光学全交叉网络与SW榕树（F＝S＝2）网络拓扑等价的多样性

本文对有关互连网络拓扑等价的分析方法作了简单评述。并采用互连网络拓扑等价的图分析法分析了自由空间光学互连全交叉网络与ＳＷ榕树网络的拓扑等价及其多样性，拓展了全交叉网络在数字光计算、光子交换及多处理机系统的潜在应用。     

Distributed Rule-Regulated Spectrum Sharing

Dynamic spectrum access is a promising technique to use spectrum efficiently. Without being restricted to any prefixed spectrum bands, nodes choose operating spectrum on-demand. Such flexibility, however, makes efficient and fair spectrum access in large-scale networks a great challenge. Prior work in this area focused on explicit coordination where nodes communicate with peers to modify local spectrum allocation, and may heavily stress the communication resource. In this paper, we introduce a distributed spectrum management architecture where nodes share spectrum resource fairly by making independent actions following spectrum rules. We present five spectrum rules to regulate node behavior and maximize system fairness and spectrum utilization, and analyze the associated complexity and overhead. We show analytically and experimentally that the proposed rule-based approach achieves similar performance with the explicit coordination approach, while significantly reducing communication cost.     

An algorithm for three-way data analysis that alternatively minimizes coupled vector (COV) resolution error and PARAFAC error.

A novel algorithm, alternatively minimizing coupled vector (COV) resolution error and PARAFAC error algorithm, is proposed in this paper. This algorithm can overcome the problem of slow convergence and is insensitive to the estimation of component number, such problems are unavoidable while using the traditional parallel factors analysis (PARAFAC) algorithm. In other words, this algorithm is capable of improving the computing speed and providing accurate resolutions provided that the number of factors used in the computation is no less than that of the actual underlying ones. The characteristic performances were demonstrated with a novel fluorescence data array.     

地方时与区时在电离层研究中的差异

本文指出混淆地时与区时两个时间概念在电离层研究中带来的差异的严重性，建议使用地方与区时这两个名词，而抛弃“本地时”和“当地时”等容易引起混淆的名词。     

Least squares approach in measurement-dependent filtering for selective medical images

An image-processing method called measurement-dependent filtering has been introduced to improve the SNR (signal-to-noise ratio) of selective images produced by various medical imaging systems. The basic algorithm involves the combination of the low-frequency information of the selective image with the high-frequency information of a nonselective image. A spatially variant control function modulates the amount of high frequency to be added at each point. A least-mean-square (LMS) control function formed from two basis images, namely the high-passed versions of the nonselective image (M(b)) and the selective image (S(b)), is introduced. The original algorithm is now viewed as a two-stage filtering method, including the low-pass filtering noise reduction and least squares filtering for the edge restoration. An appropriate linear transformation is used to convert the original basis images M(b) and S(b) into a new pair with orthogonal noise. This allows the implementation of the LMS and control function with practically obtainable a priori knowledge.     

Coriatone and corianlactone, two novel sesquiterpenes from Coriaria nepalensis

Both coriatone (1). a novel highly oxygenated picrotoxane-type sesquiterpene, and corianlactone (2). with an unprecedented sesquiterpene basic skeleton, named coriane, were isolated from Coriaria nepalensis Wall. The structures of 1 and 2 were determined by analysis of their two-dimensional NMR data, and the structure of 2 was confirmed by X-ray analysis. Compounds 1 and 2 showed no remarkable inhibitory activity toward K(562) cells. They are cytotoxic with IC(50) > 50 microg/mL (cis-platinim: IC(50) = 0.49 microg/mL).     

Microstructure of sputtered epitaxial Ni0.80Fe0.20/NixCO1−xO exchange coupled bilayers on α-Al2O3 (0001)

Epitaxial Ni_0.80Fe_0.20/Ni_xCo_1−xO bilayers have been grown on α-Al₂O₃ (0001) substrates by dc-sputtering X-ray diffraction and transmission electron microscopy have been employed to characterize these exchange-coupled films. The x-ray diffraction spectrum shows only the (111) family of peaks in both Ni_0.80Fe_0.20 and Ni_xCO_1−xO films. Growth orientation relationships have been determined from diffraction patterns taken in planar view and cross section. The relationships are: (111) Ni_0.80Fe_0.20//(111) Ni_xCo_1−xO//(0001) α−Al₂O₃ and [1 0]Ni_0.80FE_0.20//[1 0]Ni_xCo_1-xO//[1 00] α-Al₂O₃. The microstructure of these films as well as the interfacial structure between Ni_0.80Fe_0.20 and Ni_xCo_1−xO have been analyzed in high resolution electron microscopy and are described in this paper. In addition, the dependence of the exchange coupling field on interfacial roughness is discussed.     

Single-Atom Metal Sites Anchored Hydrogen-Bonded Organic Frameworks for Superior “Two-In-One” Photocatalytic Reaction

Photoredox catalysis is a green solution for organics transformation and CO₂ conversion into valuable fuels, meeting the challenges of sustainable energy and environmental concerns. However, the regulation of single-atomic active sites in organic framework not only influences the photoredox performance, but also limits the understanding of the relationship for photocatalytic selective organic conversion with CO₂ valorization into one reaction system. As a prototype, different single-atomic metal (M) sites (M²⁺ = Fe²⁺, Co²⁺, Ni²⁺, Cu²⁺, and Zn²⁺) in hydrogen-bonded organic frameworks (M-HOF) backbone with bridging structure of metal-nitrogen are constructed by a typical “two-in-one” strategy for superior photocatalytic C N coupling reactions integrated with CO₂ valorization. Remarkably, Zn-HOF achieves 100% conversion of benzylamine oxidative coupling reactions, 91% selectivity of N-benzylidenebenzylamine and CO₂ conversion in one photoredox cycle. From X-ray absorption fine structure analysis and density functional theory calculations, the superior photocatalytic performance is attributed to synergic effect of atomically dispersed metal sites and HOF host, decreasing the reaction energy barriers, enhancing CO₂ adsorption and forming benzylcarbamic acid intermediate to promote the redox recycle. This work not only affords the rational design strategy of single-atom active sites in functional HOF, but also facilitates the fundamental insights upon the mechanism of versatile photoredox coupling reaction systems.     

A 2.20 eV Bandgap Polymer Donor for Efficient Colorful Semitransparent Organic Solar Cells

Semitransparent organic solar cells (ST-OSCs) have attracted increasing attention due to their promising prospect in building-integrated photovoltaics. Generally, efficient ST-OSCs with good average visible transmittance (AVT) can be realized by developing active layer materials with light absorption far from the visible light range. Herein, the development of ultrawide bandgap polymer donors with near-ultraviolet absorption, paired with near-infrared acceptors, is proposed to achieve high-performance ST-OSCs. The key points for the design of ultrawide bandgap polymers include constructing donor–donor type conjugated skeleton, suppressing the quinoidal resonance effect, and minimizing the twist of conjugated skeleton via noncovalent conformational locks. As a proof of concept, a polymer named PBOF with an optical bandgap of 2.20 eV is synthesized, which exhibited largely reduced overlap with the human eye photopic response spectrum and afforded a power conversion efficiency (PCE) of 16.40% in opaque device. As a result, ST-OSCs with a PCE over 10% and an AVT over 30% are achieved without optical modulation. Moreover, colorful ST-OSCs with visual aesthetics can be achieved by tuning the donor/acceptor weight ratio in active layer benefiting from the ultrawide bandgap nature of PBOF. This study demonstrates the great potential of ultrawide bandgap polymers for efficient colorful ST-OSCs.