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101.
Jin Zhang Weiwei Lei Jurg Schutz Dan Liu Bin Tang Chun H. Wang Xungai Wang 《Journal of Polymer Science.Polymer Physics》2019,57(7):406-414
New multifunctional materials with both high structural and gas barrier performances are important for a range of applications. Herein we present a one‐step mechanochemical process to prepare molybdenum disulfide (MoS2) nanosheets with hydroxy functional groups that can simultaneously improve mechanical strength, thermal conductivity, and gas permittivity of a polymer composite. By homogeneously incorporating these functionalized MoS2 nanosheets at low loading of less than 1 vol %, a poly(vinyl alcohol) (PVA) polymer exhibits elongation at break of 154%, toughness of 82 MJ/m3, and in‐plane thermal conductivity of 2.31 W/m K. Furthermore, this composite exhibits significant gas barrier performance, reducing the permeability of helium by 95%. Under fire condition, the MoS2 nanosheets form thermally stable char, thus enhancing the material's resistance to fire. Hydrogen bonding has been identified as the main interaction mechanism between the nanofillers and the polymer matrix. The present results suggest that the PVA composite reinforced with 2D layered nanomaterial offers great potentials in packaging and fire retardant applications. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 406–414 相似文献
102.
Yu Xue Zexu Xue Wenwen Zhang Wenna Zhang Shuai Chen Kaiwen Lin Jingkun Xu 《Journal of polymer science. Part A, Polymer chemistry》2019,57(10):1041-1048
By employing planar thieno[3,2‐b]thiophene (TT) as end‐capped units and famous 3,4‐ethylenedioxythiophene (EDOT) or its all‐sulfur analog 3,4‐ethylenedithiathiophene (EDTT) as cores, two conjugated oligomer, TT‐EDOT‐TT and TT‐EDTT‐TT, have been synthesized and electropolymerized into electrochromic polymer films, P(TT‐EDOT‐TT) and P(TT‐EDTT‐TT), respectively. Due to strongly noncovalent inter/intramolecular interactions from S? S attraction of TT‐EDTT‐TT, it has twisted molecular configuration in contrast to planar TT‐EDOT‐TT. Spectroscopic, electrochemical, morphological as well as theoretical calculation studies of these oligomers or polymers were carried out to reveal the significant influence of such molecular geometry on their physicochemical and optoelectronic properties. According to electrochromic kinetics, P(TT‐EDTT‐TT) presented preferable electrochromic behavior such as the higher optical contrast (70.8%), favorable coloration efficiency (331.3 cm2 C?1) and fast response time (0.72 s). This research will help us deeply understand the effect of spatial organization of precursor molecules on the properties of electrochromic polymers and provides a promising strategy to develop high‐performance electrochromic materials. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 1041–1048 相似文献
103.
Aequationes mathematicae - In this paper we study estimation, continuous dependence and Hyers–Ulam stability for continuous solutions of a second order iterative equation. First we give an... 相似文献
104.
Yu Zhang Dr. Novruz G. Akhmedov Prof. Jeffrey L. Petersen Prof. Carsten Milsmann 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(12):3042-3052
Luminescent seven-coordinated zirconium and hafnium complexes bearing three mono-anionic 2,2′-pyridylpyrrolide ligands and one chloride were synthesized. Solid-state structures and the dynamic behaviors in solution were probed by X-ray crystallography and variable temperature 1H NMR experiments, respectively. Absorption spectroscopy and time-dependent density functional theory (TD-DFT) calculations supported a hybrid of ligand-to-metal charge transfer (LMCT)/ligand-to-ligand charge transfer (LLCT) for the visible light absorption band. The complexes (MePMPMe)3MCl (M=Zr, Hf, MePMPMe=3,5-dimethyl-2-(2-pyridyl)pyrrolide) are emissive in solution at room temperature upon irradiation with visible light due to a combination of phosphorescence and fluorescence characterized by excited state lifetimes in the μs and low to sub-ns timescale, respectively. Electrochemical experiments revealed that the zirconium complex possesses a reversible redox event under highly reducing condition (−2.29 V vs. Fc+/0). 相似文献
105.
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107.
Dr. Xiang-Yang Liu Yi-Jie Zhang Xiyu Fei Prof. Man-Keung Fung Prof. Jian Fan 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(27):6788-6796
Spirocyclic compounds such as 9,9′-spirobifluorene (SBF) are becoming more and more attractive for use as host materials in organic optoelectronic devices. Herein, two dispirocycles, namely, dispiro[fluorene-9,9′-anthracene-10′,9′′-fluorene] and 10,10′′-diphenyl-10H,10′′H-dispiro[acridine-9,9′-anthracene-10′,9′′-acridine], were used for the construction of host materials 1 – 4 . The attached triphenylamino group determines the thermal, photophysical, electrochemical, and charge-transport properties, and therefore they have different electroluminescent performances. The device based on dispiro[fluorene-9,9′-anthracene-10′,9′′-fluorene] ( 2 ) and 10,10′′-diphenyl-10H,10′′H-dispiro[acridine-9,9′-anthracene-10′,9′′-acridine] ( 3 ) molecular platforms exhibited external quantum efficiencies of greater than 21 % with a very high power efficiency (≈100 lm W−1). These results demonstrate the potential of extending the application of dispirocyclic molecular platforms with inherent rigidity for developing highly efficient host materials for organic light-emitting diodes. 相似文献
108.
Chen Qinlei Xia Zhengbin Zhang Yanhong Wang Shumin 《Journal of Solid State Electrochemistry》2019,23(12):3399-3408
Journal of Solid State Electrochemistry - Polyaniline/diazonium salt/TiO2 nanotube arrays (PANI/DZ/TiO2 NAs), as a supercapacitor electrode material, are fabricated by two-step anodic oxidation of... 相似文献
109.
Dr. Longhai Zhang Prof. Tong Wei Dr. Zimu Jiang Prof. Zhuangjun Fan 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(19):5022-5027
To optimize the cycle life and rate performance of lithium-ion batteries (LIBs), ultra-fine Fe2O3 nanowires with a diameter of approximately 2 nm uniformly anchored on a cross-linked graphene ribbon network are fabricated. The unique three-dimensional structure can effectively improve the electrical conductivity and facilitate ion diffusion, especially cross-plane diffusion. Moreover, Fe2O3 nanowires on graphene ribbons (Fe2O3/GR) are easily accessible for lithium ions compared with the traditional graphene sheets (Fe2O3/GS). In addition, the well-developed elastic network can not only undergo the drastic volume expansion during repetitive cycling, but also protect the bulk electrode from further pulverization. As a result, the Fe2O3/GR hybrid exhibits high rate and long cycle life Li storage performance (632 mAh g−1 at 5 A g−1, and 471 mAh g−1 capacity maintained even after 3000 cycles). Especially at high mass loading (≈4 mg cm−2), the Fe2O3/GR can still deliver higher reversible capacity (223 mAh g−1 even at 2 A g−1) compared with the Fe2O3/GS (37 mAh g−1) for LIBs. 相似文献
110.
Nonlinear Dynamics - In this paper, the current-controlled DC–DC buck converter from a new perspective are studied through the switching theory of flow, and the analytical conditions of the... 相似文献