On-Demand Local Modification of High-Tc Superconductivity in Few Unit-Cell Thick Bi2Sr2CaCu2O8+δ

High-temperature superconductors (HTSs) are important for potential applications and for understanding the origin of strong correlations. Bi₂Sr₂CaCu₂O_8+δ (BSCCO), a van der Waals material, offers a platform to probe the physics down to a unit-cell. Guiding the flow of electrons by patterning 2DEGS and oxide heterostructures has brought new functionality and access to new science. Similarly, modifying superconductivity in HTS locally, on a small length scale, is of immense interest for superconducting electronics. A route to modify superconductivity locally by depositing metal on the surface is reported here by transport studies on few unit-cell thick BSCCO. Deposition of chromium (Cr) on the surface over a selected area of BSCCO results in insulating behavior of the underlying region. Cr locally depletes oxygen in CuO₂ planes and disrupts the superconductivity in the layers below. This technique of modifying superconductivity is suitable for making sub-micrometer superconducting wires and more complex superconducting devices.     

Performance Analysis of Microstriplines Interconnect Structure with Novel Guard Trace as Parallel Links for High Speed Dram Interfaces

Wireless communication have progressed so fast in recent years with the increased frequency of operation, faster signal speed, reduced feature size and increased the integration of analog and digital blocks within a constrained space. These made the signal integrity analysis is a challengine task to printed circuit board designers. The signal integrity effects need to be mitigated by the proper design of high speed interconnects. In order to reduce crosstalk and crosstalk induced jitter in high speed parallel links to DRAM interface, a novel parallel microstriplines with U shaped guard trace interconnect structure is proposed. The crosstalk performance of the proposed interconnect structure, it can be implemented in DRAM board and compared with the conventional guard intervening scheme. The proposed structure increased the maximum data rate from 800 Mbps to 3.3 Gbps and reduced CIJ more than 2 ps.

     

SALDEFT: Self-Adaptive Learning Differential Evolution Based Optimal Physical Machine Selection for Fault Tolerance Problem in Cloud

Wireless Personal Communications - In recent years, cloud computing plays a significant role in offering several applications with high-level reliability, availability, and security as well as...     

一种抗污染攻击的传感器网络重编程方法

现有安全重编程方案无法对基于网络编码技术的新一代重编程协议提供安全保护。文章针对上述缺陷,提出了一种抗污染攻击(pollution attacks)的安全重编程方法PRMR(Pollution-ResistantMethod for Reprogramm ing)。该方法利用组合技术实现污染攻击下的编码包正常译码;并通过邻居分类系统隔离污染者(polluters)。TOSSIM仿真实验表明在一个6度的无线传感器网络中,当20%的节点为污染者时,使用PRMR方法,重编程数据分发完成时间仅是无攻击情况下的2倍;每页也仅比无攻击情况下多执行70%的译码。     

Monoclinic β-MoO(3) nanosheets produced by atmospheric microplasma: application to lithium-ion batteries

Porous high surface area thin films of nanosheet-shaped monoclinic MoO(3) were deposited onto platinized Si substrates using patch antenna-based atmospheric microplasma processing. The films were characterized by high resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM) and electrochemical analysis. The electrochemical analysis shows original redox peaks and high charge capacity, and also indicates a reversible electrochemical behaviour particularly beneficial for applications in Li-ion batteries. SEM shows that the films are highly porous and consist of nanosheets 50-100 nm thick with surface dimensions in the micrometre range. HRTEM reveals that the MoO(3) nanosheets consist of the monoclinic beta phase of MoO(3). These intricate nanoarchitectures made of monoclinic MoO(3) nanosheets have not been studied previously in the context of applications in Li-ion batteries and show superior structural and morphological features that enable effective insertion of Li ions.     

Improved phase stability and electrochemical performance of (Y,In,Ca)BaCo3ZnO7+δ cathodes for intermediate temperature solid oxide fuel cells

With an aim to combine the performance-enhancing properties of Ca with the stability-promoting properties of In in the swedenborgite YBaCo₄O_7+δ-based cathodes for solid oxide fuel cells (SOFC), cation-substituted Y_1−x−yIn_xCa_yBaCo₃ZnO_7+δ (0.2 ≤ (x + y) ≤ 0.5) oxides have been explored. All samples presented in this work are stable in air after 120 h exposure to 600, 700, and 800 °C. Increasing In content shows a negligible impact on polarization resistances (R_p), but causes an increase in the activation energies (E_a) of (Y,In,Ca)BaCo₃ZnO_7+δ + Gd_0.2Ce_0.8O_1.9 (GDC) composite cathodes on 8 mol% yttria-stabilized zirconia (8YSZ) electrolyte supported symmetric cells. Increasing Ca content shows a decrease in R_p and an increase in E_a on similar electrochemical cells. All (Y,In,Ca)BaCo₃ZnO_7+δ samples investigated here show superior performance compared to the unsubstituted YBaCo₃ZnO_7+δ + GDC cathode in the range of 400–800 °C. Especially, the Y_0.5In_0.1Ca_0.4BaCo₃ZnO_7+δ + GDC composite cathode exhibits good performance on GDC electrolytes in the range of 400–600 °C. With superior phase stability and electrochemical performance, the (Y,In,Ca)BaCo₃ZnO_7+δ series of oxides are attractive cathode candidates for intermediate temperature SOFCs.     

Novel Collision Detection and Avoidance System for Midvehicle Using Offset-Based Curvilinear Motion

In recent days, the manufacture of automotive vehicles is dramatically enhanced worldwide. Most vehicle crashes are due to the drive distraction on the real highway roads and traffic-density. In this proposed method, a novel collision detection and avoidance algorithm are coined for Midvehicle Collision Detection and Avoidance System (MCDAS), addressing two scenarios, namely, (a) A rear-end collision avoidance with host vehicle under no front-end vehicle condition and (b) offset-based curvilinear motion under critical conditions, while, suitable parallel parking manoeuvring also addressed using offset-based curvilinear motion. The Monte Carlo analysis of the proposed MCDAS is demonstrated using the Constant Velocity (CV) manoeuvring strategy and simulated with real-time data using the NGSIM database.

     

Ultra-Thin Single-Particle-Layer Sodium Beta-Alumina-Based Composite Polymer Electrolyte Membrane for Sodium-Metal Batteries

Inorganic/organic composite polymer electrolytes (CPEs) with good flexibility and electrode contact have been pursued for solid−state sodium-metal batteries. However, the application of CPEs for high energy density solid−state sodium-metal batteries is still limited by the low Na⁺ conductivity, large thickness, and low ion transference number. Herein, an ultra-thin single-particle-layer (UTSPL) composite polymer electrolyte membrane with a thickness of ≈20 µm straddled by a sodium beta−alumina ceramic electrolyte (SBACE) is presented. A ceramic Na⁺-ion electrolyte that bridges or percolates across an ultra-thin and flexible polymer membrane provides: 1) the strength and flexibility from the polymer membrane, 2) excellent electrolyte/electrode interfacial contact, and 3) a percolation path for Na⁺-ion transfer. Owing to this novel design, the obtained UTSPL-35SBACE membrane exhibits a high Na⁺-ion conductivity of 0.19 mS cm⁻¹ and a transference number of 0.91 at room temperature, contributing to long−term cycling stability of symmetric sodium cells with a small overpotential. The assembled quasi-solid-state cell with the as−prepared UTSPL-35SBACE membrane displays superior cycling performance with a discharge capacity of 105 mAh g⁻¹ at 0.5 °C rate after 100 cycles and excellent rate performance (82 mAh g⁻¹ at 5 °C rate) at room temperature with the potassium manganese hexacyanoferrate (KMHCF)@CNTs/CNFs cathode, where KMHCF refers to potassium manganese hexacyanoferrate.     

Facile synthesis of heterostructure NiO–SnO2 nanocomposite for selective electrochemical determination of l-cysteine

Journal of Materials Science: Materials in Electronics - In this present research, heterostructure NiO–SnO2 nanocomposite modified electrode was developed to determine l-cysteine molecule....