Publications by authors named "XianTao Wei"

Vanadate phosphors include [VO] tetrahedra with symmetry. Due to the charge transfer (CT) between V-O, the phosphor with [VO] tetrahedra exhibits strong emission in the visible region and can effectively absorb ultraviolet (UV) light. Garnet structured vanadate phosphors have attracted much attention due to their easily controllable composition.

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In recent years, with the growing demand for non-contact and real-time optical temperature measurements, it has become imperative to develop new luminescent thermometry materials as well as novel temperature detection schemes with higher sensitivity. In this work, a series of SrBO:Tm ( = 0.001-0.

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Self-activated phosphors have attracted considerable attention due to their low synthesis temperature, high excitation threshold, and broad emission spectrum. And self-activated tungstate phosphors are distinguished by their low cost and stable chemical properties. Generally, it is difficult to observe luminescence from tungstate phosphors at room temperature.

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Thermal imaging materials with high sensitivity and the ability to reflect real-time temperature play an important role in research areas such as biotechnology and electronic engineering. However, the temperature sensitivity and temporal resolution of the current materials are not suitable for the complicated detection situation. In this paper, we introduce a thermal imaging material - SrBO:5%Sm - with high temperature sensitivity.

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In recent years, there has been increasing effort devoted to the development of single-phase white phosphors due to drawbacks such as severe reabsorption and color deviation in traditional white light-emitting diodes (WLEDs). A new feasible strategy has emerged for achieving white light emission through the Bi-Eu energy transfer in suitable single-phase phosphors. Therefore, a series of GdTaO:Bi and GdTaO:0.

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Bi/Eu doped CsGdGeO luminescent materials were prepared by a solid-state reaction. The energy band and density of states of CsGdGeO were calculated by density functional theory. The CsGdGeO host presents a broadband emission peaking at 520 nm.

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Altering the local symmetry of an activator by lattice tuning is considered an effective strategy to optimize the luminescence performance of phosphors. Herein, the novel Mn-activated double perovskite phosphor LaMgTaO (LMTO) with A-site defects was successfully prepared. Benefiting from the random occupation of the nearest A-site by cations and vacancies, the distorted [MnO] octahedra lack the inversion center.

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Recently, using the Eu2+ → Mn2+ energy transfer strategy to explore new single-phase phosphors suitable for the near-ultraviolet (n-UV) region has become one of the major strategies in solid-state lighting applications. Therefore, a novel color-tunable K2BaCa(PO4)2 (KBCPO):[Eu2+,Si4+],Mn2+ phosphor was developed because of the preeminent thermal stability of luminescence of Eu2+-activated KBCPO. In this study, we first designed a [Eu2+, Si4+] → [K+, P5+] charge compensation strategy to optimize the luminescence properties of Eu2+ in the KBCPO matrix.

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An ideal electron transporting layer (ETL) of perovskite solar cells (PSCs) requires reasonable energy levels, high electrical conductivity and excellent charge extraction. The low processing temperature makes ZnO a promising ETL for PSCs; however the widely used solution-processed ZnO films often suffer from high-density surface defect states, which might cause severe charge recombinations at the ETL/perovskite interface and accelerate the chemical decomposition of perovskite materials. In this work, we employed the vacuum-based magnetron sputtering method to deposit ZnO ETLs, which significantly reduces the number of oxygen vacancies and hydroxyl groups on the ZnO surface.

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The thermal stability of the phosphors in phosphor-converted light-emitting diodes (LEDs) plays an important role in the practical application of lighting. Herein, the Mn-based red-emitting phosphors of pure and Eu-doped SrMnLi(PO) (SMPO) samples were prepared using the high temperature solid-state reaction method. The crystal field environment around the Mn ions was analyzed by combining the results of photoluminescence excitation spectroscopy and Tanabe-Sugano diagrams.

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Eu3+ and Er3+ co-doped YNbO4 powder phosphors were synthesized by a traditional high-temperature solid-state reaction method. A laser of 487.6 nm wavelength was selected to be the excitation source which can pump Eu3+ ions from its thermally populated low-lying 7F2 ground state to the excited state 5D2 and lift the Er3+ ions from their 4I15/2 to 4F7/2 states.

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A new strategy of optical thermometry is realized by long persistent luminescence phosphor SrAlO:Eu, Dy, Tb (SAEDT). Under different temperatures, SAEDT shows bright afterglow emissions after cessation of the UV excitation. The afterglow color of the SAEDT sample is blue at 60 K and gradually changed into green at 240 K.

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Monodisperse β-NaYF:1%Sm nanoparticles were fabricated successfully via the thermal decomposition technique. Strong temperature dependence of the Sm emission was observed when its thermally populated state H6 was directly excited to the G4 level. This strategy not only can eliminate laser heating and background Stokes-type scattering noise but also has a high quantum yield as a result of one-photon excitation process.

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Cation doped ZnGeO materials have been intensively explored owing to their excellent performance in photocatalysts, optoelectronic devices and white light-emitting diodes. However, the luminescence process and thermal quenching arising during the optical excitation of these materials are yet to be clarified. The pure and 2% Mn doped ZnGeO phosphors were prepared via the high temperature solid state reaction.

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Rare-earth doped CaInO phosphors have been widely investigated due to their excellent luminescent property, but the site occupation of rare-earth ions in CaInO is not very clear and needs to be clarified. Using Eu as a fluorescence probe, such a clarification has been made in this work. 1% and 2% Eu doped CaInO powder samples have been prepared by the sol-gel method.

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A temperature sensing scheme is proposed that is based on the dramatic temperature dependence of the photoluminescence when Sm dopants are excited from thermally populated H levels, rather than the ground level H, to the G luminescent level. The scheme has the advantage of eliminating laser heating and background Stokes-type scattering noise. Experimental realization was carried out on a (SmGd)VO sample by detecting the intensities at 550-580 nm using excitation wavelengths of 601.

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Real-time temperature imaging with high spatial resolution has been a challenging task but also one with wide potential applications. To achieve this task, temperature sensor is critical. Fluorescent materials stand out to be promising candidates due to their quick response and strong temperature dependence.

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Sm-doped SrBO was synthesized for high-sensitivity thermometry. A high thermal-sensitive fluorescence intensity ratio and fluorescence lifetime were achieved in a wide temperature range. At 500 K, the relative sensitivity of the temperature sensing was 2.

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In general, adjusting the composition of a fluorescent material is an effective way to tune its luminescent properties such as peak energy and bandwidth. In most solid-solutions, the emission peak shifts linearly with the materials' composition, which is referred to as Vegard's Law. However, we found extraordinary variations in our samples Ba2xSr2-2xV2O7, that is, both the excitation and emission peaks show nonlinear dependence on the composition x, and the same is true for the spectral bandwidths.

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The site-selective spectra and decay curves at 20 K of Eu3+ ions doped KGd2F7 were measured to study the local environment of the Eu3+ sites. The experimental results show that Eu3+ ions occupy three types of sites in the KGd2F7 host. And Eu3+ ions in different types of sites exhibit quite distinct emission spectra and have remarkably different 5D0 level decay lifetimes.

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Tm3+ and Yb3+ codoped LuPO4 phosphors were synthesized by the reverse-strike co-precipitation method. The obtained LuPO4:Tm3+,Yb3+ phosphors were characterized by X-ray diffraction (XRD), diffuse reflectance spectra, photoluminescence (PL) spectra, and decay lifetime to understand the observed near-infrared downconversion (DC) phenomena. The XRD results show that all the prepared phosphors can be readily indexed to the pure tetragonal phase of LuPO4 and exhibit good crystallinity.

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NaYF4: Nd³⁺ microprisms were synthesized by a hydrothermal method. The bands of near-infrared (NIR) luminescence originating from the 4F3/2, 4F5/2 and 4F7/2 levels of Nd³⁺ ions in NaYF4: Nd³⁺ microcrystals were measured under 574.8 nm excitation at various temperatures from 323 to 673 K.

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Optical thermometers usually make use of the fluorescence intensity ratio of two thermally coupled energy levels, with the relative sensitivity constrained by the limited energy gap. Here we develop a strategy by using the upconversion (UC) emissions originating from two multiplets with opposite temperature dependences to achieve higher relative temperature sensitivity. We show that the intensity ratio of the two UC emissions, ³F(2,3) and ¹G₄, of Tm³⁺ in β-NaYF₄:20%Yb³⁺, 0.

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In order to obtain a single-host-white-light phosphor used for near ultraviolet (NUV) light emitting diodes (LEDs), the NaSrPO4:Eu2+, Tb3+, Mn2+ powder samples were synthesized via a high temperature solid-state reaction. XRD investigation shows a single phase. Energy transfer processes is discussed by analyzing the photoluminescence (PL) and photoluminescence excitation (PLE) spectra.

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NaYF4:Eu3+ core and NaYF4:Eu3+/NaYF4 core/shell nanocrystals (NCs) were synthesized via a wet chemical method. The transmission electron microscope photographs show that the core and core/shell nanoparticles are monodisperse and uniform NCs with average diameters of 22 and 26 nm respectively. The photoluminescence (PL) properties of the samples, including the PL excitation and emission spectra, and luminescent decay curves, are investigated in detail.

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