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排序方式: 共有1299条查询结果,搜索用时 15 毫秒
1.
根据GaN氢化物气相外延生长(HVPE)的原理,设计制作了双温区卧式HVPE系统.根据实际生长中出现的问题和CaN样品的测试情况,对系统进行了逐步的调试和改进. 相似文献
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Based on the measured transverse mass spectra ofπr-, K-, and p at the RHIC energy s()NN = 130 GeV,di-omega productions from baryon-baryon reactions in hadronic matter are studied. Results about the (ΩΩ)0+ numbershow that the deeply bound state (ΩΩ)o+ can be observed at RHIC energies. 相似文献
4.
利用低压MOCVD工艺分别在(001)取向的LaAlO3,SrTiO3和重掺杂硅单晶衬底上制备PbTiO3铁电薄膜,并通过X射线衍射谱对薄膜的微结构进行分析.X射线θ-2θ扫描显示硅衬底上得到了PbTiO3多晶薄膜,另两种衬底上得到了择优取向的PbTiO3薄膜.LaAlO3衬底上的PbTiO3薄膜有a和c两个取向,也就是薄膜中存在着90°畴结构,而生长在SrTiO3衬底上的PbTiO3薄膜中只存在c方向的择优取向.由于薄膜的尺度效应,发现c轴晶格常数与块材相比均缩短.X射线的φ扫描验证了后两类薄膜的外延特性,利用同步辐射的高强度和高能量分辨率用摇摆曲线方法研究了这两种外延薄膜的品质,进一步证明了SrTiO3衬底上的PbTiO3薄膜的单畴特性.利用重掺杂的硅衬底作底电极,测量显示直接生长于硅衬底上的PbTiO3多晶薄膜具有良好的铁电性能
关键词: 相似文献
5.
Numerical Study on Left-Handed Materials Made of Ferrite and Metallic Wires 总被引:1,自引:0,他引:1 下载免费PDF全文
Due to coupling effect, we show that it is difficult to realize the left-handed material by placing metallic wires directly into a ferrite matrix. However by introducing an insulating material round the metallic wires to decouple the direct interaction between the metallic wire and ferrite matrix, we have proposed two microstructures, which are shown by numerical simulation to have negative refractive indexes. The influence of microstructure on the transmission property is also examined. 相似文献
6.
This paper presents a variational inequality (VI) approach to the problem of minimizing a sum of p-norms. First the original problem is reformulated as an equivalent linear VI. Then an improved extra-gradient method is presented
to solve the linear VI. Applications to the problem of p-norm Steiner Minimum Trees (SMT) shows that the proposed method is effective. Comparison with the general extra-gradient
method is also provided to show the improvements of the new method. 相似文献
7.
Li^+/MgO上乙烷氧化脱氢制乙烯的研究(Ⅱ):催化作用机理 总被引:3,自引:1,他引:3
借助XRD、IR、TG等技术对Li^+/MgO进行了表征,结果表明,酸、碱中心的数目,强度、催化性与Li^+的添加量相关 ,起酸碱作用的表面金属离子、表面低配位氧集团、O(L i^+O^-)是其反应的活性物种,反应机理可能由离子基、游离基协同完成。 相似文献
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9.
The Fourier transform far infrared spectra of oxalate hydrates of whole rare-earth series except Pm and Sc are investigated in the range of 100-400 cm~(-1). The assignment of vibrational frequencies is made on the basis of normal coordinate analysis using our NORVIB program. The model used for the hghter elements of the lanthanide series (La to Eu) is based on the crystal structure of Nd_2(C_2O_4)_3. 10H_2O, in which each lanthanide ion is surrounded by nine O atoms, six from three oxalate ions and three from Water molecules.The model adopted for the heavier elements of the lanthanide series (Gd to Lu) and Ytterbium is based on the crystal structure of Yb_2(C_2O_4)_3· 6H_2O, in which each ion is surrounded by eight atoms, six from three oxalate ions and two from water molecules. The variation of the metal-ligand frequencies and force constants with the atomic numbers of lanthanides is plotted and discussed. 相似文献
10.
Zhang WW Li HF Liu L Xie JL Lu CS Zhou Y Ren XM Meng QJ 《Journal of colloid and interface science》2003,261(1):82-87
A series of thiol-functionalied azobenzene derivatives (RAzoCnSH: R=H for n=3-6, abbreviated as AzoCnSH; R=CH(3)CONH for n=4, abbreviated as aaAzoC4SH) on gold electrodes were prepared and their self-assembly and electrochemical properties were studied by cyclic voltammetry. They all formed uniform and reproducible self-assembled monolayers (SAMs) on gold and showed well-behaved voltammetric responses in aqueous solution. Both the length of the alkyl chain spacer and the H-bonding of the end acetamino group had effects on the stability and the electrochemical kinetics of the SAMs, and the effect of the H-bonding was dominant. The surface coverage of the SAMs (AzoCnSH) is gradually increased with an increase of the alkyl chain spacer length, whereas the presence of the terminal acetamino group leads to a greater increase of the surface coverage. At a low scan rate, voltammetric responses corresponding to an irreversible two-electron, two-proton reduction/oxidation of the trans-azobenzene redox center were obtained in the range of +300 mV and -800 mV, which exhibited very large peak-to-peak splitting. At a high scan rate of 500 mV/s, two steps of reversible one-electron, one-proton reduction/oxidation corresponding to the cis-isomer in azobenzene-thiol SAMs (n is odd) was clearly observed between +300 and -200 mV. The apparent electron-transfer rate is decreased with increasing distance between the azobenzene redox center and the gold electrode. The existence of the end acetamino group which restricted the conformational change during the redox process also led to a decrease of the standard rate constant, and this restriction effect is more predominant than the distance effect. 相似文献