离子束引起的在Al／Cr双层薄膜界面处的原子混合

用600keV的Kr~ 离子轰击Al/Cr双层薄膜样品进行界面原子反应及相互混合的研究。实验样品是在单晶硅上蒸镀约500nm厚的铝膜,相继再蒸上所需厚度的铬膜而制成的。轰击剂量为2.0×10~(15)-2.5×10~(16)Kr~ /cm~2。用2.0MeVa粒子对轰击前后的样品进行了卢瑟福背散射(RBS)分析,发现界面处有明显的原子混合存在;当轰击剂量≥1.0×10~(16)Kr~ /cm~2时,RBS谱出现有明显的坪台,经拟合计算和x射线衍射(XRD)测量证实确有化合物Al_(13)Cr_2存在;还分别得到了原子混合量及混合效率与轰击剂量的关系;最后对界面处的原子混合机制进行了讨论。     

正则Cosine算子函数的乘积扰动定理

本文研究了正则cosine算子函数的乘积扰动性,在正则化算子C的值域不 一定稠密的一般情形下,获得了若干正则cosine算子函数的乘积扰动定理.     

非线性算子方程变号解的存在性及其应用

本文利用锥理论讨论了非线性算子方程变号解的存在性,并将抽象结果应用于Sturm-Liouville两点边值问题。所得结果无论在理论上还是在应用上都是新的.     

亚直不可约DQrC-环

在文[1]中我们引进了DQ_rC-环,本文给出了忠实的与不忠实的DQ_rC-环为亚直不可约环的充分必要条件.由于DQ_rC-环是比DQC-环更广泛的环类,所以本文推广了W.Burgess等人在DQC-环方面相应的工作.     

两个回归函数相等的Bootstrap检验

两个回归参数相等性检验一直是统计界感兴趣的问题之一．在这篇文章中，四个检验统计量被用于度量两曲线的差异，在原假设下统计量的分布采用向量数据的重复抽样来逼近，并给出了—些模拟结果．     

Birkhoff系统的Poincare—Cartan积分不变量

基于现代微分几何学，分析了作为保守系统和非保守系统的推广－Birkhoff系统的辛结构。构造Birkhoff系统的Poincare-Cartan积分不变量。最后，将一维阻尼振动作为示例，求出其Poincare积分不变量。     

Low Timing Jitter and Tunable Dual-Wavelength Picosecond Pulse Generation from a Fabry--Pérot Laser Diode with External Injection

A novel scheme to generate tunable dual-wavelength optical pulses with low timing jitter at arbitrary repetition rates is proposed and demonstrated experimentally. The pulses are generated from a gain-switched Fabry-Pérot laser diode with two external cw beams for injection seeding simultaneously. The cw light is generated by two independent distributed feedback laser diodes, and their wavelengths can be tuned independently by two temperature controllers. The dual-wavelength pulses with the pulse width of 57 ps, the timing jitter of 340 fs, are obtained. The sidemode-suppression ratio of the output pulses is better than 23dB over a 10-nm wavelength tuning range.     

Probing the Conformational Stability of Two Different Copper Proteins: A Dynamic Fluorescence Study on Azurin and Ascorbate Oxidase

Tryptophan fluorescence is extremely useful to monitor structural conformational transitions in proteins. Denaturant-induced unfolding of azurin and ascorbate oxidase has been studied by dynamic fluorescence measurements in the frequency domain and the results have been interpreted in terms of continuous distribution of lifetimes. The data add new information on the unfolding mechanism that was previously analyzed by steady-state emission spectroscopy. In particular, the existence of multiple, parallel unfolding pathways may be envisaged and correlated, in both cases, to the two protein structures. The effect of metal depletion has been also characterized by fluorescence lifetime measurements. In the case of azurin, a monomeric protein, the data demonstrate that copper removal yields a totally different unfolding pathways with respect to the holo protein, indicating that metal ion plays a fundamental structural role in the wild type, native protein. In the case of ascorbate oxidase a dimer of 140 kDa, only minor effects have been detected by copper removal. However, the analysis of the fluorescence decay in presence of different amounts of guanidinium hydrochloride gives new important insights on the unfolding intermediates. In particular the data support the hypothesis of a partial exposure of an outer layer of dimer at intermediate denaturant concentration. This ability of dynamic fluorescence to pinpoint the presence of structural micro-heterogeneity in the unfolding pathways of proteins demonstrates the greater power of this technique compared to the most commonly used steady-state measurements.     

Effect of nitrogen surface doping on the work function and field emission of hydrogenated amorphous carbon films

The effect of nitrogen surface doping on the electron field emission characteristics of hydrogenated amorphous carbon films was studied. It was found that the emission threshold electric field decreased after nitrogen surface doping which indicated the reduction of the emission barrier at the film surface. It was demonstrated that this improvement arose from the decrease of the effective work function due to the formation of a dipole layer induced by chemical termination and chemical structural change on the film surface. PACS 52.75.Xx; 73.30 +y; 73.61.Jc     

The K<Superscript>-</Superscript>α scattering length and the reaction dd↦αK<Superscript>+</Superscript>K<Superscript>-</Superscript>

We present predictions for the K^-α scattering length obtained within the framework of the multiple-scattering approach. Evaluating the pole position of the K^-α scattering amplitude within the zero-range approximation, we find a loosely bound K^-α state with a binding energy of E_R = - 2,..., - 7 MeV and a width Γ_R = 11,..., 18 MeV. We propose to measure the K^-α scattering length through the final-state interaction between the α and K^--meson produced in the reaction dd↦αK⁺K^-. It is found that the K^-α invariant-mass distribution from this reaction at energies near the threshold provides a new tool to determine the s-wave K^-α scattering length.