编码协作系统准循环重复累积码的联合设计与性能分析

重复累积(RA)码是一种特殊结构的低密度奇偶校验(LDPC)码,不仅具有LDPC码的优点,还能实现差分编码。针对LDPC编码协作系统编码复杂度高、时延长的问题,该文引入准循环RA(QC-RA)码,推导出信源节点和中继节点采用的QC-RA码对应的联合校验矩阵,基于公差构造方法设计该联合校验矩阵,并证明该方法设计的联合校验矩阵不存在围长为girth-4, girth-6的短环。理论分析和仿真结果表明,同等条件下该系统比相应点对点系统具有更优异的误码率性能。仿真结果同时表明,与采用一般构造QC-RA码或基于Z型构造QC-RA码相比,采用基于公差构造的联合设计QC-RA码的多信源多中继协作均可获得更高的编码增益。     

基于核密度估计的活动轮廓模型

基于核密度估计的活动轮廓模型如果没有适当的扰动机制,往往不能在弧度突变的边缘上获得较好的收敛结果,且在大噪声环境下鲁棒性较差。针对该问题,提出一个新的代价函数。该函数通过融合边缘映射的曲率信息,改善原算法在突变边缘的收敛效果,降低算法对初始轮廓的依赖。     

基于密度的混合属性数据流聚类算法

数据流聚类分析是当前数据挖掘研究的热点问题,为了克服数据流聚类框架CluStream算法不能处理混合属性数据流的缺陷,提出了基于密度的混合属性数据流聚类算法MCStream.在微聚类中使用面向维度的距离来度量对象之间的相似度,在宏聚类中使用改进的密度聚类算法M-DBSCAN对微簇进行聚类.实验结果表明,MCStream算法能快速有效地处理混合属性数据流聚类问题.     

基于群体智能的思维进化算法设计

针对思维进化算法（ＭＥＡ）没有充分利用公告板信息的问题,结合群体智能的优点,提出基于群体智能的思维进化算法,同时分析其算法的机制,设计利用群体信息共享进行子群体迁徙策略和拥挤浓度控制异化策略,提高了搜索速度,保证了种群的多样性．通过整个群体的总体优化特征体现了寻优方式的实现,使得收敛速度和全局收敛性均达到最好平衡．测试函数寻优及ＰＩＤ 控制器参数整定实验,验证了算法的可行性和高效性．     

基于噪声倒谱阈值频谱估计的语音活动检测

针对低方差频谱估计的语音活动检测(VAD)中Welch频谱估计方法计算量大的问题,提出利用倒谱阈值方法估计VAD中的噪声功率谱.该方法在静音时期为噪声的倒谱设置阈值,利用快速傅里叶变换计算频谱,再更新VAD中的判决阈值.算法复杂度分析与仿真结果表明,该方法的检测性能与Welch方法相当,计算量降低约18%,同时降低整个...     

A resonating rheometer using two polymer membranes for measuring liquid viscosity and mass density

A resonating sensor for mechanical liquid properties facilitating measurements at two different modes of operation is presented. One mode is more sensitive to liquid viscosity the other to mass density. A sample liquid is subjected to time-harmonic shear stress induced by two opposed vibrating polymer membranes. These membranes, placed in an external static magnetic field, carry two conductive paths each. The first path is used to actuate the membranes by means of Lorentz forces while the second acts as a pick-up coil providing an induced voltage representing the movement of the membrane. From the resulting frequency response the liquid's viscosity and mass density can be deduced. This double membrane based setup allows examining the test liquid at adjustable frequencies in the low kilohertz range from 500 Hz to 20 kHz by varying the gap between both membranes. The sensor is suitable, e.g., for low cost handheld devices with inline capabilities and disposable sensor elements for measuring Newtonian liquids such as, e.g., oils and aqueous solutions.     

一种低密度奇偶校验码矩阵的设计方法

提出一种以硬件实现的各种条件为约束设计准循环的低密度奇偶校验码的校验矩阵方法,以简化硬件结构,采用行列交换及寻找最大平均环提升译码性能的方法。设计码长为1200的校验矩阵,对该矩阵的译码电路进行RTL实现,采用SMIC0.13μm标准CMOS工艺综合实现660Mb/s吞吐率,面积为3.1mm2,以该方法设计的矩阵可用于实现低复杂度的LDPC译码电路。     

基于相对密度的孤立点和边界点识别算法

根据孤立点是数据集合中与大多数数据的属性不一致的数据,边界点是位于不同密度数据区域边缘的数据对象,提出了基于相对密度的孤立点和边界点识别算法(OBRD)。该算法判断一个数据点是否为边界点或孤立点的方法是:将以该数据点为中心、r为半径的邻域按维平分为2个半邻域,由这些半邻域与原邻域的相对密度确定该数据点的孤立度和边界度,再结合阈值作出判断。实验结果表明,该算法能精准有效地对多密度数据集的孤立点和聚类边界点进行识别。     

Exploring the potential of boron-doped nanographene as efficient charge transport and nonlinear optical material: A first-principles study

Owing to their excellent electrochemical properties, graphenes found applications in several fields ranging from semiconductors, solar cells, field effect transistors, and nanoscale electronic devices as well as in nonlinear optical (NLO) applications. The structural features, electro-optical, charge transport and nonlinear optical properties of the boron-doped graphene (BG) compound 1 were studied using density functional theory methods The BG compound comprises a central electron deficient site of boron atoms, which can serve as electron acceptor while terminal alkoxy groups as donors leading to powerful donor-π-acceptor (D-π-A) configuration. The experimental crystal structure was successfully reproduced by optimized ground state geometry at PBE0/6-311G* level of theory for isolated molecule. The experimental lattice parameters, geometries, crystal presentation and alignment of molecules in the unit cells as well as their packing orientation of BG compound 1 was also efficiently reproduced by applying periodic boundary conditions (PBC) at PBE level. The comprehensive intramolecular charge transfer (CT) was realized from terminal rings of the HOMO to the electron deficient sites of boron atoms of the LUMO. The nature of BG compound 1 might be more towards hole transport even though its hole reorganization energy is twice than that of the electron one due to the significant higher hole transfer integral values. The superior hole transfer integrals and intrinsic mobility values of the BG compound 1 might lead remarkable hole transport contender as compared to many other organic materials. The narrow band gap, density of states profile, dielectric function, uniform conductivity functions and noteworthy electronic as well as CT properties revealed that the BG compound 1 might be proficient optoelectronic contestant having intermolecular CT as well as intramolecular CT with optimal stability. A comparison of static third-order polarizability <γ> of BG compound 1, as calculated in present investigation, was also performed with some standard NLO molecules as well as graphene nanoflakes. Moreover, longitudinal component γ_zzzz of parent compound has been found 12 and 4 times larger than those of previously reported open-shell poly aromatic hydrocarbons (PAH). Interestingly, by increasing the donor ability, i.e., introduction of C₂H₂PhNH₂ groups in place of OC₄H₉ groups (BG compound 3) at terminal positions boosts the <γ> amplitude ∼ 8 times than that of its parent BG compound 1.     

Density functional theory study of adsorption geometries and electronic structures of azo-dye-based molecules on anatase TiO2 surface for dye-sensitized solar cell applications

Structural and electronic properties of eight isolated azo dyes (ArNNAr′, where Ar and Ar′ denote the aryl groups containing benzene and naphthalene skeletons, respectively) were investigated by density functional theory (DFT) based on the B3LYP/6-31G(d,p) and TD-B3LYP/6-311G(d,p) methods The effect of methanol solvent on the structural and electronic properties of the azo dyes was elucidated by employing a polarizable continuum model (PCM). Then, the azo dyes adsorbed onto the anatase TiO₂ (101) slab surface through a carboxyl group. The geometries and electronic structures of the adsorption complexes were determined using periodic DFT based on the PWC/DNP method. The calculated adsorption energies indicate that the adsorbed dyes preferentially take configuration of the bidentate bridging rather than chelating or monodentate ester-type geometries. Furthermore, the azo compounds having two carboxyl groups are coordinated to the TiO₂ surface more preferentially through the carboxyl group connecting to the benzene skeleton than through that connecting to the naphthalene skeleton. The dihedral angles (Φ_B-N) between the benzene- and naphthalene-skeleton moieties are smaller than 10° for the adsorbed azo compounds containing one carboxyl group. In contrast, Φ_B-N > 30° are obtained for the adsorbed azo compounds containing two carboxyl groups. The almost planar conformations of the former appear to strengthen both π-electrons conjugation and electronic coupling between low-lying unoccupied molecular orbitals of the azo dyes and the conduction band of TiO₂. On the other hand, such coupling is very weak for the latter, leading to a shift of the Fermi level of TiO₂ in the lower-energy direction. The obtained results are useful to the design and synthesize novel azo-dye-based molecules that give rise to higher photovoltaic performances of the dye-sensitized solar cells.