Surface modification of an up-conversion luminescence material by overcoating with SiO_2 and its characterization

The surface of an up-conversion luminescence material was modified by overcoating with SiOa, which was synthesized from a hydrolysis progress of telraethoxysilane （TEOS） in alkalescent condition. By analyzing the hydrolyzed mechanism of TEOS, it was found that there was not only physical adsorption but also chemical bonding between the up-conversion material and SiO2. At the same time, some adsorption bands at 1100, 475, 950, and 3500 cm^-1 were found by FI-IR, which were the characteristic bands of Si-OH and Si-O-Si. By analyzing the surface elements of the coated material by XPS, it was found that its surface only included Si, O, and C elements, and not F and Y. In the picture of XRD, there was no additional peak after surface modification, suggesting that the silica shell was amorphous. The small peak at 20 = 23° in the X-ray diffraction pattern of the coated material was caused by the amorphous SiO2 shell, and the TEM image also proved that the surface of the material was successfully modified by overcoating with SiO2. The amount of hydroxyls was then increased on the surface of the material, which made it easy to connect with other active groups.

Up-conversion luminescence from Nd^(3+) ions doped in NaBi(WO_4)_2 single crystal

The luminescence of Nd3+-doped in NaBi(WO4)2 single crystal was investigated from 10 K to room temperature.The excitation source was a pulsed dye laser in resonance into the(4G5/2+2G(1)7/2) levels of Nd3+ ions.Several blue emission bands in the up-conversion luminescence spectra corresponded to transitions from 2P1/2 to 4I9/2.Some violet bands corresponding to transitions of 4D3/2→(4I9/2,4I11/2,4I13/2) were also observed.For comparison,the luminescence spectra and decay curves excited by the pulsed 355 nm l...

Up-conversion luminescence tuning in Er^3+ -doped ceramic glass by femtosecond laser pulse at different laser powers

The up-conversion luminescence tuning of rare-earth ions is an important research topic for understanding luminescence mechanisms and promoting related applications. In this paper, we experimentally study the up-conversion luminescence tuning of Er3+-doped ceramic glass excited by the unshaped, V-shaped and cosine-shaped femtosecond laser field with different laser powers. The results show that green and red up-conversion luminescence can be effectively tuned by varying the power or spectral phase of the femtosecond laser field. We further analyze the up-conversion luminescence tuning mechanism by considering different excitation processes, including single-photon absorption(SPA), two-photon absorption(TPA), excited state absorption(ESA), and energy transfer up-conversion(ETU). The relative weight of TPA in the whole excitation process can increase with the increase of the laser power, thereby enhancing the intensity ratio between green and red luminescence(I547/I656). However, the second ETU(ETU2) process can generate red luminescence and reduce the green and red luminescence intensity ratio I547/I656, while the third ESA(ESA3) process can produce green luminescence and enhance its control efficiency. Moreover, the up-conversion luminescence tuning mechanism is further validated by observing the up-conversion luminescence intensity, depending on the laser power and the down-conversion luminescence spectrum under the excitation of 400-nm femtosecond laser pulse. These studies can present a clear physical picture that enables us to understand the up-conversion luminescence tuning mechanism in rare-earth ions, and can also provide an opportunity to tune up-conversion luminescence to promote its related applications.

Sensitized Up-Conversion Luminescence of Ho^(3+) in Nd^(3+)-Yb^(3+)-Ho^(3+) Co-doped ZrF_4-Based Glass

Up-conversion processes for the blue, green and red emissions were foundtwo-photon phenomenon, known as the cooperative phenomenon. This phenomenon was assisted by Nd^(3+)→ Yb^(3+) → Ho^(3+) energy transfer. The strong green emission due to the Ho^(3+) : (~5F_4, ~5S_2)→ ~5I_8 transitions was observed in Nd^(3+) - Ho^(3+) co-doped ZrF_4-based fluoride glasses under800 nm excitation. As an attempt to enhance Ho^(3+) up-conversion luminescences in the Nd^(3+) -Ho^(3+) co-doped ZrF_4-based glasses, Yb^(3+) ions were added to the glasses. As a result it wasfound that, in 800 nm excitation of 60ZrF_4. 30BaF2. (8-x)LaF_3. 1NdF_3. xYbF_3. 1HoF_3 glasses (x =0 to 7), sensitized up-conversion luminescences are observed at around 490 nm (blue), 545 nm(green), and 650 nm (red), which correspond to the Ho^(3+) : ~5F_3 → ~5I_8, ( ~5F_4, ~5S_2) →~5I_8 and ~5F_5 → ~5I_8 transitions respectively. The intensities of the green and red emissions ina 3 mol% YbF_3-containing glass were about 50 times stronger than those glasses without YbF_3. Thisis based on sensitization due to Yb^(3+) ions. In particular, the green emission was extremelystrong and the Nd^(3+) - Yb^(3+) - Ho^(3+) co-doped ZrF_4-based glasses have a high possibility ofrealizing a green up-conversion laser glass. In this paper the up-conversion mechanism in theglasses is discussed in detail.

Up-conversion luminescence properties and energy transfer of Er^(3+)/Yb^(3+)co-doped oxyfluoride glass ceramic containing CaF_2 nano-crystals

The Er^3＋/yb^3＋ co-doped transparent oxyfluoride glass-ceramics containing CaF2 nano-crystals were successfully prepared. After heat treatments, transmission electron microscopy （TEM） images showed that CaF2 nano-crystals of 20-30 nm in diameter precipitated uniformly in the glass matrix. luminescence of Er^3＋ at 540 nm and 658 nm was observed in Comparing with the host glass, high efficiency upconversion the glass ceramics under the excitation of 980 nm. Moreover, the size of the precipitated nano-crystals can be controlled by heat-treatment temperature and time. With the increase of the nano-crystal size, the intensity of the red emission increased more rapidly than that of the green emission. The energy transfer process of Er^3＋ and Yb^3＋ was convinced and the possible mechanism of Er^3＋ up-conversion was discussed.

Frequency Up-conversion Luminescence Properties and Mechanism of Tm^(3+) /Er^(3+)/Yb^(3+) Co-doped Oxyfluorogermanate Glasses

Oxyfluoride glasses were developed with composition 60GeO 2 ·10AlF 3 ·25BaF 2 ·（1.95-x）GdF 3 · 3YbF 3 ·0.05TmF 3 ·xErF 3 （x=0.02,0.05,0.08,0.11,0.14,0.17）in mole percent.Intense blue（476 nm）,green（524 and 546 nm）and red（658 nm）emissions which identified from the 1G 4 →3H 6 transition of Tm3＋and the（2H 11/2 ,4S 3/2 ）→4I 15/2 ,4F 9/2 →4I 15/2 transitions of Er3＋,respectively,were simultaneously observed under 980 nm excitation at room temperature.The results show that multicolor luminescence including white light can be adjustably tuned by changing doping concentrations of Er3＋ion or the excitation power.In addition,the energy transfer processes among Tm3＋,Er3＋and Yb3＋ions,and up-conversion mechanisms are discussed.

Comparison study of two aldehyde group finishing agents in surface modification of up-conversion luminescence materials

Surface modification of up-conversion luminescence materials （Na[Y0.57Yb0.39Er0.04]F4 modified by amino groups） by grafting and modifying with aldehyde groups was studied by means of Fourier transform infrared spectroscopy （FTIR）, scanning electron microscopy （SEM）, thermogravimetric analysis （TGA）, and emission spectrum （EM）. The surface modification effect was compared using two different finishhag agents, p-phthalaldehyde and glutaraldehyde. It was found that the surface of up-conversion luminescence materials could be modified by aldehyde groups of the two finishing agents, the systematic dispersibility and the thermostability of the up-conversion luminescence material modified by p-phthalaldehyde were better than those of the material modified by glutaraldehyde, and the luminous intensity of the material modified by p-phthalaldehyde was increased. The AI （the ratio of the suspended segmental quality in the specimen to the total mass of the specimen） of the material modified by p-phthalaldehyde was higher than that of the material modified by glutaraldehyde. It is obviously seen that the embellishment effect of p-phthalaldehyde as a finishing agent was better than that of glutaraldehyde. In addition, the reasons why p-phthalaldehyde is a good finishing agent are also explained.

Up-conversion luminescence polarization control in Er^(3+)-doped NaYF_4 nanocrystals

We propose a femtosecond laser polarization modulation scheme to control the up-conversion（UC） luminescence in Er^（3＋）-doped NaYF_4 nanocrystals dispersed in the silicate glass. We show that the UC luminescence can be suppressed when the laser polarization is changed from linear through elliptical to circular, and the higher repetition rate will yield the lower control efficiency. We theoretically analyze the physical control mechanism of the UC luminescence polarization modulation by considering on- and near-resonant two-photon absorption, energy transfer up-conversion, and excited state absorption, and show that the polarization control mainly comes from the contribution of near-resonant two-photon absorption. Furthermore, we propose a method to improve the polarization control efficiency of UC luminescence in rare-earth ions by applying a two-color femtosecond laser field.

Green up-conversion Luminescence in Nd^(3+)-Ho^(3+) Co-doped Oxyfluorotellurite Glasses

Blue, green and red up-conversion luminescence at around 490, 545 and 650 nm, which result from the Ho^3＋5F3→5I8, （5F4,5S2）→3. 5I8 and 5F5→ 5I8 transitions, respectively, were observed in Nd3＋-Ho3. co-doped oxyfiuorotellurite glasses under 800 nm excitation. Among these up-conversion luminescence, the green emission was extremely strong and the blue and red emission intensities were very weak. Selectively strong green up-conversion luminescence of these glasses indicate a high possibility for realizing a green upconversion laser. Up-conversion processes for the blue, green and red emissions are two-photon processes assisted by Nd3^＋→Ho^3＋ energy transfer. It is proposed that the up-conversion mechanism for the blue and green emissions is different from that for the red emission. The respective mechanisms are discussed.

Synthesis and Characterization of IR Up-Conversion Material SrS∶Eu, Sm

Europium and samarium co-doped strontium sulfide (SrS∶Eu, Sm) infrared up-conversion phosphor was synthesized through calcining the precursor, which prepared by wet-method with strontium carbonate (SrCO_3), sulphur (S), europium oxide (Eu_2O_3) and samarium oxide (Sm_2O_3) as the starting materials, lithium fluoride (LiF) as the fluxing agent, at 750～1200 ℃ in carbon-reducing atmosphere. XRD analysis shows that SrS crystal structure is formed at 750 ℃, most completely at 1100 ℃. The IR up-conversion luminescence properties were characterized by excitation, emission, up-conversion excitation, up-conversion emission and thermoluminescence spectra. The spectral analysis associated with the physical model of up-conversion luminescence shows that the IR up-conversion luminescence is resulted from electron trapping process of Sm 3+ energy level. The thermoluminescence peak does not appear below 500 ℃ indicating the trapping energy level is appropriately deep, 800～1400 nm near infrared light can be the release light to realize up-conversion luminescence.

Efficiency analysis of a-SiC:H thin film light emitting diodes

The hole injection,the radiative recombination and the device luminescent efficiencies of amorphous silicon carbide thin film p-i-n junction light emitting diodes are quantitatively calculated,and the effect of the carrier(especially the hole) injection and recombination processes on the device luminescent characteristics are revealed.Without considering the device junction temperature,it is found that the device luminescent efficiency mainly depends on the hole injection efficiency at low field and the hole radiative recombination efficiency at high field respectively.The theoretical analyses are in well agreement with the experimental results.

White up-conversion luminescence and highly-sensitive optical temperature sensing in Na_(3)La(VO_(4))_(2):Yb,Er,Tm,Ho phosphors

In this work,tunable white up-conversion luminescence was achieved in the Yb^(3+),Er^(3+),Tm^(3+),Ho^(3+) codoped Na_(3)La(VO_(4))_(2) phosphors under 980 nm excitation.The emissions of three primary colors are mainly attributed to the ~2H_(11/2)/~4S_(3/2)→~4I_(15/2) transitions of Er^(3+),~1G_(4)→~3H_6 transition of Tm^(3+),and_5F_5→~5I_8 transition of Ho^(3+).White luminescence characteristics and mechanisms of up-conversion system were investigated in detail.In addition,the temperature sensing behaviors of multiple levels emission combinations for Na_(3)La(VO_(4))_(2):Yb^(3+),Er^(3+),Tm^(3+),Ho^(3+) were analyzed by employing thermally coupled and non-thermally coupled energy levels.Based on the emissions of ~3F_(2,3)/~1G_(4) energy levels,the maximum relative and absolute sensitivities were obtained to be 2.20%/K and 0.279 K^(-1).The design of up-conversion luminescence materials with high-quality white luminescence and excellent sensitivity performance is critical in the field of optical applications.

Enhancement of Photoluminescence Intensity of GaInNAs/GaAs Quantum Wells by Two-Step Rapid Thermal Annealing

We investigate the effect of rapid thermal annealing on InGaNAs/GaAs quantum wells. At optimized annealing temperatures and times, the greatest enhancement of the photoluminescence intensity is obtained by a special two-step annealing process. To identify the mechanism affecting the material quality during the rapid thermal annealing, differential temperature analysis is applied, and temperature- and power-dependent photoluminescence is carried out on the samples annealed under different conditions. Our experiment reveals that some composition redistribution or other related ordering processes may occur in the quantum-well layer during annealing. Annealing at a lower temperature for a long time primarily can remove defects and dislocations while annealing at a higher temperature for a short time primarily homogenizes the composition in the quantum wells.

Structural and Luminescence Properties of Transparent Nanocrystalline ZrO2：Er^3＋ Films

The structural and luminescence properties of nanocrystalline ZrO2 ：Er^3＋ films are reported. Transparent nano-ZrO2 crystalline films doped with Er^3＋ have been prepared using a wet chemistry process. An intense roomtemperature emission at 1527nm with a full width at half-maximum of 46 nm has been observed, which is assigned to the ^4Ⅰ13/2 → ^4Ⅰ15/2 intra-4f^n electric transition of Er^3＋. Correlations between the luminescence properties and structures of the nanocrystalline ZrO2 ：Er^3＋ films have been investigated. Infrared-to-visible upconversion occurs simultaneously upon excitation of a commercially available 980-nm laser diode and the involved mechanisms have also been explained. The results indicate that the nanocrystalline ZrO2：Er^3＋ films might be suggested as promising materials for achieving broadband Er^3＋-doped waveguide amplifiers and upconversion waveguide lasers.

Quantum frequency up-conversion with a cavity

The quantum state transfer from subharmonic frequency to harmonic frequency based on asymmetrically pumped second harmonic generation in a cavity is investigated theoretically. The performance of noise-free frequency up- conversion is evaluated by the signal transfer coefficient and the conversion efficiency, in which both the quadrature fluctuation and the average photon number are taken into consideration. It is shown that the quantum property can be preserved during frequency up-conversion via operating the cavity far below the threshold. The dependences of the transfer coefficient and the conversion efficiency on pump parameter, analysing frequency, and cavity extra loss are also discussed.

Oxy-Fluoride Borate Infrared Up-Conversion Glass Ceramics

The processing parameters and infrared up-conversion properties of fluoroborate glass ceramics in composition of BaB_2O_4+AlF_3+BaF_2+PbF_2∶YbF_3+HoF_3 were reported. The emission spectrum was measured by Hitachi F-4500 spectrometer. The results show that three emission peaks located at 470,545 and 655 nm respectively are observed,(among) which the peak at 545 nm is the strongest. Photon absorption theory and energy transmission theory are used to explain the emission spectrum.

Al纳米颗粒高频局域等离激元效应对BCzVBi深蓝光有机发光器件发光效率的影响

蓝紫光有机电致发光器件难以提升发光效率.本文以BCzVBi作为深蓝荧光材料,把Al纳米颗粒引入ITO/:PEDOT:PSS/TAPC/BCzVBi:BCPO/TmPyPb/Liq/Al有机发光器件的TmPyPb电子传输层,尝试用A1纳米颗粒的高频局域等离激元效应来改善此问题.在室温真空蒸镀Al膜,厚度为1 nm时,形成尺寸在10 nm量级的分散纳米颗粒.将这种颗粒膜插入TmPyPb层内距离BCzVBi:BCPO发光层x=4,8,12 nm处,与没有Al层的对比器件相比,器件的电流密度和发光亮度都会因载流子迁移率变差而下降.但在x=8 nm,两者都显著回升.其机理可能在于,x<8 nm,会产生过强的荧光淬灭,而x>8 nm,到达Al颗粒的荧光衰减过多,又难以产生足够强的局域等离子体振荡.在x=8 nm,达到最大亮度的电压(9 V)没有变化,最大亮度从4200 Cd/m^(2)降到3500 Cd/m^(2),但电流密度也从335.19 mA/cm^(2)减小到145.71 mA/cm^(2),使得电流效率反而从0.88 Cd/A提高到2.36 Cd/A,从而把外量子效率提升了170%,效率滚降比则从78%降到30.5%,压减61%.在电流密度高达270 mA/cm^(2)时,电流效率和外量子效率也能提升66.5%.这些结果表明,Al纳米颗粒高频局域表面等离激元确实能够有效增强深蓝光有机发光二极管的发光性能.

Europium-bearing organic framework with excellent X-ray scintillating luminescence

Two europium-bearing organic frameworks,termed as EuTPO-1 and EuTPO-2(H_(3)TPO=tris(4-carboxylphenyI)-phosphineoxide),are reported in this work.A series of characterizations of EuTPO-1and EuTPO-2,such as X-ray crystallography and photoluminescence spectroscopy,was performed to expatiate their structure and physicochemical properties.Both of them are constructed by dimers of the europium-oxygen subunit of [Eu_(2)O_(16)] and TPO molecule.Benefiting from high X-ray stopping attenuation and excellent luminescence efficiency,they emit sufficient luminescence when irradiated with Xrays.Meanwhile,they possess stable light outputs when exposed to high humidities and strong radiation dose,outperforming the commercial scintillator CsI:Tl.This result paves the way for developing new scintillator and enriches the compound of europium-bearing organic framework with X-ray scintillating luminescence.

折射率对碳点基发光太阳能聚光器光电性能的影响

发光太阳能聚光器作为一种新型的实现低成本电力的潜在光伏技术已经引起了广泛的关注。选择合适的荧光基质和性能优异的光波导介质成为该技术得以推广应用的关键。目前,多数研究者把目光聚焦在荧光基质光学性能的提高上,对光波导介质性能的优化却鲜有报道。本文使用邻苯二甲酸和邻苯二胺两种前驱体,一步微波法快速高效地合成了一种晶态碳点。鉴于该碳点具有绿色荧光,荧光量子产率超过80%,并且吸收和发射光谱间存在较大的斯托克斯位移,适合作为新型太阳能聚光器用荧光基质。另外,采用预聚体法制备了高透明的聚氨酯膜,并作为发光太阳能聚光器用光波导介质研究了其光学性能。通过引入硫元素,该薄膜的折射率从1.483提高到1.547,这直接导致利用所制备的碳点作为荧光基质封装的聚氨酯薄膜型发光太阳能聚光器器件的光电转换效率提升了41%。该结果不仅证实了聚氨酯作为光波导介质的可行性,更为通过改良光波导介质的折射率来提高光传输的研究方法提供了实验依据。

Effects of Bi^(3+) on down-/up-conversion luminescence,temperature sensing and optical transition properties of Bi^(3+)/Er^(3+)co-doped YNbO_(4) phosphors

A series of YNbO_(4):Bi^(3+) and YNbO_(4):Bi^(3+)/Er^(3+) phosphors were prepared by a conventional high temperature solid-state reaction method.The results of XRD and Rietveld refinement confirm that monoclinic phase YNbO_(4)samples are achieved.The down-/up-conversion luminescence of Er^(3+) ions was investigated under the excitation of ultraviolet light(327 nm)and near infrared light(980 nm).Under 327 nm excitation,broad visible emission band from Bi^(3+) ions and characteristic green emission peaks from Er^(3+) ions are simultaneously observed,while only strong green emissions from Er^(3+) ions are detected upon excitation of 980 nm.Remarkable emission enhancement is observed in down-/up-conversion luminescence processes by introducing Bi^(3+) ions into Er^(3+)-doped YNbO_(4)phosphors.Pumped current versus up-conversion emission intensity study shows that two-photon processes are responsible for both the green and the red up-conversion emissions of Er^(3+)ion.Through the study of the temperature sensing property of Er^(3+) ion,it is affirmed that the temperature sensitivity is sensitive to the doping concentration of Bi^(3+) ions.By comparing the experimental values of the radiative transition rate ratio of the two green emission levels of Er^(3+) ions and the theoretical values calculated by Judd-Ofelt(J-O)theory,it is concluded that the temperature sensing property of Er^(3+) ions is greatly affected by the energy level splitting.