Electro-catalytic oxidation of phenol with Ti-base lead dioxide electrode

The Ti base PbO 2 electrode prepared by electrodeposition of PbO 2 on the surface of titanium was used for electro catalytic oxidation of phenol in waste water. The experimental results show that the electrodeposition of PbO 2 at a higher current density for a short time, then followed by a lower current density can get a compact and combinative PbO 2 layer. The properties of a Ti/PbO 2 electrode with an interlayer of oxide are the best. When this kind of electrode is used to treat phenol containing waste water, the phenol removal rate is higher and the slot voltage is lower. In addition, by using the phenol removal rate as an index, the influences of electrolysis current density, mass transfer condition and pH were studied and the optimal condition was confirmed.

PHOTOSPLITTING OF WATEM AT THIN FILM IRON OXIDE ELECTRODES

both theoretical and experimental findings of the photoresponse for water spliting of the pyrolytically prepared thin film iron oxide electrodes are given.Fur- ther,the spray time and the corresponding thickness of the Fe_2O_3 thin film were opti- mized to have maximum photoresponse.The effect of iodine doping on photoresponse of iron oxide was investigated.

Lowering the Operational Voltage of Single-Layer Polymer Electroluminescent Devices by Using CuO_x Modifying Indium-Tin Oxide Electrode

In this study it is demonstrated that oxygen-plasma-generated CuOx can enhance the holes injection from ITO anode into polymer layer in single-layer polymer EL devices. The possible reason for this enhancement is because the ITO anode modified with CuOx possesses much higher work function than pure ITO anode, which reduces the barrier for hole-injection and further lowers the operational voltage of the polymer EL devices. The work function shift is probable due to the oxygen-plasma-generated CuOx can store more releasable oxygen, and the releasable oxygen in turn changes the oxygen concentration just near ITO surface, which will shift the work function of ITO anode.

Immobilization of Hemoglobin on Cobalt Nanoparticles-modified Indium Tin Oxide Electrode： Direct Electrochemistry and Electrocatalytic Activity

A cobalt nanoparticles-attached indium tin oxide（CoNPs/ITO） electrode was applied to the immobilization of hemoglobin（Hb） and an Hb modified CoNPs/ITO electrode（Hb/CoNPs/ITO） was prepared. The direct electron transfer of Hb was shown by the well-behaved voltammetric responses for Hb/CoNPs/ITO electrode and the effects of scan rate and pH value were observed. Based on the catalytic activity of Hb immobilized on the CoNPs/ITO electrode toward the reduction of H2O2, a mediator-free H2O2 sensor was developed. A linear relationship existed between the catalytic current and the H2O2 concentration in a range of 1.0--100.0 μmol/L with a detection limit （S/N=3） of 0.2μmol/L.

Study on the Multi-Sensing System Based on the Tin Oxide pH Electrode

In this study,the multi-sensing system based on the tin oxide pH electrode for the ion-determination was presented. With the advantages of the real-time supervisory control apparatus,the measured values could be displayed on the liquid crystal display (LCD) immediately.In this study,the basic sensor was the tin oxide pH electrode,which was fabricated by radio frequency (r.f.) sputtering system on the indium tin oxide (ITO)/glass substrate.Moreover,the major blocks of the system consist of the tin oxide electrode-based ion selective electrodes (ISEs),an analog front-ended readout circuit,a microcontroller with built-in analog to digital (A/D) converter.In addition,by the embedded system design,the measurement results can be transmitted to a portable system or computer through the Universal Serial Bus (USB) and Universal Asynchronous Receiver Transmitter (UART) interface immediately.According to the experimental results,the multi-sensing system has high performance and reliability for pH,K^+,and Na^+ detection.

Efficient Thickness of Solid Oxide Fuel Cell Composite Electrode

The efficient thickness of a composite electrode for solid oxide fuel cells was directly calculated by developing a physical model taking into account of the charge transfer process, the oxygen ion and electron transportation, and the microstructure characteristics of the electrode. The efficient thickness, which is defined as the electrode thickness corresponding to the minimum electrode polarization resistance, is formulated as a function of charge transfer resistivity, effective resistivity to ion and electron transport, and three-phase boundary length per unit volume. The model prediction is compared with the experimental reports to check the validity. Simulation is performed to show the effect of microstructure, intrinsic material properties, and electrode reaction mechanism on the efficient thickness. The results suggest that when an electrode is fabricated, its thickness should be controlled regarding its composition, particle size of its components, the intrinsic ionic and electronic conductivities,and its reaction mechanisms as well as the expected operation temperatures. The sensitivity of electrode polarization resistance to its thickness is also discussed.

High quality Sb-doped SnO2 electrodes with high oxygen evolution potential prepared by in situ hydrothermal synthesis method

High quality Sb-doped SnO2 electrode, with high oxygen evolution potential of 3.0 V, was successfully synthesized on the Ti substrates by in situ hydrothermal synthesis method.

Nanosized Nickel Oxides Derived from the Citrate Gel Process and Performances for Electrochemical Capacitors

Nanosized nickel oxide powders were prepared by thermal decomposition of the nickel citrate gel precursors. The thermal decomposition and powder materials derived from calcination of these gel precursors with various ratios of citric acid （CA） to nickel at different temperatures and times were characterized by thermal analysis （TG/DTA）, scanning electron microscopy （SEM）, x-ray diffraction （XRD）, and measurement of specific surface area （BET） with porosity analyses. The optimized processing conditions of calcination temperature 400℃ for 1 hour with the CA/Ni ratio of 1.2, were determined to produce the nanosized nickel oxide pow- ders with a high specific surface area of 181 m^2/g, nanometer particle sizes of 15-25 nm, micro-pore diameter distribution between 4-10 nm. The capacitance characteristics of the nanosized nickel oxide electrode in various concentrations of KOH solutions were studied by the cyclic voltammetry （CV） exhibiting both a double-layer capacitance and a faradaic pseudocapacitance. The nanosized nickel oxide electrode shows a high cyclic stability and is promising for high performance electrochemical capacitors.

Nanosized Ni-Mn Oxides Prepared by the Citrate Gel Process and Performances for Electrochemical Capacitors

Nanosized Ni-Mn oxide powders have been successfully citrate gel precursors. The powder materials derived from prepared by thermal decomposition of the Ni-Mn calcination of the gel precursors with various molar ratios of nickel and manganese at different temperatures and time were characterized using thermal analysis （TG-DSC）, scanning electron microscopy （SEM）, X-ray diffraction （XRD） and Brunauer-Emmet-Teller （BET）. The optimized processing conditions of calcination at 400℃ for 1 h with Ni/Mn molar ratio 6 were proved to produce the nanosized Ni-Mn oxide powders with a high specific surface area of 109.62 m^2/g and nanometer particle sizes of 15-30 nm. The capacitance characteristics of the nanosized Ni-Mn oxide electrode in various concentrations of KOH solutions were studied by the cyclic voltammetry （CV） and exhibited both a doublelayer capacitance and a Faradaic capacitance which could be attributed to the electrode consisting of Ni-Mn oxides and residual carbons from the organic gel thermal decomposition. A specific capacitance of 194.8 F/g was obtained for the electrode at the sweep rate of 10 mV/s in 4 mol/L KOH electrolyte and the capacitor showed quite high cyclic stability and is promising for advanced electrochemical capacitors.

Electrochemical Behavior and Its Electrocatalytic Activity of A P-Mo Heteropolyanion Modified ITO Electrode

s: A new method for the preparation of an organic-inorganic composite film of the heteropolyanion has been developed by modifying P(Mo2O7)6-7 to the indium tin oxide (ITO) electrode surface. The modified electrode displayed a strong catalytic activity towards the reduction of IO3-. In the range of 1.0?0-6~5?0-4mol/L, the catalytic current was linear proportional to the IO3- concentration.

Application of Sodium Ion Sensor Based on the SnO_2/ITO Glass in the Detection of Rinsing Solution for Contact Lenses

This paper presents the studying results of the sodium ion sensor device based on the SnO_2/ITO glass structure in the detection of rinsing solution for contact lenses.The selective membrane contains poly (vinyl chloride) (PVC),bis (2-ethylhexyl) sebacate (DOS),(12-crown-4) methylmalonate (B12C4),and sodium tetrakis (4-fluoropbenyl) borate dehydrate (NaTFBD). The final weight ratios are PVC:DOS:B12C4:NaTFBD=33:66:2:2.In this condition,the sensor has performances with linear sensitivity,short response time,good repeatability and selectivity.The sensor was used to measure the rinsing solution for the contact lenses.Because the experimental results show close to the accurate value for four commercial products,this sensor can preliminary be used in detecting the rinsing solution for the contact lenses.Using this structure and sodium-sensing membrane to construct the sodium sensor is proven successfully in this application.

Fabrication and optimization of La_(0.4)Sr_(0.6)Co_(0.2)Fe_(0.7)Nb_(0.1)O_(3-δ) electrode for symmetric solid oxide fuel cell with zirconia based electrolyte

La（0.4）Sr（0.6）Co（0.2）Fe（0.7）Nb（0.1）O（3-δ）（LSCFN）was applied as both anode and cathode for symmetrical solid oxide fuel cells（SSOFCs）with zirconia based electrolyte.The cell with LSCFN electrode was fabricated by tape-casting and screen printing.Fabrication process was optimized firstly by comparing co-sintering and separate-sintering of electrode and electrolyte.To further improve the LSCFN electrode properties,oxygen ionic conductor of Gd（0.1）Ce（0.9）O（2-δ）（GDC）was added into the LSCFN electrode.The preferred composition of LSCFN-GDC composite electrode was found to be 1：1 in weight ratio with polarization resistance of 0.16Ωcm^2at 800~℃.The maximum power densities of LSCFN-GDC｜｜GDC/YSZ/GDC｜｜LSCFN-GDC tested in H2and CH4with 3%H2O were 395 m W cm^（-2）and 124 m W cm^（-2）at 850~？C,respectively,which were much higher than that of LSCFN｜｜GDC/YSZ/GDC｜｜LSCFN cells at same condition,possibly due to the extension of the triple phase boundary induced by the addition of GDC.The cell showed reasonable stability using H2and CH4with 3%H2O as fuels and no significant power output degradation was observed after total 200 h operation.

Preparation and Degradation Phenol Characterization of Ti/SnO_2-Sb-Mo Electrode Doped with Different Contents of Molybdenum

The Ti/SnO2-Sb-Mo electrodes doped with different molar ratios of molybdenum（Mo） were prepared by sol—gel method in order to investigate the effect of Mo on the characterization of Ti/SnO2-Sb—Mo electrodes.X-ray diffraction（XRD）,field-emission scanning electron microscopy（FE-SEM）,energy dispersive spectrometry（EDS）,and linear scanning voltammetry（LSV） were used to scrutinize the coating material and the electrochemical activity.The concentration of phenol,the value of total organic carbon（TOC）,the mineralization current efficiency（MCE） and the ultraviolet—visible spectroscopy（UV-Vis） spectrum of phenol solution were measured over the electrochemical degradation process of phenol to confirm the phenol degradation characterization of Ti/SnO2-Sb-Mo electrodes.Results showed that the electrode at the Mo content of 1 at.%provided optimal catalytic activity for phenol degradation and the longest life time.The removal percentage of phenol and TOC were 99.62%and82.67%,respectively.The Ti/SnO2-Sb-Mo electrode with 1 at.%of Mo reached maximum MCE of phenol oxidation.The kinetic investigation of phenol and TOC degradation displayed the pseudo-first order reaction model.The Ti/SnO2-Sb-Mo electrode coating with 7 at.%Mo presented the highest oxygen evolution overpotential,indicating the diverse effects for different Mo molar ratio doping.

Nanostructured Electrode Materials for Fuel Cells and Supercapacitors

1 Results Owing to its electrochemical stability, catalytic activity and high electrical conductivity, ruthenium-based oxides have been realized in electrochemistry as excellent electrode materials with applications ranging from electrocatalysts for industrial electrolysis to high power energy storage. Recent studies have suggested that RuOx may have an active role in electrocatalysts for fuel cells.We have been engaged in the fundamental and practical study of nanostructured RuO2-based electrodes[1-5]....

Amorphous Cobalt Boron Alloy@Graphene Oxide Nanocomposites for Pseudocapacitor Applications

Amorphous Co-B alloy nanoparticles grown on graphene sheets were synthesized via a chemical reduc- tion approach and successfully used for an application as a pseudocapacitor. This study aims to improve the capacity and cycling stability of amorphous Co-B alloy nanoparticles grown on conductive graphene sheets. The products were characterized by X-ray powder diffraction, scanning electron microscopy, and transmission electron microscopy. As electrode materials for pseudocapacitors, the amorphous Co-B alloy grown on graphene oxide （Co-B@GO） exhibits a high specific capacitance of 460 F g-1, which is nearly 1.5 times greater than that of bare Co-B nanoparticles at 1 A g-l, The specific capacitance preserved 84% of the initial capacitance even after 1000 cycles at a scan rate of 10 m V-1, suggesting its promising po- tential as pseudocapacitor materials.

A thin-layer spectroelectrochemical study of 3,3',5,5'-tetramethylbenzidine at SnO_2:F film optically transparent electrode

The electrooxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) is dependent on the pH value of Britton-Robinson (B-R) buffer solution. In this work, the electrooxidation behavior of TMB was investigated with a SnO2:F film optically transparent thin-layer spectroelectrochemical cell. TMB underwent one two-electron electrooxidation process in the pH range from 2.0 to < 4.0, and two successive one-electron electrooxidation processes in the pH range from 4.0 to < 7.0 in the B-R buffer solution. At pH 6.5, the electrooxidative product of TMB generated a subsequent chemical reaction to yield an azo compound. Several spectroelectrochemical techniques, such as thin-layer cyclic voltammetry, thin-layer cyclic voltabsorptometry, thin-layer potential-controlled electrolysis absorptometry, thin-layer single-potential-step chronoabsorptometry, thin-layer dou-ble-potential-step chronoabsorptometry, thin-layer single-potential-step open-circuit relaxation chronoabsorptometry, were applied to this investigation. The formal potential E0’ and the electron transfer number corresponding to the electrooxidation of TMB in B-R buffer solution, and the reaction rate constant of the subsequent chemical reaction were determined.

Electrocatalytic reduction of ortho nitrobenzaldehyde using modified aluminum electrode and its determination

A simple, cost effective and rapid electrochemical method has been developed for the determination of micro level ortho nitrobenzaldehyde（ONB） based on outstanding properties of modified aluminum electrode tin nanorods/anodic aluminum oxide/aluminum（SnNR/AAO/Al） for the first time. The SnNR/AAO/Al electrode was fabricated by a second step anodization, followed by electrodeposition and its electrochemical behavior was investigated in detail. The cyclic voltammetry results indicated that the SnNR/AAO/Al electrode exhibited efficient electrocatalytic activity toward reduction of ONB in the acidic solution. It provides an appreciable improvement of reduction peak for ONB at-0.721 V.Furthermore, various kinetic parameters such as transfer electron number, transfer proton number and standard heterogeneous rate constant were calculated from the scan rates.The electrocatalytic behavior was further exploited as a sensitive detection scheme for the ONB determination by differential pulse voltammetry. Under the optimized conditions, the concentration range and detection limit are 0.1-100 μmol/L and 0.05 μmol/L, respectively,for ONB. The analytical performance of this modified sensor has been evaluated for detection of real sample such as river water and recovery of ONB was achieved all-out up to102.3% under standard addition method.

Synthesis of α-Mo_2C by Carburization of α-MoO_3 Nanowires and Its Electrocatalytic Activity towards Tri-iodide Reduction for Dye-Sensitized Solar Cells

Nanowire-shaped α-Mo O3 was synthesized on a large scale by hydrothermal route.Nanocrystalline α-Mo2 C phase was obtained by the carburization of α-Mo O3 nanowires with urea as a carbon source precursor.The phase purity and crystalline size of the synthesized materials were ascertained by using powder X-ray diffraction.The shape and morphology of synthesized materials were characterized by field-emission scanning electron microscopy（FE-SEM） and high resolution transmission electron microscopy（HR-TEM）.The electrocatalytic activity of α-Mo2 C for I-/I3^-redox couple was investigated by the cyclic voltammetry.The synthesized α-Mo2 C was subsequently applied as counter electrode in dye-sensitized solar cells to replace the expensive platinum.