BaCuO_2的添加对YBa_2Cu_3O_(7-δ)临界电流密度的影响

掺入BaCuO2杂相的YBa2Cu3O7-δ(YBCO)粉末样品采用固相反应方法制备获得。XRD的Rietveld精修显示BaCuO2杂相和YBCO并存。在YBCO+xBaCuO2(x=0,0.05,0.1,0.2,0.3)的一系列样品中,当x=0.05时,样品的临界电流密度最大。在磁场中,微量BaCuO2杂相的添加,使YBCO的临界电流(Jc)提高了,但超导转变温度(Tc)稍微有所下降。临界电流密度的这些特征行为来自于两方面的共同作用,一方面是超导性的变化,另一方面纳米尺寸范围内的空间分布的非均匀性。     

LiMBO3 : Dy3+材料的发光特性

采用固相法制备了LiM(M=Ca, Sr, Ba)BO₃ : Dy³⁺材料,并研究了材料的发光特性。LiM(M=Ca, Sr, Ba)BO₃ : Dy³⁺材料的发射光谱均呈多峰发射,对应于Ca,Sr,Ba,其主发射峰分别是Dy³⁺的⁴F_9/2→⁶H_15/2(484,486,486 nm),⁶H_13/2(577,578,578 nm)和⁶H_11/2(668,668,666 nm)跃迁。监测黄色发射峰时,所得激发光 谱峰值位置相同,主激发峰分别为331,368, 397,433,462,478 nm,对应Dy³⁺的⁶H_15/2→ ⁴D_7/2,⁶P_7/2,⁶M_21/2,⁴G_11/2,⁴I_15/2和⁶F_9/2跃迁。研究了敏化剂Ce³⁺及电荷补偿剂Li⁺、Na⁺和K⁺对LiM(M=Ca, Sr, Ba)BO₃ : Dy³⁺材料发光强度的影响。结果显示:加入敏化剂Ce³⁺提高了材料的发光强度,发光强度最大处对应的Ce³⁺浓度为3%;加入电荷补偿剂Li⁺、Na⁺和K⁺后,材料的发光强度也得到了明显提高,但发光强度最大处对应的Li⁺、Na⁺和K⁺浓度不同,依次为4%、4%和3%。     

InxGa1-xN/InyGa1-yN多量子阱结构 发光特性的测量与分析

利用MOCVD方法在蓝宝石衬底上生长了In_xGa_1-xN/In_yGa_1-yN多量子阱结构外延层,并用变温光致发光(PL)光谱、选择激发光谱以及激发(PLE)光谱等手段研究了该结构的量子效率、多峰效应的起源以及峰位随温度变化等信息。变温PL光谱的结果表明:在温度从30 K变化到300 K时,其峰值强度只下降了1.36倍且发光波长发生了蓝移。通过选择激发光谱证明了其发光峰位的独立性。PLE结果表明了GaN和势垒层的Stokes位移很小,但是In_xGa_1-xN阱层的Stokes位移变化很大。同时,提出了一种可同时获得多个吸收边的数据处理方法。     

Mass of Open Cluster NGC 7789

Mass of open duster NGC 7789 in the Galaxy is determined by three methods： the photometric method based on mass-luminosity relations of stars in the duster Mpho= 7712.5M⊙; the dynamical method based on virial theorem Mvir=6996.1M⊙; and the tidal radius method based on the interaction between the cluster and the Galaxy Mtid= 5152.5M⊙. The mean mass of this cluster is estimated to be Mc =6620.4 4- 762.5M⊙.     

(1-x)(K0.5Na0.5)NbO3-xSrTiO3陶瓷的弛豫铁电性能

通过对(1-x)(K0.5Na0.5)NbO3-xSrTiO3(0≤x≤0.15)陶瓷的相组成、晶体结构和介电性能的研究发现,该陶瓷为单一的钙钛矿结构相.当x含量较小(x＜0.1)时为正交相结构,x≥0.1时转变为四方相结构.随着SrTiO3掺杂量的增加,样品的致密度增加,样品由正常铁电相逐渐向弥散铁电相转变,且相变温度明显下降,其相变峰的半高宽D和临界指数γ,随 x 的增加而增加.样品损耗ε″r(复介电常数虚部)随温度T的变化表明低温时弛豫极化损耗起主要作用,高温时漏导损耗起主要作用.同时介电常数实部ε′r随频率的变化显示(1-x)(K0.5Na0.5)NbO3-xSrTiO3弛豫为德拜弛豫.     

封离式He-N2-CO2激光器横模特性的测量与分析

利用激光光束分析仪,实时在线测量了一根He-N2-CO2封离式激光管的横模分布特性,得到了激光模式随放电电流的变化关系.实验表明该激光器在最佳工作电流时,容易形成低阶模运转,但很难获得基模运转,通过改善对称性以及加快冷却水流速可以获得基模运转.通过激光动力学过程分析了模式变化的形成原因,为大功率激光器模式控制与改善提供了一定的理论和实验借鉴.     

Zn(Ⅱ)-槲皮素螯合机理的紫外分光光度法研究

采用紫外分光光度法研究Zn^2＋离子与槲皮素在乙醇溶液中形成螯合物量配比及螯合机理。通过定量的槲皮素、山萘酚、柚皮素乙醇溶液与Zn^2＋离子作用,在426nm处测其溶液的吸光度,从而确定Zn^2＋）离子与槲皮素的螯合比为2：1。且螯合位置发生在槲皮素分子3-羟基和4-羰基上与3′,4′-OH位置。     

Phase control of maximal atomic coherence

The atomic coherence in a three-level Λ atom is studied, in which each optical transition is driven by a coherent field and the metastable states are coupled to each other via a microwave field. It’s shown that the atomic coherence crucially depends on the relative phase delay between the envelopes of the amplitudes of the three coupling fields. In particular, when the phase delay is adjusted to 0 or π, the maximal atomic coherence arises, while the maximal atomic coherence doesn’t occur once the phase delay is changed to π/2. The maximal atomic coherence is attributed to the trapping of the population in the lower sublevels.     

Sideband structure spontaneous spectrum without the rotating wave approximation

The effects of the non-rotating wave approximation (non-RWA) on the spontaneous emission of a V-type three-level atom are studied, where the excited states are coupled to a common ground state by a weak laser field and the upper-level doublet is driven by a strong microwave field. When the non-RWA is applied to the interaction of the atom with the microwave field, for some values of the parameters involved, the spontaneous emission spectrum is comprised of a central peak and a series of sidebands with a constant spacing of the microwave frequency, and the central peak and/or sidebands can be split into two components. The physical interpretation of the spectral characteristics is given in light of the dressed states.     

First-principles study of palladium atom adsorption on the boron- or nitrogen-doped carbon nanotubes

We have performed first-principles calculation to investigate the adsorption of a single palladium atom on the surface of the pristine and boron- or nitrogen-doped carbon nanotubes (CNTs). The results show that for the adsorption of a single palladium atom on the pristine CNT surface, the most stable site is Bridge1 site above the axial carbon–carbon bond. Either boron- or nitrogen-doped CNTs can assist palladium surface adsorption, but the detailed mechanisms are different. The enhanced palladium adsorption on boron-doped CNT is attributed to the palladium d orbital strongly hybridized with both boron p orbital and carbon p orbital. The enhancement in palladium adsorption on nitrogen-doped CNT results from activating the nitrogen-neighboring carbon atoms due to the large electron affinity of nitrogen. Furthermore, the axial bond is preferred over the zigzag bond for a palladium atom adsorbed on the surface of all three types of CNTs. The most energetically favorable site for a palladium atom adsorbed on three types of CNTs is above the axial boron–carbon bond in boron-doped CNT. The enhancement in palladium adsorption is more significant for the boron-doped CNT than it is for nitrogen-doped CNT with a similar configuration. So we conclude that accordingly, the preferred adsorption site is determined by the competition between the electron affinity of doped and adsorbed atoms and preferred degree of the axial bond over the zigzag bond.