SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Endrődi Balázs 1987 ) "

Sökning: WFRF:(Endrődi Balázs 1987 )

  • Resultat 1-10 av 15
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Bencsik, G., et al. (författare)
  • Conducting polymer based multifunctional composite electrodes
  • 2009
  • Ingår i: Reaction Kinetics and Catalysis Letters. - : Springer. - 0133-1736 .- 1588-2837. ; 96, s. 421-428
  • Tidskriftsartikel (refereegranskat)abstract
    • In this paper, we report a novel pattern of composite electrocatalysts. PPy/iron-oxalate films exhibit photo-electrochemical activity. The PPy/B12 composite electrode on stainless steal (SS) support shows high catalytic activity in the electrochemical reduction of methylviologen. Thin polymer layers filled with magnetite particles can be applicable in magneto-selective electrochemical reactions.In this paper, we report a novel pattern of composite electrocatalysts. PPy/iron-oxalate films exhibit photo-electrochemical activity. The PPy/B12 composite electrode on stainless steal (SS) support shows high catalytic activity in the electrochemical reduction of methylviologen. Thin polymer layers filled with magnetite particles can be applicable in magneto-selective electrochemical reactions.
  •  
2.
  • Bencsik, Gábor, et al. (författare)
  • Electrocatalytic properties of the polypyrrole/magnetite hybrid modified electrode towards the reduction of hydrogen peroxide in the presence of dissolved oxygen
  • 2012
  • Ingår i: Electrochimica Acta. - : Elsevier. - 0013-4686 .- 1873-3859. ; 73, s. 53-58
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study, we report on the electrocatalytic behaviour of a polypyrrole/magnetite hybrid electrode towards the reduction of hydrogen peroxide. The electrocatalytic activity of the composite electrode was demonstrated by cyclic voltammetric and chrono-amperometric measurements in comparison with the identically prepared neat polymer film. The stationary reduction currents, measured at an appropriately chosen potential (here at E = -0.3 V), plotted against the peroxide concentration gave a perfect linear correlation in nitrogen atmosphere in the micromolar concentration range. The performance of the composite electrode was not affected by the presence of sulphate, nitrate or chloride anions. In the presence of dissolved oxygen a complex electrocatalytic activity was observed, involving the reduction of both oxygen and H2O2. However, a linear dependence was found also in oxygen containing media, although with much higher currents, but with the same slope (even at different oxygen concentrations). This fact may trigger the development of such hybrid electrodes towards hydrogen peroxide sensors in different aqueous (including natural) samples.
  •  
3.
  • Endrődi, Balázs, 1987-, et al. (författare)
  • Challenges and rewards of the electrosynthesis of macroscopic aligned carbon nanotube array/conducting polymer hybrid assemblies
  • 2015
  • Ingår i: Journal of Polymer Science Part B. - : Wiley. - 0887-6266 .- 1099-0488. ; 53, s. 1507-1518
  • Tidskriftsartikel (refereegranskat)abstract
    • Hybrid assemblies based on conducting polymers and carbon nanomaterials with organized nanoscale structure are excellent candidates for various application schemes ranging from thermal management to electrochemical energy conversion and storage. In the case of macroscopic samples, however, precise control of the nanoscale structure has remained a major challenge to be solved for the scientific community. In this study we demonstrate possible routes to homogeneously infiltrate poly(3-hexylthiophene), poly(3,4-ethylenedioxythiophene), and polyaniline into macroscopic arrays of vertically aligned multiwalled carbon nanotubes (MWCNTAs). Electron microscopic images and Raman spectroscopic analysis (performed along the longitudinal dimension of the hybrid samples) both confirmed that optimization of the electropolymerization circumstances allowed fine tuning of the hybrid structure towards the targeted application. In this vein, three different application avenues were tested. The remarkable anisotropy in both the electrical and thermal conductivity of the nanocomposites makes them eminently attractive candidates to be deployed in thermal management. Thermoelectric studies, aimed to understand the effect of organized nanoscale morphology on the important parameters (Seebeck coefficient, electrical-, and thermal conductivity) compared to their non-organized hybrid counterparts. Finally, extraordinary high charge storage capacity values were registered for the MWCNTA/PANI hybrids (500 F g−1 and 1–3 F cm−2). 
  •  
4.
  • Endrődi, Balázs, 1987-, et al. (författare)
  • Electrochemical synthesis and characterization of poly(3-hexylthiophene)/single-walled carbon nanotube array hybrid materials
  • 2016
  • Ingår i: Journal of Solid State Electrochemistry. - : Springer. - 1432-8488 .- 1433-0768. ; 20:11, s. 3179-3187
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study, we demonstrate that by directly employing single-walled carbon nanotube arrays (SWCNT-arrays)-grown on conductive substrates-as working electrodes, selective and uniform electrodeposition of a conducting polymer, namely poly(3-hexylthiophene), can be achieved on the surface of the nanotubes. The overall kinetic pattern of the electrodeposition was studied by separating the deposition charge from the one related to the redox transformation of the polymer film deposited during the precedent cycles. Both the structure and the electrochemical properties of the hybrid materials were studied as a function of the electrodeposition cycles, thus the amount of the formed polymer. The hybrids were characterized by electron microscopic (SEM, TEM) and vibrational spectroscopic (Raman spectroscopy) means. The obtained results were compared and contrasted with those gathered on macroscopic-sized multi-walled carbon nanotube array-based composites in our group recently. Overall, we conclude that electrochemical polymerization is an attractive tool to synthesize conducting polymer/SWCNT hybrid materials with controlled composition and morphology.
  •  
5.
  • Endrődi, Balázs, 1987-, et al. (författare)
  • Fixation of laccase enzyme into polypyrrole, assisted by chemical interaction with modified magnetite nanoparticles : A facile route to synthesize stable electroactive bionanocomposite catalysts
  • 2014
  • Ingår i: Electrochimica Acta. - : Elsevier. - 0013-4686 .- 1873-3859. ; 122, s. 282-288
  • Tidskriftsartikel (refereegranskat)abstract
    • Effective bio-electrocatalysts require stable immobilization of sufficient amounts of the bioactive component. In this study, a novel and efficient method for specific binding of laccase enzyme onto magnetite nanoparticles (NPs) is presented. The interaction between the chemically modified magnetite NPs and the enzyme was evidenced by both infrared (FT-IR) and X-ray photoelectron spectroscopy (XPS). Subsequently, the enzyme-coated magnetite NPs were successfully incorporated into polypyrrole (PPy) matrix during galvanostatic electropolymerization. The encapsulation of laccase covered NPs was proved by EQCN, TEM, and FT-IR spectroscopy; whereas the electrochemical behaviour of the formed bionanocomposite was characterized by cyclic voltammetiy. In oxygen saturated solution a cathodic charge surplus was observed, related to the electrochemical reduction of oxygen. This surplus was two times higher in the case of the laccase containing layer compared to its only magnetite containing counterpart. Kinetic aspects of the oxygen reduction reaction (ORR) on the laccase containing films were investigated by hydrodynamic voltammetry, and the four-electron route was found to be exclusive, which is promising from the fuel cell perspective. Such synergistic combination of inorganic NPs and enzymes may open new avenues in the application of these bio-nanocomposite materials.
  •  
6.
  • Endrődi, Balázs, 1987-, et al. (författare)
  • Layer by layer growth of electroactive conducting polymer/magnetite hybrid assemblies
  • 2013
  • Ingår i: Synthetic metals. - : Elsevier. - 0379-6779 .- 1879-3290. ; 171, s. 62-68
  • Tidskriftsartikel (refereegranskat)abstract
    • Poly(thiophene-acetic-acid)/magnetite nanocomposite electrodes were fabricated from aqueous solutions on PDADMA (polydiallyldimethylammonium chloride) pre-treated ITO covered glass electrodes, employing layer by layer (LBL) technique. This approach was selected on the ground of the interaction between the surface OH-groups of the magnetite and the carboxylic group of the thiophene derivative. The gradual development of the hybrid assembly was followed by UV-vis spectroscopy, and was found to be continuous up to 30 bilayers. Moreover, the absorbance increase at the characteristic wavelengths was linear in the whole examined region. Importantly, the LBL-prepared composites proved to be electroactive, in aqueous phosphate buffer the Fe3+/Fe2+ redox transformation was observed. The electrocatalytic activity of the modified electrodes was demonstrated for electrooxidation of dopamine (DA), and the role of both components as well as their synergistic contribution was elucidated. Preliminary results indicate possible utilization of such hybrid assemblies in the amperometric detection of this analyte.
  •  
7.
  • Janáky, C., et al. (författare)
  • Electro- and Photoreduction of Carbon Dioxide: The Twain Shall Meet at Copper Oxide/Copper Interfaces
  • 2016
  • Ingår i: ACS Energy Letters. - : American Chemical Society (ACS). - 2380-8195. ; 1, s. 332-338
  • Tidskriftsartikel (refereegranskat)abstract
    • Of the myriad electrode materials that have been used for electrochemical (EC) and photoelectrochemical (PEC) reduction of carbon dioxide in aqueous media, copper oxide/copper interfaces have shown a remarkable range of hydrocarbon and oxygenated products including acids, aldehydes, ketones, and alcohols. This Perspective highlights experimental evidence for the fact that both EC and PEC reduction scenarios have similar chemical and morphological underpinnings in the in situ formation of copper nano- or microcubes on the (photo)cathode surface. Recent rapid developments in our fundamental understanding of these interfaces and areas requiring further studies are discussed in light of recent studies in the authors' laboratories and elsewhere.
  •  
8.
  • Kecsenovity, E., et al. (författare)
  • Enhanced Photoelectrochemical Performance of Cuprous Oxide/Graphene Nanohybrids
  • 2017
  • Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 139:19, s. 6682-6692
  • Tidskriftsartikel (refereegranskat)abstract
    • Combination of an oxide semiconductor with a highly conductive nanocarbon framework (such as graphene or carbon nanotubes) is an attractive avenue to assemble efficient photo electrodes for solar fuel generation. To fully-exploit the possible synergies of the hybrid formation, however, precise knowledge of these systems is required to allow rational design and morphological engineering. In this paper, we present the controlled electrochemical deposition of nanocrystalline p-Cu2O on the surface of different graphene substrates. The developed synthetic protocol allowed tuning of the-morphological features of the hybrids as, deduced from electron microscopy. (Photo)electrochemical measurements (including photovoltammetry, electrochemical impedance spectroscopy, photocurrent transient analysis) demonstrated better performance for the 2D graphene containing photoelectrodes, compared to the bare Cu2O films, the enhanced performance being rooted in suppressed charge carrier recombination. To elucidate the precise role of graphene, comparative studies were performed with carbon nanotube (CNT) films and 3D graphene foams. These studies revealed, after allowing for the effect of increased surface area, that the 3D graphene substrate outperformed the other two nanocarbons. Its interconnected structure facilitated effective charge separation and transport, leading to better harvesting of the generated photoelectrons. These hybrid assemblies are shown to be potentially attractive candidates in photoelectrochemical energy conversion schemes, namely CO2 reduction.
  •  
9.
  • Samu, G. F., et al. (författare)
  • Bandgap-engineered quaternary MxBi2-xTi2O7 (M: Fe, Mn) semiconductor nanoparticles : Solution combustion synthesis, characterization, and photocatalysis
  • 2017
  • Ingår i: Applied Catalysis B. - : Elsevier. - 0926-3373 .- 1873-3883. ; 208, s. 148-160
  • Tidskriftsartikel (refereegranskat)abstract
    • Ternary and quaternary metal oxides form a rapidly emerging class of new functional materials tackling the grand challenge of efficient solar energy harvesting. Currently the main interest is devoted to the characteristics of these materials and little consideration has been given to their preparation. Solution combustion synthesis (SCS) is considered a green and sustainable alternative to the widely employed energy-and/or time-consuming synthesis methods. In this study, SCS was employed to prepare Bi2Ti2O7 and to perform bandgap engineering through foreign ion (Fe, Mn) incorporation. The synthesized materials were characterized by powder X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray microanalysis, diffuse reflectance UV-vis and Raman spectroscopy, and surface area determination via N-2 adsorption. We found that nanocrystalline materials were formed during the SCS synthesis. Further, the phase composition of these materials and the amount of the foreign metal ions incorporated in the parent structure, could be effectively controlled. Consequently, the SCS technique provided a simple and reliable tool for bandgap engineering. The photocatalytic activity of the materials was tested through methyl orange degradation, and the intrinsic photocatalytic activity of the various samples were compared after deconvoluting the effect of their vastly different specific surface areas.
  •  
10.
  • Szabó, T., et al. (författare)
  • Charge stabilization by reaction center protein immobilized to carbon nanotubes functionalized by amine groups and poly(3-thiophene acetic acid) conducting polymer
  • 2012
  • Ingår i: Physica status solidi. B, Basic research. - : Wiley-VCH Verlagsgesellschaft. - 0370-1972 .- 1521-3951. ; 249:12, s. 2386-2389
  • Tidskriftsartikel (refereegranskat)abstract
    • A large number of studies have indicated recently that photosynthetic reaction center proteins (RC) bind successfully to nanostructures and their functional activity is largely retained. The major goal of current research is to find the most efficient systems and conditions for the photoelectric energy conversion and for the stability of this bio-nanocomposite. In our studies, we immobilized the RC protein on multiwalled carbon nanotubes (MWNT) through specific chemical binding to amine functional groups and through conducting polymer (poly(3-thiophene acetic acid), PTAA). Both structural (TEM, AFM) and functional (absorption change and conductivity) measurements has shown that RCs could be bound effectively to functionalized CNTs. The kinetics of the light induced absorption change indicated that RCs were still active in the composite and there was an interaction between the protein cofactors and the CNTs. The light generated photocurrent was measured in an electrochemical cell with transparent CNT electrode designed specially for this experiment.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 15

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy