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Cyclic voltammetry

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Full-Text Articles in Chemistry

Cyclic Voltammetric Studies In Adsorption Of Cetyltrimethylammonium Bromide (Ctab) On Au(111) Electrode, Ling Chen, Chang-Deng Xu, Jin-Yu Ye, Chun-Hua Zhen, Shi-Gang Sun Aug 2014

Cyclic Voltammetric Studies In Adsorption Of Cetyltrimethylammonium Bromide (Ctab) On Au(111) Electrode, Ling Chen, Chang-Deng Xu, Jin-Yu Ye, Chun-Hua Zhen, Shi-Gang Sun

Journal of Electrochemistry

Adsorption of cetyltrimethylammonium bromide (CTAB) on Au(111) electrode was investigated by cyclic voltammetry (CV). The results demonstrate that the adsorption of CTAB on Au(111) yields particular CV features. Both the adsorption of CTA+ and the phase change of the surfactant film are surface structure selective. Two pairs of stable sharp peaks that depend on halide species appear upon the adsorption of cationic surfactant on Au(111) electrode. The relationship between the peak current density and the scan rate indicates that the electron transfer reaction was controlled by diffusion process. These CV features are observed for the first time, and reflect …

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Phosphorous Acid Route Synthesis Of Iron Tavorite Phases, Lifepo₄(Oh)ₓf₁₋ₓ [0 ≤ X ≤ 1] And Comparative Study Of Their Electrochemical Activities, Hooman Yaghoobnejad Asl, Amitava Choudhury Aug 2014

Phosphorous Acid Route Synthesis Of Iron Tavorite Phases, Lifepo₄(Oh)ₓf₁₋ₓ [0 ≤ X ≤ 1] And Comparative Study Of Their Electrochemical Activities, Hooman Yaghoobnejad Asl, Amitava Choudhury

Chemistry Faculty Research & Creative Works

New synthesis routes were employed for the synthesis of three derivatives of iron hydroxo-, fluoro-, and mixed hydroxo-fluoro phosphates LiFePO 4(OH)xF1-x where 0 ? x ? 1 with the tavorite structure type, and their detail electrochemical activities have been presented. The hydrothermal synthesis of the pure hydroxo-derivative, LiFePO4OH, using phosphorous acid as a source of phosphate yielded good quality crystals from which the crystal structure was solved for the first time using SC-XRD (single crystal X-ray diffraction). The fluoro derivative, LiFePO4F, was prepared as a very fine powder at low temperature in …

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Fabrication And Electrochemical Properties Of Graphene-Zno Nanocomposite, Chuan-Ling Men, Wan Wang, Jun Cao Apr 2014

Fabrication And Electrochemical Properties Of Graphene-Zno Nanocomposite, Chuan-Ling Men, Wan Wang, Jun Cao

Journal of Electrochemistry

In this work, the graphene-ZnO nanocomposite was successfully synthesized through a one-step solvothermal approach, using ethylene glycol as the solvent and reducing agent. The ZnO particles could be attached to the surfaces and edges of graphene sheet. The electrochemical performance of the nanocomposite was investigated by performing cyclic voltammetry, A.C. impedance and chronopotentiometry tests in 6 mol·L-1 KOH. The results showed that the graphene-ZnO nanocomposite exhibited a nice electrochemical specific capacitance of 115 F·g-1 determined in cyclic voltammetry test, or 71 F·g-1 evaluated in chronopotentiometry test and good reversible charge/discharge behavior.

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Electrodeposition Of Copper From A Choline Chloride Based Ionic Liquid, Rostom Ali M., Ziaur Rahman Md., Sankarsaha S. Apr 2014

Electrodeposition Of Copper From A Choline Chloride Based Ionic Liquid, Rostom Ali M., Ziaur Rahman Md., Sankarsaha S.

Journal of Electrochemistry

The electrodeposition of copper from a solution containing copper chloride in either an ethylene glycol (EG)-choline chloride based or a urea-choline chloride based ionic liquid has been carried out onto a steel cathode by constant current and constant potential methods at room temperature. The influences of various experimental conditions on electrodeposition and the morphology of the deposited layers have been investigated by scanning electron microscopy (SEM) and X-ray diffraction (XRD). It is shown that very smooth, shiny and dense with good adherence and bright metallic coloured copper coatings can be obtained from both EG and urea based ionic liquids at …

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Synthesis And Electrochemical And Spectroelectrochemical Characterization Of Chloromanganese(Iii) Phthalocyanines, Mukaddes Özçeşmeci̇, Ilgin Nar, Esi̇n Hamuryudan Jan 2014

Synthesis And Electrochemical And Spectroelectrochemical Characterization Of Chloromanganese(Iii) Phthalocyanines, Mukaddes Özçeşmeci̇, Ilgin Nar, Esi̇n Hamuryudan

Turkish Journal of Chemistry

The synthesis of novel, symmetrical, tetrasubstituted manganese phthalocyanine complexes bearing 4 hexylthio, 2',3',4',5',6'-pentafluorobenzyloxy, 2',3',5',6'-tetrafluoro-4'-hexylthio-benzyloxy, and 2',3',5',6'-tetrafluoro-4'-pentoxy-benzyloxy units is reported. The new compounds have been characterized by using elemental analyses and UV-Vis, FT-IR, and mass spectroscopic data. The electrochemical properties of the manganese phthalocyanine complexes were investigated by cyclic and square wave voltammetry and the nature of the observed redox processes was studied by spectroelectrochemistry.

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Electrochemical Properties Of 1,3-Disubstituted Methyl Methoxy Phenyl-5-Phenylformazans And Comparison With Spectral Properties, Habi̇be Tezcan, Güler Ekmekci̇, Mehmet Levent Aksu Jan 2013

Electrochemical Properties Of 1,3-Disubstituted Methyl Methoxy Phenyl-5-Phenylformazans And Comparison With Spectral Properties, Habi̇be Tezcan, Güler Ekmekci̇, Mehmet Levent Aksu

Turkish Journal of Chemistry

In this study, electrochemical behaviors of formazans were investigated. The compounds contained CH_3 and OCH_3 groups at the o-, m-, and p-positions of the 1-phenyl ring and an OCH_3 group at the p-position of the 3-phenyl ring. Their electrochemical behaviors, such as the number of electrons transferred, diffusion coefficients, and heterogeneous rate constants, were studied by cyclic voltammetry, ultramicrodisk electrode, and chronoamperometry. Possible mechanisms were proposed based upon the data obtained. There was a correlation between the absorption and electrochemical properties. A linear correlation was obtained between \lambda_{\max} and E_{red2} and Hammett substituent coefficients with E_{red2} and k_s values.

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Acid-Base Catalysis In Proton-Coupled Electron Transfer Reactions (Pcet): The Effects Of Brönsted Bases On The Oxidation Of Glutathione And Hydroquinone, Ramos Jonnathan Medina Dec 2012

Acid-Base Catalysis In Proton-Coupled Electron Transfer Reactions (Pcet): The Effects Of Brönsted Bases On The Oxidation Of Glutathione And Hydroquinone, Ramos Jonnathan Medina

Theses and Dissertations

This thesis presents the results and discussion of the investigation of the effects of Brönsted bases on the kinetics and thermodynamics of two proton-coupled electron transfer processes: the mediated oxidation of glutathione and the electrochemical oxidation of hydroquinone. Proton-coupled electron transfer (PCET) is the name given to reactions that involve the transfer of electron(s) accompanied by the exchange of proton(s). PCETs are found in many chemical and biological processes, some of current technological relevance such as the oxygen reduction reaction in fuel cells, which involves the transfer of four electrons and four protons (4e-, 4H+); or the splitting of water …

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Electrochemical Detection Of Ammonia In Aqueous Solution Using Fluorescamine: A Comparison Of Fluorometric Versus Voltammetric Analysis, Panchompoo Janjira, G. Compton Richard Oct 2012

Electrochemical Detection Of Ammonia In Aqueous Solution Using Fluorescamine: A Comparison Of Fluorometric Versus Voltammetric Analysis, Panchompoo Janjira, G. Compton Richard

Journal of Electrochemistry

Fluorescamine is a non-fluorescent reagent widely used for the quantitative determination of primary amines by fluorescence spectroscopy as it reacts readily with primary amines to form a fluorescent product. In this work, a new sensitive voltammetric method for the detection of ammonia in aqueous solution by the reaction with fluorescamine has been developed. First, the electrochemical behaviour of fluorescamine in the absence and presence of ammonia was investigated in 0.1 mol L-1 borate buffer solution (pH 9.0) by cyclic voltammetry using a glassy carbon (GC) electrode. As for fluorescamine itself, a well-defined irreversible oxidation peak could be observed at …

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Ethanol Electrooxidation On Pt/Mo2/Cnts Catalysts, Yu-Long Cheng, Jie Sun, Ji-Gang Li, Li-Gong Zhang, Tian Zhou, Geng Chang, Zhong-Chao Dong Apr 2012

Ethanol Electrooxidation On Pt/Mo2/Cnts Catalysts, Yu-Long Cheng, Jie Sun, Ji-Gang Li, Li-Gong Zhang, Tian Zhou, Geng Chang, Zhong-Chao Dong

Journal of Electrochemistry

The ethanol electrooxidation behaviors on Pt/MO2/CNTs（M=Sn, Ti, Ce）and Pt/CNTs catalysts in H2SO4 solutions were researched by cyclic voltammetry. It has revealed that the catalysts with the addition of metal oxides presented higher electrooxidation activity for ethanol, in particular, the Pt/CeO2/CNTs catalyst showed the best activity for ethanol electrooxidation intermediate. The Pt/SnO2/CNTs catalyst demonstrated the best ethanol electrooxidation activity when considering the synthetic effects of such parameters as the onset oxidation potential, peak current densities and total oxidation area.

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Electrochemical Properties Of The Keggin-Type Lacunary Heteropolysilicate Anion And Its Eectrocatalysis For H2O2 Reduction, Xi-Long Liu, Chun-Yan Wu, Fang Zhou, Hong-Sheng Liu, Ying-Jie Hua, Chong-Tai Wang, Xiao-Yang Liu Apr 2012

Electrochemical Properties Of The Keggin-Type Lacunary Heteropolysilicate Anion And Its Eectrocatalysis For H2O2 Reduction, Xi-Long Liu, Chun-Yan Wu, Fang Zhou, Hong-Sheng Liu, Ying-Jie Hua, Chong-Tai Wang, Xiao-Yang Liu

Journal of Electrochemistry

Electrochemical properties of the Keggin-type lacunary heteropolysilicate anion SiW11O398- (SiW11) and its indirect electrocatalysis for H2O2 reduction in the supporting electrolyte containing 0.1 mol·L-1 NaHSO4 and Na2SO4 solutions were investigated using cyclic voltammetry, square wave voltammetry and alternating current impedance spectroscopy. Experimental results indicated that SiW11 showed two pairs of reversible redox waves on the glassy carbon (GC) electrode in an acidic solution. The electron transfer number corresponding to the two pairs of waves was one, and the proton transfer number involved was two during …

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Electrochemical Behavior Of Imidacloprid, Jie-Qiong Wang, Wang Zhang, Ming Chen, Guo-Wang Diao Feb 2012

Electrochemical Behavior Of Imidacloprid, Jie-Qiong Wang, Wang Zhang, Ming Chen, Guo-Wang Diao

Journal of Electrochemistry

The electrochemical behavior of imidacloprid（IDP）on glassy carbon electrode has been investigated by cyclic voltammetry. The result shows that the electrochemical reduction of IDP is irreversible and controlled by diffusion. At 25 ℃, the numbers of the electrons transferred of IDP in the electrochemical reaction are four. The diffusion coefficient of IDP is 2.44×106 cm2·s-1 and the diffusion activation energy is calculated to be 9.33 kJ·mol-1.

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Characterization And Electrochromic Properties Of Poly(2,3,5,6-Tetrafluoroaniline): Progress Towards A Transparent Conducting Polymer, Lavinia Astratine, Edmond Magner, John Cassidy, Tony Betts Jan 2012

Characterization And Electrochromic Properties Of Poly(2,3,5,6-Tetrafluoroaniline): Progress Towards A Transparent Conducting Polymer, Lavinia Astratine, Edmond Magner, John Cassidy, Tony Betts

Articles

Electrochromic films of poly(2,3,5,6-tetrafluoroaniline) (PTFA) were formed on ITO substrates from aqueous solutions utilising perchloric acid (HClO4) as dopant. Electrochemical and spectroscopic characterization of PTFA films was performed in background electrolyte and in solutions with the addition of tetrahydrofuran. When the PTFA film was removed from its growth medium, a significant decrease in the faradaic current was observed. The faradaic response increased on addition of tetrahydrofuran which facilitates ion movement through the polymer matrix. PTFA films deposited on ITO substrate were orange and light orange in the oxidized and reduced forms, respectively. The films were ca. 25 nm …

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Properties Of The Mixed Adsorption Layer: Neutral Detergent-Tetramethylthiourea At Interface Electrode/Solution, Jolanta Nieszporek, Dorota Sienko, Dorota Gugala-Fekner, Malgorzata Klin Jan 2012

Properties Of The Mixed Adsorption Layer: Neutral Detergent-Tetramethylthiourea At Interface Electrode/Solution, Jolanta Nieszporek, Dorota Sienko, Dorota Gugala-Fekner, Malgorzata Klin

Turkish Journal of Chemistry

The mixed adsorption layers of tetramethylthiourea and a neutral detergent formed at the electrode surface in 1 M NaClO_4 are described in this paper. The systems were characterized by the measurement of differential capacity, zero charge potential, and surface tension at the same potential. The data were analyzed to obtain the surface pressure and relative surface excess of tetramethylthiourea as a function of electrode charge and bulk concentration of the studied compounds. The values of the lateral interaction parameters, obtained in the presence and in the absence of decanoyl-N-methylglucamide (C_{17}H_{35}NO_6), change differently depending on the isotherm used, but \Delta G° …

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Synthesis And Structural And Electrochemical Characterization Of Novel Macrocyclic Vic-Dioxime Ligand And Its Mononuclear Transition And Nontransition Metal Complexes, Pervi̇n Deveci̇, Bi̇lge Taner, Zeynel Kiliç, Ali̇ Osman Solak, Emi̇ne Özcan Jan 2012

Synthesis And Structural And Electrochemical Characterization Of Novel Macrocyclic Vic-Dioxime Ligand And Its Mononuclear Transition And Nontransition Metal Complexes, Pervi̇n Deveci̇, Bi̇lge Taner, Zeynel Kiliç, Ali̇ Osman Solak, Emi̇ne Özcan

Turkish Journal of Chemistry

The reaction of N-(4-aminophenyl)aza-15-crown-5 (1) with anti-chlorophenylglyoxime (2) produces a novel azacrown ether containing vic-dioxime, N-(4-aminophenyl)aza-15-crown-5-phenylglyoxime (LH_2). LH_2 reacts with Ni(II), Cu(II), Co(II), Cd(II), and Zn(II) ions to yield the mononuclear transition and nontransition metal complexes [M(LH)_2] (M = Ni and Cu), [M(LH)_2(H_2O)_2] (M = Co), and [M(LH)(H_2O)(Cl)] (M = Cd and Zn). The structural features of LH_2 were studied using several techniques including elemental analysis, Fourier transform infrared spectroscopy (FT-IR), ultraviolet visible (UV-Vis), mass spectrometry (MS), 1-dimensional (1D) ^1H-NMR and ^{13}CNMR, distortionless enhancement by polarization transfer (DEPT) 2-dimensional (2D) heteronuclear single-quantum coherence (HSQC), and heteronuclear multiple-bond correlation (HMBC) techniques. …

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Electrochemistry Of Pani/Metal Composites In Basic Solutions, Tamthinhan Quy Dec 2011

Electrochemistry Of Pani/Metal Composites In Basic Solutions, Tamthinhan Quy

UNLV Theses, Dissertations, Professional Papers, and Capstones

Polyaniline (PANI) has been extensively investigated due to its unique conductivity, which is primarily dependent on the oxidation state of the material and the solution pH. PANI is an insulator when it is oxidized, and the solution pH exceeds four. Numerous attempts to extend PANI's conductivity to neutral and alkaline environments have been unsuccessful. However, our previous study has demonstrated that PANI/Pd composite is conductive and catalytically active in a basic solution, pH ∼ 12. Therefore, the conductivity and the electrochemical properties of PANI composites including PANI/Au, PANI/Pd and PANI/Pt were evaluated in basic solutions. The fundamental studies of PANI/metal …

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Determinations In Reducing Degree Of Iron-Amine Complex By Cyclic Voltammetry, Yu-Kun Lai, Wei Wang Feb 2011

Determinations In Reducing Degree Of Iron-Amine Complex By Cyclic Voltammetry, Yu-Kun Lai, Wei Wang

Journal of Electrochemistry

The veracity and influence factors in reducing degree on iron-amine complex were tested by cyclic voltammetry.The types of cathode electrolytes including ferric nitrate,triethanolamine,sodium hydroxide and calcium nitrate were optimized.Compared with dip-dyeing coloration method,the cyclic voltammetry method can be used to measure the reducing degree of iron-amine complex more accurately with better stability,easier and faster operation.Potential applications of cyclic voltammetric determination method can be found in the fields of electrochemical dye production and related quality control.

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Electrooxidation Of Methanol On Multilayer Films Of Polypyrrole-Platinum Electrode, Ling Zhang, Long-Zhen Zheng Feb 2011

Electrooxidation Of Methanol On Multilayer Films Of Polypyrrole-Platinum Electrode, Ling Zhang, Long-Zhen Zheng

Journal of Electrochemistry

Multilayer films of polypyrrole-platinum electrode were fabricated by cyclic voltammetric technique.Electro-oxidation of methanol on this electrode was investigated with the aid of cyclic voltammetry and chronoamperometry.Results demonstrated that the multilayer of polypyrrole-platinum electrode behaved better electrocatalytic performance for electro-oxidaton of methanol and better poison resistant.Furthermore,with the increase of deposited platinum loadings,the rate controlling step on electro-oxidation reaction of methanol was changed from CO oxidation to sorption-desorption of hydrogen.

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Electrochemical Studies Of Quinone On Clay-Modified Platinum Electrodes, Thomas Edward Nelson Jan 2011

Electrochemical Studies Of Quinone On Clay-Modified Platinum Electrodes, Thomas Edward Nelson

Theses (2 year embargo)

No abstract provided.

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Characterization Of Triggerable Quinones For The Development Of Enzyme-Responsive Liposomes, Maria Fabiana Mendoza Jan 2011

Characterization Of Triggerable Quinones For The Development Of Enzyme-Responsive Liposomes, Maria Fabiana Mendoza

LSU Doctoral Dissertations

For decades, there has been a lot of focus on the development of new carriers for drug delivery applications. From all of the carriers, stimuli-responsive liposomes have been studied extensively, but only a handful have been enzyme-responsive liposomes. Therefore, the field of endogenous proteins as activators of liposomes is a fertile field worthy of exploration. The research described in this dissertation involves how structural changes on the quinone moiety altered their electronic properties, as well as their behavior toward the human enzyme NAD(P)H:quinone oxidoreductase type-1 (hNQO1, over expressed in certain tumor tissues), thus yielding a series of triggerable quinones to …

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Electrochemical Performance Of Zinc Tetra (Trifluoroethoxy) Phthalocyaninate In Aqueous And Nonaqueous Solvents, Xiao-Shan Wu, Li-Ying Huang, Jin-Que Zhang, Shan-Lan Zhu Nov 2010

Electrochemical Performance Of Zinc Tetra (Trifluoroethoxy) Phthalocyaninate In Aqueous And Nonaqueous Solvents, Xiao-Shan Wu, Li-Ying Huang, Jin-Que Zhang, Shan-Lan Zhu

Journal of Electrochemistry

The cyclic voltammetric performance of ZnPcF in N,N-dimethylformaide(DMF),dimethyl sulfoxide(DMSO) solution and phosphate buffer solutions(PBS) has been examined.The results showed that four pairs of redox peaks appeared in nonaqueous solvents,and the values of half-wave redox potential were 0.558 V,-0.761 V,-1.034 V,-1.417 V,respectively,exhibiting four quasi-reversible phthalocyanine ligand based one-electron transfers.In PBS only two redox peaks were observed and the values of half-wave redox potential were-0.885 V,-1.104 V,exhibiting irreversible behavior characteristics.Comparing to the zinc phthalocyanine(unsubstitute ZnPc),introducing electron-withdrawing groups-trifluoroethoxyl to the peripheral sites of the phthalocyanines shifts the redox processes of the complex toward positive potentials.

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Synthesis Of Cosalen Composite In Apo-5 And Its Electrocatalytic Behaviour For Reaction Of Dioxygen Reduction, Rong Zhang, Li-Hua Tang, Bin-Bin Fan, Jing-Hong Ma, Rui-Feng Li May 2010

Synthesis Of Cosalen Composite In Apo-5 And Its Electrocatalytic Behaviour For Reaction Of Dioxygen Reduction, Rong Zhang, Li-Hua Tang, Bin-Bin Fan, Jing-Hong Ma, Rui-Feng Li

Journal of Electrochemistry

CoAPO-5 molecular sieve was hydrothermally synthesized. The Cobalt ions in CoAPO-5 were coordinated with the SALEN ligend diffusing into the channels of the molecular sieve to form CoSALEN complexes. The electrochemical behaviors and electrocatalysis for dioxygen reduction of the CoSALEN complex immobilized in APO-5 modified glassy carbon electrodes (GCEs) have been investigated by cyclic voltammetry (CV) and chronoamperometry (CA) in differrent pH aqueous solutions. The results showed that the PS/CoSALEN/APO-5 /GC modified electrode is of the high electrocatalytic activity towards dioxygen reduction in pH 6. 86 buffer solution with a reduced overpotential of 447 mV lower than bare GC electrode. …

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Electrochemical Behavior Of Europium(Ⅲ) In 1-Butyl-3-Methylimidazolium, Qiu-Yue Zhang, Hui He, Xiao-Hong Huang, Guo-An Ye Feb 2010

Electrochemical Behavior Of Europium(Ⅲ) In 1-Butyl-3-Methylimidazolium, Qiu-Yue Zhang, Hui He, Xiao-Hong Huang, Guo-An Ye

Journal of Electrochemistry

The electrochemical behavior of EuCl3 in 1-butyl-3-methylimidazolium chlorid([BMIM]Cl) has been investigated in the temperature range of 328 ～ 348 K by cyclic voltammetry.Influences of scan speed and temperature in [BMIM]Cl have been examined.The electrochemical window of [BMIM]Cl was-1.7 V ～ 0.80 V(vs.Ag/AgCl),when the working electrode was glassy carbon electrode.Eu3+ in[BMIM]Cl underwent a single step one-electron transfer reduction to Eu2 +,which is quasi-reversible reaction controlled by both electron transfer and diffusion of ions.The diffusion coefficient of Eu3 + in [BMIM]Cl increased with increase of temperature from 3.75 × 10-9 cm2 /s at 328 K …

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Electrochemical Properties Of 1-(O-, M-, P-Nitrophenyl)-3-(M-Nitrophenyl)- 5-Phenylformazans And Their Nickel Complexes, Habi̇be Tezcan, Mehmet Levent Aksu Jan 2010

Electrochemical Properties Of 1-(O-, M-, P-Nitrophenyl)-3-(M-Nitrophenyl)- 5-Phenylformazans And Their Nickel Complexes, Habi̇be Tezcan, Mehmet Levent Aksu

Turkish Journal of Chemistry

The electrochemical properties of NO_2 formazans and their Ni(II) complexes were investigated. The investigated formazans included a NO_2 group at the o-, m-, and p-positions of the 1-phenyl ring and at the m-position of the 3-phenyl ring. The oxidation and reduction peak potentials, number of electrons transferred, diffusion coefficient, heterogeneous rate constant, and possible reaction mechanism of the compounds were determined with the use of cyclic voltammetry (CV), ultramicrodisc electrodes (UMEs), and chronoamperometry (CA). The peak potentials (E}_{ox1}) were observed to shift towards more anodic potentials in formazans and more cathodic potentials in their respective Ni complexes compared to unsubstituted …

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Performance Evaluation Of Platinum-Based Catalysts For The Development Of Proton Exchange Membrane Fuel Cells, Abdul Sattar Ali Khan, Riaz Ahmed, Muhammad Latif Mirza Jan 2010

Performance Evaluation Of Platinum-Based Catalysts For The Development Of Proton Exchange Membrane Fuel Cells, Abdul Sattar Ali Khan, Riaz Ahmed, Muhammad Latif Mirza

Turkish Journal of Chemistry

Platinum-based catalysts are considered the most efficient catalysts for triggering electrochemical reactions in proton exchange membrane (PEM) fuel cells. In the present study, commercial catalysts containing 10% and 30% Pt supported on Vulcan XC-72 carbon were studied to assess their performance in PEM fuel cells. Both catalysts consisted of Pt particles of almost the same size. The utility of these catalysts in PEM fuel cells was studied by finding the real surface area and rate of electro-oxidation of methanol in 0.5 M H_2SO_4 by using cyclic voltammetry. The methanol oxidation reaction was used for characterization of catalysts of PEM fuel …

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Cyclic Voltammetric And In-Situ Ftir Spectroscopic Studies Of Adsorption And Reduction Of No On Electrode Of Pt Nanoparticles, Qian Cheng, Yan-Xia Jiang, Dong-Mei Zeng, Shi-Gang Sun Nov 2009

Cyclic Voltammetric And In-Situ Ftir Spectroscopic Studies Of Adsorption And Reduction Of No On Electrode Of Pt Nanoparticles, Qian Cheng, Yan-Xia Jiang, Dong-Mei Zeng, Shi-Gang Sun

Journal of Electrochemistry

Adsorption and reduction of NO on electrode of Pt nanoparticles in acid solutions were studied by means of cyclic voltammetry(CV) and in-situ FTIR spectroscopy.The results indicated that the reduction of NO is a complicated process including the adsorption of NO on electrode surface.Two types of surface-bonded NO were determined on Pt nanoparticles.The weakly adsorbed NO was reduced between 0.6 V and-0.05 V,which yielded nitrous oxide(N2O) and ammonium(NH4+) as products;while the strongly bonded NO was reduced at more negative potentials between-0.05V and-0.15V,producing only NH4+ species.

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Synthesis Of α-Mno2 Microspheres For The Application In Supercapacitor, Liang Wang, Gui-Chang Liu, Zhi-Cong Shi Nov 2009

Synthesis Of α-Mno2 Microspheres For The Application In Supercapacitor, Liang Wang, Gui-Chang Liu, Zhi-Cong Shi

Journal of Electrochemistry

The MnO2 microspheres were prepared through the oxidation of KMnO4 and MnCO3 microspheres precursor.The microstructure and supercapacitor properties of MnO2 were characterized by XRD,SEM and CV.The results show that MnO2 was in a poorly crystalline state with α-crystallographic form,the size of microspheres typically ranged from 0.5 to 2 μm.Loading 5 mg·cm-2 MnO2 microspheres had excellent capacitance behaviors in 2 mol·L-1(NH4)2SO4 solution.The specific capacitance was 135.6 F·g-1 with the scan rate at 2 mV·s-1,and 118.8 F·g-1 with the large scan rate at 100 …

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Electrochemical Reduction Of Nitrobenzene In Different Ionic Liquids, Jun-Li Fan, Wei-Lin Ye, Rong Wang, Li-Qun Xu, Xia-Qin Wu Aug 2009

Electrochemical Reduction Of Nitrobenzene In Different Ionic Liquids, Jun-Li Fan, Wei-Lin Ye, Rong Wang, Li-Qun Xu, Xia-Qin Wu

Journal of Electrochemistry

Electrochemical reduction of nitrobenzene at glassy carbon electrode in different ionic liquids,such as N-methylimidazolium-p-toluene sulfonic acid ([Mim][PhSO3]) and ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate ([Bmim][PF6]) have been investigated by cyclic voltammetry. Experimental results showed that only a cathodic current peak was observed in [Mim][PhSO3],which is a diffusional controlled irreversible reaction. And two pairs of current peaks were obtained in [Bmim][PF6] in the same potential range,indicating showed that the reduction products of nitrobenzene were different in different ionic liquids.

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The Electrochemical Behavior And Determination Of Carbendazim On Iron Montmorillonite Modified Electrode, Xiao-Li Jiang, Rong Li, Xiao-Ying He, Jiang Li, Ying Li Feb 2009

The Electrochemical Behavior And Determination Of Carbendazim On Iron Montmorillonite Modified Electrode, Xiao-Li Jiang, Rong Li, Xiao-Ying He, Jiang Li, Ying Li

Journal of Electrochemistry

The FeCl3 modified clay electrode was made.The electrochemical behavior of carbendazim(BCM) on the modified electrode was studied by cyclic voltammetry.The impacts of pH,scan rate and dosages of modifier were discussed and the important kinetic parameters of the electrochemical process were determined.The results indicated that the process was controlled by diffusion.The effective area of FeMM-CMC/GCE(A)=0.027 cm2,the transfer electron numbers(n)=2 and the diffusion coefficient(D)=5.115×10-6cm2/s.Under the optimized conditions,a good linearity was found between the first order derivative of peak current and concentration of BCM in the range of 2.00×10-5～8.00×10-4mol/L,with i′p=-8.045×10-7-0.0237c,correlation …

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A Study Of Growth And Breakdown Of Passive Film On Copper Surface By Electrochemical Impedance Spectroscopy, Amtul Naseer, Athar Yaseen Khan Jan 2009

A Study Of Growth And Breakdown Of Passive Film On Copper Surface By Electrochemical Impedance Spectroscopy, Amtul Naseer, Athar Yaseen Khan

Turkish Journal of Chemistry

Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry were used to investigate the oxide layer formed on a copper disc electrode and the changes that took place when treated potentiostatically in the range of -0.3 V to 0.9 V in aqueous buffer solution of pH 9.2. Equivalent circuits were used to model the response of the electrode, initially at equilibrium to an applied potential. These circuits were proposed for different potential ranges in order to illustrate the Cu/oxide/electrolyte system and its properties in terms of 2 interfaces. A criterion for the applicability of equivalent circuit models was discussed. Changes in the …

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Primary Study Of Tiron As Active Materials For The Redox Flow Battery, Yan Xu, Yue-Hua Wen, Jie Cheng, Yu-Sheng Yang, Zi-Li Xie Nov 2008

Primary Study Of Tiron As Active Materials For The Redox Flow Battery, Yan Xu, Yue-Hua Wen, Jie Cheng, Yu-Sheng Yang, Zi-Li Xie

Journal of Electrochemistry

Effects of solution pH on the electrochemical behavior of tiron(sodium 4,5-dihydroxy-1,3-benzendisulfonic) couple(on a graphite electrode) were studied by cyclic voltammetry in aqueous solutions.It is shown that at pH<4,tiron exhibited a redox process at a relatively high potential with a good reversibility.A redox flow battery was formed employing tiron as the positive active species and V(III)/V(II) as the negative redox couple.In sulfuric acid medium,the coulombic efficiency of the tiron-V redox flow cell was more than 90% with a good cycle life.The decay in the cycle performance was minimal.Therefore,the feasibility of tiron as active materials for redox flow battery application is demonstrated.

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