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1.
Graphene oxide (GO) is an attractive freestanding support that can be decorated with ultrathin organic layers for facile and low‐cost fabrication of novel devices with controllable functional properties and microstructures. Here, it is reported that a hybrid material consisting of an ultrathin iron phthalocyanine (FePc) layer self‐assembled on reduced graphene oxide (rGO) exhibits excellent catalytic activity that is superior to that of commercial Pt/C for an oxygen reduction reaction (ORR). During solution processing, the FePc layer is first self‐organized onto GO sheets and then reduced electrochemically to form an FePc/rGO hybrid electrocatalyst. Kinetics studies reveal that the hybrid architecture affords an ultrafast ORR rate caused by a strongly dominant four‐electron process, and the durability of the catalyst shows significant improvement by forming the hybrid structure. Spectroscopic studies suggest that these advantages are afforded by synergistic effects between FePc and rGO, which are enriched by the hybrid structure and the appropriate reduction step.  相似文献   

2.
We report the use of the spray pyrolysis method to design self‐assembled isotropic ternary architectures made up of reduced graphene oxide (GO), functionalized multiwalled carbon nanotubes, and nickel oxide nanoparticles for cost‐effective high‐performance supercapacitor devices. Electrodes fabricated from this novel ternary system exhibit exceptionally high capacitance (2074 Fg?1) due to the highly conductive network, synergistic link between GO and carbon nanotubes and achieving high surface area monodispersed NiO decorated rGO/CNTs composite employing the liquid crystallinity of GO dispersions. To further assess the practicality of this material for supercapacitor manufacture, we assembled an asymmetric supercapacitor device incorporating activated carbon as the anode. The asymmetric supercapacitor device showed remarkable capacity retention (>96%), high energy density (23 Wh kg?1), and a coulombic efficiency of 99.5%.  相似文献   

3.
We report the influence of electron‐beam (E‐beam) irradiation on the structural and physical properties modification of monolayer graphene (Gr), reduced graphene oxide (rGO) and graphene oxide (GO) with ultradispersed diamond (UDD) forming novel hybrid composite ensembles. The films were subjected to a constant energy of 200 keV (40 nA over 100 nm region or electron flux of 3.9 × 1019 cm−2s−1) from a transmission electron microscope gun for 0 (pristine) to 20 min with an interval of 2.5 min continuously – such conditions resemble increased temperature and/or pressure regime, enabling a degree of structural fluidity. To assess the modifications induced by E‐beam, the films were analyzed prior to and post‐irradiation. We focus on the characterization of hierarchical defects evolution using in situ transmission electron microscopy combined with selected area electron diffraction, Raman spectroscopy (RS) and Raman mapping techniques. The experiments showed that the E‐beam irradiation generates microscopic defects (most likely, interstitials and vacancies) in a hierarchical manner much below the amorphization threshold and hybrids stabilized with UDD becomes radiation resilient, elucidated through the intensity, bandwidth, and position variation in prominent RS signatures and mapping, revealing the defects density distribution. The graphene sheet edges start bending, shrinking, and generating gaps (holes) at ~10–12.5 min owing to E‐beam surface sputtering and primary knock‐on damage mechanisms that suffer catastrophic destruction at ~20 min. The microscopic point defects are stabilized by UDD for hybrids in the order of GO > rGO ≥ Gr besides geometric influence, i.e. the int erplay of curvature‐induced (planar vs curved) energy dispersion/absorption effects. Furthermore, an attempt was made to identify the nature of defects (charged vs residual) through inter‐defect distance (i.e. LD). The trends of LD for graphene‐based hybrids with E‐beam irradiation implies charged defects described in terms of dangling bonds in contrast to passivated residual or neutral defects. More importantly, they provided a contrasting comparison among variants of graphene and their hybrids with UDD. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

4.
In this study, inorganic cesium lead iodide (CsPbI3) perovskite nanoparticles (PNPs) and perovskite nanowires (PNWs) with single‐layer graphene (SLG) are combined to obtain 0D–2D PNP–SLG and 1D–2D PNW–SLG hybrids with improved light harvesting. Time‐resolved single‐nanostructure photoluminescence studies of PNPs, PNWs, and related hybrids reveal (i) quasi‐two‐state photoluminescence blinking in PNPs, (ii) highly polarized photoluminescence emitted by PNWs and (iii) efficient interfacial electron transfer between perovskite nanostructures and SLG in both PNP–SLG and PNW–SLG hybrids. Doping of poorly absorbing, highly conductive SLG with perovskite nanocrystals and nanowires provides a simple, yet efficient path to obtain hybrids with increased light‐harvesting properties for potential utilization in the next‐generation photodetectors and photovoltaic devices, including polarization sensitive photodetectors.  相似文献   

5.
We investigate with Raman spectroscopy how gold nanostructures of different shape, size and geometry locally modify a graphene cover layer through strain. The resulting phonon softening translates into frequency downshifts of up to 85 cm–1 for the 2D‐mode of graphene. With spatially resolved and excitation dependent Raman measurements we demonstrate that the downshifted Raman peaks exclusively arise from strained graphene subject to plasmonic enhancement by the nanostructures. The signals arise from an area well below the size of the laser spot. They serve as a local probe for the interaction between graphene and intense light fields. (© 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

6.
Liquid phase transmission electron microscopy (LP‐TEM) is a novel and highly promising technique for the in situ study of important nanoscale processes, in particular the synthesis and modification of various nanostructures in a liquid. Destabilization of the samples, including reduction, oxidation, or dissolution by interactions between electron beam, liquid, and sample, is still one of the main challenges of this technique. This work focuses on amorphous silica nanospheres and the phenomena behind their reshaping and dissolution in LP‐TEM. It is proposed that silica degradation is primarily the result of reducing radical formation in the liquid phase and the subsequent accelerated hydroxylation of the silica, while alterations in silica solid structure, pH, and oxidizing species formation had limited influence. Furthermore, the presence of water vapor instead of liquid water also results in degradation of silica. Most importantly however, it is shown that the addition of scavengers for reducing radicals significantly improved amorphous silica stability during LP‐TEM imaging. Devising such methods to overcome adverse effects in LP‐TEM is of the utmost importance for further development and implementation of this technique in studies of nanoscale processes in liquid.  相似文献   

7.
Reduced graphene oxide (rGO) is a two-dimensional material, which is attracting increasing attention due to its special properties. It can be obtained by laser or ion beam irradiations of pristine graphene oxide (GO). It shows high mechanical resistance, considerable electric and thermal conductivity. All these rGO characteristics together with the high number of molecular species that can be embedded between its layers, make graphene oxide a potential material for electronic sensors or efficient support on which conductive strips, condensers, and micrometric electronic devices can be designed. In particular, as it is described in this paper, it is possible to carry out high spatial resolution lithography in GO by using a focused laser or micro ion beam in order to design macro, micro, and submicron geometrical structures. The use of the reduced graphene oxide for the laser and ion beam fabrication of electrical resistances and capacitances is presented.  相似文献   

8.
In this article, a simple and novel photochemical synthesis of different gold nanostructures is proposed using solar radiation. This method is rapid, convenient and of low cost, and can be performed under ambient conditions. By adjusting the concentration of sodium acetate (NaAc), different morphologies of the products can be easily obtained. Without NaAc, the products obtained are mainly polyhedral gold particles; lower concentration of NaAc (0.05 and 0.1 M) accelerates the formation of flowerlike gold nanostructures; while higher concentration of NaAc (0.5 M) facilitates the formation of a variety of gold nanowires and nanobelts. It is found that the morphology change of gold nanaostructures is the result of the synergistic effect of poly(diallyl dimethylammonium) chloride (PDDA), Ac ions, and the pH value. In addition, the different gold nanostructures thus obtained were used as substrates for surface‐enhanced Raman scattering (SERS) with p‐aminothiophenol (p‐ATP) as the probe molecule. In comparison, the flowerlike gold nanostructures show stronger SERS effect than the other gold nanostructures, which is associated with their unique geometrical shapes providing highly localized electromagnetic (EM) field for the optical enhancement to the probe molecules. These gold nanostructures, with different geometrical shapes, might have potential applications in the areas of photonics, optoelectronics and optical sensing. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

9.
The comparison between two different approaches based on the use of the laser ablation in medium to synthetise gold nanoparticles is presented and discussed. Deionised water as well as a graphene oxide (GO) suspension in deionised water have been employed as solution to produce gold nanoparticles by laser ablation. In the former case, the nanoparticles assembly has been stabilised by using surfactants, but in the latter case to avoid undesired effects the use of chemicals was not necessary and Au reduced graphene oxide (Au-rGO) nanocomposites have been obtained. The structure, size and composition of the gold nanoparticles and of the Au–rGO nanocomposites have been monitored by UV–Vis–NIR absorption spectroscopy and Raman spectroscopy, the transmission and scanning electron microscopies and the X-ray energy-dispersive spectroscopy. The presented methodology of Au rGO nanocomposites preparation could represent a green alternative on the production of metallic nanoparticles in biocompatible environment.  相似文献   

10.
A method is introduced for the design of invisibility cloaks inspired by fluid dynamics that is different from traditional transformation optics. The inhomogeneous refractive index of the liquid cloak controlled by the natural liquid diffusion is analogous to its counterpart designed by transformation optics. Here, a tunable liquid visible cloak is experimentally presented by the natural diffusion of miscible flows. This method avoids the use of complex nanostructures in its solid counterpart, and provides a simple and low‐cost approach. This implies that optofluidics can be used as a technology to make real‐time reconfigurable transformation optic devices.  相似文献   

11.
Electrochemical synthesis employing porous membranes previously metalized with a gold layer as a template is an easy and widespread method to obtain 1D nanostructures. Nevertheless, experimental factors for tuning the morphology and structural details of such nanostructures are still investigated. The influence of the amount of gold on morphology and structure of the 1D systems is studied for the first time. For this purpose, CeO2 nanotubes are synthesized via template‐based electrodeposition inside the pores of gold‐sputtered anodic aluminum oxide (AAO). X‐ray diffraction and electron microscopy techniques, including 3D electron tomography, are applied for the characterization of the template and the nanostructures. On one hand, the results reveal how gold is deposited on top and inside the pores of the AAO as a thin layer or as particles. On the other hand, the 1D systems consist of nanotubes formed by randomly oriented fluorite‐like nanocrystals (2–5 nm), which features a network of inner walls whose compactness directly relates to the thickness of the gold‐sputtered layer. From the combined analysis of voltage–time curves recorded during electrodeposition and the 2D, 3D structural information, a growth mechanism is proposed, which may enlighten paths to tailor the morphology and properties of CeO2 1D nanostructures.  相似文献   

12.
The sliver nanoparticles (AgNPs) with diameters of 30~50 nm were self-assembled onto the surfaces of reduced graphene oxide (rGO) sheets simply by mixing AgNO3 aqueous solution and GO dispersion via a synchronous reduction process. Structure and morphology of the rGO–AgNPs hybrids were well characterized. More significantly, the surface-enhanced Raman scattering (SERS) spectrum of 2-mercaptobenzimidazole (MBI) adsorbed on the solid rGO–AgNPs surface shown that the rGO–AgNPs system gives a very strong SERS intensity at in-plane vibrational modes in comparison to the out-of-plane vibrational modes. This large enhancement effect is most likely a result of charge-transfer (CT) mechanism. Based on the surface selection rules and the information provided by the highly enhanced in-plane vibrational modes, it can be found that MBI molecule was adsorbed on AgNPs surface as a thiol form via the sulphur and nitrogen atoms with a slightly tilted geometric conformation.  相似文献   

13.
2D MoS2 has a significant capacity decay due to the stack of layers during the charge/discharge process, which has seriously restricted its practical application in lithium‐ion batteries. Herein, a simple preform‐in situ process to fabricate vertically grown MoS2 nanosheets with 8–12 layers anchored on reduced graphene oxide (rGO) flexible supports is presented. As an anode in MoS2/rGO//Li half‐cell, the MoS2/rGO electrode shows a high initial coulomb efficiency (84.1%) and excellent capacity retention (84.7% after 100 cycles) at a current density of 100 mA g?1. Moreover, the MoS2/rGO electrode keeps capacity as high as 786 mAh g?1 after 1000 cycles with minimum degradation of 54 µAh g?1 cycle?1 after being further tested at a high current density of 1000 mA g?1. When evaluated in a MoS2/rGO//LiCoO2 full‐cell, it delivers an initial charge capacity of 153 mAh g?1 at a current density of 100 mA g?1 and achieves an energy density of 208 Wh kg?1 under the power density of 220 W kg?1.  相似文献   

14.
Si nanoparticle (Si‐NP) composite anode with high rate and long cycle life is an attractive anode material for lithium‐ion battery (LIB) in hybrid electric vehicle (HEV)/pure electric vehicle (PEV). In this work, a carbon nanotube (CNT)/reduced graphene oxide (rGO)/Si nanoparticle composite with alternated structure as Li‐ion battery anode is prepared. In this structure, rGO completely wraps the entire Si/CNT networks by different layers and CNT networks provide fast electron transport pathways with reduced solid‐state diffusion, so that the stable solid‐electrolyte interphase layer can form on the whole surface of the matrix instead of on single Si nanoparticle, which ensure the high cycle stability to achieve the excellent cycle performance. As a result, the CNT/rGO/Si‐NP anode exhibits high performances with long cycle life (≈455 mAh g?1 at 15 A g?1 after 2000 cycles), high specific charge capacity (≈2250 mAh g?1 at 0.2 A g?1, ≈650 mAh g?1 at 15 A g?1), and fast charge/discharge rates (up to 16 A g?1). This nanostructure anode with facile and low‐cost synthesis method, as well as excellent electrochemical performances, makes it attractive for the long life cycles at high rate of the next generation LIB applications in HEV/PEV.  相似文献   

15.
Graphene is a valuable and useful nanomaterial due to its exceptionally high tensile strength, electrical conductivity and transparency, as well as the ability to tune its materials properties via functionalization. One of the most important features needed to integrate functionalized graphene into products via scalable processing is the effectiveness of graphene dispersion in aqueous and organic solvents. In this study, we aimed to achieve the functionalization of reduced graphene oxide (rGO) by sonication in a one-step process using polyvinyl alcohol (PVA) as a model molecule to be bound to the rGO surface. We investigated the influence of the sonication energy on the efficacy of rGO functionalization. The correlation between the performance of the high-intensity ultrasonic horn and the synthesis of the PVA functionalized rGO was thoroughly investigated by TGA coupled with MS, and IR, Raman, XPS, Laser diffraction, and SEM analysis. The results show that the most soluble PVA-functionalized rGO is achieved at 50% of the ultrasonic horn amplitude. Analysis of cavitation dynamics revealed that in the near vicinity of the horn it is most aggressive at the highest amplitude (60%). This causes rGO flakes to break into smaller domains, which negatively affects the functionalization process. On the other hand, the maximum of the pressure pulsations far away from the horn is reached at 40% amplitude, as the pressure oscillations are attenuated significantly in the 2-phase flow region at higher amplitudes. These observations corelate well with the measured degree of functionalization, where the optimum functionalized rGO dispersion is reached at 50% horn amplitude, and generally imply that cavitation intensity must be carefully adjusted to achieve optimal rGO functionalization.  相似文献   

16.
In this paper, a novel strategy for the fabrication of reduced graphene oxide (rGO)/Cu8S5/polypyrrole (PPy) composite nanosheets with Cu8S5 nanoparticles and PPy layer anchored on the surface of rGO as peroxidase‐like nanocatalyst is reported. During the synthesis, graphene oxide (GO)/CuO composite nanosheets are prepared first and used as templates, then the sulfuration of CuO and polymerization of pyrrole are accompanied with the reduction of GO, resulting in ternary rGO/Cu8S5/PPy composite nanosheets. The synthesized Cu8S5 nanoparticles with a diameter in the range from tens to hundreds of nanometers are dispersed within PPy decorated rGO nanosheets. The resultant ternary rGO/Cu8S5/PPy composite nanosheets exhibit a higher peroxidase‐like catalytic activity toward the oxidation of 3,3′,5,5′‐tetramethylbenzidine in the presence of H2O2 than GO/CuO and rGO/CuS composite nanosheets, revealing a synergistic effect on their activity. The as‐prepared rGO/Cu8S5/PPy platform provides a simple colorimetric approach for the detection of H2O2 and phenol with a high sensitivity. This work offers a new way for the fabrication of rGO‐based nanocomposite with superior enzyme‐like activity, which displays great potential applications in biocatalysis and environmental monitoring.  相似文献   

17.
Single-crystal Au nanosheets and fcc gold nanocrystals of uniform size were synthesized by a novel and simple route. The results of field-emission scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD) indicated the formation of the single-crystal structure of gold nanosheets and fcc nanocrystals. Energy-dispersive analysis of X-ray (EDAX) showed absorbance of cetyltrimethylammonium bromide (CTAB) molecules onto the surface of gold nanostructures. Moreover, zeta potential measurements showed that CTAB-coated nanostructures were positively charged and the zeta potential remained almost the same upon centrifugation and redispersion of the resulting nanostructures in methanol, confirming the high stability of the surfactant-protected nanocomposites. Evolution of the nanostructures during the reaction was monitored by TEM observations. The results indicated that the formation of the gold nanostructures followed a two-step mechanism with a bilayer CTAB structure on the surface of the gold nanostructures.  相似文献   

18.
《Current Applied Physics》2018,18(8):879-885
Several studies have been done on physiochemical properties of thin films of graphene materials, but less on their mechanical properties. The mechanical properties such as tensile and storage modulus of films of graphene oxide (GO), different reduced graphene oxides (rGO), functionalised reduced graphene oxide (frGO) and a few layers graphene (graphene) were analysed in this study. During syntheses processes, a range of variations occurs due to different reducing agents and functionalising components used; this affects or changes the mechanical properties of the materials. In addition, it has become vital to comprehend the mechanical properties of these films as the potential applications such as sensor and electrodes demand extended life cycles or lifetime. It has been found that the ultimate tensile strength (UTS), tensile modulus, and storage modulus vary across all the samples that highly depend on nature/efficiency of reducing agent used, amount of impurities such as oxygen functional groups and defect density such as discrepancies/holes in the aromatic structure. The highest UTS and modulus have been identified with a few layers graphene and with hydroiodic acid reduced GO among the rGOs. The frGO shows almost similar properties to that of graphene.  相似文献   

19.
为了有效研究液晶环境对金属纳米结构表面等离子体的调制作用,基于时域有限差分方法,对液晶环境下金纳米柱结构进行了建模,上下边界采用完全吸收边界条件,四周为周期边界条件.数值模拟了液晶厚度、倾角、光栅距离以及周期结构等参数对金纳米柱的消光特性的调制作用.分析结果表明:随着液晶光轴角度增加,谐振波长出现红移现象,且调制范围为40nm;光栅距离越大,金纳米柱之间的相互作用越弱,谐振波长越小;增加周期长度,谐振波长红移,且随着周期长度增加,次峰作用越明显.利用液晶光学性质可调节金属纳米结构的表面等离子体特性,结果对液晶环境中表面等离子体结构在新的光子器件等方面的研究提供了理论依据.  相似文献   

20.
MgO-reduced graphene oxide nanocomposites (NCs) were synthesized by a simple two-step chemical method. The microstructure, surface morphology, and composition of the prepared samples have been studied. X-ray diffractometer (XRD) analysis confirmed the crystalline cubic MgO nanoparticle and rGO sheets. Scanning electron microscope (SEM) showed the spherical MgO nanoparticles well dispersed over the graphene sheets. UV–visible spectroscopy analysis demonstrated that a red shift in the wavelength dependent absorbance curve. The band gap of the samples was found to be decreased with the increase of rGO content. The dielectric studies have been examined in the frequency range 500 Hz−5 MHz and found significant improvement in the dielectric constant, dielectric loss, and electric properties due to rGO addition.This is mainly attributed to the strong interfacial polarization (Maxwell–Wagner polarization) between MgO and rGO sheets. Further, the modulation of charge carrier density with rGO additions help to enhance the electrical conductivity of NCs and thus, encouraging to have wider application in electronic and energy technologies.  相似文献   

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