Non-equilibrium dynamics for impurities in semiconductors

This paper summarizes the ‘first-principles’ calculations of the vibrational properties of impurities, which are critical to the optical identification of defects. The issue of temperature control for non-equilibrium molecular dynamics (NEMD) is discussed. Applications of NEMD include the calculations of the temperature-dependence of vibrational lifetimes and of the thermal conductivity of semiconductors as a function of their impurity content.     

m次幂等矩阵的等价条件

利用矩阵的秩和齐次线性方程组解空间的维数,给出了m(m≥2)次幂等矩阵的一些等价条件,推广了2,3次幂等矩阵的相应结果.此外,所获结果还给推广到了m次幂等线性变换中.     

Orientational order parameter studies on 3.Om and 3O.Om liquid crystals

Orientational order parameter S is evaluated in the nematic phase of six liquid crystal compounds, N-(p-n-propyl benzylidene)-p-n-alkoxy anilines, 3.Om and N-(p-n-propyloxy benzylidene)-p-n-alkoxy anilines, 3O.Om compounds with m = 6, 7 and 8, using different methods. The techniques employed are S from birefringence δn, Haller's approximation from (1?T/T_c) ^β, effective geometry parameter α_g and Vuks’ scaling factor S_C. The values of S obtained using the above methods are compared with one another and with the results on a number of liquid crystals; the liquid crystals favor isotropic Vuks’ method.     

环状硅酸盐图的友好指数集

Let G be a graph with vertex set V(G) and edge set E(G). A labeling f : V(G) →Z2 induces an edge labeling f*: E(G) → Z2 defined by f*(xy) = f(x) + f(y), for each edge xy ∈ E(G). For i ∈ Z2, let vf(i) = |{v ∈ V(G) : f(v) = i}| and ef(i) = |{e ∈ E(G) : f*(e) =i}|. A labeling f of a graph G is said to be friendly if |vf(0)- vf(1)| ≤ 1. The friendly index set of the graph G, denoted FI(G), is defined as {|ef(0)- ef(1)|: the vertex labeling f is friendly}. This is a generalization of graph cordiality. We investigate the friendly index sets of cyclic silicates CS(n, m).     

DS-SS/EBPSK调制的码分多址研究

为了实现直序扩频扩展的二元相移键控(DS-SS/EBPSK)调制的多址通信,研究了一种DS-SS/EBPSK调制的码分多址实现方法.首先对DS-SS/EBPSK调制信号进行分析,公式化表述了DS-SS/EBPSK的调制过程,得到了可用于解扩和码分多址的等效扩频序列;在此基础上,设计了相关接收机对DS-SS/EBPSK调制信号进行检测,利用不同用户扩频序列互相关很小的特点实现多址传输;最后以m序列为例,仿真了期望用户的误码性能与用户数量和m序列周期长度的关系.仿真结果验证了此种码分多址实现方式的可行性,同时也表明多用户的于扰程度取决于扩频序列之间的互相关性.     

改进谱聚类算法在MCI患者检测中的应用研究

为了利用功能核磁影像（fMRI, functional magnetic resonance imaging）数据进行轻度认知障碍（MCI, mild cognitive impairment）自动检测,对患者的fMRI数据进行聚类分析,得到患者大脑血氧依赖水平(BOLD, blood oxygen level dependence)的变化模式,并将异常模式用于疾病检测中。由于传统谱聚类算法需要计算相似矩阵所有的特征值和特征向量、时间与空间复杂度较高。提出一种改进的谱聚类方法,在相似矩阵的构造以及σ与k值的确定等方面进行了改进,将其用于MCI fMRI数据的聚类与诊断研究中。与传统谱聚类及Nystr?m算法进行的对比实验结果表明,改进的谱聚类方法可以更准确得到患者异常BOLD模式,分类正确率较高,且时间和空间复杂度均小于传统算法。     

基于0.35μm CMOS工艺的APD器件仿真分析

提出了一种基于0.35μm CMOS工艺的、具有p+/n阱二极管结构的雪崩光电二极管(APD),器件引入了p阱保护环结构.采用silvaco软件对CMOS-APD器件的关键性能指标进行了仿真分析.仿真结果表明:p阱保护环的应用,明显降低了击穿电压下pn结边缘电场强度,避免了器件的提前击穿.CMOS APD器件的击穿电压为9.2V,工作电压下响应率为0.65 A/W,最大内部量子效率达到90％以上,响应速度能够达到6.3 GHz,在400～900 nm波长范围内,能够得到很大的响应度.     

大直径重掺硅单晶工艺研究

重掺单晶一些独有的特性,能有效解决目前集成电路面临的一些难题。对大直径重掺硅单晶生长过程中的一些工艺进行了研究,主要包括掺杂方式和拉速设定两个方面,通过实验分析,选取了适宜的掺杂方式与拉速,最终生长出外形良好,符合电阻率目标要求的单晶。     

Green ultra‐fast high‐performance liquid chromatographic method using a short narrow‐bore column packed with fully porous sub‐2 μm particles for the simultaneous determination of selected pharmaceuticals as surface water and wastewater pollutants

Fast separations are very desirable in laboratories that analyze large numbers of samples per day or those needing short turn‐around times. Traditional HPLC methods using conventional stationary phases and standard column dimensions require significant amounts of organic solvents and generate large volumes of waste. With growing awareness about the environment, the development of green technologies has been receiving increasing attention. In this work, a very fast green analytical method based on LC‐UV using a short narrow bore column packed with fully porous sub‐2 μm particles has been developed for simultaneous determination of nine pharmaceuticals in wastewater and surface water. The chromatographic separation was optimized in order to achieve short analysis time and good resolution for all analytes in a single run. All analytes could be separated in 1 min with good resolution. Sample preparation was executed by solid phase extraction using Oasis HLB cartridges. The method developed was validated based on parameters such as linearity, precision, accuracy, detection, and quantification limits. The recovery ranged from 70.9 to 92.5% with SDs not higher than 5.4%, except for acetaminophen and sulphanilamide. LODs ranged from 0.6–2.5 μg/L, while the LOQs were in the range 2–8 μg/L.     

Quantification of L‐ergothioneine in whole blood by hydrophilic interaction ultra‐performance liquid chromatography and UV‐detection

A new hydrophilic interaction ultra‐performance LC method was established for the whole blood measurement of L‐ergothioneine. Chromatographic separation was achieved in a fairly short time, less than 4 min, on a 100 × 2.1 mm Acquity UPLC BEH HILIC 1.7 μm column with a mobile phase consisting of a mixture of 100 mmol/L ammonium acetate/ACN/water (5:85:10, v/v/v) that flowed isocratically at 0.250 mL/min. The LOD and the limit of quantification were 3.85 and 11.67 μmol/L, respectively. The method exhibited linearity in a concentration range of 15.63–1000 μmol/L (R² > 0.999). Mean recovery was 96.34% whereas intraassay and interassay precision were 1.52 and 1.82% RSD, respectively. On the whole, the developed method is simple, fast, precise, accurate, and sensitive and may be useful for routine analyses.