The electrodeposition of nickel-silicon carbide coatings on a copper electrode was done by mixing SiC particles in the nickel electrodeposition solution.The influence of surfactants and silicon carbide particle size o...The electrodeposition of nickel-silicon carbide coatings on a copper electrode was done by mixing SiC particles in the nickel electrodeposition solution.The influence of surfactants and silicon carbide particle size on uniformity and quantity of silicon carbide particles in nickel-silicon carbide composite coatings was investigated.It was found that particle size affects the nucleation overpotential,with 40 nm silicon carbide nanoparticles more effective in promoting nickel nucleation than 500 nm particles due to an increase in active nucleation sites.In terms of surfactants,anionic surfactant sodium dodecyl sulfate(SDS)produced better dispersion of 40 nm silicon carbide particles than cationic surfactant cetyltrimethyl ammonium bromide(CTAB),but little difference was found between the two when 500 nm silicon carbide particles were used.Thus,although the suspension of silicon carbide particles can be improved and their co-deposition can be promoted with a cationic surfactant CTAB,it is less effective than an anionic surfactant SDS in terms of surface finish.展开更多
The initial stage of Ni-TiO2 composite system electrodeposition on glassy carbon electrode from an acidic solution of nickel sulfate was investigated using cyclic voltammetry （CV）, chronoamperometry （CA） and elect...The initial stage of Ni-TiO2 composite system electrodeposition on glassy carbon electrode from an acidic solution of nickel sulfate was investigated using cyclic voltammetry （CV）, chronoamperometry （CA） and electrochemical impedance spectroscopy （EIS）. Analysis of current density-time transients was performed using the nonlinear fitting procedure and electrochemical impedance spectroscopy was simulated by Z-view software. Besides, the surface morphology of Ni-TiO2 co-deposition at the initial stage was observed by scanning electron microscopy （SEM）. The results show that, in the case of low overpotential （-790 mV vs SCE）, the presence of TiO2 particles in the plating bath makes the nucleation relaxation time tm^x decreased clearly. Meanwhile, the electro-crystallization of Ni-TiO2 system follows a Scharifker-Hills （SH） progressive nucleation/growth mechanism. While in the case of higher overpotential, the presence of the TiO2 particles in solution makes the nucleation relaxation time tmax increased. At -850 mV （vs SCE）, the co-deposition of Ni-TiO2 system meets SH instantaneous nucleation/growth mechanism. The results of impedance spectra show that the appearance of the characteristic inductive loops represents the nucleation/growth of nickel and the presence of TiO2 particles reduces the charge transfer resistance of solution. The SEM observation confirms that TiO2 particles can be considered as favorable sites for nickel nucleating.展开更多
Porous platinum electrodes were prepared by adding YSZ,as an active material,in platinum paste.Relationship between microstructure and electrochemical performance of O 2(g),Pt/YSZ electrode have been characterized by ...Porous platinum electrodes were prepared by adding YSZ,as an active material,in platinum paste.Relationship between microstructure and electrochemical performance of O 2(g),Pt/YSZ electrode have been characterized by SEM and cyclic voltammetry.Results showed that the microstructure of platinum electrode is a significant impact on the cyclic voltammetry.With the increase of platinum electrode's porosity,the area of three-phase boundary of O 2(g) /Pt/YSZ was increased.The electrochemical reactivity was also enhanced.These were presented as the increase of current density and cathode voltage in cyclic voltammetry.展开更多
The electrocatalytic oxidation of contraflam was investigated in alkaline solution on nickel and nickel–copper alloy modified glassy carbon electrodes(GC/Ni and GC/NiCu). We prepared these electrodes by galvanostatic...The electrocatalytic oxidation of contraflam was investigated in alkaline solution on nickel and nickel–copper alloy modified glassy carbon electrodes(GC/Ni and GC/NiCu). We prepared these electrodes by galvanostatic deposition and the surface morphologies and compositions of electrodes were determined by energy-dispersive X-ray(EDX) and scanning electron microscopy(SEM). Cyclic voltammetry and chronoamperometric methods were employed to characterize the oxidation process and its kinetics. Voltammetric studies exhibit one pair of well-defined redox peaks, which is ascribed to the redox process of the nickel and followed by the greatly enhanced current response of the anodic peak in the presence of contraflam and a decrease in the corresponding cathodic current peak. This indicates that the immobilized redox mediator on the electrode surface was oxidized contraflam via an electrocatalytic mechanism. The catalytic currents increased linearly with the concentration of contraflam in the range of 0.25– 1.5 mmol/L. The anodic peak currents were linearly proportional to the square root of scan rate. This behaviour is the characteristic of a diffusion-controlled process. The determination of contraflam in capsules is applied satisfactorily by modified electrode.展开更多
Electrochimcal behaviors of rusticyanin （Rus.） isolated from Acidithiobacillus ferrooxidans were investigated through Rus.-ZnS-QDs/L-Cys/Au electrode. The cyclic voltammetric results indicate that rusticyanin immobi...Electrochimcal behaviors of rusticyanin （Rus.） isolated from Acidithiobacillus ferrooxidans were investigated through Rus.-ZnS-QDs/L-Cys/Au electrode. The cyclic voltammetric results indicate that rusticyanin immobilized on the surface of Rus.-ZnS-QDs/L-Cys/Au electrode can undergo a direct quasi-reversible electrochemical reaction. The immobilized rusticyanin is not denatured and still retains its activity in the temperature range of 19-43 ℃. The reduction ability of the protein increases and its oxidation ability becomes weak with the increase of pH from 6.0 to 7.8. Fe^2＋ ions in the solution can promote the electron transfer kinetics of the immobilized rusticyanin and make its peak potentials （φp） markedly move negatively.展开更多
The high-temperature requirement for liquid iron smelting via molten oxide electrolysis presents significant challenges.This study investigates the electrochemical reduction of Fe(Ⅲ)in a novel low-temperature electro...The high-temperature requirement for liquid iron smelting via molten oxide electrolysis presents significant challenges.This study investigates the electrochemical reduction of Fe(Ⅲ)in a novel low-temperature electrolyte,Na_(2)SiO_(3)-SiO_(2)-Fe_(2)O_(3),utilizing cyclic voltammetry and square wave voltammetry techniques.The results show that Fe(Ⅲ)reduction occurs in two steps:Fe(Ⅲ)+e^(−)→Fe(Ⅱ),Fe(Ⅱ)+2e^(−)→Fe,and that the redox process of Fe(Ⅲ)/Fe(Ⅱ)at the tungsten electrode is an irreversible reaction controlled by diffusion.The diffusion coefficients of Fe(Ⅲ)in the molten Na_(2)SiO_(3)-SiO_(2)-Fe_(2)O_(3)in the temperature range of 1248–1278 K are between 1.86×10^(−6)cm^(2)/s and 1.58×10^(−4)cm^(2)/s.The diffusion activation energy of Fe(Ⅲ)in the molten salt is 1825.41 kJ/mol.As confirmed by XRD analysis,potentiostatic electrolysis at−0.857 V(vs.O_(2)/O_(complex)^(2-))for 6 h produces metallic iron on the cathode.展开更多
The electrochemical behavior of Al(Ⅲ)in urea-1-butyl-3-methylimidazolium chloride-aluminum chloride(urea-BMIC-AlCl_(3))ionic liquids,and the effect of potential and temperature on the characterization of cathode prod...The electrochemical behavior of Al(Ⅲ)in urea-1-butyl-3-methylimidazolium chloride-aluminum chloride(urea-BMIC-AlCl_(3))ionic liquids,and the effect of potential and temperature on the characterization of cathode products,current efficiency and energy consumption of aluminum electrorefining have been investigated.Cyclic voltammetry showed that the electrochemical reduction of Al(Ⅲ)was a one-step three-electron-transfer irreversible reaction,and the electrochemical reaction was controlled by diffusion.The diffusion coefficient of Al(Ⅲ)in urea-BMIC-AlCl_(3)ionic liquids at 313 K was 1.94×10^(−7)cm^(2)/s.The 7075 aluminum alloy was used as an anode for electrorefining,and the cathode products were analyzed by XRD,SEM and EDS.The results from XRD analysis indicated that the main phase of the cathode products was aluminum.The results from SEM and EDS characterization revealed that the cathode product obtained by electrorefining−1.2 V(vs.Al)was dense and uniform,and the mass fraction of aluminum decreased from 99.61%to 99.10%as the experimental temperature increased from 313 K to 333 K.In this work,the optimum experimental conditions were−1.2 V(vs.Al)and 313 K.At this time,the cathode current efficiency was 97.80%,while the energy consumption was 3.72 kW·h/kg.展开更多
Cyclic voltammetry was used to investigate the reaction of erythromycin （EM） with dissolved oxygen on gold nanopartiele-modified electrodes prepared via electrodeposition. A well-defined reduction peak at -0.420 V a...Cyclic voltammetry was used to investigate the reaction of erythromycin （EM） with dissolved oxygen on gold nanopartiele-modified electrodes prepared via electrodeposition. A well-defined reduction peak at -0.420 V and a reoxidation peak at -0.055 V were observed. With the addition of EM into the NaOH solution containing dissolved oxygen, the oxidation peak at -0.055 V was still indiscernible. However, a new oxidation peak at 0.200 V appeared, which suggests the interaction between EM and dissolved oxygen. Therefore, this method can be used for the analysis of EM in tablets. The present method is simple, reproducible, and does not require complex analytical instruments.展开更多
The electrochemical behavior of CoCl2 in 1-butyl-3-methylimidazolium hexafluorophosphate (bmim]PF6) was investigated by cyclic voltammetry. The cyclic voltammograms were obtained from electrochemical measurement under...The electrochemical behavior of CoCl2 in 1-butyl-3-methylimidazolium hexafluorophosphate (bmim]PF6) was investigated by cyclic voltammetry. The cyclic voltammograms were obtained from electrochemical measurement under different temperatures, and the reversible behavior for Co2+/Co3+ redox couple on glassy carbon electrode in bmim]PF6 was confirmed by the characteristic of the peak currents. The diffusion coefficients (about 10-11 m2/s) of Co2+ in bmim]PF6 under different temperatures were evaluated from the dependence of the peak current density on the potential scan rates in cyclic voltammograms. It is found that the diffusion coefficient increases with increasing temperature. Diffusion activation energy of Co2+ in bmim]PF6 is also calculated to be 23.4 kJ/mol according to the relationship between diffusion coefficient and temperature.展开更多
The electro-polymerization behavior of aniline in reverse(W/O) microemulsion was investigated. The experiment results show that the cyclic voltammetry polymerization behavior of aniline in W/O microemulsion is differe...The electro-polymerization behavior of aniline in reverse(W/O) microemulsion was investigated. The experiment results show that the cyclic voltammetry polymerization behavior of aniline in W/O microemulsion is different from that in aqueous solution remarkably. With the increase of scan cycle, the oxidation potential shifts positively and the reduction potential shifts negatively, i.e., the redox potential difference increases. H+ apparent concentration affects the aniline polymerization evidently. When H+ concentration is lower than 0.08 mol/L, the electro-polymerization of aniline is difficult. With the increase of H+ concentration, the polymerization current of aniline increases gradually. Only when H+ concentration is high enough(0.5 mol/L), aniline can be well electro-polymerized. Moreover, under the same condition, the aniline polymerization current in W/O microemulsion is higher than that in aqueous solution. The scanning electron microscopy image shows that the deposited polyaniline(PANI) has uniform fiber morphology with diameter of about 100 nm. Further study result suggests that the electrochemical activity of the PANI in HCl is similar to that of the PANI prepared in aqueous solution.展开更多
基金Project(20180550242)supported by the Liaoning Science and Technology Plan,China。
文摘The electrodeposition of nickel-silicon carbide coatings on a copper electrode was done by mixing SiC particles in the nickel electrodeposition solution.The influence of surfactants and silicon carbide particle size on uniformity and quantity of silicon carbide particles in nickel-silicon carbide composite coatings was investigated.It was found that particle size affects the nucleation overpotential,with 40 nm silicon carbide nanoparticles more effective in promoting nickel nucleation than 500 nm particles due to an increase in active nucleation sites.In terms of surfactants,anionic surfactant sodium dodecyl sulfate(SDS)produced better dispersion of 40 nm silicon carbide particles than cationic surfactant cetyltrimethyl ammonium bromide(CTAB),but little difference was found between the two when 500 nm silicon carbide particles were used.Thus,although the suspension of silicon carbide particles can be improved and their co-deposition can be promoted with a cationic surfactant CTAB,it is less effective than an anionic surfactant SDS in terms of surface finish.
基金Project(MKPT-04-106) supported by the Project of National Defense of China
文摘The initial stage of Ni-TiO2 composite system electrodeposition on glassy carbon electrode from an acidic solution of nickel sulfate was investigated using cyclic voltammetry （CV）, chronoamperometry （CA） and electrochemical impedance spectroscopy （EIS）. Analysis of current density-time transients was performed using the nonlinear fitting procedure and electrochemical impedance spectroscopy was simulated by Z-view software. Besides, the surface morphology of Ni-TiO2 co-deposition at the initial stage was observed by scanning electron microscopy （SEM）. The results show that, in the case of low overpotential （-790 mV vs SCE）, the presence of TiO2 particles in the plating bath makes the nucleation relaxation time tm^x decreased clearly. Meanwhile, the electro-crystallization of Ni-TiO2 system follows a Scharifker-Hills （SH） progressive nucleation/growth mechanism. While in the case of higher overpotential, the presence of the TiO2 particles in solution makes the nucleation relaxation time tmax increased. At -850 mV （vs SCE）, the co-deposition of Ni-TiO2 system meets SH instantaneous nucleation/growth mechanism. The results of impedance spectra show that the appearance of the characteristic inductive loops represents the nucleation/growth of nickel and the presence of TiO2 particles reduces the charge transfer resistance of solution. The SEM observation confirms that TiO2 particles can be considered as favorable sites for nickel nucleating.
文摘Porous platinum electrodes were prepared by adding YSZ,as an active material,in platinum paste.Relationship between microstructure and electrochemical performance of O 2(g),Pt/YSZ electrode have been characterized by SEM and cyclic voltammetry.Results showed that the microstructure of platinum electrode is a significant impact on the cyclic voltammetry.With the increase of platinum electrode's porosity,the area of three-phase boundary of O 2(g) /Pt/YSZ was increased.The electrochemical reactivity was also enhanced.These were presented as the increase of current density and cathode voltage in cyclic voltammetry.
基金financial assistance from Tehran University of Medical Sciences,Tehran,Iran
文摘The electrocatalytic oxidation of contraflam was investigated in alkaline solution on nickel and nickel–copper alloy modified glassy carbon electrodes(GC/Ni and GC/NiCu). We prepared these electrodes by galvanostatic deposition and the surface morphologies and compositions of electrodes were determined by energy-dispersive X-ray(EDX) and scanning electron microscopy(SEM). Cyclic voltammetry and chronoamperometric methods were employed to characterize the oxidation process and its kinetics. Voltammetric studies exhibit one pair of well-defined redox peaks, which is ascribed to the redox process of the nickel and followed by the greatly enhanced current response of the anodic peak in the presence of contraflam and a decrease in the corresponding cathodic current peak. This indicates that the immobilized redox mediator on the electrode surface was oxidized contraflam via an electrocatalytic mechanism. The catalytic currents increased linearly with the concentration of contraflam in the range of 0.25– 1.5 mmol/L. The anodic peak currents were linearly proportional to the square root of scan rate. This behaviour is the characteristic of a diffusion-controlled process. The determination of contraflam in capsules is applied satisfactorily by modified electrode.
基金Project(2010CB630903) supported by the National Basic Research Program of ChinaProject(50621063) supported by the National Natural Science Foundation of China
文摘Electrochimcal behaviors of rusticyanin （Rus.） isolated from Acidithiobacillus ferrooxidans were investigated through Rus.-ZnS-QDs/L-Cys/Au electrode. The cyclic voltammetric results indicate that rusticyanin immobilized on the surface of Rus.-ZnS-QDs/L-Cys/Au electrode can undergo a direct quasi-reversible electrochemical reaction. The immobilized rusticyanin is not denatured and still retains its activity in the temperature range of 19-43 ℃. The reduction ability of the protein increases and its oxidation ability becomes weak with the increase of pH from 6.0 to 7.8. Fe^2＋ ions in the solution can promote the electron transfer kinetics of the immobilized rusticyanin and make its peak potentials （φp） markedly move negatively.
基金Project(52074084)supported by the National Natural Science Foundation of China。
文摘The high-temperature requirement for liquid iron smelting via molten oxide electrolysis presents significant challenges.This study investigates the electrochemical reduction of Fe(Ⅲ)in a novel low-temperature electrolyte,Na_(2)SiO_(3)-SiO_(2)-Fe_(2)O_(3),utilizing cyclic voltammetry and square wave voltammetry techniques.The results show that Fe(Ⅲ)reduction occurs in two steps:Fe(Ⅲ)+e^(−)→Fe(Ⅱ),Fe(Ⅱ)+2e^(−)→Fe,and that the redox process of Fe(Ⅲ)/Fe(Ⅱ)at the tungsten electrode is an irreversible reaction controlled by diffusion.The diffusion coefficients of Fe(Ⅲ)in the molten Na_(2)SiO_(3)-SiO_(2)-Fe_(2)O_(3)in the temperature range of 1248–1278 K are between 1.86×10^(−6)cm^(2)/s and 1.58×10^(−4)cm^(2)/s.The diffusion activation energy of Fe(Ⅲ)in the molten salt is 1825.41 kJ/mol.As confirmed by XRD analysis,potentiostatic electrolysis at−0.857 V(vs.O_(2)/O_(complex)^(2-))for 6 h produces metallic iron on the cathode.
基金Project(52004062)supported by the National Natural Science Foundation of ChinaProject(2020-MS-084)supported by the Natural Science Foundation of Liaoning Province,ChinaProject(N2125014)supported by the Fundamental Research Funds for the Central Universities,China。
文摘The electrochemical behavior of Al(Ⅲ)in urea-1-butyl-3-methylimidazolium chloride-aluminum chloride(urea-BMIC-AlCl_(3))ionic liquids,and the effect of potential and temperature on the characterization of cathode products,current efficiency and energy consumption of aluminum electrorefining have been investigated.Cyclic voltammetry showed that the electrochemical reduction of Al(Ⅲ)was a one-step three-electron-transfer irreversible reaction,and the electrochemical reaction was controlled by diffusion.The diffusion coefficient of Al(Ⅲ)in urea-BMIC-AlCl_(3)ionic liquids at 313 K was 1.94×10^(−7)cm^(2)/s.The 7075 aluminum alloy was used as an anode for electrorefining,and the cathode products were analyzed by XRD,SEM and EDS.The results from XRD analysis indicated that the main phase of the cathode products was aluminum.The results from SEM and EDS characterization revealed that the cathode product obtained by electrorefining−1.2 V(vs.Al)was dense and uniform,and the mass fraction of aluminum decreased from 99.61%to 99.10%as the experimental temperature increased from 313 K to 333 K.In this work,the optimum experimental conditions were−1.2 V(vs.Al)and 313 K.At this time,the cathode current efficiency was 97.80%,while the energy consumption was 3.72 kW·h/kg.
基金Project(2005037207) supported by Postdoctoral Science Foundation of China
文摘Cyclic voltammetry was used to investigate the reaction of erythromycin （EM） with dissolved oxygen on gold nanopartiele-modified electrodes prepared via electrodeposition. A well-defined reduction peak at -0.420 V and a reoxidation peak at -0.055 V were observed. With the addition of EM into the NaOH solution containing dissolved oxygen, the oxidation peak at -0.055 V was still indiscernible. However, a new oxidation peak at 0.200 V appeared, which suggests the interaction between EM and dissolved oxygen. Therefore, this method can be used for the analysis of EM in tablets. The present method is simple, reproducible, and does not require complex analytical instruments.
基金Project(2005-383) supported by the Scientific Research Foundation for the Returned Overseas Chinese Scholars, Ministry of Education, China
文摘The electrochemical behavior of CoCl2 in 1-butyl-3-methylimidazolium hexafluorophosphate (bmim]PF6) was investigated by cyclic voltammetry. The cyclic voltammograms were obtained from electrochemical measurement under different temperatures, and the reversible behavior for Co2+/Co3+ redox couple on glassy carbon electrode in bmim]PF6 was confirmed by the characteristic of the peak currents. The diffusion coefficients (about 10-11 m2/s) of Co2+ in bmim]PF6 under different temperatures were evaluated from the dependence of the peak current density on the potential scan rates in cyclic voltammograms. It is found that the diffusion coefficient increases with increasing temperature. Diffusion activation energy of Co2+ in bmim]PF6 is also calculated to be 23.4 kJ/mol according to the relationship between diffusion coefficient and temperature.
基金Projects(51071067,21271069,20673036,J1210040,50473022) supported by National Natural Science Foundation of ChinaProject(2013GK3015) supported by the Science and Technology Program of Hunan Province,China
文摘The electro-polymerization behavior of aniline in reverse(W/O) microemulsion was investigated. The experiment results show that the cyclic voltammetry polymerization behavior of aniline in W/O microemulsion is different from that in aqueous solution remarkably. With the increase of scan cycle, the oxidation potential shifts positively and the reduction potential shifts negatively, i.e., the redox potential difference increases. H+ apparent concentration affects the aniline polymerization evidently. When H+ concentration is lower than 0.08 mol/L, the electro-polymerization of aniline is difficult. With the increase of H+ concentration, the polymerization current of aniline increases gradually. Only when H+ concentration is high enough(0.5 mol/L), aniline can be well electro-polymerized. Moreover, under the same condition, the aniline polymerization current in W/O microemulsion is higher than that in aqueous solution. The scanning electron microscopy image shows that the deposited polyaniline(PANI) has uniform fiber morphology with diameter of about 100 nm. Further study result suggests that the electrochemical activity of the PANI in HCl is similar to that of the PANI prepared in aqueous solution.
