the enhanced ISC at low temperatures. This work provides considerable insight into the different mechanisms that occur when a high density of excited states exist in rubrene and reasonable reasons for the absence of EL efficiency roll-off in rubrene-based OLEDs.
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http://dx.doi.org/10.1021/acsami.7b17695 | DOI Listing |
Chem Sci
December 2024
Department of Physical Chemistry, University of Málaga, Andalucia-Tech Campus de Teatinos s/n 29071 Málaga Spain
The synthesis, electrochemical, spectroelectrochemical, photophysical and light induced electron transfer reactions in two new anthanthrene quinodimethanes have been studied and analyzed in the context of dynamic electrochemistry. Their properties are dependent on the interconversion between folded and twisted forms, which are separated by a relatively small energy range, thus allowing to explore their interconversion by variable temperature measurements. The photophysics of these molecules is mediated by a diradical excited state with a twisted structure that habilitates rapid intersystem crossing.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Department of Physics and Astronomy, University of Sheffield, Hounsfield Road, Sheffield S3 7RH, U.K.
Activated intramolecular singlet fission is known to occur in the conjugated polymer polythienylene-vinylene (P3TV). Instead, efficient intersystem crossing has been observed in a short 3-alkyl(thienylene-vinylene) dimer. Here, we investigate a series of oligomers covering the conjugation length gap between the dimer and polymer.
View Article and Find Full Text PDFPhotochem Photobiol
December 2024
Department of Chemistry, The Gandhigram Rural Institute-Deemed to be University, Dindigul, Tamilnadu, India.
Modulating the photophysical properties of photosensitizers is an effective approach to enhance singlet oxygen generation for photodynamic therapy. Porphyrins are the most widely used photosensitizers due to their biocompatible nature. Aggregation-induced emission (AIE) characteristics of photosensitizers are one of the advantageous features that will enhance fluorescence, intersystem crossing, and efficient triplet state generation.
View Article and Find Full Text PDFNano Lett
December 2024
School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, P. R. China.
Room-temperature phosphorescent (RTP) carbon dots (CDs) demonstrate significant potential applications in the field of information anticounterfeiting due to their excellent optical properties. However, RTP emission of CDs remains significantly limited due to the spin-forbidden properties of triplet exciton transitions. In this work, an in situ nitrogen doping strategy was employed to design and construct strong spin-orbit coupling nitrogen-doped CDs with mesoporous silica with alumina (N-CDs@MS@AlO) RTP composites.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Department of Chemistry, NIS Interdepartmental and INSTM Reference Centre, University of Torino, Via G. Quarello 15/A, 10135 and Via P. Giuria 7, 10125 Turin, Italy.
In this study, we present for the first time the incorporation of two distinct nonsymmetrical squaraines (SQ) into hierarchically porous Hafnium-based UiO-66 Metal-Organic Frameworks (MOFs), each functionalized with various moieties, for application as photosensitizers in photodynamic therapy. SQs are meticulously designed to feature COOH moieties for interaction with the MOF's metallic cluster and bromine atoms to enhance intersystem crossing and reactive oxygen species (ROS) production. The distinct central functionalizations, one with squaric acid and the other with a dicyanovinyl-substituted squaric acid derivative, result in unique geometric conformations.
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