基于DSP的光纤捷联惯导系统设计与实现

介绍了一种基于DSP的光纤陀螺捷联惯导系统的设计与实现方法;系统采用DSP+MCU的体系结构,DSP主要完成导航计算,利用单片机实现对数据采集模块的控制,并通过双口RAM实现单片机和DSP的数据通信,构成了一套小型捷联惯导系统,同时给出了一种捷联惯导算法编排,简要介绍了SPI通信和TMS320C6713的二次bootloder方式;经测试,系统速度和精度都满足了设计要求,已应用于实际系统。     

内存数据库一种紧凑的存储结构

文章分析和研究了当前针对内存数据库的存储结构,提出了索引与记录相结合的存储结构,通过索引与记录数据的结合存储,以提高内存数据库存储空间利用率和操作的效率。     

一种基于完全独立集的排课算法

班级、教师、课程、教室、时间是课表的基本要素,通过把排课转化为求图的完全独立集,解决了时间冲突问题和合班课问题;根据教室资源限制,对独立集的个数和大小进行控制,解决了教室完全匹配问题和一门课程的不同教室安排问题.为实现排课软件提供了一个面向实际的算法.     

Stabilizing Redox-Active Hexaazatriphenylene in a 2D Conductive Metal–Organic Framework for Improved Lithium Storage Performance

Organic redox-active materials are promising electrode candidates for lithium-ion batteries by virtue of their designable structure and cost-effectiveness. However, their poor electrical conductivity and high solubility in organic electrolytes limit the device's performance and practical applications. Herein, the π-conjugated nitrogen-containing heteroaromatic molecule hexaazatriphenylene (HATN) is strategically embedded with redox-active centers in the skeleton of a Cu-based 2D conductive metal–organic framework (2D c-MOF) to optimize the lithium (Li) storage performance of organic electrodes, which delivers improved specific capacity (763 mAh g⁻¹ at 300 mA g⁻¹), long-term cycling stability (≈90% capacity retention after 600 cycles at 300 mA g⁻¹), and excellent rate performance. The correlation of experimental and computational results confirms that this high Li storage performance derives from the maximum number of active sites (CN sites in the HATN unit and CO sites in the CuO₄ unit), favorable electrical conductivity, and efficient mass transfer channels. This strategy of integrating multiple redox-active moieties into the 2D c-MOF opens up a new avenue for the design of high-performance electrode materials.     

Lightweight deep learning methods for panoramic dental X-ray image segmentation

Neural Computing and Applications - Dental X-ray image segmentation is helpful for assisting clinicians to examine tooth conditions and identify dental diseases. Fast and lightweight segmentation...     

Avoiding negative elastic moduli when using Lagrange interpolation for material grading in finite element analysis

Polynomial interpolations, one of the most common interpolations used in finite element methods (FEMs), are a workhorse of many FEM codes. These interpolations are readily available for all kinds of elements, and using them for modeling the variation of elastic moduli in graded elements is thus both convenient and natural. Yet, like all polynomial interpolations, they can be prone to oscillations that can result in regions of negative elastic modulus in the element, even with only positive nodal values of elastic moduli. The result of these negative modulus regions, even if the region is small, can be unexpected singularities in the solution. This defeats the purpose of using polynomial interpolations for capturing material grading in the element. We demonstrate the issue using three-node quadratic Lagrange interpolations of material grading in otherwise isoparametric p-type elements and show how to avoid this problem.     

Array SSL VPN如何保障番禺有线办公网的安全运行

企业办公自动化系统的应用十分广泛,随着互联网的高速发展,WEB应用成为主流,OA系统在互联网上的延伸成为大趋势,本文阐述在WEB应用中如何保障数据和系统安全的手段和方法。     

Structures and spectroscopic properties of nonperipherally and peripherally substituted metal-free phthalocyanines: a substitution effect study based on density functional theory calculations

The molecular structures, molecular orbitals, atomic charges, electronic absorption spectra, and infrared (IR) and Raman spectra of a series of substituted metal-free phthalocyanine compounds with four (1, 3, 5, 7) or eight (2, 4, 6, 8) methoxyl (1, 2, 5, 6) or methylthio groups (3, 4, 7, 8) on the nonperipheral (1-4) or peripheral positions (5-8) of the phthalocyanine ring are studied by density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations. The calculated structural parameters and simulated electronic absorption and IR spectra are compared with the X-ray crystallography structures and the experimentally observed electronic absorption and IR spectra of the similar molecules, and good agreement between the calculated and experimental results is found. The substitution of the methoxyl or methylthio groups at the nonperipheral positions of the phthalocyanine ring has obvious effects on the molecular structure and spectroscopic properties of the metal-free phthalocyanine. Nonperipheral substitution has a more significant influence than peripheral substitution. The substitution effect increases with an increase in the number of substituents. The methylthio group shows more significant influence than the methoxyl group, despite the stronger electron-donating property of the methoxyl group than the methylthio group. The octa-methylthio-substituted metal-free phthalocyanine compounds have nonplanar structures whose low-lying occupied molecular orbitals and electronic absorption spectra are significantly changed by the substituents. The present systematical study will be helpful for understanding the relationship between structures and properties in phthalocyanine compounds and designing phthalocyanines with typical properties.