石墨烯纳米片的简易合成及其超级电容性能研究

以硫代氨基脲(CH₅N₃S)为还原剂, 通过还原氧化石墨(GO)制备了石墨烯纳米片(GNS)。利用XRD, FE-SEM, AFM和UV-Vis光谱对产物的结构和形貌进行分析, 并使用循环伏安和恒流充放电等测试手段来表征其超级电容性能。实验结果表明, 所制备的GNS具有良好的结晶状态, 并且在水溶液中具有良好的分散性。以GNS纳米片为电极材料, 在3 mol/L KOH电解质溶液中, 在500 mA/g电流密度测试条件下所得比电容量为75 F/g。而且GNS纳米片显示出了良好的电化学循环稳定性。     

Facile preparation and electrochemical characterization of graphene/ZnO nanocomposite for supercapacitor applications

Graphene/ZnO nanocomposites were successfully synthesized by microwave-assisted method. The structure, morphology, optical and composition of the obtained samples were characterized using XRD, FT-IR, laser Raman, UV–Vis spectroscopy and XPS analysis. XRD analysis confirmed the presence of graphene/ZnO nanocomposite. FE-SEM image reveals that the homogenous distribution of ZnO nanoparticles on the graphene nanosheets. The electrochemical properties of the graphene/ZnO electrodes were analyzed by cyclic voltammetry and impedance spectroscopy. The results confirmed that the incorporation of ZnO nanoparticles enhanced the capacitive performance of graphene electrode. Graphene/ZnO nanocomposite electrode showed higher capacitance value of 109 F g⁻¹ at a scan rate of 5 mV s⁻¹ in 1 M KCl solution as compared to the graphene electrodes. These results demonstrated the importance and great potential of graphene based composites in the development of high-performance energy-storage systems.     

Facile approach for temperature-responsive polymeric nanocapsules with movable magnetic cores

A novel facile approach was developed to prepare the well-defined temperature-responsive polymeric nanocapsules with movable magnetic cores (TPNMCs) based on the organic/inorganic sandwich-structured composite nanoparticles with temperature-responsive crosslinked shells via the one-pot approach surface-initiated atom transfer radical copolymerization (SI-ATRP) of N-isopropyl acrylamide (NIPAM) and N,N′-methylenebisacrylamide (MBA) from the surfaces of the Fe₃O₄@SiO₂ core-shell nanoparticles, followed by the selective removal of the silica layer. Based on the temperature-induced volume phase transition and impressive magnetic response, the TPNMCs are expected to be used for the targeted controlled release of sensitive molecules, such as enzymes, proteins or DNA, by responding to the changing the environmental temperature.     

Au/ZnO nanocomposites: Facile fabrication and enhanced photocatalytic activity for degradation of benzene

Au nanoparticles supported on highly uniform one-dimensional ZnO nanowires (Au/ZnO hybrids) have been successfully fabricated through a simple wet chemical method, which were first used for photodegradation of gas-phase benzene. Compared with bare ZnO nanowires, the as-prepared Au/ZnO hybrids were found to possess higher photocatalytic activity for degradation of benzene under UV and visible light (degradation efficiencies reach about 56.0% and 33.7% after 24 h under UV and visible light irradiation, respectively). Depending on excitation happening on ZnO semiconductor or on the surface plasmon band of Au, the efficiency and operating mechanism are different. Under UV light irradiation, Au nanoparticles serve as an electron buffer and ZnO nanowires act as the reactive sites for benzene degradation. When visible light is used as the light irradiation source, Au nanoparticles act as the light harvesters and photocatalytic sites alongside of charge-transfer process, simultaneously.     

Synthesis of Janus composite particles by the template of dumbbell-like silica/polystyrene

Janus particles possess promising performances. It is challenging to develop new methods to control composition and microstructure of the particles. In this report, we describe a general template synthesis of several non-spherical Janus composite particles by the template of dumbbell-like silica/polystyrene (PS) Janus particles. Both PS and silica can be modified to introduce desired functional groups respectively, or induce crystallization of other materials on the particle surface. Especially, by favorable growth of materials within the sulfonated PS gel forming the core–shell structure at the polymer part, several new Janus hollow particles are obtained after removal of the PS core.     

Effect of Graphene Oxide as a Dopant on the Electrochemical Performance of Graphene Oxide/Polyaniline Composite

A method for preparing a graphene oxide/polyaniline （GO/PANI） composite electrode was developed to investigate the effect of GO doped in PANI. PANI was first prepared by the polymerisation of aniline and then dedoped by NH4OH to form emeraldine base （EB）. The dedoped PANI and as-prepared GO were dissolved in N-methyl-2-pyrrolidone （NMP） to generate a homogeneous dispersion. The GO/PANI composites were redoped in HCI before use as electrode materials. These composites were characterised by Raman spectroscopy, X-ray diffraction, UV-vis adsorption spectroscopy, scanning electron microscopy, atomic force microscopy and electrochemical measurements. The GO/PANI composite electrode （containing 2.5% GO） has an initial gravimetric capacitance of 896 F g-1 at a scan rate of 5 mV s-1 and a retention life of 51% after 500 cycles, which is an improvement over that of pure PANI （23%）. The results show that the synergy of GO and PANI attributes to the good electrochemical performance of the GO/PANI composite electrode.     

Microstructure and room temperature fracture toughness of cast Nbss/silicides composites alloyed with Hf

The effect of Hf addition on microstructure and room temperature fracture toughness of cast Nb-16Si alloy was investigated. The Hf addition changes significantly the microstructural morphology of Nb-16Si alloys, which includes microstructure refinement and disappearance of eutectic colonies. Fracture toughness of the alloys improves with increasing Hf content. The improvement in fracture toughness is mainly attributed to the microstructural change by Hf addition. The Hf addition leads to a transition of Nb solid solution fracture manner from brittle cleavage to plastic stretching.     

Facile Synthesis Optimization and Structure Characterization of Zinc Tungstate Nanoparticles

The study involves a direct precipitation method developed for the facile and efficient synthesis of ZnWO₄ nanoparticles. Effects of various parameters such as zinc and tungstate ion solution concentrations, flow rate of reagent addition, and reactor temperature on diameter of synthesized zinc tungstate nanoparticles were investigated experimentally by the aid of orthogonal array design. The findings of the study revealed that the diameter of the produced ZnWO₄ nanoparticles can be fine-tuned through the adjustment of the reaction parameters, including zinc and tungstate ion solution concentrations and the reaction temperature, and at optimum conditions of synthesis procedure, the size of the produced zinc tungstate particles was about 33 nm. Finally, scanning electron microscopy, X-ray diffraction, FTIR, and photoluminescence techniques were used for structural and morphological characterization of the product, so as to monitor the role of the mentioned parameters on the targeted properties in the product.     

Facile preparation of poly(vinyl alcohol) nanocomposites with pristine layered double hydroxides

In this paper, nano-sized Mg–Al layered double hydroxide (LDH) was synthesized by a fast nucleation and slow aging method. The structures of LDH were characterized by transmission electron microscopy (TEM), atomic force microscopy (AFM) and photon correlation spectroscopy (PCS). Poly(vinyl alcohol) (PVA) nanocomposites with different LDH loadings were prepared by water solution casting method. TEM observations show that the LDH nanoplatelets are uniformly dispersed in the PVA matrix. Tensile tests indicate that the elastic modulus and the tensile strength of PVA are improved by about 15% and 54%, respectively, when incorporating with 2 wt% LDH. The improvement of mechanical properties of PVA can be attributed to fine dispersion of LDH, good compatibility and strong interaction between PVA and LDH. In addition, the presence of LDH decreases the decomposition rates at the second stage and improves the amount of residues of PVA. Meanwhile, the transparency of the nanocomposite films is maintained compared with neat PVA.     

Fabrication of toughened Cf/SiC whisker composites and their mechanical properties

In this paper, dense short carbon fiber reinforced silicon carbide matrix composites had been fabricated by hot-pressed (HP) sintering using Al₂O₃ and La₂O₃ as sintering additives. The results showed that the combination of Al₂O₃ and La₂O₃ system was effective to promote densification of short cut carbon fiber reinforced silicon carbide composites (Cf/SiC). The whisker structure of silicon carbide was formed during the annealed treatment at 2023 K for 1 h. However, it was noted that this structure was not observed in the as-received HP material. The mechanism of forming whisker structure was not clear, but this kind of whisker structure was helpful to improve mechanical properties. The combination of grain bridging, crack deflection and whisker debonding would improve the fracture toughness of the Cf/SiC composites.     

Processing of Al/B4C composites by cross-roll accumulative roll bonding

In the present study, Al/B₄C composites were successfully produced in the form of sheets, through accumulative roll bonding (ARB) and cross-roll accumulative roll bonding (CRARB) processes. The CRARB process was performed in two steps. In the first step, the strips were roll-bonded with a draft percentage of 66% reduction, while in the second step the strips were roll-bonded with a draft percentage of 50%. The results indicated that the dispersion of the B₄C particles in the CRARB process is more homogeneous than the ARB process. In addition, the tensile strength of the CRARBed composite is higher than that of the ARBed composite.     

Bending properties of epoxy resin matrix composites filled with Ni-Mn-Ga ferromagnetic shape memory alloy powders

Two types of epoxy resin matrix composites filled with Ni-Mn-Ga ferromagnetic shape memory alloy powders, with and without magnetic field during curing, were prepared, aiming to create anisotropic and isotropic alignments of the Ni-Mn-Ga particles. The bending properties of the composites are found to be significantly influenced by the distribution of Ni-Mn-Ga particles in the epoxy matrix. The composites without magnetic field during curing exhibit larger bending strength and fracture strain than the composites with magnetic field during curing. The fractography reveals that the Ni-Mn-Ga particle chains formed in the composites with magnetic field during curing facilitate the initiation and propagation of cracks, thus weakening the bending properties.     

Effect of sintering condition on microstructure and dielectric properties of BSTN composite ceramics

The effect of sintering condition on the phase composition, microstructure and dielectric properties of barium strontium titanate niobate (BSTN) composite ceramics, in which the perovskite phase and the tungsten bronze phase coexisted, was investigated by XRD, SEM and LCZ Meter. The results show that more Sr²⁺ ions dissolved from the grain boundaries into the crystal lattice of the pervoskite phase and the tungsten bronze phase, especially, into the lattice of the pervoskite phase with the increasing of sintering temperature and sintering time, respectively. So the Curie temperature point decreases with the increasing of sintering temperature. The crystal growth rate of the tungsten bronze phase is higher than that of the perovskite phase in BSTN composite ceramics as the sintering temperature increases. The reasonable sintering temperature is about 1275 °C for BSTN composite ceramics. The activation energy to setting up polarization in BSTN composite ceramics increases with the increase of the applied frequency.     

Synthesis,characterization and dielectric behavior of (ES)-form polyaniline/cerium(III)-nitrate-hexahydrate composites

In this study, morphological, thermal and dielectric properties of chemically synthesized polyaniline (PANI) and its cerium(III)-nitrate-hexahydrate (Ce(NO₃)₃·6H₂O) doped composites with various doping levels were investigated. Characteristic bands of emeraldine salt (ES)-form of PANI was clearly observed in UV–visible (UV–vis) and Fourier transform infrared (FTIR) spectroscopies. Thermal analyses carried out by Differential scanning calorimetry (DSC) indicated that there was a glass transition at about 70 °C and the doping process increased thermal stability of the polymer. In the surface morphologies examined by scanning electron microscopy (SEM), various microstructures depending on the doping level were observed. Real dielectric constant exhibited a significant decrease due to the increase in the doping level especially at higher frequencies. Conductivity mechanisms of PANI and its composites were investigated by universal power law as conventional models could not provide a complete picture for all the samples. Dramatic increases up to 45, 35 and 30 times in the conductivity of 10% doped PANI were observed for 300, 350 and 400 K, respectively.     

Facile coordinating decoration of salophen Al on graphene nanosheet: Salophen Al complex functionalized graphene nanocomposite with electrochemical properties

Salophen Al complex functionalized graphene (SCFG) nanocomposite was synthesized by simple coordination of phenol functionalized graphene (PFG) and as-prepared salophen Al complex. This process is facile, convenient and high efficient. We also investigated the structure, optical properties and electrochemical properties of the obtained SCFG composites. The results showed that salophen Al conjugated and incorporated onto the graphene sheet surface and the composites maintained the micro-structure of graphene sheets without agglomeration. The photoluminescence of salophen Al was completely quenched by graphene, due to the charge transfer between the salophen Al and the graphene nanosheets. Moreover, a significant electrochemical signal emerged on the SCFG modified electrodes compared with those of the graphene sheets or salophen Al complex. Owing to preliminary results of the excellent electrochemical property, SCFG nanocomposite is a promising electrochemical redox probe material.     

Effects of surface modification of β-CaSiO3 on electrospun poly(butylene succinate)/β-CaSiO3 composite fibers

In this experiment, pure PBSU fibers, PBSU/12.5% β-CaSiO₃, and PBSU/25% β-CaSiO₃ composite fibers were fabricated by electrospinning. In order to investigate the effects of surface modification of β-CaSiO₃ on composite fibers, β-CaSiO₃ nanowires were surface esterified using dodecyl alcohol. SEM micrographs showed that composite materials with modified β-CaSiO₃ have homogeneous fibrous structures similar as that of pure PBSU fibers, while the fibers containing unmodified β-CaSiO₃ were inhomogeneous and much larger in diameter, and also junctions where β-CaSiO₃ agglomerated could be found. Mechanical testing showed that with the addition of unmodified β-CaSiO₃ into PBSU matrix, the tensile strength of fibrous materials decreased obviously, and the decrease degree increased with increased β-CaSiO₃ content. However, the tensile stresses of composite materials after surface modification of β-CaSiO₃ turned back and increased about 40% compared to those containing unmodified β-CaSiO₃. All of these results suggested surface modification of β-CaSiO₃ was an effective approach to obtain composite fibrous materials with better morphologies and enhanced mechanical properties, and this method is supposed to be feasible in other fibrous material systems.     

Facile Carbothermal Reduction Synthesis of ZrB2 Nanoparticles: The Effect of Starting Precursors

Zirconium diboride (ZrB₂) ceramic nanoparticles were synthesized by using zirconium (IV) complexes as new precursors. The citrate sol–gel process, which included the mixing of ions at the atomic scale, affected hydrolysis reactions and finally led to the formation of the pure phase of the sample. Results showed that the different sizes of ZrB₂ nanocrystals were produced by adjusting four potential chelating agents of bi- and tetra-dentate (N₂O₂ donor set) ligands by the sol-gel process during carbothermal reduction. The samples were characterized by thermal gravimetric analysis (TGA), X-ray diffraction, fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM). The results obtained from microscopic observations indicated that pure and homogeneous ZrB₂ nanostructures have been formed by using 2-hydroxyacetophenone (hap).     

Synthesis and super capacitance of goethite/reduced graphene oxide for supercapacitors

We report a one-step fabrication of α-iron oxyhydroxide/reduced graphene oxide (α-FeOOH/rGO) composites, in which the ferrous sulfate (FeSO₄·7H₂O) are used as the iron raw and reducing agent to grow goethite (α-FeOOH) and reduce graphite oxide (GO) to rGO in the same time. The morphology, composition and microstructure of the as-obtained samples are systematically characterized by thermogravimetric (TG) analysis, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and FT-IR. Moreover, their electrochemical properties are investigated using cyclic voltammetry and galvanostatic charge/discharge techniques. The specific capacitance of 452 F g⁻¹ is obtained at a specific current of 1 A g⁻¹ when the mass ratio of α-FeOOH to rGO is up to 80.3:19.7. In addition, the α-FeOOH/rGO composite electrodes exhibit the excellent rate capability (more than 79% retention at 10 A g⁻¹ relative to 1 A g⁻¹) and well cycling stability (13% capacitance decay after 1000 cycles). These results suggest the importance and great potential of α-FeOOH/rGO composites in the applications of high-performance energy-storage.