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.

Improving luminescent property of SrIn_2 O_4 :Eu^(3+) by co-doped A^+ (A = Li, Na, K) or Sm^(3+)

A series of SrIn2 O4 ：Eu^3＋ phosphors are synthesized by a high temperature solid-state method, and their luminescent properties are investigated. They can be excited by 395-nm radiation, and produce red emission （619 nm）; however, they have a low absorption of near-ultraviolet light with the wavelength of 400nm–405 nm. When co-doped with A^＋ （A=Li, Na, K）, the emission intensity of SrIn2O4 ：Eu^3＋ is significantly enhanced, but its emission and excitation spectral profile is unchanged. With co-doping Sm^3＋ , not only is the emission intensity of SrIn2 O4 ：Eu^3＋ enhanced, but also the absorption is broadened and strengthened in the range of 400 nm–405nm. The effect of Sm^3＋ -doped content on the emission intensity of SrIn2O4 ：Eu^3＋ , Sm^3＋ is investigated, and the optimal Sm^3＋ content is 0.02 mol.

Preparation of CaS∶Eu^(2+), Sm^(3+) by Solid Reaction Method and Its Photostimulated Luminescence

The CaS∶Eu^(2+), Sm^(3+) powders were prepared by high-temperature solid method in a reducing atmosphere. The influences of temperature and fired-time on properties of samples were studied. XRD analysis shows that crystal structure of CaS has formed at 700 ℃. Spectrum analysis results show that the samples which were stimulated by 980 nm laser after excited by ultraviolet lamp emit red luminescence peaking at 649 nm.

Rb-Sr and Sm-Nd Isochron Ages of the Dongmozhazhua and Mohailaheng Pb-Zn Ore Deposits in the Yushu area, southern Qinghai and Their Geological Implications

Located on the northeast margin of the Qiangtang terrane between the Jinshajiang suture zone and Bangonghu-Nujiang suture zone,the Dongmozhazhua and Mohailaheng Pb-Zn deposits in the Yushu area of Qinghai Province are representative Pb-Zn deposits of the Pb-Zn-Cu polymetallic mineralization belt in the northern part of the Nujiang-Lancangjiang-Jinshajiang area,which are in the front belt of the Yushu thrust nappe system.The formed environments of these two deposits are different from those of sediment-hosted base metal deposits elsewhere in the world.The authors hold that they were formed during the Indian-Asian continental collision and developed within the fold-thrust belt combined with thrust and strike-slip-related Cenozoic basins in the interior of the collisional zone.Studying on the metallogenic epochs of these two deposits is helpful to the understanding of ore-forming regularity of the regional Pb-Zn-Cu mineralization belt and also to the search for new deposits in this region.The age of the Dongmozhazhua deposit has been determined by the Rb-Sr isochron method for sphalerite residues,whereas the age of the Mohailaheng deposit has been determined by the Rb-Sr isochron method for sphalerite residues and the Sm-Nd isochron method for fluorite.The age of the Dongmozhazhua deposit is 35.0-±0.0 Ma （（87Sr/86Sr）0=0.708807） for sphalerite residues.The age of the Mohailaheng deposit is 32.2±0.4 Ma （（87Sr/86Sr）o=0.708514） for sphalerite residues and 31.8±0.3 Ma （（143Nd/144Nd）o=0.512362） for fluorite with an average of 32.0 Ma.Together with the regional geological setting during mineralization,a possible tectonic model for metallogeny of the Dongmozhazhua and Mohailaheng Pb-Zn deposits has been established.These two ages are close to the ages of the Pb-Zn deposits in the Lanping and Tuotuohe basins,indicating that it is possible that the narrow 1000-kilometer-long belt controlled by a thrust nappe system on the eastern and northern margins of the Tibetan plateau could be a giant Pb-Zn mineralized belt.

Effect of Sm content on microstructure evolution and mechanical properties of as-cast Mg-6Al-2Sr alloys

Mg-6Al-2Sr alloys with different Sm contents(0%, 0.5%, 1%, 1.5%, 2%, mass fraction) were prepared by melting and casting method. The effects of Sm on the microstructure and mechanical properties of as-cast Mg-6Al-2Sr alloys were studied by optical microscope, scanning electron microscope, energy dispersive spectrometer, transmission electron microscope, X-ray diffraction and tensile test. The results show that the microstructure of as-cast Mg-6Al-2Sr alloy is composed of α-Mg, Mg_(17)Al_(12), Mg_(13)Al_(3)Sr and lamellar acicular Al_(4)Sr phase. After adding Sm element, granular block Al2Sm phase appears in the grain. With the increase of Sm content, the discontinuous long strip reticular Mg_(17)Al_(12)phase and the lamellar acicular Al4Sr phase gradually decrease, and the Al_(2)Sm phase increases and distributes more dispersedly, so the alloy microstructure is continuously refined. The average grain size of the alloys decreases at first and then increases with the increase of Sm content. When the Sm content is 1.5 wt%, the average grain size reaches the minimum value of 94.6 μm. With the increase of Sm content, the mechanical properties of the alloy at room temperature first increase and then decrease. When the Sm content is 1.5 wt%, the alloy has the best comprehensive mechanical properties at room temperature.

Separation of Neighboring REElementsfrom Sm_2O_3Eu_2O_3Gd_2O_3 System by a Stepwise ChlorinationChemical Vapor Transport Reaction

The mutual separation characteristics were investigated for the neighboring Sm, Eu and Gd from their ternary oxide mixture Sm 2O 3 Eu 2O 3 Gd 2O 3 by a stepwise chlorination chemical vapor transport reaction within 6 h using AlCl 3 as complex former. The rare earth chlorides were more readily transported and concentrated in the middle temperature range of 980～1100 K and the transport efficiency was in the order of Sm≈Gd>Eu. The separation factor, expressed as molar ratio for the resulting chlorides, was 1 70 for Eu∶Sm, 1 88 for Eu∶Gd, 1 24 for Sm∶Gd in the higher temperature region, and 2 76 for Sm∶Eu, 2 83 for Gd∶Eu and 1 12 for Gd∶Sm in the lower temperature region, respectively. All results are much higher than those of the conventional wet process.

Solvent extraction kinetics of Sm(Ⅲ),Eu(Ⅲ) and Gd(Ⅲ) with 2-ethylhexyl phosphoric acid-2-ethylhexyl ester

Solvent extraction kinetics of Sm（Ⅲ）, Eu（Ⅲ） and Gd（Ⅲ） from hydrochloric acid have been focused on using 2-ethylhexyl phosphoric acid-2-ethylhexyl ester （P507） with Anordning for Kontinuerlig Undersokning av Fordelningsfaktore rid Vatske Extraction （AKUFVE）. Compared with the conventional set-up, some advantages emerge obviously, for example, fast phase separation, easy operation and convenience of kinetic data acquisition. First of all, the extraction mechanism was discussed based on the dimeric model of P507. Secondly, the effects of stirring speed were investigated and 420 r-min-1 was determined of the following experiments. The effects of pH, concentration of rare earth elements （REEs） and P507 on the extraction rate were analyzed. The results indicated that the extraction mechanism changed with the increasing concentration of P507. Then, the experiments with different temperature were carried out. It turned out that the values of apparent activation energy （Ea） for Sm（Ⅲ）, Eu（Ⅲ） and Gd（Ⅲ） extracted by P507 were 26.80 kJ-mol-1, 13.40 kJ.mol-1 and 1.10 kJ- mol- 1 respectively, the resistance of the entire process was limited by diffusion or both of diffusion and reaction. Finally, the correlation equations were obtained, and the theoretical results fit with the experimental data well, most relative error was within ± 30%.

新型红色荧光粉Sr_(3)CaNb_(2)O_(9):Sm^(3+),Eu^(3+)的发光特性和能量传递分析

利用高温固相反应法制备一系列单基质荧光粉Sr_(3)CaNb_(2)O_(9):xSm^(3+),yEu^(3+)(x=0.04~0.09,y=0.03~0.15),并对样品的物相形貌、发光性能、能量传递机制和CIE色坐标进行分析。研究表明,Sr_(3)CaNb_(2)O_(9):xSm^(3+)荧光粉在激发波长为407 nm时的浓度淬灭点为x=0.07。在Sr_(3)CaNb_(2)O_(9):0.07Sm^(3+),yEu^(3+)荧光粉中,随着Eu^(3+)掺杂浓度的增加,Sm^(3+)的发光强度降低而Eu^(3+)发光强度却先增加后降低,Eu^(3+)的浓度淬灭点为y=0.09。Sm^(3+)→Eu^(3+)的能量传递以电偶极-电偶极相互作用为主,能量传递效率达到76.6%。色坐标图表明Eu^(3+)离子的加入可使色坐标从橙红色区域向纯红色区域移动。此外,样品还具有较高的色纯度和较低的色温。结果表明,Sr_(3)CaNb_(2)O_(9)∶Sm^(3+),Eu^(3+)荧光粉有望成为白光LED发出红光物质的候选材料。

Effects of Doping Trace Sm^(3+) and Gd^(3+) on Luminescent Character of Y_2O_2S∶Eu^(3+)

After trace Sm^3＋ ions and Gd^3＋ ions doping, the emission intensity of red phosphors Y2O2S： Eu^3 ＋ was enhanced and the voltage character （relation between emission intensity and excitation voltage） was improved while the other properties of physics and chemistry were not changed. The origins of enhancement and improvement are discussed. Probably the distortion and the defect of crystals are decreased by the substitution of Gd^3＋ for Y^3＋ instead of Eu^3＋ for Y^3＋ , and thus the Eu^3＋ crystal field is improved, and radiationless process and energy loss resulted from crystal defect are weakened, which leads to increased luminescence intensity and voltage character improvement. The overlapping fluorescent spectra of Y2O2S： Sm^3＋ emission and Y2O2S：Eu^3＋ excitation as well as Eu^3 ＋ excitation spectra transitions spectra lead to energy transfer from Sm^3 ＋ sensitization of Sm^3＋ ions fectively. containing Sm^3＋ excitation the possibility of resonance ions to Eu^3＋ ions, and the to Eu^3＋ ions is achieved effectively.

SrS:Eu,Sm荧光粉的制备及性能表征

制备了用于宽频谱红外上转换的SrS：Eu，Sin荧光粉。XRD分析表明，在1100℃，灼烧1h获得的SrS：Eu，Sm样品较理想，为SrS的面心立方结构；激发光谱表明，样品可被紫外和可见光有效激发；样品的荧光发射光谱由4个发射峰组成，峰值分别位于567，589，602和648nm。红外上转换发光光谱是峰值位于595nm附近的宽带谱，样品的红外响应范围主要位于800～1400nm。

SrS：Eu，Sm光存储材料的制备及表征

采用湿法在还原气氛下制备了SrS:Eu,Sm电子俘获光存储材料,研究了制备条件(灼烧温度、灼烧时间、助熔剂含量)对样品光激励发光性能的影响。XRD图谱表明,样品在750°C就可以形成SrS晶格。光谱分析表明,先将样品用紫外光饱和激发后,再用980nm半导体激光照射,具有光激励发光现象,发光峰值位于599 nm。对这种稀土掺杂硫化物材料的光存储机理进行了探讨。

SrS∶Eu,Sm光存储机理的研究

采用高温固相反应法在还原气氛下制备了SrS∶Eu,Sm样品,利用荧光光谱仪测量了这种光存储材料的激发光谱和发射光谱。将样品用紫外灯(265nm)照射激发饱和后,再用980nm的红外激光器激励,利用荧光光谱仪测试得到了峰值位于599nm的光激励发光光谱。此外还利用热释光谱仪测试了样品的热释光谱。探讨了SrS∶Eu,Sm的光存储机理,认为引入的稀土离子在SrS的带隙中形成分裂能级。当用紫外光照射材料时,Eu的电子从基态被激发到激发态或基质材料的导带,其中一部分电子被辅助激活剂Sm的陷阱俘获,实现信息写入。当材料被与陷阱深度相当的红外光激励时,电子陷阱Sm2+俘获的电子才可能跃出俘获能级,与空穴在Eu的激发态和基态能级上复合,多余的能量以可见光的形式释放出来,实现信息读出。

SrS∶Eu,Sm的制备与光谱性能

采用高温固相法制备了SrS：Eu，Sm光激励发光材料。研究了稀土掺杂量对样品光激励发光性能的影响。XRD分析表明，在1000℃灼烧1h的样品为SrS面心立方结构，晶格常数a=0．6020nm；激发光谱表明，样品在紫外和可见光均有较强激发峰；样品的荧光发射光谱由3个发射峰组成，其主峰位于602．1nm。红外光激励发射光谱是峰值位于602nm附近的宽带谱，样品的光激励激发光谱是峰值位于1046nm宽带谱，带宽在800—1400nm。最佳稀土掺杂量为0．15％。

红色LiM(M=Ca,Sr,Ba)BO_3∶Re^(3+)(Re=Eu,Sm)发光材料的特性

采用固相法制备了红色LiM(M=Ca,Sr,Ba)BO3∶Re3+(Re=Eu,Sm)发光材料,研究了材料的发光性能。研究发现LiM(M=Ca,Sr,Ba)BO3∶Eu3+材料呈现多峰发射,最强发射分别位于610,615,613 nm处,分别监测这三个最强峰,所得激发光谱峰值位于369,400,470 nm。LiM(M=Ca,Sr,Ba)BO3∶Sm3+材料也呈多峰发射,分别对应Sm3+的4G5/2→6H5/2、4G5/2→6H7/2和4G5/2→6H9/2跃迁发射;分别监测602,599,597 nm三个最强发射峰,所得激发光谱峰值位于374,405 nm。研究了激活剂浓度对材料发射强度的影响,结果随激活剂浓度的增大,发射强度先增强后减弱,即,存在浓度猝灭效应。实验表明,加入电荷补偿剂Li+、Na+或K+均可提高LiM(M=Ca,Sr,Ba)BO3∶Re3+(Re=Eu,Sm)材料的发射强度。

发光颜色可调谐的新型荧光体Sr_2CeO_4:RE^(3+)(RE=Eu,Sm,Dy)的发光性能

Sr2CeO4既是一种有重要应用价值的新型蓝色荧光体,又是一种适合稀土掺杂的发光基质。近年来人们对稀土掺杂的Sr2CeO4的荧光性能进行了研究。本文结合作者的工作,分析了Sr2CeO4的结构特点和光谱特性;综述了Eu3+,Sm3+,Dy3+等稀土离子掺杂Sr2CeO4的发光性能的研究现状,并对今后的研究工作提出了一些设想。

近紫外光LED芯片用红色荧光粉SrIn_2O_4:Eu^(3+),Sm^(3+)的制备及性能研究

利用高温固相法制备了Eu^(3+)、Sm^(3+)单掺杂及共掺杂的SrIn_2O_4荧光材料.通过XRD、激发光谱、发射光谱等对SrIn_2O_4∶Eu^(3+)、Sr In_2O_4∶Sm^(3+)、Sr In2O4∶Eu^(3+),Sm^(3+)进行表征。结果表明,Sr In2O4∶Eu^(3+)在近紫外光395 nm激发下能够有效的产生616 nm的红光发射.在Sr In2O4∶Sm^(3+)体系中发现,该系列样品适合于407 nm的紫光激发,发射峰位于607 nm.在Sr In_2O_4∶Eu3^(3+)Sm^(3+)体系中,通过光谱分析发现,基质中存在Eu^(3+)和Sm^(3+)激活剂之间的相互能量传递过程.该能量传递过程使Sr In2O4∶Eu^(3+),Sm^(3+)更适合于390~410 nm紫外芯片激发的LED用红色荧光粉。

新型橙红色荧光粉Sr_(3)CaNb_(2)O_(9)∶Sm^(3+)的制备及发光性能研究

通过高温固相法制备了一系列Sr_(3)CaNb_(2)O_(9)∶xSm^(3+)(0.04≤x≤0.1)新型橙红色荧光粉。研究了其物相、形貌、发光性能、热稳定性和CIE色度坐标。X射线衍射(XRD)物相分析和Rietveld精修结果表明合成了Sr_(3)CaNb_(2)O_(9)的纯相。在407nm的紫光激发下,Sr_(3)CaNb_(2)O_(9)∶Sm^(3+)在645nm处发红光,可归因于Sm^(3+)的^(4)G_(5/2)→^(6)H_(9/2)跃迁。实验表明Sr_(3)CaNb_(2)O_(9)∶xSm^(3+)的最佳掺杂浓度为x=0.07,根据Dexter理论分析,其浓度猝灭机理为电偶极-电偶极相互作用。Sr_(3)CaNb_(2)O_(9)∶Sm^(3+)在423K下发光强度是室温下的90.3%,表现出良好的热稳定性。Sr_(3)CaNb_(2)O_(9)∶xSm^(3+)的发光色坐标均位于橙红色区域,且具有较高的色纯度。结果表明Sr_(3)CaNb_(2)O_(9)∶Sm^(3+)荧光粉在白光发光二极管(WLED)中具有潜在的应用前景。

添加S及掺杂Dy^(3+)对SrS:Eu^(2+)荧光粉发光性能的影响

采用高温固相法,以糊精为还原剂,在温度为1 150℃、N2-H2(10∶1)的还原气氛中合成了S、Dy^(3+)掺杂的SrS:Eu^(2+)红色荧光粉材料。采用X射线衍射分析(XRD)、荧光分光光度计等对其物相与光学性能进行表征。结果表明,样品在蓝光(波长498nm)激发下,添加的S的质量分数为2%时,SrS:Eu^(2+)荧光粉发出的红光强度最强;Dy^(3+)的掺杂摩尔分数为1%时,试样发出的红光最强。其激发光谱是400~600nm的宽带激发光谱。

Energy transfer mechanism of Sr_4Al_(14)O_(25):Eu^(2+) phosphor

Long lasting blue-green-emitting Sr4Al14O25:Eu2+ phosphors were synthesized by solid-state reactions.The phosphors were investigated by X-ray diffraction(XRD) and fluorescence spectrophotometer.A pure phase of Sr4Al14O25:Eu2+ phosphor was obtained at 1250 °C.There are two different types of Eu emission centers in Sr4Al14O25:Eu2+ phosphor.The effects of the Eu2+ concentration and the reducing temperature on the distribution of Eu2+ among different sites were investigated.The energy transfer mechanism between...

Sm^(3+)掺杂SrMoO_4∶Eu^(3+)发光材料制备及性能研究

采用水热法制备了铕、钐共掺杂的钼酸锶(Sr_(1-x-y)MoO_4∶xEu^(3+),ySm^(3+))系列发光材料,对样品的晶体结构、微观形貌和发光特性进行了研究。结果表明:制备的样品均具有体心四方白钨矿结构;样品的颗粒比较均一,分散性较好,颗粒粒径1~2μm;三价稀土铕离子(Eu^(3+))和钐离子(Sm^(3+))共同掺杂样品的激发光谱由位于350~500nm的系列激发峰构成,同时存在Eu^(3+)和Sm^(3+)的特征激发峰,激发主峰位于395nm和465nm,表明样品能被近紫外光和蓝光有效激发;其发射主峰位于615nm,Sm^(3+)的掺杂能对Eu^(3+)起敏化作用,增强Eu^(3+)的红光发射强度;Eu^(3+)、Sm^(3+)的最佳掺杂量分别为x=0.04,y=0.03,制得的Sr_(1-x-y)MoO_4∶xEu^(3+),ySm^(3+)发光材料的最强相对发射强度达5000(光栅狭窄缝均为5.0测试条件下),具有较好的发光性能。