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1.
In this study, we fabricated optically transparent and electrically conductive multi-walled carbon nanotube (MWCNT) thin films using a spray-coating technique. The transparency and the electrical resistance of thin film are dependent on the nanotube content deposited on the polyethylene terephthalate (PET) substrate. Poly(acrylic acid) (PAA) and poly(N-vinyl pyrrolidone) (PVP) were used as adhesion promoters to improve MWCNT coating more significantly. The cross-linked polymer resulted in a superior bond between the MWCNTs and the substrates. The surface electrical resistance was significantly lower than the original sheet after nitric acid (HNO3) treatment because of the removed surfactant and the increased interconnecting networks of MWCNT bundles, thus improving the electrical and optical properties of the films. Stronger interaction between the MWCNTs and the substrates resulted in lower decomposition of the polymer chain and less amounts of MWCNTs separated into the HNO3 solution. The lower sheet electrical resistance of PVP/PAA-g-MWCNT conductive films on the PET substrate was because of a more complete conductive path with the cross-linked polymer than that without. Such an improved sheet of electrical resistance varied from 8.83 × 104 Ω/□ to 2.65 × 103 Ω/□ with 5.0 wt.% PVP/PAA-g-MWCNT sprayed on the PET after acid treatment.  相似文献   

2.
Combustion synthesis (CS) is characterized by extremely high heating rates (up to 106 K/s) and temperatures (up to 4000 K), as well as short times of reaction completion (usually less than 1 s, sometimes even 10−3–10−2 s). The above unique conditions lead to materials microstructure formation mechanisms that cannot be observed in the isothermal or quasi-isothermal cases. In turn, evolution of the reaction media microstructure influences characteristics (temperature, velocity) of the combustion wave. In this work, such microstructural effects are demonstrated on the examples of CS in different gas–solid systems (i.e., Si–N2, Al–N2, and Nb–N2). It is shown that dilution of the reaction media by inert high surface area precursors with phase compositions similar to the CS product leads to a significant increase in combustion velocity in the Si–N system, while the temperature remains constant. Also, it is revealed that dispersion of the metal (Nb) particles in the preheating zone might be responsible for constancy of the combustion velocity as a function of the size of the initial reactants. Finally, a complex two-stage mechanism of AlN formation explains the non-monotonic shape of the temperature–time profile observed during CS in this system.  相似文献   

3.
Ag–Ni nanoparticles were prepared with a chemical reduction method in the presence of polyvinylpyrrolidone (PVP) used as a stabilizing agent. During the synthesis of Ag–Ni nanoparticles, silver nitrate was used as the Ag+ source while nickel sulfate hexahydrate was used as Ni2+ source. Mixed solutions of Ag+ source and Ni2+ source were used as the precursors and sodium borohydride was used as the reducing agent. Five ratios of Ag+/Ni2+ (9:1, 3:1, 1:1, 1:3, and 1:9) suspensions were prepared in the corresponding precursors. Ag–Ni alloy nanoparticles were obtained with this method at room temperature. Scanning electronic microscope (SEM), energy dispersive spectrum (EDS), high resolution transmission electron microscope (HRTEM) were used to characterize the morphology, composition and crystal structure of the nanoparticles. The crystal structure was also investigated with X-ray diffraction (XRD). In all five Ag/Ni ratios, two kinds of particle structures were observed that are single crystal structure and five-fold twinned structure respectively. Free energy of nanoparticles with different crystal structures were calculated at each Ag/Ni ratio. Calculated results revealed that, with identical volume, free energy of single crystal particle is lower than multi-twinned particle and the difference becomes smaller with the increase of particle size; increase of Ni content will lead the increase of free energy for both structures. Formation of different crystal structures are decided by the structure of the original nuclei at the very early stage of the reduction process.  相似文献   

4.
Igarashi  T.  Ihara  M.  Kusunoki  T.  Ohno  K.  Isobe  T.  Senna  M. 《Journal of nanoparticle research》2001,3(1):51-56
Coordination states of Mn2+ inside and near the surface of ZnS:Mn nanocrystal (NC) (ca. 1.8 nm in particle radius) coated with poly(acrylic acid) (PAA) were examined by the detailed analysis of electron paramagnetic resonance (EPR). The symmetry of both Mn2+ sites inside and near the surface of NC is lower than that of submicron particles (0.125 m in particle radius), because of larger lattice distortion and larger zero field splitting constant. Temperature dependence of line width ( H pp) of EPR signals from Mn2+ inside and near surface sites of ZnS:Mn disappears when the particle radius of ZnS:Mn decreases from 0.125 m to 1.8 nm. These indicate increasing extent of d–d transition and stronger interaction between Mn2+ and ZnS as well as between Mn2+ and PAA in NC, leading to more effective energy transfer from ZnS and PAA to Mn2+. These phenomena explain the high luminescence intensity of ZnS:Mn nanocrystal coated with PAA.  相似文献   

5.
In this study, we developed a facile and benign green synthesis approach for the successful fabrication of well-dispersed urchin-like Au@Pt core–shell nanoparticles (NPs) using gallic acid (GA) as both a reducing and protecting agent. The proposed one-step synthesis exploits the differences in the reduction potentials of AuCl4 and PtCl62−, where the AuCl4 ions are preferentially reduced to Au cores and the PtCl62− ions are then deposited continuously onto the Au core surface as a Pt shell. The as-prepared Au@Pt NPs were characterized by transmission electron microscope (TEM); high-resolution transmission electron microscope (HR-TEM); scanning electron microscope (SEM); UV-vis absorption spectra (UV-vis); X-ray diffraction (XRD); Fourier transmission infrared spectra (FT-IR). We systematically investigated the effects of some experimental parameters on the formation of the Au@Pt NPs, i.e., the reaction temperature, the molar ratios of HAuCl4/H2PtCl6, and the amount of GA. When polyvinylpyrrolidone K-30 (PVP) was used as a protecting agent, the Au@Pt core–shell NPs obtained using this green synthesis method were better dispersed and smaller in size. The as-prepared Au@Pt NPs exhibited better catalytic activity in the reaction where NaBH4 reduced p-nitrophenol to p-aminophenol. However, the results showed that the Au@Pt bimetallic NPs had a lower catalytic activity than the pure Au NPs obtained by the same method, which confirmed the formation of Au@Pt core–shell nanostructures because the active sites on the surfaces of the Au NPs were covered with a Pt shell.  相似文献   

6.
In the article, the Co/Pd/TiO2, Co/TiO2 and Pd/TiO2 catalysts prepared by the impregnation and sol–gel method are studied by using X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The result shows that Co2+ and metal Pd may act as the active center for the direct synthesis of acetic acid from CH4 and CO2 by a two-step reaction sequence. When the catalysts are prepared by the sol–gel, Co2+ can enter the crystal lattice of the TiO2, causing the phase transition from anatase to rutile at lower temperature, but existence of Pd2+ can prevent from the phase transition. When the catalysts are prepared by the impregnation, the phase transition is inhibited not only Co2+ but also Pd2+.  相似文献   

7.
A novel synthetic process for producing aromatic polycarbonate (PC) nanoparticles using supercritical CO2 was developed. The objective of the present research work was to synthesize high molecular weight PC nanoparticles using transesterification between bisphenol-A (BPA) and diphenyl carbonate (DPC) in supercritical CO2 which is an excellent plasticizing agent and a good solvent for phenol, a by-product of the reaction. Poly(propylene oxide)–poly(ethylene oxide)–poly(propylene oxide) tri-block copolymer with CO2-phobic anchor and CO2-philic tail group was used as a stabilizer for the preparation of stable dispersions of BPA–DPC mixture in a CO2 continuous phase. As the reaction was proceeding, phenol formed from the reaction was dissolved and diffused into supercritical CO2 phase. The PC nanoparticles were isolated by simple venting of the supercritical CO2 from the reactor. Spherical morphology of PC particles was confirmed by scanning electron microscopy. Particle size and morphology of PC particles were modified upon variation of the process conditions. The resulting PC particles with a nano-size of 30–140nm have a high molecular weight (M w) of 3.1×105 (g/mol).  相似文献   

8.
Silver-decorated silica spheres of submicrometer-sized silica spheres with a core-shell structure were obtained based on a seed-mediated growth process, where silver nanoparticles were firstly formed from reducing Ag+ to Ag0 in N,N-dimethylformamide (DMF) in the presence of poly(vinylpyrrolidone) (PVP) as protective agent under ultrasound irradiation, followed by the growth of silver shell served silver nanoparticles as nucleation sites and formaldehyde as reducer. The results revealed that the terms of PVP addition and ultrasonic surroundings had great influence on the fabrication of silver seeds.  相似文献   

9.
Vanadium dioxide nanorods were synthesized through a hydrothermal reaction from V2O5 xerogel, poly(vinyl pyrrolidone) (PVP) and lithium perchlorate (LiClO4). The prepared samples were characterized by X-ray diffraction, infrared spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and electrochemical discharge–charge cycling in lithium battery. SEM images reveal the nanorods to have dimensions on the order of 1–3 μm in length and 10–50 nm in diameter. The measured initial discharge capacity of the lithium battery with a cathode made of VO2 (B) nanorods was 152 mA h/g.  相似文献   

10.
Nanospheres of AgSCN with an average radius of 30–80 nm have been prepared by a simple reaction between AgCl suspension and KSCN in the presence of gelatin. Gelatin played a decisive role as an inhibitor of the direct attack of SCN ions to AgCl surfaces and coagulation of the growing AgSCN in producing the spherical AgSCN nanoparticles. The products were characterized by X-ray powder diffraction, transmission electron microscopy and X-ray photoelectron spectra techniques. The electrical conductivity of thin films of as-prepared AgSCN nanoparticles and polyethylene oxide (PEO) at room temperature was measured. The maximum value of electrical conductivity of as-prepared AgSCN–PEO was 1.53 × 10−5 S cm−1.  相似文献   

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