菲并咪唑类双极发光材料的合成及其性能

以菲醌、对苯二甲醛、异佛尔酮和丙二腈等为原料,合成了一种新型菲并咪唑类双极发光材料3-(4-(2-菲并咪唑基)苯基)乙烯基-5,5-二甲基-2-环己烯亚基丙二腈(PIPCM)。利用FTIR、1H NMR、UV-Vis、荧光光谱、DSC和电化学等方法对PIPCM的结构、荧光性能、电化学行为及热稳定性进行了研究。实验结果表明,PIPCM溶于二甲基甲酰胺中时发射较强蓝色荧光,而在薄膜状态下发射红色荧光;PIPCM的电子亲和势为2.96 eV,电离势为5.84 eV,因此既具有电子传输性能又具有空穴传输性能;PIPCM的热稳定性优良,是一种具有潜在应用前景的新型双极发光材料。

有机电致发光器件中的新型双极主体材料的合成及应用

设计并合成了一种由咔唑和噁二唑基团构成的,具有双极载流子传导特性的新型主体材料C1PBD。通过对C1PBD的光物理和电化学性能进行研究,证明这种新型的双极主体材料可以用作为蓝色荧光器件的主体材料.利用传统蓝色荧光掺杂材料TBPe,制备了C1PBD作为主体材料的器件,并对其性能进行了表征,器件开启电压约为3.2 V,最大电流效率达到2.26 cd/A,器件表现出稳定的蓝色发光,CIE值稳定在(0.14,0.14),展现了C1PBD作为主体材料的良好性能.

双极绿色磷光主体材料1-甲基-3-[4-(9-咔唑基)苯基]-4-苯基喹啉-2(1H)-酮的合成与性能研究

设计并合成了一种基于喹诺酮衍生物的双极绿色磷光主体材料1-甲基-3-[4-(9-咔唑基)苯基]-4-苯基喹啉-2(1 H)-酮.计算发现,化合物的HOMO轨道的电子云位于咔唑基团,LUMO轨道的电子云位于喹诺酮基团,是一种良好的双极材料.化合物的磷光发射峰为515 nm(2.41 eV),符合绿色磷光主体材料的基本要求(>2.4 eV).热失重和差热分析结果表明,该化合物具有较高的热稳定性,分解温度和玻璃化转变温度分别为312℃和105℃.研究结果表明:该新型化合物是一种潜在的具有双极特性的绿色磷光主体材料.

基于咪唑并吡啶的双极性绿色磷光主体材料合成及其性能

高效的磷光有机电致发光器件有赖于主体材料,而双极性主体材料相对于传统主体材料不仅能降低驱动电压,提高电流效率和功率效率,还能加快载流子迁移率和平衡载流子的通量。因此本文基于咪唑并吡啶设计了两种给体-受体型双极性绿光主体材料,即9-苯基-3-(9-(4-(3-苯基咪唑并[1,2-a]吡啶-2-基)苯基)二苯并[b,d]呋喃-2-基)-9H-咔唑(CzDFDp)和9-苯基-3-(3-(9-(4-(3-苯基咪唑并[1,2-a]吡啶-2-基)苯基)二苯并[b,d]呋喃-2-基)苯基)-9H-咔唑(CzPDFDp),对其结构进行核磁表征。通过光物理研究表明CzDFDp和CzPDFDp具有较高的三线态能级2.8 eV和2.49 eV,和较高的分解(509℃和529℃)与玻璃转化(130℃和138℃)温度,十分有利于磷光器件效率和器件的热稳定提升。以CzDFDp或CzPDFDp为主体、三(4-甲基-2,5-二苯基吡啶)合铱(GD-Ir)为发光掺杂材料制作绿光器件,启亮电压只有2.6 V,最大电流效率分别达到44.9 cd·A^(-1)和47.2 cd·A^(-1),最大功率效率达到50.4 lm·W^(-1)和57 lm·W^(-1),远优于CBP为主体材料参比的器件(3.6 V,14.4 cd·A^(-1),5.8 lm·W^(-1)),两个主体材料的启亮电压降低了1 V,电流效率提高3倍以上,且功率效率提高了8倍以上,表明本文两个双极性主体材料具有良好的传输性质,能够有效地平衡载流子通量,是优异的绿光主体材料。

钛基层状材料在钠离子储能电池中的关键应用

钠元素在地壳中储量丰富,价格低廉,并且具有和锂元素类似的物理化学性质,因而钠离子电池被认为是最有希望商业化的新型储能技术之一。然而,钠离子的半径和质量较大,极大地限制了钠离子的迁移和电化学反应,所以发展新型安全稳定储钠电极材料是提升钠离子电池性能和推动其商业化的关键。在众多的电极材料当中,钛基层状材料具有低价、安全和稳定的特点,是近年来钠离子电池的阴极和阳极材料研究的热点之一。因此,本文综述了钛基层状材料在钠离子电池中的研究现状,包括钛基层状材料作为阳极材料、阴极材料和双极材料等方面,并详细探讨和分析该材料所面临的主要科学问题,最后展望钛基层状材料的未来发展趋势。

1,2-亚乙基桥联咔唑和芳基噁二唑的双极传输材料的合成及光电性能研究

设计合成了三种1,2-亚乙基桥联咔唑和2,5-二芳基-1,3,4-噁二唑衍生物的双极传输材料,并通过核磁氢谱、碳谱、元素分析表征了它们的分子结构,研究了它们的紫外-可见吸收、光致发光、电化学和热稳定等性能.研究结果表明,这类双极传输材料具有咔唑和芳基噁二唑双功能基的紫外可见吸收和光致发光综合特性.热分解温度超过了340℃.与共轭基团桥联咔唑和芳基噁二唑的双极传输材料相比,HOMO/LUMO能级相应地提高,热稳定性能增强.

Effects of polyaniline on electrochemical properties of composite inert anodes used in zinc electrowinning

In order to search for a suitable anode material used in zinc electrowinning in place of Pb-Ag alloy,Al/Pb-PANI（polyaniline）-WC（tungsten carbide） composite inert anodes were prepared on aluminum alloy substrate by double pulse electrodeposition（DPE） of PANI and WC particles with Pb2＋ from an original plating bath.Thereafter,anodic polarization curves,cyclic voltammetry curves and Tafel polarization curves for the composite inert anodes obtained under different PANI concentrations in the original plating bath were measured,and the microstructural features were also investigated by scanning electron microscopy（SEM）.The results show that Al/Pb-PANI-WC composite inert anode obtained under PANI concentration of 20 g/L in the original plating bath possesses uniform microstructures and composition distributions,higher electrocatalytic activity,better reversibility of electrode reaction and corrosion resistance in a synthetic zinc electrowinning electrolyte of 50 g/L Zn2＋,150 g/L H2SO4 at 35 °C.Compared with Pb-1%Ag alloy,the overpotential of oxygen evolutions for the composite inert anode are decreased by 185 mV and 166 mV,respectively,under 500 A/m2 and 1000 A/m2.

Microstructure and mechanical properties of rutile-reinforced AA6061 matrix composites produced via stir casting process

A novel process of fabricating aluminium matrix composites(AMCs)with requisite properties by dispersing rutile particles in the aluminum matrix was studied.A novel bi-stage stir casting method was employed to prepare composites,by varying the mass fractions of the rutile particles as 1%,2%,3%and 4%in AA6061 matrix.The density,tensile strength,hardness and microstructures of composites were investigated.Bi-stage stir casting method engendered AMCs with uniform distribution of the reinforced rutile particles in the AA6061 matrix.This was confirmed by the enhancement of the properties of AMCs over the parent base material.Rutile-reinforced AMCs exhibited higher tensile strength and hardness as compared with unreinforced parent material.The properties of the composites were enhanced with the increase in the mass fraction of the rutile particles.However,beyond 3 wt.%of rutile particles,the tensile strength decreased.The hardness and tensile strength of the AMCs reinforced with 3 wt.%of rutile were improved by 36%and 14%respectively in comparison with those of matrix alone.

Influence of graphite particle size and its shape on performance of carbon composite bipolar plate

Bipolar plates for proton exchange membrane fuel cell (PEMFC) where polymer is used as binder and graphite is used as electric filler were prepared by means of compression molding technology. Study on the effects of graphite particle size and shape on the bipolar plate performance, such as electrical conductivity, strength, etc. showed that with decrease of graphite particle size, bulk electrical conductivity and thermometric conductivity decreased, but that flexural strength was enhanced. After spherical graphite occurrence in flake-like form, the flexural strength of the bipolar plate was enhanced, electrical conductivity increased but thermal conductivity decreased in direction paralleling pressure direction, and both electrical conductivity and thermometric conductivity reduced in direction perpendicular to pressure direction.

Improving electrochemical performance of Ni-rich layered oxide cathodes via one-step dual modification strategy

A one-step overall strategy from surface to bulk was proposed to simultaneously synthesize the Nb-doped and LiNbO_(3)-coated LiNi_(0.83)Co_(0.12)Mn_(0.05)O_(2) cathode materials.The incorporation of LiNbO_(3) coating can regulate the interface and facilitate the diffusion of Li-ions.Simultaneously,the stronger Nb—O bond can effectively suppress Li^(+)/Ni^(2+) cation mixing and strengthen the stability of crystal structure,which helps to mitigate the anisotropic variations of lattice parameters during Li^(+) de/intercalation.The results showed that the dual-modified materials exhibited good structural stability and distinguished electrochemical performance.The optimal NCM-Nb2 sample showed an excellent capacity retention of 90.78%after 100 cycles at 1C rate between 2.7 and 4.3 V,while only 67.90%for the pristine one.Meanwhile,it displayed a superior rate capability of 149.1 mA·h/g at the 10C rate.These results highlight the feasibility of one-step dual modification strategy to synchronously improve the electrochemical performance of Ni-rich layered oxide cathodes.

Aplication of Corncob-Based Activated Carbon as Electrode Material for Electric Double-Layer Capacitors

To investigate the influence of expansion pretreatment for materials on carbon structure, activated carbons （ACs） were prepared from corncob with/without expansion pretreatment by KOH activation, the structure properties of which were determined based on N2 adsorption isotherm at 77 K. The results show that the expansion pretreatment for corncobs is beneficial to the preparation of ACs with high surface area. The specific surface area of the AC derived from corncob with expansion pretreatment （AC-1） is 32.5% larger than that without expansion pretreatment （AC-2）. Furthermore, to probe the potential application of corncob-based ACs in electric double-layer capacitor （EDLC）, the prepared ACs were used as electrode materials to assemble EDLC, and its electrochemical performance was investi- gated. The results indicate that the specific capacitance of AC-I is 276 F/g at 50 mA/g, which increases by 27% com- pared with that of AC-2 （217 F/g）. As electrode materials, AC-1 presents a better electrochemical performance than AC-2, including a higher voltage maintenance ratio and a lower leakage current.

Fabrication of micro-flow channels on graphite composite bipolar plates using microplaning

A new method of manufacturing micro-flow channels on graphite composite bipolar plate(GCBPP) microplaning using specially designed multi-tooth tool is proposed. In this method, several or even dozens of parallel micro-flow channels ranging from 100 μm to 500 μm in width can be produced simultaneously. But, edge chippings easily occur on the rib surface of GCBPP during microplaning due to brittleness of graphite composites. Experimental results show that edge chippings result in the increase of contact resistance between bipolar plate and carbon paper at low compaction force. While the edge chippings scarcely exert influence on the contact resistance at high compaction force. Contrary to conventional view, the edge chippings can significantly improve performance of microfuel cell and big edge chippings outperform small edge chippings. In addition, the influence of technical parameters on edge chippings was investigated in order to obtain big, but not oversized edge chippings.

Study on Electrode Material for Carbon Based Double-layer Capacitors

Activated carbon （AC） was fabricated by using phenolic resin as carbon source, silica gel as inorganic template, KOH as activator. The samples were analyzed by N2 adsorption, scanning electron microscopy （SEM）. Cyclic voltammetry and galvanostatic charge-discharge were used to characterize the electrochemical performance of the samples. The results showed that the pore size was mainly in the range of 0.5 9.0 nm. Supercapacitors based on the sample AC-3 have low equivalent series resistanceb （ESR） and excellent power property.

Investigation on Fracture Behavior of FRP-Concrete Interface under Direct Shear

In this study, the authors reviewed and compared the existing researches on debonding performance of FRP-Concrete Interface under direct shear firstly. Following that, two determinants of the debonding ultimate bearing capacity of FRP-Concrete Interface under pure shear are introduced into this study, namely fracture-resisting force at the undamaged area and friction stress transferred along the already debonded surface. The authors deduced the formulae on fracture energy for FRP-Concrete Interface and obtained the values for fracture energy and friction stress at FRP-Concrete Interface based on the experimental results of eight specimens of FRP-Concrete Interface. On the basis of theoretical frame mentioned above, the authors concluded that the friction-resisting stress transferred along the deteriorated bi-material interface is independent of length of FRP bonded onto concrete substrates and concrete strength, but it relies on the tension rigidity （i.e., the layers of the bonding FRP, it is found that the friction stress declines substantially while the layers of FRP increases bonded to concrete substrate）. On the contrary, cohesive fracture energy is dependent on length of FRP bonded to concrete substrate and the tension stiffness of bi-material interface. In addition, the percentage of the fracture-resisting force in the ultimate debonding load at the interface decreases with the bonding length of FRP increasing, but increases with the increase of the layers of the FRP.

In-situ electropolymerized bipolar organic cathode for stable and high-rate lithium-ion batteries

To address the dissolution issue and enhance the electrochemical performance of organic electrode materials,herein, a bipolar organic cathode was prepared by in-situ electropolymerization of amino-phenyl carbazole naphthalene diimide(APCNDI). APCNDI is composed of n-type 1,4,5,8-naphthalene tetracarboxylic diimide that stores Li cations and p-type carbazole groups which react with anions and serve as polymerization sites. Electropolymerization completely eliminated the dissolution problem of APCNDI, and the electropolymerized cathode demonstrated a bipolar reaction with excellent electrochemical performance, stable cycling performance with a capacity retention of 92 mA h g;after1000 cycles, and a superior rate performance of 72 mA h g;at 10 A g;. The bipolar feature and reactions of APCNDI were systematically investigated and verified by multiple characterization techniques. Our findings provide a novel strategy for the design and fabrication of electrodes for high-performance organic batteries.

A novel composite(FMC)to serve as a durable 3D-clam-shaped bifunctional cathode catalyst for both primary and rechargeable zinc-air batteries

Novel and highly durable air cathode electrocatalyst with three dimensional （3D）-clam-shaped structure, MnO2 nanotubes-supported Fe2O3 （Fe2O3/MnO2） composited by carbon nanotubes （CNTs） （（Fe2O3/ MnO2）3/4-（CNTs）1/4） is synthesized using a facile hydrothermal process and a following direct heat- treatment in the air. The morphology and composition of this catalyst are analyzed using scanning elec- tronic microscopy （SEM）, transmission electron microscopy （TEM）, X-ray diffraction （XRD） and energy dispersive X-ray spectroscopy （EDX）. The morphology characteristics reveal that flower-like Fe2O3 parti- cles are highly dispersed on both MnO2 nanotubes and CNT surfaces, coupling all three components firmly. Electrochemical measurements indicate that the synergy of catalyst exhibit superior bi- functional catalytic activity for both oxygen reduction reaction （ORR） and oxygen evolution reaction （OER） as well as stability than Pt/C and lrO2 catalysts. Using these catalysts for air-cathodes, both primary and rechargeable zinc-air batteries （ZABs） are assembled for performance validation. In a primary ZAB, this 3D-clamed catalyst shows a decent open circuit voltage （OCV, -1.48 V） and a high discharge peak power density （349 mW cm 2）, corresponding to a coulomhic efficiency of 92%. In a rechargeahle ZABs with this bifunctional catalyst, high OCV （〉1.3 V） and small charge-discharge voltage gap （〈1.1 V） are achieved along with high specific capacity （780 mAh g 1 at 30 mA cm-2） and robust cycle-life （1,390 cycles at cycle profile of 20 mA/10 min）.