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A major goal within the CO2 electrolysis community is to replace the generally used Ir anode catalyst with a more abundant material, which is stable and active for water oxidation under process conditions. Ni is widely applied in alkaline water electrolysis, and it has been considered as a potential anode catalyst in CO2 electrolysis. Here we compare the operation of electrolyzer cells with Ir and Ni anodes and demonstrate that, while Ir is stable under process conditions, the degradation of Ni leads to a rapid cell failure. This is caused by two parallel mechanisms: (i) a pH decrease of the anolyte to a near neutral value and (ii) the local chemical environment developing at the anode (i.e., high carbonate concentration). The latter is detrimental for zero-gap electrolyzer cells only, but the first mechanism is universal, occurring in any kind of CO2 electrolyzer after prolonged operation with recirculated anolyte.

Sodium dichromate is an essential solution additive for the electrocatalytic production of sodium chlorate, assuring selective hydrogen evolution. Unfortunately, the serious environmental and health concerns related to hexavalent chromium mean there is an urgent need to find an alternative solution to achieve the required selectivity. In this study sodium permanganate is evaluated as a possible alternative to chromate, with positive results. The permanganate additive is stable in hypochlorite-containing solutions, and during electrolysis a thin film is reductively deposited on the cathode. The deposit is identified as amorphous manganese oxide by Raman spectroscopic and X-ray diffraction studies. Using different electrochemical techniques (potentiodynamic measurements, galvanostatic polarization curves) we demonstrate that the reduction of hypochlorite is suppressed, while the hydrogen evolution reaction can still proceed. In addition, the formed manganese oxide film acts as a barrier for the reduction of dissolved oxygen. The extent of hydrogen evolution selectivity in hypochlorite solutions was quantified in an undivided electrochemical cell using mass spectrometry. The cathodic current efficiency is significantly enhanced after the addition of permanganate, while the effect on the anodic selectivity and the decomposition of hypochlorite in solution is negligible. Importantly, similar results were obtained using electrodes with manganese oxide films formed ex situ. In conclusion, manganese oxides show great promise in inducing selective hydrogen evolution, and may open new research avenues to the rational design of selective cathodes, both for the chlorate process and for related processes such as photocatalytic water splitting.

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 Bi 2 Ti 2 O 7 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.

Sodium chlorate is industrially produced by electrolysis of an aqueous salt solution, in which chromium(VI) constitutes an important excipient component. It is added to a concentration of a few grams Na2Cr2O7/liter to the electrolyte and has several functions in the process, the most important being to increase the Faradaic efficiency for hydrogen evolution in the undivided electrochemical cells. A thin film of Cr(OH)3 × nH2O formed by reductive deposition on the cathodes decreases the rate of unwanted side reactions, while still enabling hydrogen evolution to occur. In addition chromium(VI) buffers the electrolyte at the optimum pH for operation and promotes the desired homogeneous reactions in the electrolyte bulk. Chromium species also affect the rates of hydrogen and oxygen evolution at the electrodes and are said to protect the steel cathodes from corrosion. Although chromium(VI) stays in a closed loop during chlorate production, chromate is a highly toxic compound and new REACH legislation therefore intends to phase out its use in Europe from 2017. A production without chromium(VI), with no other process modifications is not possible, and today there are no commercially available alternatives to its addition. Thus, there is an urgent need for European chlorate producers to find solutions to this problem. It is expected that chromium-free production will be a requirement also in other parts of the world, following the European example. As the chromium(VI) addition affects the chlorate process in many ways its replacement might require a combination of solutions targeting each function separately. The aim of this paper is to explain the role and importance of chromium(VI) in the chlorate manufacturing process. Previous achievements in its replacement are summarized and critically evaluated to expose the current state of the field, and to highlight the most promising avenues to be followed. An attempt is also made to reveal connections with other research fields (e.g. photochemical water splitting, corrosion science) facing similar problems. Allied effort of these different communities is expected to open up research avenues to the mutual benefit of these fields.

In situ electrochemical techniques are widely applied to study the synthesis and properties of redox active materials. These combined methods enable the in–depth understanding of the complex processes, since they are able to furnish extra information about the given process from some additional aspect. Thus, detection of spectral modifications, changes in mass, structure, volume and conductivity, occurring in parallel with the redox transformations, complete the knowledge by enlightening secondary effects of the electrochemical perturbation. Various combinations of two in situ electrochemical methods extend further the understanding of the behaviour of electroactive materials by furnishing information from several aspects at the same time from the self-same layer. In this work these advantageous hyphenations are summarized, which combinations enable to correlate additive or secondary effects, provoked by the same background: the electrochemical process. The presented methods can be implemented and used ubiquitously in studies of divers modified electrodes.

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.

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.

Water oxidation (i.e., oxygen evolution) reaction is the most often used, green anodic pair of carbon dioxide (CO2) electroreduction, mimicking the natural photosynthetic process. At the same time, it requires high energy input and generates a product of little commercial value (i.e., oxygen). Finding appropriate alternative anode processes to be coupled with CO2 reduction is a major undertaking. Several factors need to be considered, such as (i) the value of the product, (ii) abundance and cost of the substrate, (iii) necessary cell voltage (energy input), (iv) needed catalysts, (v) cell structure and components, and (vi) ease/complexity of product analysis and separation. This opinion discusses all these aspects and outlines the main questions to be answered through future research activity.

[Image: see text] Electrochemical reduction of CO(2) is a value-added approach to both decrease the atmospheric emission of carbon dioxide and form valuable chemicals. We present a zero gap electrolyzer cell, which continuously converts gas phase CO(2) to products without using any liquid catholyte. This is the first report of a multilayer CO(2) electrolyzer stack for scaling up the electrolysis process. CO formation with partial current densities above 250 mA cm(–2) were achieved routinely, which was further increased to 300 mA cm(–2) (with ∼95% faradic efficiency) by pressurizing the CO(2) inlet (up to 10 bar). Evenly distributing the CO(2) gas among the layers, the electrolyzer operates identically to the sum of multiple single-layer electrolyzer cells. When passing the CO(2) gas through the layers consecutively, the CO(2) conversion efficiency increased. The electrolyzer simultaneously provides high partial current density, low cell voltage (−3.0 V), high conversion efficiency (up to 40%), and high selectivity for CO production.

To efficiently harness the possible synergies, stemming from the combination of organic conducting polymers and inorganic semiconductors, sophisticated assembling methods are required to control the composition and morphology at the nanoscale. In this proof-of-concept study, we demonstrate the in situ photocatalytic deposition of CdS nanoparticles on poly(3-hexylthiophene) (P3HT) nanofibers, exploiting the semiconducting nature of this polymer. The formation of the hybrid assembly was monitored by UV–vis and Raman spectroscopy, Energy-dispersive X-ray microanalysis, and X-ray diffraction (XRD). Transmission electron microscopic studies and AFM images confirmed that both the particle size and the loading can be tuned by the deposition time. Photoelectrochemical studies revealed the facile transfer of photogenerated electrons from P3HT to CdS, as well as that of the holes from CdS to P3HT. It is believed that ensuring intimate contact between the components in these nanohybrids will open new avenues in vari...

An optoelectronic device, which converts light energy to electric potential, was designed and fabricated by using photosynthetic reaction centre (RC) proteins of purple bacterium Rhodobacter sphaeroides R-26, based on the structure and function of the dye sensitised organic solar cells. First, an electrochemical cell with three electrodes was created especially for this measurement. ITO covered by the MWCNT-RC containing sample served as the working electrode and the counter and the reference electrodes were platinum and Ag\AgCl, respectively. Water soluble ubiquinone-0 and ferrocene, in some experiments were used as mediators. In another experiment, the presence of the RCs in the active layer under dried conditions assured tuneable wavelength sensitivity, in general in the visible, but specially, in the near infrared (700-1000 nm) spectral range. The lifetime of the primary charge separation is in the ps time scale and that of the charge stabilisation can be modulated (at least theoretically) between ps and seconds. A successful combination of RC protein with a light energy converter device in spectroelectrochemical cell (wet conditions in buffered electrolyte) and in dried multilayer structure will be presented here. (C) 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

With the rapid development of renewable energy technologies there is an urgent need to find synthesis routes that address the needs of materials in a reproducible and affordable way. In this study, we present a one-step electrochemical method for the deposition of nanocrystalline titanium dioxide films on different carbon substrates. By optimizing the synthetic conditions, electrodeposition of nanocrystalline and porous titanium dioxide layers was achieved in only a few minutes. To deconvolute the complex effect of the solution pH and temperature, as well as the deposition potential, a set of systematic experiments was carried out on glassy carbon electrodes. The robustness and general applicability of this synthetic approach is demonstrated by extending it to graphene film electrodes. The phase composition of TiO2 was controlled by varying the solution composition. The photoelectrochemical performance of the electrodeposited titanium dioxide films was better than, or at least comparable to the benchmark...

Investigation of ionic motion in connection with the redox transformation of conjugated polymers (CP) has always been at the leading edge of research. Motivated by recent proofs for the chemical bond formation between chloride ion and α-positioned carbon in poly (3,4–ethylenedioxythiophene) (PEDOT), comprehensive studies have been extended to another strongly electronegative halide (F−) and to another CP, polypyrrole (PPy). As the electrochemical quartz crystal nanobalance (EQCN) results proved, the movement of the bulky Bu4N+ cations has been exclusively experienced during the redox processes of both systems. Moreover, the decisive role of the anions being present in the polymerization solution in determining the redox capacity and, consequently, the maximum doping level of the films was evidenced. On the grounds of the systematic experiments, the strong and permanent chemical interaction of highly electronegative anions and the polymer has been demonstrated as a general phenomenon. Importantly, this observation requires the necessary reconsideration of specific polymer–dopant interactions and calls attention to the necessity of careful design of the polymerization procedure.

In this study, we investigated the impact of molecular and supramolecular structure of conducting polymers (CPs) on their thermoelectric properties. As a model system, poly(3-alkylthiophene)s (P3ATs) with different side-chain lengths were prepared through oxidative chemical polymerization and were recrystallized to a well-ordered lamellar structure, resulting in one-dimensional self-assembled nanofibers (evidenced by transmission electron microscopy, X-ray diffraction, and UV–vis spectroscopic measurements). Thermoelectric characterization was performed at different doping levels (precisely tuned by doping in the redox reaction with Ag+ and Fe3+ cations), and the highly doped samples exhibited the best performance for all studied polymers. By varying the length of the alkyl side chain, the supramolecular structure and consequently the electronic properties were varied. The highest electrical conductivity was measured for poly(3-butylthiophene), rooted in its densely packed structure. The established struc...

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 voltammetry. 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.

Enhanced thermoelectric properties of poly(3-hexylthiophene) nanofiber networks, doped in their reaction with silver cations, are presented. The role of charge carrier concentration and mobility (influenced by the supramolecular structure and nanoscale morphology) is discussed. The nanonet structure leads to a six fold increase in the ZT value compared to the bulk polymer counterpart.

The redox transformations of polyaniline (PANI) have been studied in acidic solutions of pH in situ optical electrochemistry and in situ ac conductance technique applied both separately and by using them in a hyphenated mode. For the combination of the two in situ electrochemical techniques, thin layers have been deposited on a special double-band ITO electrode (dbITO), with a gap of 15 μm. The structure of the dbITO printed circuit electrode made possible to monitor simultaneously the electrochemical, the optical and the conductance changes during the redox processes, occurring in the self-same film. Spectral features confirmed the existence of protonated segments in the reduced film, formed in these strongly acidic media, assumingly via the proton partition at the reduced film/solution interface, coupled also with anion uptake to fulfil electroneutrality. The simultaneous in situ spectral and ac conductance data gave evidence that the development of the conducting state starts only with the oxidative transformation of emeraldine type radical cations coupled with anion entry, leading to the increase in the quinoid/benzonoid ratio in the charge carriers.

H2O2 is a product of reactions catalysed by several oxidase enzymes and it is essential in environmental and pharmaceutical analyses. The most commonly used enzyme in understanding the biological behaviour of catalysed oxidation of H2O2 is horseradish peroxidase (HRP). In our experiments HRP was bound to carboxyl-functionalized multiwalled carbon nanotubes (MWNT-COOH) by N-hydroxysuccinimide (NHS) and 1-[3-dimethylaminopropyl]-3-ethyl-carbodiimide (EDC) crosslinkers. The activity of this bio-nanocomposite and the limit of detection (LOD) for H2O2 were determined by measuring the fluorescence of tetraguaiacol (which chemical is the product of guaiacol oxidation after addition of H2O2 to the reaction mixture) as a function of time. The hydrogen peroxide biosensor we developed exhibited a detection limit of 1.2 mu MH(2)O(2)s(-1) which resolution was better than the one measured in solution by about a factor of eight (it was 10 mu MH(2)O(2)s(-1) in solution). An attempt has been made to measure the concentration of H2O2 in an electrochemical cell with HRP immobilized on the surface of an electrode made of indium tin oxide (ITO, a transparent conductive oxide) and MWNT. (C) 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

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.

Combination of an oxide semiconductor with a highly conductive nanocarbon framework (such as graphene or carbon nanotubes) is an attractive avenue to assemble efficient photoelectrodes 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.

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 H 2 O 2 . 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.

Conducting polymers are getting more and more interest as both supporting matrixes and electrocatalysts in the oxygen reduction reaction (ORR). A polypyrrole−magnetite nanocomposite layer has been synthesized by using potassium tetraoxalate as the conducting electrolyte. FT-IR measurements proved that chemical modification of the iron oxide by a reaction between the nanoparticles and the salt—leading to an iron oxalate layer on their surface—endows a negative charge to the particles, which leads to their penetration into the polymeric film as a part of the charge compensation. The new hybrid material showed significant photoelectrocatalytic behavior in the ORR. The ratio observed between the stabilized stationary currents under and without illumination is 2.0 for this hybrid. Separate studies on the electrochemical decomposition of H2O2 also indicated an enhanced catalytic activity of the polypyrrole/magnetite hybrid compared with the neat polymer. The results may open new opportunities in the next genera...

Conducting polymer-based magnetic composites with controlled magnetic behaviour have been synthesized by chemical polymerization in nanoparticle containing organic media. Poly(3-thiophene-acetic-acid)–Fe3O4 hybrids have been prepared with five different iron-oxide contents, up to 20 m/m%, according to the results obtained by thermogravimetric analysis (TGA) and inductively coupled plasma atomic emission spectroscopic (ICP-AES) measurements. X-ray diffraction (XRD) and Mossbauer spectroscopic results gave direct evidences for the incorporation of both maghemite and magnetite. Photoacoustic Fourier transform infrared spectroscopic (PAS-FT-IR) measurements showed a chemical interaction between the polymer and the iron-oxide particles. SQUID investigations indicated a typical superparamagnetic behaviour for all samples, where saturation magnetization values proved to be tunable by the Fe3O4 content. After coating them onto electrode surfaces, basic electrochemical activity of the composite samples was demonstrated by cyclic voltammetry.

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.

Hybrid materials of electrically conducting polymers and inorganic semiconductors form an exciting class of functional materials. To fully exploit the potential synergies of the hybrid formation, however, sophisticated synthetic methods are required that allow for the fine-tuning of the nanoscale structure of the organic/inorganic interface. Here we present the photocatalytic deposition of a conducting polymer (polyaniline) on the surface of silicon carbide (SiC) nanoparticles. The polymerization is facilitated on the SiC surface, via the oxidation of the monomer molecules by ultraviolet-visible (UV-vis) light irradiation through the photogenerated holes. The synthesized core–shell nanostructures were characterized by UV-vis, Raman, and Fourier Transformed Infrared (FT-IR) Spectroscopy, thermogravimetric analysis, transmission and scanning electron microscopy, and electrochemical methods. It was found that the composition of the hybrids can be varied by simply changing the irradiation time. In addition, we proved the crucial importance of the irradiation wavelength in forming conductive polyaniline, instead of its overoxidized, insulating counterpart. Overall, we conclude that photocatalytic deposition is a promising and versatile approach for the synthesis of conducting polymers with controlled properties on semiconductor surfaces. The presented findings may trigger further studies using photocatalysis as a synthetic strategy to obtain nanoscale hybrid architectures of different semiconductors.

The precipitation reaction of calcium oxalate is studied experimentally in the presence of spatial gradients by controlled flow of calcium into oxalate solution. The density difference between the reactants leads to strong convection in the form of a gravity current that drives the spatiotemporal pattern formation. The phase diagram of the system is constructed, the evolving precipitate patterns are analyzed and quantitatively characterized by their diameters and the average height of the gravity flow. The compact structures of calcium oxalate monohydrate produced at low flow rates are replaced by the thermodynamically unstable calcium oxalate dihydrate favored in the presence of a strong gravity current.

A poly(aryl piperidinium)-based anion exchange membrane (PiperION) with high carbonate conductance is employed for CO2 electrolysis to CO in conjunction with a tailored electrolyzer cell structure. This combination results in unprecedentedly high partial current densities in zero-gap cells (jCO > 1.0 A cm−2), while maintaining high conversion (20–45%), selectivity (up to 90%) and low cell voltage (2.6–3.4 V).

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)). (C) 2015 Wiley Periodicals, Inc.

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. (C) 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim