Ultrahigh‐Working‐Frequency Embedded Supercapacitors with 1T Phase MoSe2 Nanosheets for System‐in‐Package Application

Commercial aluminium electrolyte capacitors (AECs) are too large for integration in future highly integrated electronic systems. Supercapacitors, in comparison, possess a much higher capacitance per unit volume and can be embedded as passive capacitors to address such challenges in electronics scaling. However, the slow frequency response (<10¹ Hz) typical of supercapacitors is a major hurdle to their practical application. Here, it is demonstrated that 1T‐phase MoSe₂ nanosheets obtained by laser‐induced phase transformation can be used as an electrode material in embedded micro‐supercapacitors. The metallic nature of MoSe₂ nanosheet‐based electrodes provides excellent electron‐ and ion‐transport properties, which leads to an unprecedented high‐frequency response (up to 10⁴ Hz) and cycle stability (up to 10⁶ cycles) when integrated in supercapacitors, and their power density can be ten times higher than that of commercial AECs. Furthermore, fabrication processes of the present device are fully compatible with system‐in‐package device manufacturing to meet stringent specifications for the size of embedded components. The present research represents a critical step forward in in‐package and on‐chip applications of electrolytic capacitors.     

Laminated Modulation of Tricritical Ferroelectrics Exhibiting Highly Enhanced Dielectric Permittivity and Temperature Stability

Ferroelectric materials with large dielectric response and high temperature‐stability have found significant applications in advanced electronics and electrical power/storage equipment. The effective approaches explored up to now mainly focus on improving dielectric response by employing the phase instability caused by the ferroelectric transition. Nevertheless, one inherent shortcoming is that the enhancement of dielectric permittivity is at the expense of the deterioration of its temperature stability. Here, a strategy that successfully achieves both enhanced dielectric response as well as excellent temperature reliability (with ε_r ≈ 2 × 10⁴ from 30 to 85 °C) by designing a laminated structure of tricritical ferroelectrics (LTF) with successive Curie temperatures is proposed. Moreover, the improvement in dielectric performance triggers the temperature‐stable energy‐storage performance as well as electrocaloric property in LTF specimens. Further microstructure investigation and phase‐field modeling reveal that these remarkable properties of laminated layers originate from the successive occurrence of tricritical transition with a nanodomain structure in a wide temperature range. The findings may shed a new light on developing advanced ferroelectrics with high performance and thermal reliability.     

Evaluation Method of Classroom Teaching Effect Under Intelligent Teaching Mode

Mobile Networks and Applications - In order to improve the accuracy and performance of classroom teaching effect evaluation, an intelligent teaching mode classroom teaching effect evaluation method...     

基于RFID高校运动会信息管理系统实现

为了便于高校运动会中信息的管理,提出了基于RFID高校运动会的信息管理系统。本文分析了高校运动会信息管理系统的需求,设计了基于RFID运动会信息管理的整体系统,并详细设计了识别系统即RFID系统。     

基于SKOS的知识管理研究

文章首先介绍了SKOS和SKOS Core的基本概念,然后深入探讨了SK0S在数字图书馆知识管理中的若干关键问题.这些问题包括:基于SKOS的Web资源通用框架、词表映射框架、规范网络语义描述、推进数字图书馆知识组织语义互联等四个方面.     

考虑钟差修正的脉冲星与多普勒差分组合导航

为了提高导航系统长时间航行的导航精度和钟差修正能力, 提出了一种钟差修正的X射线脉冲星与多普勒差分组合导航方法.X射线脉冲星导航(X-ray pulsar navigation, XPNAV)使用脉冲到达时间作为导航量测量, 多普勒差分导航测量两个时刻航天器相对于太阳的多普勒速度, 并将两个多普勒速度的差值作为导航的量测量, 这里采用两个多普勒速度的差值可避免多普勒速度偏差; 在此基础上, 将星载时钟钟差增广为新的状态变量, 建立组合导航系统, 使用联邦无迹卡尔曼滤波器(unscented Kalman filter, UKF)融合导航信息.仿真结果表明, 该方法可以抑制多普勒速度偏差对导航的影响, 控制星载时钟钟差, 并提供更高的导航估计精度.     

Ternary Emission of Fluorescence and Dual Phosphorescence at Room Temperature: A Single‐Molecule White Light Emitter Based on Pure Organic Aza‐Aromatic Material

Herein, a simple aza‐aromatic compound dibenzo[a,c]phenazine (DPPZ), which exhibits single‐molecule white light with a ternary emission, consisting of simultaneous fluorescence (S₁→S₀) and dual room‐temperature phosphorescence (RTP, T₂→S₀ and T₁→S₀) is reported. The Commission Internationale de l' Éclairage coordinates of DPPZ powder are (0.28, 0.33). To everyone's knowledge, this is the first case to achieve single‐molecule white emission with ternary emission of fluorescence and dual RTP. This finding provides a prototype strategy to realize low‐cost, stable pure organic single‐molecule white light emission with three standard primary colors through further precise modulation of excited states.