{"title":"SrAl2O4:Eu2+, Dy3+复合材料修饰的Sm(DBM)3phen复合物中的多光谱发射和拉长的红色发射衰减","authors":"Kiran Kalkal, Pooja Uttam, Y. Dwivedi","doi":"10.1016/j.ceramint.2024.10.125","DOIUrl":null,"url":null,"abstract":"<div><div>In the present study, we report elongated red emission decay in Sm(DBM)<sub>3</sub>phen (SDp) complex stimulated via radiative transfer from a persistent luminescent phosphor SrAl<sub>2</sub>O<sub>4</sub>:Eu<sup>2+</sup>,Dy<sup>3+</sup> (SrAl) in the Polyvinyl alcohol (PVA) matrix. The detailed spectroscopic investigations carried out on 405 nm laser excitation reveal the predominating broad emission, centered at 520 nm with a prolonged decay time, while the SDp complex in PVA yields characteristic yellow-red emissions with a decay time of ∼535 μs. The PVA composite yields an amalgam of emissions with modified intensities and changes in peak shape due to the lattice effect. We report spectroscopic analysis of the emission spectrum with varying concentrations, layer stacking, lattice effect, etc. The lattice leads the emission peak broadening, facilitating improved interaction between the SDp complex and SrAl phosphor. The radiative decay analysis of red emission for transition <sup>4</sup>G<sub>5/2</sub> → <sup>6</sup>H<sub>9/2</sub> (Sm<sup>3+</sup> ion) reveals that in PVA host, it decays slower (∼535μs) than in the pure complex (∼260μs). Further, red emission was present even after cessation of excitation due to the elongated radiative decay (∼3.5 ms) in the presence of SrAl phosphor in PVA, indicating efficient radiative transfer (transfer rate of ∼1580 s<sup>−1</sup>) from the phosphor to Sm(DBM)<sub>3</sub>phen complex. Detailed photophysics and CIE coordinate calculations were presented.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"51 12","pages":"Pages 16484-16491"},"PeriodicalIF":5.1000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multispectral emissive and elongated red emission decay in Sm(DBM)3phen complex modified by SrAl2O4:Eu2+, Dy3+ composite\",\"authors\":\"Kiran Kalkal, Pooja Uttam, Y. Dwivedi\",\"doi\":\"10.1016/j.ceramint.2024.10.125\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In the present study, we report elongated red emission decay in Sm(DBM)<sub>3</sub>phen (SDp) complex stimulated via radiative transfer from a persistent luminescent phosphor SrAl<sub>2</sub>O<sub>4</sub>:Eu<sup>2+</sup>,Dy<sup>3+</sup> (SrAl) in the Polyvinyl alcohol (PVA) matrix. The detailed spectroscopic investigations carried out on 405 nm laser excitation reveal the predominating broad emission, centered at 520 nm with a prolonged decay time, while the SDp complex in PVA yields characteristic yellow-red emissions with a decay time of ∼535 μs. The PVA composite yields an amalgam of emissions with modified intensities and changes in peak shape due to the lattice effect. We report spectroscopic analysis of the emission spectrum with varying concentrations, layer stacking, lattice effect, etc. The lattice leads the emission peak broadening, facilitating improved interaction between the SDp complex and SrAl phosphor. The radiative decay analysis of red emission for transition <sup>4</sup>G<sub>5/2</sub> → <sup>6</sup>H<sub>9/2</sub> (Sm<sup>3+</sup> ion) reveals that in PVA host, it decays slower (∼535μs) than in the pure complex (∼260μs). Further, red emission was present even after cessation of excitation due to the elongated radiative decay (∼3.5 ms) in the presence of SrAl phosphor in PVA, indicating efficient radiative transfer (transfer rate of ∼1580 s<sup>−1</sup>) from the phosphor to Sm(DBM)<sub>3</sub>phen complex. Detailed photophysics and CIE coordinate calculations were presented.</div></div>\",\"PeriodicalId\":267,\"journal\":{\"name\":\"Ceramics International\",\"volume\":\"51 12\",\"pages\":\"Pages 16484-16491\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2024-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ceramics International\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0272884224046388\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, CERAMICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ceramics International","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0272884224046388","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, CERAMICS","Score":null,"Total":0}
Multispectral emissive and elongated red emission decay in Sm(DBM)3phen complex modified by SrAl2O4:Eu2+, Dy3+ composite
In the present study, we report elongated red emission decay in Sm(DBM)3phen (SDp) complex stimulated via radiative transfer from a persistent luminescent phosphor SrAl2O4:Eu2+,Dy3+ (SrAl) in the Polyvinyl alcohol (PVA) matrix. The detailed spectroscopic investigations carried out on 405 nm laser excitation reveal the predominating broad emission, centered at 520 nm with a prolonged decay time, while the SDp complex in PVA yields characteristic yellow-red emissions with a decay time of ∼535 μs. The PVA composite yields an amalgam of emissions with modified intensities and changes in peak shape due to the lattice effect. We report spectroscopic analysis of the emission spectrum with varying concentrations, layer stacking, lattice effect, etc. The lattice leads the emission peak broadening, facilitating improved interaction between the SDp complex and SrAl phosphor. The radiative decay analysis of red emission for transition 4G5/2 → 6H9/2 (Sm3+ ion) reveals that in PVA host, it decays slower (∼535μs) than in the pure complex (∼260μs). Further, red emission was present even after cessation of excitation due to the elongated radiative decay (∼3.5 ms) in the presence of SrAl phosphor in PVA, indicating efficient radiative transfer (transfer rate of ∼1580 s−1) from the phosphor to Sm(DBM)3phen complex. Detailed photophysics and CIE coordinate calculations were presented.
期刊介绍:
Ceramics International covers the science of advanced ceramic materials. The journal encourages contributions that demonstrate how an understanding of the basic chemical and physical phenomena may direct materials design and stimulate ideas for new or improved processing techniques, in order to obtain materials with desired structural features and properties.
Ceramics International covers oxide and non-oxide ceramics, functional glasses, glass ceramics, amorphous inorganic non-metallic materials (and their combinations with metal and organic materials), in the form of particulates, dense or porous bodies, thin/thick films and laminated, graded and composite structures. Process related topics such as ceramic-ceramic joints or joining ceramics with dissimilar materials, as well as surface finishing and conditioning are also covered. Besides traditional processing techniques, manufacturing routes of interest include innovative procedures benefiting from externally applied stresses, electromagnetic fields and energetic beams, as well as top-down and self-assembly nanotechnology approaches. In addition, the journal welcomes submissions on bio-inspired and bio-enabled materials designs, experimentally validated multi scale modelling and simulation for materials design, and the use of the most advanced chemical and physical characterization techniques of structure, properties and behaviour.
Technologically relevant low-dimensional systems are a particular focus of Ceramics International. These include 0, 1 and 2-D nanomaterials (also covering CNTs, graphene and related materials, and diamond-like carbons), their nanocomposites, as well as nano-hybrids and hierarchical multifunctional nanostructures that might integrate molecular, biological and electronic components.