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Solid polymer electrolytes with relatively low ionic conductivity at room temperature and poor mechanical strength greatly restrict their practical applications. Herein, we design semi-interpenetrating network polymer (SNP) electrolyte composed of an ultraviolet-crosslinked polymer network (ethoxylated trimethylolpropane triacrylate), linear polymer chains (polyvinylidene fluoride-co-hexafluoropropylene) and lithium salt solution to satisfy the demand of high ionic conductivity, good mechanical flexibility, and electrochemical stability for lithium metal batteries. The semi-interpenetrating network has a pivotal effect in improving chain relaxation, facilitating the local segmental motion of polymer chains and reducing the polymer crystallinity. Thanks to these advantages, the SNP electrolyte shows a high ionic conductivity (1.12 mS cm−1 at 30 °C), wide electrochemical stability window (4.6 V vs. Li+/Li), good bendability and shape versatility. The promoted ion transport combined with suppressed impedance growth during cycling contribute to good cell performance. The assembled quasi-solid-state lithium metal batteries (LiFePO4/SNP/Li) exhibit good cycling stability and rate capability at room temperature.  相似文献   
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Six new complexes: [Ln2(pzda)3(H2O)2] · 2.5H2O (Ln = Nd, (1); Eu, (2)), [Co(pzda) (bpe)] · 0.125(bpe) · 1.75H2O (3), [Mn(pzda)(H2O)1.5] (4), [Co2(pzda)2(bpe)(H2O)4] · 0.5(CH3OH) · H2O (5) and [Co(pzda)(2,2′-bpy)(H2O)] · 0.5H2O (6) (H2pzda = pyrazine-2,6-dicarboxylic acid, bpe = 1,2-bis(4-pyridyl)ethane, 2,2′-bpy = 2,2′-bipyridine) were obtained from metal salts and H2pzda under hydro(solvo)thermal conditions. The single crystal X-ray structural analysis reveals that the title complexes have different structures, ranging from zero- to three- dimensions, which are mainly due to the different metal ions, and especially the coordination modes of the pzda ligands. Complexes 1 and 2 have 3D metal-organic frameworks containing a 1D tri-strand array, in which the pzda ligand adopts a pentadentate mode to link lanthanide ions. Complex 3 has a 2D metal-organic framework, in which the pzda ligand acts in a tetradentate mode to connect Co(II) ions into 1D chains, which are further connected by bpe spacers into a 2D framework. While in 4, both of the two carboxylate groups of the pzda ligand adopt μ2-O bridging modes to link Mn(II) ions into a 1D coordination polymer, which is further assembled into a 2D supramolecular network containing double-stranded hydrogen-bonded helical chains. In both 5 and 6, the pzda ligand binds metal ions as a tridentate ligand (ONO mode) to form zero dimensional structures. Complex 5 is a binuclear molecule, while 6 is a mononuclear complex, which can be attributed to the bridging ligand bpe for 5 and the terminal auxiliary ligand 2,2′-bpy for 6.  相似文献   
3.
Semivalues are shown to exhibit a capability of modification that enables us to introduce additional information in the evaluation of games. After using a general method to design modified versions of the Shapley and Banzhaf values, we apply them to some political, economic and sociological problems.  相似文献   
4.
In this paper, some results concerning the PageRank versatility measure for multiplex networks are given. This measure extends to the multiplex setting the well-known classic PageRank. Particularly, we focus on some spectral properties of the Laplacian matrix of the multiplex and on obtaining boundaries for the ranking value of a given node when some personalization vector is added, as in the classic setting.  相似文献   
5.
Dielectric relaxations of several poly(diitaconate)s with cyclobutyl, cycloheptyl, and cyclooctyl groups in the side chain were investigated. The study was performed by determining the dielectric permittivity and loss, depending on the frequency and temperature. Dynamic dielectric measurements indicated several relaxations according to the chemical structure of the polymers. The dielectric behavior of these polymers was compared with those of poly(dicyclohexyl itaconate), previously reported. The α relaxations were analyzed with the Havriliak–Negami equation. Significant differences in the subglass relaxations were observed. A tentative explanation of the molecular origin of each absorption was proposed in terms of the number of carbon atoms of the ring and their conformational versatility. Strong conductive processes were observed in these polymers at low frequencies and high temperatures. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 1059–1069, 2003  相似文献   
6.
There is a great need for effective transformations and a broad range of novel chemical entities. Continuous‐flow (CF) approaches are of considerable current interest: highly efficient and selective reactions can be performed in CF reactors. The reaction setup of CF reactors offers a wide variety of possible points where versatility can be introduced. This article presents a number of selective and highly efficient gas–liquid–solid and liquid–solid reactions involving a range of reagents and immobilized catalysts. Enantioselective transformations through catalytic hydrogenation and organocatalytic reactions are included, and isotopically labelled compounds and pharmaceutically relevant 1,2,3‐triazoles are synthesized in CF reactors. Importantly, the catalyst bed can be changed to a solid‐phase peptide synthesis resin, with which peptide synthesis can be performed with the utilization of only 1.5 equivalents of the amino acid.

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7.
基于嵌入式技术,设计了一套集控制、测试和分析于一体的伺服综合测控平台。该平台采用集散式结构,在硬件上提供了多种通信与测控接口,软件上以Linux嵌入式操作系统和Windows系统为基础,提供了友好的人机交互界面。可以根据现场状况工作在便携的单机模式或者功能完备的联机模式。平台同时为网络型伺服系统预留了网络接口,有很好的通用性和可扩展性等优点。经测试,该平台操作便捷,运行稳定,可用于多种类伺服系统的测控分析。  相似文献   
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