Gold nanonetwork film on the ITO surface exhibiting one-dimensional optical properties

A network of gold nanostructures exhibiting one-dimensional gold nanostructure properties may become a prospective novel structure for optical, electrical and catalytic applications benefited by its unusual characteristics resulting from the collective properties of individual nanostructures in the network. In this paper, we demonstrate a facile method for the formation of high-density gold nanonetwork film on the substrate surface composed of quasi-1D nanoparticles (typically fusiform) with length ca. 10 nm - via reduction of gold ions in the presence of nanoseeds attached surface, binary surfactants of cetyltrimethylammonium bromide and hexamethyleneteramine and Ag(+) ions. The length of the nanonetworks can be up to ca. 100 nm, which corresponds to the aspect ratio of ca. 10. The quasi-1D gold nanostructures as well as the nanonetworks were found to be sensitive to the binary surfactants system and the Ag(+) ions as they can only be formed if all the chemicals are available in the reaction. The nanonetworks exhibit unique 1D optical properties with the presence of transverse and longitudinal surface plasmon resonance absorption. Owing to their peculiar structures that are composed of small quasi-1D nanoparticles, the nanonetworks may produce unusual optical and catalytic properties, which are potentially used in surface-enhanced Raman scattering, catalysis and optical and non-linear optical applications

Codeposition of Platinum and Gold on Nickel Wire Electrodes via Galvanic Replacement Reactions for Electrocatalytic Oxidation of Alcohols

Codeposition of Pt and Au on Ni wire was performed using a simple treatment of immersing Ni wire in aqueous solutions containing both K₂PtCl₄ and HAuCl₄. For evaluating the electrochemical properties of the thus-prepared electrodes, cyclic voltammograms (CVs) of 1.0 M ethanol in 1.0 M NaOH aqueous solutions were recorded. Compared with Pt- or Au-deposited Ni wire electrodes prepared by treating Ni wire in aqueous solutions of a single component, e.g., 1.0 mM K₂PtCl₄ or 1.0 mM HAuCl₄, a noteworthy increase in the electrocatalytic current was observed for the oxidation of ethanol with a PtAu-codeposited Ni (PtAu/Ni) wire electrode even when it was prepared in an aqueous solution containing both 0.10 mM K₂PtCl₄ and 0.10 mM HAuCl₄. In addition, the shape and the peak potentials of CVs recorded using PtAu/Ni wire electrodes were found to be different from those recorded with the Pt- or Au-deposited Ni wire electrodes. Because the CV responses typical of the PtAu/Ni wire electrodes were observed even when a PtAu/Ni wire electrode was prepared in an aqueous solution containing both 0.010 mM K₂PtCl₄ and 1.0 mM HAuCl₄, it is considered that a small amount of Pt was effectively modified or incorporated and affected the electrochemical properties significantly. The CV results for ethanol oxidation were compared with those for the electrocatalytic oxidations of methanol, 1-propanol, and 2-propanol. Besides, the CV results recorded with the present PtAu/Ni wire electrodes are discussed in comparison with some previous results obtained using other PtAu nanoelectrocatalysts

Modification with platinum of silver-deposited nickel wire electrodes for electrocatalytic oxidation of alcohols

A silver-deposited nickel (Ag/Ni) wire electrode was prepared via a galvanic replacement reaction between Ag⁺ and Ni wire in aqueous solution. It was then found that the Ag/Ni wire electrode could be modified with Pt simply by treating it in an aqueous solution of K₂PtCl₄. Although the deposition of Ag on Ni wire was limited in amount, forming Ag deposits less than 100 nm in size, a considerable increase in the electrocatalytic currents for the oxidation of alcohols could be observed after further modification of the Ag/Ni wire electrodes with Pt. This is in contrast to the fact that it was difficult to produce sufficient electrocatalytic response by modifying Ni wire with Pt directly via a simple galvanic replacement between PtCl₄²⁻ and Ni wire. Thus, the prior deposition of Ag was found to strongly promote modification with Pt via a simple stepwise treatment using AgNO₃ and K₂PtCl₄. This approach should be effective in modifying various Ni materials with Pt, including Ni microparticles

A simple route to vertical array of quasi-1D ZnO nanofilms on FTO surfaces: 1D-crystal growth of nanoseeds under ammonia-assisted hydrolysis process

A simple method for the synthesis of ZnO nanofilms composed of vertical array of quasi-1D ZnO nanostructures (quasi-NRs) on the surface was demonstrated via a 1D crystal growth of the attached nanoseeds under a rapid hydrolysis process of zinc salts in the presence of ammonia at room temperature. In a typical procedure, by simply controlling the concentration of zinc acetate and ammonia in the reaction, a high density of vertically oriented nanorod-like morphology could be successfully obtained in a relatively short growth period (approximately 4 to 5 min) and at a room-temperature process. The average diameter and the length of the nanostructures are approximately 30 and 110 nm, respectively. The as-prepared quasi-NRs products were pure ZnO phase in nature without the presence of any zinc complexes as confirmed by the XRD characterisation. Room-temperature optical absorption spectroscopy exhibits the presence of two separate excitonic characters inferring that the as-prepared ZnO quasi-NRs are high-crystallinity properties in nature. The mechanism of growth for the ZnO quasi-NRs will be proposed. Due to their simplicity, the method should become a potential alternative for a rapid and cost-effective preparation of high-quality ZnO quasi-NRs nanofilms for use in photovoltaic or photocatalytics applications

Green synthesis of graphene-PtPd alloy nanoparticles with high electrocatalytic performance for ethanol oxidation

Japan Society for the Promotion of Science (JSPS); National Natural Science Foundation of China [21305050, 21375112]; JSPS KAKENHI [2402335, 24550100]A facile and green method is described for the fabrication of PtPd alloy nanoparticles on graphene nanosheets (PtPdNPs/GNs). The keys of the synthesis strategy were to employ a low-cost and green solvent, ethanol, as the reductant, and a two-dimensional carbon material, GNs, as the supporting material. The morphology, structure and composition of the as-prepared PtPdNPs/GNs were characterized by transmission electron microscopy (TEM), high resolution TEM, energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. It was found that by changing the preparation procedures and varying the molar ratio of the starting precursors, NPs with different shapes such as spherical NPs (Pt(1)Pd(1)NPs), nanoflowers (Pd@PtNFs) and nanodentrites (Pt(3)Pd(1)NPs) could be produced on GNs. Based on these observations, a plausible growth mechanism of PtPdNPs/GNs was discussed. In addition, the electrocatalytic properties of PtPdNPs/GNs for direct ethanol oxidation in alkaline media were systematically investigated. Due to the synergetic effects of Pt and Pd, and the enhanced electron transfer properties enhanced of GNs, PtPdNPs/GNs exhibited higher electrocatalytic ability and better tolerance to reaction intermediate poisoning in the electrooxidation of ethanol compared with Pt nanoflowers supported on GNs (PtNFs/GNs), PdNPs/GNs and PtPdNPs supported on carbon black (PtPdNPs/C). The presented method is a general, facile and green approach for the synthesis of GN-supported bimetallic PtM electrocatalysts, which is significant for the development of high performance electrocatalysts

AuPd bimetallic nanoparticles decorated on graphene nanosheets: their green synthesis, growth mechanism and high catalytic ability in 4-nitrophenol reduction

Japan Society for the Promotion of Science (JSPS); National Natural Science Foundation of China [21305050, 21175112]; Scientific Research Foundation of Shangda Li, Jimei University [ZC2013005]; JSPS KAKENHI [2402335, 24550100]A one-pot green method to synthesize ultrafine AuPd nanoparticles (NPs) monodispersed on graphene nanosheets (GNs) is reported. Due to the reducing capability, moderate number of deposition sites and large surface area, GNs are used as a three-functional agent such as reductant, stabilizer and support in this synthesis. The morphology, structure and composition of thus-prepared AuPdNPs/GNs were characterized by transmission electron microscopy (TEM), high resolution TEM, energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. As it is a surfactant-free formation process, the as-prepared AuPdNPs/GNs are very clean and can exhibit a high activity towards the reduction of 4-nitrophenol. Moreover, the optical properties and catalytic activities of the AuPdNPs/GNs composite are tunable via controlling the Au versus Pd atomic ratio during their synthesis. The catalytic activity of bimetallic AuPdNPs/GNs composites is highly enhanced over the monometallic AuNPs/GNs and PdNPs/GNs composites. This straightforward method is of significance for deposition of bimetallic NPs with high catalytic performance on graphene-based materials

Au nanoparticles on citrate-functionalized graphene nanosheets with a high peroxidase-like performance

Japan Society for Promotion of Science (JSPS); National Natural Science Foundation of China [21305050]; Special Foundation for Young researchers of Health Department of Fujian [2013-2-106]; Scientific Research Foundation of Shangda Li, Jimei University [ZC2013005]; JSPS KAKENHI [2402335, 24550100]In this paper, Au nanoparticles (AuNPs) have been homogeneously deposited on citrate-functionalized graphene nanosheets (Cit-GNs) by a simple one-pot reducing method. The morphology and composition of the thus-prepared AuNPs/Cit-GNs were characterized by transmission electron microscopy (TEM), high resolution TEM, energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. The results showed that the AuNPs with a uniform size are well dispersed on the surface of the Cit-GNs. Significantly, the as-prepared AuNPs/Cit-GNs possess intrinsic peroxidase-like activity, which can catalyze the oxidation of the peroxidase substrate 3,3,5,5-tetramethylbenzidine (TMB) by hydrogen peroxide (H2O2) to develop a blue color in aqueous solution. The catalysis was in accordance with Michaelis-Menten kinetics and the AuNPs/Cit-GNs showed a strong affinity for both H2O2 and TMB. Moreover, by comparing with Cit-AuNPs, AuNPs/GNs and AuNPs/PVP-GNs, the AuNPs/Cit-GNs composite exhibits a higher catalytic ability with a lower Michaelis constant (Km) value, suggesting that the GNs with a large surface area and the citrate ions with more carboxyl groups around the AuNPs can greatly enhance the peroxidase-like activity of AuNPs/Cit-GNs. Taking the advantages of the high catalytic activity, the good stability and the low cost, the novel AuNPs/Cit-GNs represent a promising candidate as an enzyme mimic and may find a wide range of new applications in biochemistry and biotechnology

Non-enzymatic oxalic acid sensor using platinum nanoparticles modified on graphene nanosheets

Japan Society for the Promotion of Science (JSPS); National Natural Science Foundation of China (NSFC) [21175112]; Science and Technology Planning Project of Fujian Province, China [2012Y0052]An enzyme-free oxalic acid (OA) electrochemical sensor was assembled using a platinum nanoparticle-loaded graphene nanosheets (PtNPGNs)-modified electrode. The PtNPGNs, with a high yield of PtNPs dispersed on the graphene nanosheets, were successfully achieved by a green, rapid, one-step and template-free method. The resulting PtNPGNs were characterized by transmission electron microscopy (TEM), high-resolution TEM, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and an X-ray diffraction technique. Electrochemical oxidation of OA on the PtNPGNs-modified electrode was investigated by cyclic voltammetry and differential pulse voltammetry methods. Based on the results, the modified electrode exhibited high electrochemical activity with well-defined peaks of OA oxidation and a notably decreased overpotential compared to the bare or even the GNs-modified electrode. Under optimized conditions, a good linear response was observed for the concentration of OA and its current response was in the range of 0.1-15 mM and 15-50 mM with a detection limit (S/N = 3) of 10 mM. Furthermore, the electrochemical sensor presented good characteristics in terms of stability and reproducibility, promising the applicability of the sensor in practical analysis

High-performance aqueous asymmetric electrochemical capacitors based on graphene oxide/cobalt(ii)-tetrapyrazinoporphyrazine hybrids

A novel asymmetric electrochemical capacitor (AEC) with high energy and power densities has been developed using a graphene oxide/cobalt(II)tetrapyrazinoporphyrazine composite (GO/CoTPyzPz) as the positive electrode and graphene oxide/carbon black (GO/CB) as the negative electrode in a neutral aqueous Na2SO4 electrolyte. The excellent specific capacitance, energy and power densities ( 500 F g 1, 44 W h kg 1 and 31 kW kg 1) coupled with long cycle life, excellent short response time, and low equivalent series resistance clearly indicate that this new material has great potential for the development of low-cost and ‘green’ aqueous AECs that operate at high energy and power densities. Interestingly, the energy density of the GO/CoTPyzPz//GOCB based AEC falls within the range usually observed for nickel metal hydride (NiMH) batteries (30–100 W h kg 1), but more importantly, shows better power performance than NiMH batteries (0.25–1 kW kg 1) widely used in hybrid vehicles such as Toyota Prius and Honda Insight.The University of Pretoria, CSIR and NRF Nanotechnology flagship programme (K.I.O), and the US National Science Foundation (CHE-1012258 and DMR-0804049, S.W.C.).http://www.rsc.org/MaterialsAam201