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Optical investigation of radiation-induced color centers in lithium fluoride thin films for low-energy proton-beam detectors
摘要： In the last few years, the peculiar photoluminescence properties of radiation-induced color centers in lithium fluoride (LiF) films have been successfully used for advanced diagnostics of low-energy proton beams produced by the TOP-IMPLART linear accelerator for protontheraphy under development at ENEA C.R. Frascati. The two-dimensional spatial dose map of the transversal section of proton beams was fully reconstructed in a wide interval of doses. In this work the optical emission properties of LiF thin films, grown by thermal evaporation on glass and Si (100) substrates and subsequently irradiated by proton beams of nominal energy 3 MeV at doses higher than 105 Gy, were carefully investigated. Their structural and morphological analyses were performed by X-ray diffraction and atomic force microscopy. A careful comparison of the photoluminescence and photoluminescence-excitation spectra of F2 and F3+ electronic defects was performed. Substrate-enhanced photoluminescence intensity increase up to 100% was observed in colored LiF films grown on Si substrates with respect to glass ones. This behavior can be substantially ascribed to the reflective properties of the Si substrate at the emission wavelengths of F2 and F3+ CCs, although other complex effects due to the polycrystalline nature of the films cannot be excluded.
关键词： Photoluminescence,Lithium fluoride,Radiation detectors,Color centers,Thin films
更新于2025-09-23 15:23:52
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Conjugate Electrospinning Construction of Microyarns with Synchronous Color-Tuned Photoluminescence and Tunable Electrical Conductivity
摘要： Here, we report a strategy for constructing {[Tb(BA)3phen + Eu(BA)3phen]/PAN}//[PANI/PAN] (BA = benzoic acid, phen = phenanthroline, PANI = polyaniline, PAN = polyacrylonitrile) hetero-structured microyarns simultaneously endowed with the bi-functionality of tunable luminescence colors and electrical conductivity by using a conjugate electrospinning technique. The obtained hetero-structured microyarns are composed of [Tb(BA)3phen + Eu(BA)3phen]/PAN luminescent nano?bers and PANI/PAN electrically conductive nano?bers, realizing ef?cient separation of dark-colored PANI from rare earth (RE) complexes, and thus the enhanced luminescent performance is obtained. Under 276-nm ultraviolet light excitation, the emitting light color of the hetero-structured microyarns can be adjusted in a broad range of green–yellow–red by changing the proportion of RE complexes. The electrical conductivity of the hetero-structured microyarns also can be modulated via tuning the percentages of PANI. These hetero-structured microyarns, by virtue of their luminescent properties and electrical performance, are expected to be applied in multifunctional applications.
关键词： photoluminescence,conjugate electrospinning,Microyarn,electrical properties
更新于2025-09-23 15:23:52
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Effect of Macro-scale Mechanical Stress of Silicon Wafer on Room Temperature Photoluminescence Signals
摘要： Mechanical stress was applied to single side polished and double side polished Si wafers in polypropylene wafer containers for different localized stress levels and durations. Room temperature photoluminescence (RTPL) spectra from Si wafers were measured before and after applying localized mechanical stress. Significant changes (up to 26% increase) in RTPL intensity were measured from areas under different stress levels even 1 year after the fixtures for mechanical stress generation were removed. Significant effects of localized mechanical stress on RTPL intensity variations were measured up to 49 days after the fixture removal. Nearly fully relaxed RTPL signatures for localized mechanical stress were measured 450 days after the fixture removal. RTPL intensity is found to be very sensitive to the externally applied macro-scale mechanical stress of Si wafers and residual (or memorized) internal stress even after removal of fixtures for external mechanical stress generation.
关键词： Silicon,room temperature photoluminescence,stress relaxation,mechanical stress
更新于2025-09-23 15:23:52
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Broadband Emission in Hybrid Organic–Inorganic Halides of Group 12 Metals
摘要： We report syntheses, crystal and electronic structures, and characterization of three new hybrid organic?inorganic halides (R)ZnBr3(DMSO), (R)2CdBr4·DMSO, and (R)CdI3(DMSO) (where (R) = C6(CH3)5CH2N(CH3)3, and DMSO = dimethyl sulfoxide). The compounds can be conveniently prepared as single crystals and bulk polycrystalline powders using a DMSO?methanol solvent system. On the basis of the single-crystal X-ray diffraction results carried out at room temperature and 100 K, all compounds have zero-dimensional (0D) crystal structures featuring alternating layers of bulky organic cations and molecular inorganic anions based on a tetrahedral coordination around group 12 metal cations. The presence of discrete molecular building blocks in the 0D structures results in localized charges and tunable room-temperature light emission, including white light for (R)ZnBr3(DMSO), bluish-white light for (R)2CdBr4·DMSO, and green for (R)CdI3(DMSO). The highest photoluminescence quantum yield (PLQY) value of 3.07% was measured for (R)ZnBr3(DMSO), which emits cold white light based on the calculated correlated color temperature (CCT) of 11,044 K. All compounds exhibit fast photoluminescence lifetimes on the timescale of tens of nanoseconds, consistent with the fast luminescence decay observed in π-conjugated organic molecules. Temperature dependence photoluminescence study showed the appearance of additional peaks around 550 nm, resulting from the organic salt emission. Density functional theory calculations show that the incorporation of both the low-gap aromatic molecule R and the relatively electropositive Zn and Cd metals can lead to exciton localization at the aromatic molecular cations, which act as luminescence centers.
关键词： zero-dimensional structures,broadband emission,group 12 metals,exciton localization,photoluminescence quantum yield,hybrid organic?inorganic halides
更新于2025-09-23 15:23:52
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Novel emission bands of Na2TiF6:Mn4+ phosphors induced by the cation exchange method
摘要： A series of Na2TiF6:xMn4+ samples were prepared by the cation exchange method. Visible QC behavior and the strongest ZPL peaks were observed for these samples. The characteristic of the visible QC behavior is that PL intensity at 620 nm is 1.61 times as high as PLE intensity at 476 nm. The mechanisms of these phenomena were discussed, and the color purity, crystal-field and nephelauxetic effect, the critical distance and the multipolar interaction for the samples were determined. The result shows that the Mn4+ ions are located at a strong crystal field and the concentration quenching of Mn4+ is from the quadrupole-quadrupole interaction. The slightly increase of nephelauxetic ratio causes the slightly blue shift of emission. The color-purity and chromaticity coordinates of the optimal sample suggests that the strongest ZPL makes its red emission with high color-purity. Thus, Na2TiF6:0.08Mn4+ is a potential red-emitting phosphor for blue light-based WLEDs.
关键词： Fluorides,Photoluminescence,Mn4+,Red emitting phosphor,Visible quantum cutting
更新于2025-09-23 15:23:52
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Red-light Emission of Li-doped Ga2O3 One-dimensional Nanostructures and the Luminescence Mechanism
摘要： Li-doped Ga2O3 one-dimensional nanostructures were synthesized by thermal evaporation. The observation results of morphology show that there are plenty of one-dimensional nanostructures in the sample. Raman spectra of samples show excellent crystallinity and the Raman peaks of the Li-doped Ga2O3 have red-shifted compared to the “undoped” Ga2O3 in the low wavenumber section. Comparing the photoluminescence behavior of the two samples at room temperature, they were found to have blue light emission peaks, but the emission peak of Li-doped Ga2O3 is blue-shifted. Additionally, there is a strong red light emission peak centered at 692 nm in the spectrum of Li-doped Ga2O3.
关键词： Li-doped,Nanostructures,Photoluminescence,Ga2O3,Raman spectrum
更新于2025-09-23 15:23:52
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Synthesis, characterization and photophysical properties of meso-indole-boron-dipyrromethene derivatives and their cell imaging and viscosity sensing
摘要： Based on the molecular design and structural modification of boron-dipyrromethene (BODIPY), two new BODIPY derivatives with meso-substituted functional indole moieties were successfully prepared. These new compounds were characterized by NMR, HRMS and FTIR, exhibiting the different UV-vis and PL spectral phenomena because of their varied molecular structures in various solvents and different degrees of negative solvatochromism. Theoretical calculations and CV results show that the substituted NO2 group at 5-position of indole is favorable for increasing the oxidation potential of the molecules, while the NH2 group is the opposite. These two BODIPY derivatives have different sensitivities to pH changes, and can be appropriately applied as cell imaging materials due to their good physical chemical characteristics and excellent biocompatibility. In particular, the fluorescence characteristics of BODIPY derivative with the substituted NH2 group at 5-position of indole show a good solvent viscosity dependence, highlighting its potential application for testing the intracellular viscosity changes of the living cell in disease diagnosis.
关键词： meso-indole boron-dipyrromethene derivatives,photoluminescence,fluorescence characteristics,cell imaging,viscosity sensing
更新于2025-09-23 15:23:52
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Modulated up-conversion luminescence and low-temperature sensing of Gd3Ga5O12:Yb3+/Er3+ by incorporation of Fe3+ ions
摘要： Yb3+/Er3+ co-doped crystals show strong up-conversion luminescence and their temperature dependence of luminescence intensity enable the application of temperature sensors. Such sensors usually work at hundreds Kelvin with high sensitivity, while the sensors appropriate to very low temperatures are rarely reported. In this study, we report the low temperature sensing of Gd3Ga5O12:Yb3+/Er3+ nanocrystals by partial or total substitution of Ga3+ by Fe3+ ions. The up-conversion photoluminescence of the nanocrystals is measured on cooling from 300 to 4.2 K. The low-temperature sensing performance is improved, and the structure, magnetic and optical properties are modulated by the substitution of Fe3+ ions, rendering the nanocrystal useful for multi-functional sensing application.
关键词： Temperature sensor,Magnetic doping,Photoluminescence,Up-conversion
更新于2025-09-23 15:23:52
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Host Sensitized Lanthanide Photoluminescence from Post-synthetically Modified Semiconductor Nanoparticles Depends on Reactant Identity
摘要： This work investigates the photoluminescence characteristics where cadmium selenide (CdSe) and zinc sulfide (ZnS) nanoparticles are treated post-synthetically by the trivalent lanthanide cations (Ln3+) [Ln = Pr, Nd, Sm, Eu, Tb, Dy, Ho, Er, Tm, Yb] separately to form either CdSe/Ln or ZnS/Ln nanoparticles. Host sensitized Ln3+ emission was found to be present only in CdSe/Eu, CdSe/Tb, ZnS/Eu, ZnS/Tb and ZnS/Yb nanoparticles. In all the cases tuning of emission of the nanoparticles has been observed, irrespective of the presence or absence of host sensitization. The elemental compositions of CdSe and ZnS nanoparticles upon post-synthetic treatment show a remarkable difference. Incorporation of lanthanides in the nanoparticles is evident with significant alteration in the anionic content, and complete cation exchange of either Cd2+ or Zn2+ by Ln3+ has not been detected; as evaluated from energy dispersive X-ray spectroscopy. Further evaluation on this comes from considering thermodynamic parameters of inter cation interaction. In cases where the host sensitized Ln3+ emission have been observed, luminescence lifetime measurements reveal significant protection of Ln3+ in the nanoparticles. Noticeable difference in photophysical properties for a given Ln3+ has been realized in the two hosts. The photophysical observations have been rationalized using (i) charge trapping mediated host sensitized dopant emission, (ii) autoionization of excited electrons, and (iii) environment induced photoluminescence quenching. The post-synthetic modification discussed in the present work provides an easy and less synthetically demanding room temperature based protocol to avail lanthanide incorporated (doped) semiconductor nanoparticles that can potentially use the unique emission properties of the lanthanide cations.
关键词： Semiconductor Nanoparticles,Host Sensitization,Trivalent Lanthanides,Photoluminescence,Post-synthetic Modification
更新于2025-09-23 15:23:52
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Synthesis and photoluminescence properties of different structural cuprous complexes regulated by benzoxazole ligands and halogen/pseudohalide ions
摘要： Reaction of 2-(2’-pyridyl)benzoxazole (2-PBO), 2-(4’-pyridyl)benzoxazole (4-PBO) and 2,2-(1,4-butanediyl)bis-1,3-benzoxazole (BBO) ligands with CuX (X = I, Br, SCN) afforded a binuclear copper(I) complex [Cu(2-PBO)(μ2-I)]2 (1) and three copper(I) coordination polymers [Cu4(4-PBO)4(μ3-I)4]n (2), {[Cu(4-PBO)(μ3-SCN)]2}n (3) and {[Cu(BBO)(μ2-Br)]2}n (4). The structural analysis revealed that the all copper(I) ions are four-coordinated and the geometric structure around the central copper(I) atom possessing slightly distorted tetrahedral geometry in complexes 1-4. Halogen or pseudohalide ions can not only act as counter anions, but also as ligands participation in coordination when the cuprous ion coordination sites are not saturated. Due to the different coordination modes of the benzoxazole ligands, in order to satisfy the tetra-coordination of cuprous ions, halogen or pseudohalide ions adopt μ2 and/or μ3-bridging modes to synergistically complete coordination. Photoluminescence investigation show that complexes 1, 3 and 4 have two emission peaks, the high energy band peak is attributed to MLCT[d10(Cu)→π*] and XMCT, the low energy band peak is caused by the 3CC emission. This may be due to the presence of μ2-X (X=I, Br, S) in these complexes. However complex 2 only had one emission peak, which may be attributed to MLCT[d10(Cu)→π*] and XMCT.
关键词： Cuprous complex,Charge-transfer,Photoluminescence,Crystal structure,Benzoxazole
更新于2025-09-23 15:23:52