Direct preparation of K0.5Na0.5NbO3 powders

K_0.5Na_0.5NbO₃ powders have been directly synthesized by an alternative solid–state method. Stoichimometric mixture of ammonium niobium oxalate and C₄H₄O₆KNa·4H₂O were calcined in temperature range from 500 to 800 °C for 3 h. The precursor and calcination products were characterized with respect to stoichiometry, purity, crystalline structure, particle size and powder morphology using X–ray diffraction (XRD), X‐ray fluorescence (XRF) spectrometer, scanning electron microscope (SEM), Fourier transform infrared (FTIR) spectra, thermogravimetric (TG) analysis, differential scanning calorimetry (DSC) and UV–Vis diffuse reflectance (UV–Vis) spectroscopy. XRD and XRF results reveal that stoichiometric K_0.5Na_0.5NbO₃ powders could be synthesized by the method. The particle size is about 68 nm for the precursor calcined at 500 °C according to XRD data, which is in good agreement with SEM data. The average band gap energy is estimated to be 3.18 eV by UV–vis diffuse reflectance spectra. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

A novel intramolecular reversible reaction between the hydroxyl group and isobutenylene chain in a cyclophane-type macrocycle

A novel Hg²⁺ ion induced reversible ring contraction was achieved employing the intramolecular reaction of isobutylene with an aromatic hydroxyl group of cyclophane; reversibility of the reaction was facilitated by excess addition of NaBH₄ which also resulted in complexation. The ring contraction and expansion was monitored by UV-VIS absorption, and by fluorescence and ¹H NMR spectra. Switchable fluorescence behavior (on—off—on) was observed when the ring-size was tuned from a 19-membered ring to an 18-membered and vice versa. This fine tuning has the potential to be applied in the construction of new supramolecular devices.     

Optimizing Optoelectronic Properties of Pyrimidine‐Based TADF Emitters by Changing the Substituent for Organic Light‐Emitting Diodes with External Quantum Efficiency Close to 25 % and Slow Efficiency Roll‐Off

A series of green butterfly‐shaped thermally activated delayed fluorescence (TADF) emitters, namely PXZPM , PXZMePM , and PXZPhPM , are developed by integrating an electron‐donor (D) phenoxazine unit and electron‐acceptor (A) 2‐substituted pyrimidine moiety into one molecule via a phenyl‐bridge π linkage to form a D –π–A–π–D configuration. Changing the substituent at pyrimidine unit in these emitters can finely tune their emissive characteristics, thermal properties, and energy gaps between the singlet and triplet states while maintaining frontier molecular orbital levels, and thereby optimizing their optoelectronic properties. Employing these TADF emitters results in a green fluorescent organic light‐emitting diode (OLED) that exhibits a peak forward‐viewing external quantum efficiency (EQE) close to 25 % and a slow efficiency roll‐off characteristic at high luminance.     

140GHz大功率交错双栅行波管的设计和模拟研究

采用交错双栅结构,结合带状电子注,研究了一种工作在140 GHz频段的大功率行波管. 本振模数值计算表明该结构具有良好的色散特性和耦合阻抗.针对所采用的慢波结构, 提出了慢波过渡结构、输入输出耦合器和集中衰减器,保证了行波管的良好工作. 利用三维大信号模拟计算的方法得到的结果显示,当电子注直流功率为5.115 kW,输入信号功率为0.1 W时, 所研究的行波管能在132-152 GHz范围内提供大于300 W的峰值功率,其中在138 GHz时得到最大功率546 W, 对应增益为37.37 dB.当在0.027-0.46 W内调节输入信号功率,可以保持该行波管在128-152 GHz 频带内得到大于440 W的峰值功率,对应的电子效率大于8.6%. 结果显示该行波管将在大功率短毫米波领域具有重要意义和潜在应用价值.     

Effects of Current on Microcosmic Properties of Catalyst and Reforming of Bio-oil

通过低温电催化重整方法(电流通过催化剂床),用传统的镍基重整催化剂NiO-Al2O3重整生物油制取氢气是一种高效的生物油产氢方法．还探索了电流对生物油重整的促进影响,发现通过催化剂的电流明显地提高了生物油的重整．通过BET、XRD、XPS和SEM的测试,研究了电流对催化剂微观结构的影响,包括比表面、孔径、孔体积、晶粒尺寸和氧化镍的还原程度．从通电的催化剂表面脱附的热电子直接由飞行时间质谱测量．讨论了电催化重整生物油的机理．     

强流脉冲离子束辐照靶材烧蚀效应二维数值研究

对强流脉冲离子束(IPIB)辐照Ti靶的烧蚀效应进行了二维数值研究.得到了表面烧蚀物质随脉冲时间的变化关系.得出TEMP Ⅱ 型加速器产生的脉冲束流辐照靶材时引起的汽、液化均是从表面开始、并且汽化过程中表面物质被层层烧蚀的结论.同时，得到中心区的平均烧蚀速度为10m/s 数量级，它远小于产生的烧蚀等离子体的喷发速度.得到脉冲期间靶材内部不同位置烧蚀斑痕形状的时间演化过程，以及束流中含有的离子种类分额不同时IPIB辐照过程产生的不同效果. 关键词： 强流脉冲离子束 靶 烧蚀过程 二维数值模拟     

+3价离子掺杂钨酸铅晶体发光性能和微观缺陷的研究

通过透射光谱、x射线激发发射光谱（XSL）的测试，研究了Bridgman法生长的几种不同+3价离子掺杂钨酸铅晶体的发光性能，并利用正电子湮没寿命谱（PAT）和x光电子能谱（XPS）的实验手段，对不同钨酸铅晶体的微观缺陷进行研究.实验表明，不同的+3价离子掺杂，对钨酸铅晶体发光性能的改善不同，并使得晶体中正电子俘获中心和低价氧的浓度发生不同变化.其中掺镧晶体的正电子俘获中心和低价氧浓度均上升，而掺钇和掺铋晶体的正电子俘获中心和低价氧浓度均下降，掺锑晶体则出现了正电子俘获中心浓度上升、低价氧浓度下降的情况.提 关键词： 钨酸铅晶体 +3价离子掺杂 正电子湮没寿命谱 x光电子能谱