{"title":"金纳米结构对多域 HTTH 染料激发态分子内质子转移的影响","authors":"I. I. Hudzenko, A. Lopatynskyi, V. Chegel","doi":"10.15407/spqeo26.04.457","DOIUrl":null,"url":null,"abstract":"Organic multidomain dyes exhibiting excited state intramolecular proton transfer (ESIPT) are known due to large Stokes shifts and dependence of their luminescence spectral characteristics on the properties of the environment. In this work, influence of gold nanostructures on the spectral characteristics of a “polycarbonate matrix – gold nanostructures – HTTH” system was studied using thiazole dye HTTH as an example. A hypothesis about the possibility of plasmon resonance energy transfer (PRET) between the HTTH molecules in different states, namely the ground state (enol form) and the state after proton transfer (keto form), mediated by gold nanostructures was experimentally tested. Presence of gold nanostructures in the vicinity of HTTH molecules was found to lead to the changes in the ratio of the luminescence peak intensities for the enol and keto form of these molecules. This phenomenon opens up the possibility of additional regulation of the spectral characteristics and may evidence the PRET effect in the systems containing ESIPT-exhibiting dyes and plasmonic nanostructures. The obtained results improve our understanding of the physical processes in the systems similar to the studied one and imply new practical applications of them such as fabrication of organic light-emitting diodes, sensors, super-resolution microscopy tools and ultraviolet-to-visible radiation convertors.","PeriodicalId":21598,"journal":{"name":"Semiconductor physics, quantum electronics and optoelectronics","volume":"137 21","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Influence of gold nanostructures on excited state intramolecular proton transfer in multidomain HTTH dye\",\"authors\":\"I. I. Hudzenko, A. Lopatynskyi, V. Chegel\",\"doi\":\"10.15407/spqeo26.04.457\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Organic multidomain dyes exhibiting excited state intramolecular proton transfer (ESIPT) are known due to large Stokes shifts and dependence of their luminescence spectral characteristics on the properties of the environment. In this work, influence of gold nanostructures on the spectral characteristics of a “polycarbonate matrix – gold nanostructures – HTTH” system was studied using thiazole dye HTTH as an example. A hypothesis about the possibility of plasmon resonance energy transfer (PRET) between the HTTH molecules in different states, namely the ground state (enol form) and the state after proton transfer (keto form), mediated by gold nanostructures was experimentally tested. Presence of gold nanostructures in the vicinity of HTTH molecules was found to lead to the changes in the ratio of the luminescence peak intensities for the enol and keto form of these molecules. This phenomenon opens up the possibility of additional regulation of the spectral characteristics and may evidence the PRET effect in the systems containing ESIPT-exhibiting dyes and plasmonic nanostructures. The obtained results improve our understanding of the physical processes in the systems similar to the studied one and imply new practical applications of them such as fabrication of organic light-emitting diodes, sensors, super-resolution microscopy tools and ultraviolet-to-visible radiation convertors.\",\"PeriodicalId\":21598,\"journal\":{\"name\":\"Semiconductor physics, quantum electronics and optoelectronics\",\"volume\":\"137 21\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Semiconductor physics, quantum electronics and optoelectronics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15407/spqeo26.04.457\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Semiconductor physics, quantum electronics and optoelectronics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15407/spqeo26.04.457","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Influence of gold nanostructures on excited state intramolecular proton transfer in multidomain HTTH dye
Organic multidomain dyes exhibiting excited state intramolecular proton transfer (ESIPT) are known due to large Stokes shifts and dependence of their luminescence spectral characteristics on the properties of the environment. In this work, influence of gold nanostructures on the spectral characteristics of a “polycarbonate matrix – gold nanostructures – HTTH” system was studied using thiazole dye HTTH as an example. A hypothesis about the possibility of plasmon resonance energy transfer (PRET) between the HTTH molecules in different states, namely the ground state (enol form) and the state after proton transfer (keto form), mediated by gold nanostructures was experimentally tested. Presence of gold nanostructures in the vicinity of HTTH molecules was found to lead to the changes in the ratio of the luminescence peak intensities for the enol and keto form of these molecules. This phenomenon opens up the possibility of additional regulation of the spectral characteristics and may evidence the PRET effect in the systems containing ESIPT-exhibiting dyes and plasmonic nanostructures. The obtained results improve our understanding of the physical processes in the systems similar to the studied one and imply new practical applications of them such as fabrication of organic light-emitting diodes, sensors, super-resolution microscopy tools and ultraviolet-to-visible radiation convertors.