Enhanced electrocatalytic performance of processed, ultrathin, supported Pd-Pt core-shell nanowire catalysts for the oxygen reduction reaction.

We report on the synthesis, characterization, and electrochemical performance of novel, ultrathin Pt monolayer shell-Pd nanowire core catalysts. Initially, ultrathin Pd nanowires with diameters of 2.0 ± 0.5 nm were generated, and a method has been developed to achieve highly uniform distributions of these catalysts onto the Vulcan XC-72 carbon support. As-prepared wires are activated by the use of two distinctive treatment protocols followed by selective CO adsorption in order to selectively remove undesirable organic residues. Subsequently, the desired nanowire core-Pt monolayer shell motif was reliably achieved by Cu underpotential deposition followed by galvanic displacement of the Cu adatoms. The surface area and mass activity of the acid and ozone-treated nanowires were assessed, and the ozone-treated nanowires were found to maintain outstanding area and mass specific activities of 0.77 mA/cm(2) and 1.83 A/mg(Pt), respectively, which were significantly enhanced as compared with conventional commercial Pt nanoparticles, core-shell nanoparticles, and acid-treated nanowires. The ozone-treated nanowires also maintained excellent electrochemical durability under accelerated half-cell testing, and it was found that the area-specific activity increased by ~1.5 fold after a simulated catalyst lifetime.

Platinum-monolayer shell on AuNi(0.5)Fe nanoparticle core electrocatalyst with high activity and stability for the oxygen reduction reaction.

We describe a simple method for preparing multimetallic nanoparticles by in situ decomposition of the corresponding Prussian blue analogue, which is adsorbed on carbon black. The example involves the AuNi(0.5)Fe core of the Pt(ML)/Au(1)Ni(0.5)Fe core-shell electrocatalyst for the oxygen reduction reaction. The core contains 3-5 surface atomic layers of Au, which play an essential role in determining the activity and stability of the catalyst. The Pt(ML)/AuNi(0.5)Fe electrocatalyst exhibited Pt mass and specific activities of 1.38 A/mg(Pt) and 1.12 × 10(-3) A/cm(2)(Pt), respectively, both of which are several times higher than those of commercial Pt/C catalysts. Its all-noble-metal mass activity (0.18 A/mg(Pt,Au)) is higher than or comparable to those of commercial samples. Stability tests showed an insignificant loss in activity after 15,000 triangular-potential cycles. We ascribe the high activity and stability of the Pt(ML)/AuNi(0.5)Fe electrocatalyst to its hierarchical structural properties, the Pt-core interaction, and the high electrochemical stability of the gold shell that precludes exposure to the electrolyte of the relatively active inner-core materials.

Layer-by-layer assembled carbon nanotubes for selective determination of dopamine in the presence of ascorbic acid.

Multilayer films of shortened multi-walled carbon nanotubes (MWNTs) are homogeneously and stably assembled on glassy carbon (GC) electrodes using layer-by-layer (LBL) method based on electrostatic interaction of positively charged poly(diallyldimethylammonium chloride) (PDDA) and negatively charged shortened MWNTs. The assembled MWNT multilayer films were studied with respect to the electrocatalytic activity toward ascorbic acid (AA) and dopamine (DA) and were further applied for selective determination of DA in the presence of AA. Scanning electron microscopy (SEM) used for characterization of MWNT films indicates that the assembled MWNTs are almost in a form of small bundles or single nanotubes on the electrodes. Cyclic voltammetric results with assembled MWNT electrode indicate that the strategy based on the LBL method for assembling the MWNT multilayer films on substrate well retains the electrochemical catalytic activity of the MWNTs toward AA and DA, offering some advantages particularly attractive for analytical applications, such as the form of MWNTs assembled on the substrate, i.e., small bundles or single tubes, homogeneity and stability of the as-assembled MWNT films. These features make the assembled MWNTs relatively potential for selective and sensitive determination of DA in the presence of AA.

Electrochemistry and electroanalytical applications of carbon nanotubes: a review.

This review addresses recent developments in electrochemistry and electroanalytical chemistry of carbon nanotubes (CNTs). CNTs have been proved to possess unique electronic, chemical and structural features that make them very attractive for electrochemical studies and electrochemical applications. For example, the structural and electronic properties of the CNTs endow them with distinct electrocatalytic activities and capabilities for facilitating direct electrochemistry of proteins and enzymes from other kinds of carbon materials. These striking electrochemical properties of the CNTs pave the way to CNT-based bioelectrochemistry and to bioelectronic nanodevices, such as electrochemical sensors and biosensors. The electrochemistry and bioelectrochemistry of the CNTs are summarized and discussed, along with some common methods for CNT electrode preparation and some recent advances in the rational functionalization of the CNTs for electroanalytical applications.

Vertically-aligned sandwich nanowires enhance the photoelectrochemical reduction of hydrogen peroxide: hierarchical formation on carbon nanotubes of cadmium sulfide quantum dots and Prussian blue nanocoatings.

We describe a vertically-aligned array of sandwiched nanowires comprising Prussian blue (PB) nanocoating-carbon nanotube (CNT) core-shell structures with CdS particles positioning at the core/shell interface, viz. PB/CdS/CNT. The PB/CdS/CNT electrode thus constructed are noticeable in synchronically harvesting photon-, ionic-, and chemical-energies, respectively, from visible light radiation, K(+) uptaking and releasing, and the reduction of H2O2. In 0.2 M K2SO4 aqueous solution, the photoelectrocatalytic reduction of 1.5 mM H2O2 at PB/CdS/CNT delivered the current density as high as 1.91 mA/cm(2) at reduced overpotential, that is, three times that at the Pt/C. This superb performance is causally linked to the judicious choice of materials and their assembly into defining sandwich nanostructures wherein the three components closely cooperate with each other in the photoelectrocatalytic reduction of H2O2, including photo-induced charge separation in CdS, spontaneous electron injection into PB due to its relatively low Fermi level, and the electrocatalytic reduction of H2O2 by PB via an electrochemical-chemical-electrochemical reaction mechanism. The structural alignment of PB/CdS/CNT ensures the simplest pathway for the mass diffusion and electron shuttle, and a high surface area accessible to the chemical and electrochemical reactions, so as to minimize the concentration- and electrochemical-polarization and thus ensure the fast overall kinetics of the electrode reaction.

Novel electrochemical method for sensitive determination of homocysteine with carbon nanotube-based electrodes.

An electrochemical method has been successfully demonstrated for sensitive determination of homocysteine (HcySH) with carbon nanotube (CNT)-modified glassy carbon (GC) electrodes. Cyclic voltammetric results clearly show that carbon nanotubes, especially those pretreated with nitric acid, possess an excellent electrocatalytic activity toward the oxidation of HcySH at a low potential (0.0 V versus Ag/AgCl). The remarkable catalytic property of the acid-pretreated CNTs, which is essentially associated with oxygen-containing moieties introduced on the tube surface, has been further exploited as a sensitive determination scheme for HcySH. Continuous-flow amperometric results suggest that the CNT-based electrodes (p-CNT/Nafion/GC), which were prepared by using Nafion to solubilize and further immobilize CNTs on GC electrodes, show striking analytical properties of good stability and reproducibility and strong ability against electrode fouling. Such analytical properties, along with the low operation potential, substantially enable a reliable and sensitive determination of HcySH with a good dynamic linearity up to 60 microM and a detection limit of 0.06 microM (S/N = 3). The catalytic mechanism and the possible application of the as-prepared p-CNT/Nafion/GC electrodes for the study of the auto-oxidation of HcySH are also demonstrated and discussed.

Heterojunction nanowires having high activity and stability for the reduction of oxygen: formation by self-assembly of iron phthalocyanine with single walled carbon nanotubes (FePc/SWNTs).

A self-assembly approach to preparing iron phthalocyanine/single-walled carbon nanotube (FePc/SWNT) heterojunction nanowires as a new oxygen reduction reaction (ORR) electrocatalyst has been developed by virtue of water-adjusted dispersing in 1-cyclohexyl-pyrrolidone (CHP) of the two components. The FePc/SWNT nanowires have a higher Fermi level compared to pure FePc (d-band center, DFT=-0.69 eV versus -0.87 eV, respectively). Consequently, an efficient channel for transferring electron to the FePc surface is readily created, facilitating the interaction between FePc and oxygen, so enhancing the ORR kinetics. This heterojunction-determined activity in ORR illustrates a new stratagem to preparing non-noble ORR electrocatalysts of significant importance in constructing real-world fuel cells.

Vertically-aligned Prussian blue/carbon nanotube nanocomposites on a carbon microfiber as a biosensing scaffold for ultrasensitively detecting glucose.

We describe our assembly and the analytical performance of a glucose biosensor consisting of an array of carbon nanotubes (CNTs) that perpendicularly fall on a 7-µm-diameter carbon fiber and are modified by a "dual" enzymatic system-viz. glucose oxidase (GOx) and Prussian blue (PB, an artificial peroxidase). We chose to use the PB-catalyzed reduction reaction of hydrogen peroxide, an end-product of the GOx-catalyzed oxidation of glucose, to "relay" electrons from GOx to the substrate electrode. We highlight that the electrode-structural alignment of this novel biosensing system plays a crucial role in optimizing the electrochemical- and catalytic-reactions of the enzymes with their substrates. The vertical alignment of enzyme-modified CNTs with the pores located between neighboring individual CNTs creates the simplest optimized pathways for substrates to diffuse to the enzymes and for the generated electrical signals to transport along the nanotube's length to an electronic analyzer. Consequently, the glucose biosensor thus constructed exhibits a high sensitivity of 4.9 µA/mM with a detection limit of 0.05 mmol/L and long-term stability in amperometrically detecting glucose. Our long-range-order assembling of electroactive biomolecules and microscale/nanoscale materials into a multifunctional biocomposite accounts for this superb performance of vital importance in their realistic applications in deciphering glucose and hydrogen peroxide.

Nitrogen-doped carbon nanotube arrays with high electrocatalytic activity for oxygen reduction.

The large-scale practical application of fuel cells will be difficult to realize if the expensive platinum-based electrocatalysts for oxygen reduction reactions (ORRs) cannot be replaced by other efficient, low-cost, and stable electrodes. Here, we report that vertically aligned nitrogen-containing carbon nanotubes (VA-NCNTs) can act as a metal-free electrode with a much better electrocatalytic activity, long-term operation stability, and tolerance to crossover effect than platinum for oxygen reduction in alkaline fuel cells. In air-saturated 0.1 molar potassium hydroxide, we observed a steady-state output potential of -80 millivolts and a current density of 4.1 milliamps per square centimeter at -0.22 volts, compared with -85 millivolts and 1.1 milliamps per square centimeter at -0.20 volts for a platinum-carbon electrode. The incorporation of electron-accepting nitrogen atoms in the conjugated nanotube carbon plane appears to impart a relatively high positive charge density on adjacent carbon atoms. This effect, coupled with aligning the NCNTs, provides a four-electron pathway for the ORR on VA-NCNTs with a superb performance.

Rational attachment of synthetic triptycene orthoquinone onto carbon nanotubes for electrocatalysis and sensitive detection of thiols.

This study demonstrates a novel electrochemical method for sensitive determination of biological thiols including homocysteine, cysteine, and glutathione based on rational functionalization of single-walled carbon nanotubes (SWNTs) with synthetic triptycene orthoquinone (TOQ). Unlike previous strategies used for the functionalization of the carbon nanotubes to fabricate new kind of electrochemically functional nanostructures, the method demonstrated here is essentially based on understanding of the redox properties inherent in the SWNTs themselves. It is demonstrated that the electrochemical oxidation of the thiols at the SWNT-modified electrode is redox-mediated by the quinone-like functional groups at the tube ends and that the low density of such functional groups leads to a follow-up oxidation of the thiols at a more positive potential at the electrode. To mimic the redox properties of the SWNTs and thus to increase the catalytic sites onto the SWNTs, we rationally choose the synthetic TOQ and attach such a compound onto the SWNTs. As a result, it is found that the rational attachment of TOQ onto the SWNTs substantially results in a sufficient electrocatalysis toward the thiols at a low potential of 0.0 V with enhanced sensitivities (i.e., almost by a factor of 10-fold) for the determination of such kind of species in relative to those at the SWNT-modified electrode. The high sensitivity and the good stability as well as the high reproducibility of the TOQ/SWNT-modified electrodes substantially make them very useful for reliable and durable determination of the biological thiols.

Continuous on-line monitoring of extracellular ascorbate depletion in the rat striatum induced by global ischemia with carbon nanotube-modified glassy carbon electrode integrated into a thin-layer radial flow cell.

This study describes a novel analytical system integrating in vivo microdialysis sampling with a radial thin-layer flow cell with a single-walled carbon nanotube (SWNT)-modified glassy carbon electrode as working electrode for continuous and on-line monitoring of ascorbate depletion in the rat striatum induced by global ischemia. The SWNTs, especially those after vacuum heat treatment at 500 degrees C, are found to be able to enhance the electron-transfer kinetics of ascorbate oxidation at a low potential (ca. -50 mV) and possess a strong ability against electrode fouling. These properties essentially make it possible to determine ascorbate with a good stability and high selectivity against catecholamines and their metabolites and other electroactive species of physiological levels. While being integrated with in vivo microdialysis to assemble an on-line analytical system, the electrode is proved useful for continuous and sensitive monitoring of the basal dialysate level of ascorbate and its depletion in the rat striatum induced by global ischemia. The basal dialysate level of ascorbate is determined to be 5.0 +/- 0.5 microM (n = 5) and a 50 +/- 10% (n = 3) depletion is recorded for the basal ascorbate after 4 h of global ischemia.

Sol-gel-derived ceramic-carbon nanotube nanocomposite electrodes: tunable electrode dimension and potential electrochemical applications.

Nanocomposite electrodes made of sol-gel-derived ceramic-carbon nanotube are fabricated by doping mutliwalled carbon nanotubes (MWNTs) into a silicate gel matrix. The electrochemical behavior and potential electrochemical applications of the ceramic-carbon nanotube nanocomposite electrodes (CCNNEs) are also studied. The as-prepared CCNNEs exhibit a tunable dimension ranging from conventional electrode to nanoelectrode ensemble (NEE), depending on the amount of the MWNT dispersed in the silica sol and finally doped within the gel matrix. A high content of the MWNT (i.e., higher than 1.5 mg/mL in the sol) leads to the formation of the CCNNE characteristic of an electrode of conventional dimension, while a low content (typically lower than 0.10 mg/mL) essentially yields the CCNNE like a nanoelectrode ensemble. The NEE is demonstrated to possess good electrocatalytic activity toward the oxidation of ascorbic acid (AA), and the CCNNE of conventional dimension is found to possess remarkable electrocatalytic activity toward the oxidation of glutathione (both reduced and oxidized forms, GSH and GSSG). These properties of the CCNNEs essentially offer a new electrochemical approach for the detection of AA, GSH, and GSSG. The possible essence of the tailor-made dimensions of the CCNNEs is also presented and discussed.

Electrostatic layer-by-layer assembled carbon nanotube multilayer film and its electrocatalytic activity for O2 reduction.

Multilayer films of shortened multiwalled carbon nanotubes (MWNTs) are homogeneously and stably assembled on glassy carbon electrodes with the layer-by-layer (LBL) method, based on electrostatic interaction of positively charged poly(diallyldimethylammonium chloride) and negatively charged and shortened MWNTs. The film assembly and electrochemical property as well as the electrocatalytic activity toward O2 reduction of the MWNT multilayer film are studied. Scanning electron microscopy, the quartz crystal microbalance technique, ultraviolet-visible-near-infrared spectroscopy, and cyclic voltammetry are used for characterization of film assembly. Experimental results revealed that film growth is uniform, almost with the same coverage of the MWNTs in each layer, and that the assembled MWNTs are mainly in the form of small bundles or single tubes on the electrodes. Electrochemical studies indicate that the LBL assembled MWNT films possess a remarkable electrocatalytic activity toward O2 reduction in alkaline media. This property, combined with the well-dispersed, porous and conductive features of the MWNT film illustrated with the LBL method, suggests the potential application of the MWNT film for constructing an efficient alkaline air electrode for energy conversions.