掺铒硼酸钙氧钆(GdCOB:Er)晶体的光谱分析

生长并测量了新型激光晶体GdCa4O(BO3)3:Er(简称GdCOB:Er)的透过谱,计算了Er3+离子在晶体中的吸收截面.由积分吸收截面的公式拟合出唯象强度参量Ω2＝2.531×10-20cm2,Ω4＝2.716×10-20cm2,Ω6＝1.891×10-20cm2,并应用Judd-Ofelt理论计算出振子强度fJ,J、辐射跃迁几率AJ,J、荧光辐射寿命τ及积分发射截面σ.并根据这些光学参量,讨论了GdCa4O(BO3)3:Er晶体用作激光晶体的可能性.     

掺镝近化学计量比铌酸锂晶体的光谱性质

利用提拉法,在锂铌比为58.5/41.5的富锂熔体中生长了质量良好的掺镝近化学计量比铌酸锂(Oy:NSLN)单晶,生长晶体的尺寸为φ25mm×35 mm.测量了晶体的室温吸收谱,并根据Judd-Ofeh理论,拟合出Oy3 离子的晶体场唯象强度参数:Ω2=4.8130×10-20,Ω4 =2.6140 × 10-20, Ω6=2.2448×10-20.计算了各能级的跃迁辐射几率A1,1,振子强度P1,1, 辐射寿命r,荧光分支比β1等,并根据这些光学参量讨论了该晶体的部分性能和应用前景.     

Er3+,Yb3+:YAl3(BO3)4晶体的光谱性质研究

采用助熔剂法生长了Er3+,Yb3+共掺的YAl3(BO3)4晶体,测量了晶体的室温吸收谱.由此吸收谱,根据JuddOfelt理论计算了Er3+在Er3+,Yb3+:YAl3(BO3)4晶体中的强度参数、自发辐射几率、积分发射截面等参数.强度参数为Ω2=2.44×10-20cm2、Ω4=2.00×10-20cm2、Ω6=6.10×10-20cm2.研究了晶体的荧光特性,并在976nm激光泵浦下得到了上转换绿色荧光.     

Cr:Nd:YCa4O(BO3)3光谱参数的计算

采用Czochralski法生长了透明均匀的Cr:Nd:YCaO(BO3)3晶体,生长的晶体尺寸为φ42.5×50mm,生长参数为提拉速度为0.6mm/h,转速为25r/min.测定了其室温吸收谱.根据Judd-Ofelt理论拟合了Nd3+离子的强度参数Ωλ:Ω2=0.734×10-20,Ω4=6.814×10-20,Ω6=2.476×10-20;并计算了各能级跃迁的自发辐射跃迁几率、辐射寿命、荧光分支比.其中4F3/2能级的寿命τtot=271.64μs,4F3/2→4I9/2的荧光分支比βc=58.01;.并对实验结果进行了讨论.     

PSN-PMN-PT∶Er3+晶体Judd-Ofelt理论分析

为了探索Er3+在铁电晶体场中的发光特性,采用高温溶液法生长了Er3+掺杂Pb(Sc1/2Nb1/2)O3-Pb(Mg1/3Nb2/3)O3-PbTiO3弛豫铁电单晶.该晶体在紫外-可见-近红外吸收光谱380～1800 nm波段出现了7个吸收峰;在980 nm泵浦光源照射下,该晶体的发射光谱出现了强绿光和强红光上转换发射带,分别对应于Er3+的4S3/2→4I15/2和4F9/2→4I15/2跃迁;利用Judd-Ofelt理论计算了晶体的振子强度三参数(Ω2＝2.54×10-20 cm2,Ω4＝1.36×10-20 cm2,Ω6 ＝2.38× 10-20 cm2)以及Er3+在PSN-PMN-PT晶体场中的跃迁几率、能级寿命和荧光分支比.研究结果表明 PSN-PMN-PT∶Er3+弛豫铁电晶体是一种新型发光晶体.     

Nd:LuVO4晶体光谱参数的计算及其分析

测定了Nd:LuVO4晶体的室温吸收谱;根据Judd-Ofelt理论拟合了Nd3+离子的三个晶场调节参数Ωt(t=2,4,6)的值分别为8.235×10-20cm2,4.683×10-20cm2,6.090×10-20cm2;计算了各个能级跃迁的谱线强度、振子强度、吸收截面等,进而计算了4F3/2态的自发跃迁几率、辐射寿命、荧光分支比和积分发射截面,并对结果作了分析.     

Er~(3 ),Yb~(3 )∶YAl_3(BO_3)_4晶体的光谱性质研究

采用助熔剂法生长了Er3 ,Yb3 共掺的YAl3 (BO3 ) 4 晶体 ,测量了晶体的室温吸收谱。由此吸收谱 ,根据Judd Ofelt理论计算了Er3 在Er3 ,Yb3 ∶YAl3 (BO3 ) 4 晶体中的强度参数、自发辐射几率、积分发射截面等参数。强度参数为Ω2 =2 .4 4× 10 -2 0 cm2 、Ω4=2 .0 0× 10 -2 0 cm2 、Ω6=6 .10× 10 -2 0 cm2 。研究了晶体的荧光特性 ,并在 976nm激光泵浦下得到了上转换绿色荧光。     

NaGd(MoO4)2单晶及其钕离子掺杂的晶体生长和性能分析

使用提拉法生长了φ15 mm ×40 mm的掺Nd3+∶NaGd(MoO4)2以及纯的NaGd(MoO4)2晶体,通过XRD分析了晶体的结构.测量了晶体的TG-DSC曲线以表征晶体的热学性质,晶体的熔点为1182℃,比热为0.51 J/g·K.测量了晶体的拉曼光谱,其拉曼频移为886 cm-1.研究了Nd3+∶NaGd(MoO4)2的吸收光谱和荧光光谱,在806 nm谱带的吸收截面为3.862 × 10-19 cm2,半高宽为17 nm.在1058 nm处的发射截面为2.900×10-20 cm2.运用J-O理论,获得振子强度参数(Ω2,Ω4,Ω6),跃迁几率,荧光分支比,辐射寿命等参数.     

双掺Er~(3+)/Yb~(3+)∶Sr_3La_2(BO_3)_4晶体的生长与光谱特性

采用提拉法生长了尺寸为20mm×30mm的Er3+/Yb3+∶Sr3La2(BO3)4晶体,研究了Er3+/Yb3+∶Sr3La2(BO3)4晶体的吸收光谱和荧光光谱。根据Judd-Ofelt理论分析并计算了辐射跃迁几率、辐射寿命、荧光分支比等光谱参数,获得的唯象参数为:Ω2=15.59×10-20cm2,Ω4=2.25×10-20cm2,Ω6=1.49×10-20cm2。在Er3+/Yb3+∶Sr3La2(BO3)4晶体中Er3+在1533nm处发射跃迁截面为7.88×10-21cm2,Er3+的4I13/2→4I15/2能级跃迁的荧光寿命和辐射寿命分别为0.728ms和4.24ms,结果表明Yb3+对Er3+有敏化作用,提高了对泵浦光的吸收能力,Er3+/Yb3+∶Sr3La2(BO3)4晶体可望作为1.55μm波段的一种有潜力的激光材料。     

Nd~(3+)掺杂的Sr_3Y_2(BO_3)_4晶体光谱特性研究

采用提拉法生长出25mm×40mm的Nd3+∶Sr3Y2(BO3)4晶体,测试了该晶体的吸收光谱、荧光光谱及荧光寿命。结果表明:Nd3+∶Sr3Y2(BO3)4晶体在807nm附近有最强的吸收峰,其半峰宽(FWHM)为16nm,宽的吸收半峰宽适合于LD泵浦;从荧光光谱得到发射波长分别为910.8nm、1065.2nm和1399nm的荧光峰。根据吸收和荧光光谱,计算了晶体的吸收截面和发射截面。采用J-O理论计算了Nd3+在Sr3Y2(BO3)4中的强度参数、各能级的振子强度、自发辐射几率、荧光分支比等参数。计算结果表明,其强度参数Ω2=3.816×10-20cm2,Ω4=10.895×10-20cm2,Ω6=12.44×10-20cm2,辐射寿命为104μs,量子效率η=49.7%,荧光分支比β1(0.88μm)=0.429,β2(1.06μm)=0.461,β3(1.35μm)=0.107,β4(1.88μm)=0.003。     

Triethyl ammonium salt of O,O′-bis(p-tolyl)dithiophosphate, [Et3NH]+[(4-MeC6H4O)2PS2]−

Triethyl ammonium Salt of O,O′-bis(p-tolyl)dithiophosphate and O,O′-bis(m-tolyl)dithiophosphate have been obtained by reaction of p- and m-cresol, respectively with P₂S₅ in toluene and have been characterized by elemental analysis, IR, ¹H and ³¹P NMR spectroscopy. The molecular structure of O,O′-bis(p-tolyl)dithiophosphate has been determined. Crystal data: [Et₃NH]⁺[(4-MeC₆H₄O)₂PS₂]⁻: Monoclinic, P2₁/c, a=15.2441(9) ?, b=10.415(2) ?, c=3.9726(9) ?, β=91.709(7)°, V=2217.5(1) ?⁻³, Z=4.Supplementary materials Additional material available from the Cambridge Crystallographic Data Centre (CCDC no. 600927 for [Et₃NH]⁺[(4-MeC₆H₄O)₂PS₂]⁻ comprises the final atomic coordinates for all atoms, thermal parameters, and a complete listing of bond distances and angles. Copies of this information may be obtained free of charge on application to The Director, 12 Union Road, Cambridge CB2 2EZ, UK (fax: +44-1223-336033; email: deposit@ccdc.cam.ac.uk or www:http://www.ccdc.cam.ac.uk).     

First-principles coexistence simulations of supercooled liquid silicon

We perform first-principles coexistence simulations of the low-density and the high-density phases of supercooled liquid silicon and find a negative slope for the coexisting line in the temperature-pressure plane. Electron density maps and electron-localization function plots of the two phases of silicon show marked differences. The calculated differences suggest more localized electrons in the low-density liquid compared to the high-density liquid, coming from an increased population of covalent bonds, which further explain the calculated negative slope in the two phase coexistence regime. This is consistent with the presence of a pseudo-gap in low-density liquid silicon, absent in the high-density liquid which shows a metallic behavior.     

Crystal structures of thecis andtrans isomers of dithiahexahydro[3.3]metacyclophane

Structures of both thecis andtrans isomers of dithiahexahydro[3.3]metacyclophane, ?C₆H₄?CH₂SCH₂?C₆H₁₀?CH₂SCH₂?, have been determined, wherecis andtrans refer to the attachments to the cyclohexane ring. Thecis form crystallizes in the monoclinic space groupP2₁/c witha=8.4299(11)Å,b=21.772(2)Å,c=8.9724(13)Å, β=116.574(11)^o, andZ=4. Thetrans isomer packs into the monoclinic space groupP2₁ witha=8.159(16)Å,b=10.185(5)Å,c=9.558(2)Å, β=112.435(18)^o, andZ=2. The cyclohexane ring of thecis isomer is in the chair conformation, while the cyclohexane of thetrans isomer is found in a twisted boat conformation.     

CTAB与SDBS对碳酸锶粒子生长形态调控及机理研究

以表面活性剂CTAB和SDBS为化学添加剂,采用化学共沉淀法对碳酸锶晶体的生长形态进行调控,成功地制备出了实心的树枝状和花瓣为空心的花状碳酸锶粉体,并用X射线衍射(XRD)、扫描电子显微镜(SEM)和傅里叶变换红外光谱(FT-IR)等分析手段对样品进行了表征;最后重点对化学添加剂可能产生的影响机理进行了初步的探讨.结果表明,CTAB和SDBS在晶体生长的过程中能起到显著的影响作用,两者对粒子分散性能的作用效果相反,而且后者对晶体(013)和(213)晶面表面能降低的贡献明显大于前者.     

Crystal structures of the cis and trans isomers of a tetrathia[3.3.3.3]cyclophane

Both the cis and trans isomers of 3,11,18,26-tetrathiatricyclo[26.2.2.1^5,9.2^13,16.1^20,24] hexatriaconta-5,7,9,20,22,24-hexene have been prepared and structurally characterized. Each of these centrosymmetric tetrathia dimers includes two cyclohexane rings in chair conformations with either 1,4-cis or 1,4-trans bonding and two meta-substituted benzene rings. The cis isomer packs into the monoclinic space group P2₁/a with a = 10.485(3)Å, b = 10.3956(18)Å, c = 14.1343(10)Å, = 105.200(13)°, Z = 2 and refined to an R factor of 0.046. The trans isomer crystallizes in the monoclinic space group P2₁/c with a = 10.7217(12)Å, b = 5.6797(7)Å, c = 25.415(5)Å, = 96.001(12)°, Z = 2 and refined to an R factor of 0.043. In the cis structure each benzene ring faces a cyclohexane ring while in the trans structure the cyclohexane rings face one another.     

Crystal structure of Zn4Na(OH)6SO4Cl·6H2O

The structure of Zn₄Na(OH)₆SO₄Cl·6H₂O, a secondary mineral from Hettstedt, Germany, was determined by single-crystal X-ray diffraction. The crystals are hexagonal,a=8.413(8),c=13.095(24) Å, space group $P\bar 3$ , Z=2. The structure was refined to R=0.0554 and R_w=0.0903 for 970 reflections with I≥3σ(I). The structure can be described as zinc hydroxide layers perpendicular toc, from which sulfates and chlorides extend. The layers are held together by a system of hydrogen bonds involving hexaaquo Na⁺ ions which occupy the interlayer space.     

Synthesis and Crystal Structure of 5-[2-(6-bromonaphthalenyloxymethyl)]-3-(4-morpholinomethyl)-1,3,4-oxadiazole-2(3<Emphasis Type="Italic">H</Emphasis>)-thione

Abstract  The title compound, C₁₈H₁₈BrN₃O₃S, a derivative of 1,3,4-oxadiazole, crystallizes in the triclinic space group P-1 with unit cell parameters a = 6.8731(3), b = 8.9994(4), c = 15.7099(6) ?, α = 92.779(3)°, β = 130.575(3)°, γ = 107.868(4)°, Z = 2. The dihedral angle between the mean planes of the planar naphthyl and morpholine (chair) rings with the planar oxadiazol ring is 50.1(8) and 76.8(6)°, respectively. The planar naphthyl ring is twisted 52.2(5)° with the mean plane of the morpholine ring. A group of four intermolecular close contacts are observed between a bromine atom and hydrogen atoms from the closely packed naphthyl, morpholine and oxy–methyl groups in the unit cell. These molecular interactions in concert with an additional series of π–π stacking interactions that occur between the center of gravity of the two 6-membered rings of the naphthalene group influence the twist angles of each of these three groups. A MOPAC AM1 calculation of the conformation energy of the crystal structure [226.0128(9) kcal] compared to that of the minimum energy structure after geometry optimization [29.9744(1) kcal] reveals a significantly reduced value. The twist angles of the three groups above also change after the AM1 calculation giving support to the influence of both intermolecular C–H···Br short-range interactions and Cg π–π stacking interactions on these angles which therefore play a role in stabilizing crystal packing. Graphical Abstract  Crystal structure of 5-{[(6-bromonaphthalen-2-yl)oxy]methyl}-3-(morpholin-4-ylmethyl)-1,3,4-oxadiazole-2(3H)-thione, C₁₈H₁₈BrN₃O₃S, is reported and its geometric and packing parameters described and compared to a MOPAC computational calculation. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

电沉积法制备ZnO纳米棒阵列及其发光特性

本文以掺F的SnO2导电玻璃为基板,以硝酸锌水溶液为电解液,采用三电极恒电位体系电沉积制备ZnO纳米棒阵列,系统考察了硝酸锌浓度和沉积电位等工艺参数对ZnO纳米棒阵列的微观形貌及其发光性能的影响规律.结果表明,硝酸锌浓度和沉积电位对纳米棒阵列的形貌有显著影响,控制适宜的工艺条件可以制备出直径分布均匀、结晶性好且纯度高的六方纤锌矿ZnO纳米棒阵列.荧光光谱分析表明,电沉积制备出的ZnO纳米棒阵列在385 nm附近有一个强荧光发射峰,且发光性能稳定、对纳米棒阵列微观形貌的细微变化不敏感,使其在发光二极管和激光器等领域具有广阔的应用前景.     

Crystal structure of irisolidone from the flowers of Pueraia lobata

Irisolidone (5,7-dihydroxy-6,4′-dimethoxyisoflavone) was isolated from the flowers of Pueraia lobata and its crystal structure was examined by X-ray single crystal diffraction. The crystal structure of irisolidone is monoclinic, space group P2₁/c with a = 15.491(9) ?, b = 7.895(4) ?, c = 13.321(7) ?, β = 110.546(9)° and Z = 4. Hydrogen bonding and aromatic π–π stacking assemble the title compound into a three-dimensional networking structure.