~(146)Tb的能级结构研究

利用能量为161—175MeV的~(32)S束流,通过反应~(118)Sn(~(32)S,1p3n)~(146)Tb研究了双奇核~(146)Tb的高自旋态能级结构。实验进行了γ射线的激发函数、γ射线的各向异性度、X-γ和γ-γ-t符合测量。基于这些测量结果,建立了激发能达8390kev的~(146)Tb核的能级纲图,其中包括新发现的41条γ射线和新建立的27个能级,并指定了~(146)Tb新发现能级的自旋值。用一个h_(11/2)价质子和一个h_(11/2)~(-1)价中子空穴耦合、πh_(11/2)υh_(11/2)~(-1)与~(146)Gd核实激发态的耦合对~(146)Tb的能级结构进行了定性地讨论。

~(145)Tb的高自旋态能级纲图

利用能量为 1 61— 1 75MeV的32 S束流 ,通过反应118Sn( 32 S ,1p4n)产生了145 　Tb的高自旋态 .进行了γ射线的激发函数、γ γ t符合测量 .首先建议了由 2 4条能级和 4 2条γ跃迁组成的145 Tb核的能级纲图 ,并指定了各条能级的自旋值及部分低位能级的宇称 .用一个πh11/ 2 价质子与144 Gd核芯激发态的耦合定性地解释了145 Tb的一些低位激发态

~(130)Nd和~(140)Tb的EC/β~+衰变研究

利用能量为１７０ＭｅＶ左右的３６Ａｒ重离子束轰击９６Ｒｕ和１０６Ｃｄ浓缩同位素靶，分别生成缺中子同位素１３０Ｎｄ和１４０Ｔｂ．借助氦喷嘴带传输系统，用 Ｘ－γ和 γ－γ符合方法，分离鉴别了这两种核素，并进一步测定了它们的衰变性质．得到１３０ Ｎｄ的半衰期为（１３± ３）ｓ，首次建议了它的ＥＣ／β＋衰变纲图，推测了其子核１３０Ｐｒ的基态和低位能级的自旋宇称．修订了１４０Ｔｂ的原有极简单的ＥＣ／β＋衰变纲图并指认１４０Ｔｂ的基态自旋宇称为７＋．

具有Pb衬的Tb薄靶的制备

采用滚压法制备Ｔｂ靶，采用滚压法或真空蒸发法制得Ｐｂ膜，两者通过滚压或真空蒸发法结合制得了带Ｐｂ村的Ｔｂ薄靶。

beta-delayed proton decays of Tb-140 and Dy-140 as well as the spin and parity of Dy-143

Tb-140 and Dy-141 were produced via fusion evaporation in the reaction Ca-40+Cd-106. Their beta-delayed proton decays were studied by means of "p-gamma" coincidence in combination with a He-jet tape transport system, including half-lives, proton energy spectra, gamma-transitions following the proton emissions, and the branching ratios to the low-lying states in the grand-daughter nuclei. The ground-state spins and parities of Tb-140 and Dy-141 were extracted as 7(+/-) and 9/2(+/-), respectively, by fitting the experimental data with a statistical model calculation. The configuration-constrained nuclear potential energy surfaces (NPES) of Tb-140 and Dy-141 were calculated by using the Woods-Saxon Strutinsky method, which indicate the ground-state spins and parities of Tb-140 and Dy-147 to be 7(+) and 9/2(-), respectively. In addition, the configuration-constrained NPES of Dy-143 was also calculated by using the same method. From the NPES a 1/2(+) ground state and a 11/2(-) isomer with the excitation energy of 198keV were found. The calculated results are consistent with our experimental data on the decay of Dy-143 reported in Eur. Phys. J., 2003, A16: 347-351.

beta-delayed proton decays and spin assignments for Tb-140, Dy-141 and Dy-143

The proton-rich isotopes Tb-140 and Dy-141 were produced via the fusion evaporation reaction Ca-40+ Cd-106. Their beta-delayed proton decays were studied by p-gamma coincidence in combination with a He-jet tape transport system, and half-lives, proton energy spectra, gamma-transitions following the proton emission, as well as beta-delayed proton branching ratios to the low-lying states in the grand-daughter nuclei were determined. Comparing the experimental data with statistical model calculations, the ground-state spins of Tb-140 and Dy-141 were found to be consistent with 7 and 9/2, respectively. The configuration-constrained nuclear potential energy surfaces (NPES) of Tb-140 and Dy-141 were calculated using the Woods-Saxon-Strutinsky method, which suggest the ground-state spins and parities of Tb-140 and Dy-141 to be 7(+) and 9/2(-), respectively. In addition, the configuration-constrained NPES of Dy-143 were calculated, which predict a 1/2(+) ground state and a 11/2(-) isomer with excitation energy of 198 keV. These findings are consistent with our previous experimental data on Dy-143 reported in Eur. Phys. J. A 16, 347 (2003).

中能区~(40)Ar + ~(197)Au/~(159)Tb/~(nat)Ag反应中高激发热核性质研究

通过对中能区Ar+Au/Tb/Ag反应中高激发核的发射时标、发射次序、发射机制、核温度、集体运动等衰变特性的研究，提取了轻粒子和中等质量碎片（IMF）的发射时间，IMF发射时间随束流能的升高而变短，发射机制逐渐由相继衰变过渡至多重碎裂。研究了轻粒子和碎片间的发射次序，对高能粒子和碎片，轻粒子先于碎片发射，而低能时，则为碎片先于轻粒子发射。IMF发射成分与角度和碰撞参数有关，前角区来自于弹核碎裂，后角区来自于类靶热核的蒸发。在平面和出平面研究表明，中速粒子和碎片为在平面发射占主导，即存在类转动效应；对轻粒子，转动效应随粒子质量增加而增加；对中速产物均观测到该效应随碰撞参数饿增大而增大。采用几种不同的方法提取了热核的核温度，研究了不同方法之间的区别。

Synthesis and luminescent properties of Lu3Ga5O12 : RE3+ (RE = Eu, Tb, and Pr) nanocrystalline phosphors via sol-gel process

Lu3Ga5O12:Eu3+, Lu3Ga5O12:Tb3+, and Lu3Ga5O12:Pr3+ phosphors were prepared through a Pechini-type sol-gel process. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), photoluminescence, and cathodoluminescence spectra were utilized to characterize the synthesized phosphors. The XRD results reveal that the sample begins to crystallize at 800 degrees C and fully crystallined pure Lu3Ga5O12 phase can be obtained at 1000 degrees C. The FESEM image indicates that the phosphor sample is composed of aggregated rice grainlike particles with sizes around 80-120 nm.

Lanthanide-hinged calixarene bicapsules: Discrete hexanuclear Ln(III)/phenanthroline/p-sulfonatocalix[4]arene oligomers (Ln = Gd, Tb)

The dumbbell-like calixarene bicapsule in two novel Ln(III)-C4AS compounds was found to be a hexanuclear Ln(III)/phenanthroline/p-sulfonatocalix[4]arene oligomer. The magnetic and luminescent properties of these compounds were examined.

Synthesis and photoluminescent properties of silica-coated LaCeF3 : Tb nanocrystals

La0.45Ce0.45F3:Tb (10 mol% Tb) nanoparticles was synthesized via sonochemical method and then coated with silica (SiO2) shells through a microemulsion process, resulting in the formation of core/shell structured LaCeF3:Tb/SiO2 nanoparticles. The obtained core/shell LaCeF3:Tb/SiO2 nanoparticles are spherical and uniform in size (average size about 60 nm), strongly fluorescent, and long fluorescence lifetime (1.87 ms). This kind of nanoparticles was water-soluble, which could be applied in biological labeling and other fields.

Energy transfer from Tb3+ to Mn2+ in LaMgAl11O19:Tb, Mn phosphors

Luminescent properties of LaMgAl11O19:Tb, Mn phosphors were investigated. It was observed that the energy distributions of the Tb3+-emission bands associated with transitions from the D-5(3) and D-5(4) levels to F-7(J) depend on the Tb3+-concentration, which is due to the cross-relaxation between Tb 31 ions. The emission band at about 516 nm is attributed to the T-4(1) -> (6)A(1) transition of the Mn2+ ions. We observed an energy transfer from the Tb 3, to Mn2+ ions in LaMgAl11O19:Tb, Mn.

Novel hybrid periodic mesoporous organosilica material grafting with Tb complex: Synthesis, characterization and photoluminescence property

A novel periodic mesoporous organosilica (PMO) material was synthesized through one-step co-condensation of 1,2-bis(triethoxysilyl)ethane (BTESE) and benzoic acid-functionalized organosilane (BA-Si) using cetyltrimethylammonium bromide (CTAB) as a structure-directing agent under basic conditions. The materials were fully characterized by FTIR, XRD, N-2 adsorption-desorption isotherms and FESEM. FTIR spectra proved that BA-Si was successfully incorporated into the PMO materials (PMOs) via benzyl group as a linker. XRD and N-2 adsorption-desorption isotherms revealed the characteristic mesoporous structure with highly uniform pore size distributions. FESEM confirmed that the morphology of the PMOs was significantly dependent cri the molar ratio of two organosilica precursors.

Thiacalix[4]arene-Supported Planar Ln(4) (Ln = Tb-III, Dy-III) Clusters: Toward Luminescent and Magnetic Bifunctional Materials

This paper reports the syntheses, crystal structures, and luminescent and magnetic properties of four tetranuclear Tb-III (1 and 3) and Dy-III (2 and 4) complexes supported by p-phenylthiacalix[4]arene (H(4)PTC4A) and p-tert-butylthiacalix-[4]arene (H(4)TC4A). All four frameworks can be formulated as [Ln(4)(III)(PTC4A/TC4A)(2)(mu(4)-OH)Cl-3(CH3OH)(2)(H2O)(3)], and some methanol and water solvent molecules are occupied in the interstices. The compounds are featured with a sandwichlike unit constructed by two tail-to-tail calixarene molecules and a planar tetragonal (mu(4)-OH)Ln(4) cluster. The photoluminescent analyses suggest that there is an efficient ligand-to-Ln(III) energy transfer for compounds 1-3 and H(4)PTC4A is a more efficient "antenna" than H(4)TC4A.

Controlled Synthesis of Ln(3+) (Ln = Tb, Eu, Dy) and V5+ Ion-Doped YPO4 Nano-/Microstructures with Tunable Luminescent Colors

YPO4 nano/microcrystals with multiform crystal phases and morphologies, such as hexagonal nano/submicroprisms, spherical-like nanoparticles, and nanorods with different length/diameter ratios as well as tetragonal nanospindles, have been synthesized via a facile hydrothermal route. A series of controlled experiments indicate that the pH values in the initial solution, phosphorus sources, and the organic additive trisodium citrate (Cit(3-)) are responsible for crystal phase and shape determination of final products. It is found that Cit(3-) as a ligand and shape modifier has the dynamic effect by adjusting the growth rate of different facets under different experimental conditions, resulting in the formation of various geometries of the final products. The possible formation mechanisms for products with diverse architectures have been presented.