Komal Vasant Barhate , Mohammad Amir Ahemad , Juhi Dutta , Sangita Bose , Neeraj Agarwal
{"title":"揭示了粉末形式的吖啶酮-胺衍生物和具有12% EQE的高效oled","authors":"Komal Vasant Barhate , Mohammad Amir Ahemad , Juhi Dutta , Sangita Bose , Neeraj Agarwal","doi":"10.1016/j.jphotochem.2025.116468","DOIUrl":null,"url":null,"abstract":"<div><div>Fluorescence-based organic light-emitting diodes (OLEDs) are explicitly appealing due to their extended operational lifetimes, high color purity of electroluminescence, and unmatched potential for low-cost manufacturing in next-generation full-colour display and lighting applications. Here, we designed N-substituted acridone-dibenzoazepine derivatives (<strong>Aze-Me-Acr</strong> and <strong>Aze-Anisyl-Acr)</strong>. Twisted electron rich dibenzoazepine provides limited rotation at donor–acceptor bond. Both, <strong>Aze-Me-Acr</strong> and <strong>Aze-Anisyl-Acr</strong> show solvent polarity dependent fluorescence in a range of 490 to 525 nm at room temperature (RT), whereas at 77 K, triplet emission at around 620 nm was observed having life time of ∼435–547 ms. Both these emitters showed dual emission <em>i.e.</em>, fluorescence and phosphorescence in powder form. Fluorescence was observed at 550 & 544 nm while phosphorescence was seen at 670 & 655 nm, respectively for <strong>Aze-Me-Acr</strong> and <strong>Aze-Anisyl-Acr</strong>. Long excited lifetimes in the range of 8 to 15 μs were found in red region (>600 nm). OLEDs with <strong>Aze-Me-Acr</strong> and <strong>Aze-Anisyl-Acr</strong> as active emitters were also fabricated which showed green (CIE: 0.28, 0.65) and yellowish green (CIE: 0.39, 0.56) electroluminescence, respectively. Doped devices of <strong>Aze-Me-Acr</strong> in CBP blend resulted in high external quantum efficiency (EQE) of 12.8 %.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"468 ","pages":"Article 116468"},"PeriodicalIF":4.1000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unveiling dual emission in powder form of acridone-amine derivatives and efficient OLEDs with 12% EQE\",\"authors\":\"Komal Vasant Barhate , Mohammad Amir Ahemad , Juhi Dutta , Sangita Bose , Neeraj Agarwal\",\"doi\":\"10.1016/j.jphotochem.2025.116468\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Fluorescence-based organic light-emitting diodes (OLEDs) are explicitly appealing due to their extended operational lifetimes, high color purity of electroluminescence, and unmatched potential for low-cost manufacturing in next-generation full-colour display and lighting applications. Here, we designed N-substituted acridone-dibenzoazepine derivatives (<strong>Aze-Me-Acr</strong> and <strong>Aze-Anisyl-Acr)</strong>. Twisted electron rich dibenzoazepine provides limited rotation at donor–acceptor bond. Both, <strong>Aze-Me-Acr</strong> and <strong>Aze-Anisyl-Acr</strong> show solvent polarity dependent fluorescence in a range of 490 to 525 nm at room temperature (RT), whereas at 77 K, triplet emission at around 620 nm was observed having life time of ∼435–547 ms. Both these emitters showed dual emission <em>i.e.</em>, fluorescence and phosphorescence in powder form. Fluorescence was observed at 550 & 544 nm while phosphorescence was seen at 670 & 655 nm, respectively for <strong>Aze-Me-Acr</strong> and <strong>Aze-Anisyl-Acr</strong>. Long excited lifetimes in the range of 8 to 15 μs were found in red region (>600 nm). OLEDs with <strong>Aze-Me-Acr</strong> and <strong>Aze-Anisyl-Acr</strong> as active emitters were also fabricated which showed green (CIE: 0.28, 0.65) and yellowish green (CIE: 0.39, 0.56) electroluminescence, respectively. Doped devices of <strong>Aze-Me-Acr</strong> in CBP blend resulted in high external quantum efficiency (EQE) of 12.8 %.</div></div>\",\"PeriodicalId\":16782,\"journal\":{\"name\":\"Journal of Photochemistry and Photobiology A-chemistry\",\"volume\":\"468 \",\"pages\":\"Article 116468\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Photochemistry and Photobiology A-chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1010603025002084\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Photochemistry and Photobiology A-chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1010603025002084","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Unveiling dual emission in powder form of acridone-amine derivatives and efficient OLEDs with 12% EQE
Fluorescence-based organic light-emitting diodes (OLEDs) are explicitly appealing due to their extended operational lifetimes, high color purity of electroluminescence, and unmatched potential for low-cost manufacturing in next-generation full-colour display and lighting applications. Here, we designed N-substituted acridone-dibenzoazepine derivatives (Aze-Me-Acr and Aze-Anisyl-Acr). Twisted electron rich dibenzoazepine provides limited rotation at donor–acceptor bond. Both, Aze-Me-Acr and Aze-Anisyl-Acr show solvent polarity dependent fluorescence in a range of 490 to 525 nm at room temperature (RT), whereas at 77 K, triplet emission at around 620 nm was observed having life time of ∼435–547 ms. Both these emitters showed dual emission i.e., fluorescence and phosphorescence in powder form. Fluorescence was observed at 550 & 544 nm while phosphorescence was seen at 670 & 655 nm, respectively for Aze-Me-Acr and Aze-Anisyl-Acr. Long excited lifetimes in the range of 8 to 15 μs were found in red region (>600 nm). OLEDs with Aze-Me-Acr and Aze-Anisyl-Acr as active emitters were also fabricated which showed green (CIE: 0.28, 0.65) and yellowish green (CIE: 0.39, 0.56) electroluminescence, respectively. Doped devices of Aze-Me-Acr in CBP blend resulted in high external quantum efficiency (EQE) of 12.8 %.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.