MgF2对Mn4+掺杂锗酸盐红色荧光粉发光的影响

3.5MgO·0.5MgF₂·GeO₂∶Mn⁴⁺作为优异热稳定性和良好发光性能的红色荧光粉而被市场应用,然而,该粉体中MgF₂的作用影响机理尚不明晰,阻碍其性能进一步优化和发展。采用高温固相法制备了系列Mn⁴⁺激活的锗酸盐荧光粉,通过对比加入MgF₂、H₃BO₃(助熔剂),研究了该粉体的结构、形貌、发光性能等变化规律,阐明了MgF₂的发光影响作用。研究表明,加入MgF₂、H₃BO₃和不加任何助熔剂时的样品,其最佳烧结温度分别为1 150、1 250和1 350 ℃,上述温度下发光强度均为最佳值,其中加入MgF₂、H₃BO₃的样品在最佳温度处生成了纯相。MgF₂的添加,一方面同H₃BO₃一样作为助熔剂对生成纯相、提高样品结晶度起了积极的作用;另一方面,通过研究分析,确认F^-离子成功掺杂进入晶格,促使样品生成的晶体结构为Mg₁₄Ge₅(O,F)₂₄。加入MgF₂、H₃BO₃在最佳烧结温度的样品的荧光寿命分别为0.93和0.75 ms。     

基于四甲基取代胍环的四核稀土镝簇合物的慢磁弛豫

报道了2个基于四甲基取代胍环的三明治型四核稀土簇合物, [Ln₄(μ₃-OH)₄(μ₂-OH)₂(H₂O)₄(NO₃)₂(TMeQ[6])₂]·(NO₃)₄·26H₂O(Ln=Dy, 1; Ln=Tb, 2)。晶体结构分析显示2个簇合物包含2个四甲基取代胍环夹心的四核稀土立方烷结构, [Ln₄(μ₃-OH)₄]⁸⁺。磁性研究显示化合物1显示了慢磁弛豫行为。由于胍环配体可以有效的传递能量给稀土铽离子, 化合物2具有较好的发光性能。     

Br-掺杂Bi2WO6的水热法合成及其可见光催化性能

以Bi（NO₃）₃·5H₂O和Na₂WO₄·2H₂O为主要原料,采用水热法合成了纯相Bi₂WO₆,并对其进行非金属离子Br^-掺杂改性。采用XRD、SEM、TEM、XPS、Raman、PL和DRS研究了Br^-掺杂对Bi₂WO₆的物相结构、形貌和可见光催化性能的影响。结果表明,Br^-掺杂可有效提高Bi₂WO₆的可见光催化性能,当掺杂量（物质的量百分数）为8%时,溴掺杂Bi₂WO₆的光催化性能最好,可见光照射40 min后,可降解96.73%的罗丹明-B,与未掺杂Bi₂WO₆相比,其降解率提高了36.32%。     

Conceptual design of an intense positron source based on an LIA

Accelerator based positron sources are widely used due to their high intensity. Most of these accelerators are RF accelerators. An LIA (linear induction accelerator) is a kind of high current pulsed accelerator used for radiography. A conceptual design of an intense pulsed positron source based on an LIA is presented in the paper. One advantage of an LIA is its pulsed power being higher than conventional accelerators, which means a higher amount of primary electrons for positron generations per pulse. Another advantage of an LIA is that it is very suitable to decelerate the positron bunch generated by bremsstrahlung pair process due to its ability to adjustably shape the voltage pulse. By implementing LIA cavities to decelerate the positron bunch before it is moderated, the positron yield could be greatly increased. These features may make the LIA based positron source become a high intensity pulsed positron source.     

A design study of a magnifying magnetic lens for proton radiography

Magnifying magnetic lenses can be used in high-energy proton microscopes. The -I lens suggested by Zumbro is analyzed in this paper, and a new type of magnetic lens called a lengthened lens is introduced. Theoretical analysis shows that the lengthened lens can form a magnifying lens, and at the same time the main advantages of a Zumbro lens are inherited. Using the My-BOC beam dynamics code, an example of the design is shown. The results show that the method of designing magnifying magnetic lenses is effective.     

Formation of multiple dark photovoltaic spatial solitons

We theoretically study the formation of multiple dark photovoltaic soliton splitting in the quasi-steady-state and steady-state regimes under open-circuit conditions. We find that the initial width of the dark notch at the entrance face of the crystal is a key parameter for generating an even (or odd) number sequence of dark coherent photovoltaic solitons. If the initial width of the dark notch is small, only a fundamental soliton or Y-junction soliton pair is generated. As the initial width of the dark notch is increased, the dark notch tends to split into an odd (or even) number of multiple dark photovoltaic solitons, which realizes a progressive transition from a low-order soliton to a sequence of higher-order solitons. The soliton pairs far away from the centre have bigger width and less visibility. In addition, when the distance from the centre of the dark notch increases, the separations between adjacent dark stripes become slightly smaller.     

巧用Excel处理大学物理实验数据

以霍尔元件测量磁场为例,介绍了用Excel软件对实验数据进行分析处理的一般过程.结果表明利用Excel处理物理实验数据能大大减轻学生繁杂的数据计算及处理步骤,有效避免了手工处理所带来的误差,并且能满足一般的实验作图要求,适宜在大学物理实验数据处理方面推广应用.     

浊点萃取-胶束增稳室温燐光法测定水样中痕量α-萘乙酸

提出了用非离子表面活性剂Triton X-100作萃取剂的浊点萃取-胶束增稳室温燐光法测定痕量α-萘乙酸的新方法.就溶液pH、试剂浓度、平衡温度和时间等实验条件对浊点萃取的影响及后续使用的胶束增稳室温燐光法的测定条件进行了探讨.在最佳条件下,线性范围为3.0×10-8～2.0×10-6 mol/L;检出限1.3×10-8 mol/L;方法用于强化水样中痕量α-萘乙酸的测定,回收率95%～104%;相对标准偏差2.0%～3.5%.     

Studies on Chem icalCom position ofIron-m olybdenum Cofactor fromNitrogenase by Fluorescence Analysis

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