The influence of temperature on calcareous deposits formed under galvanostatic polarization mode was studied. The deposition was monitored by electrochemical impedance spectrum, and a supplementary loop in Nyquist dia...The influence of temperature on calcareous deposits formed under galvanostatic polarization mode was studied. The deposition was monitored by electrochemical impedance spectrum, and a supplementary loop in Nyquist diagram at high frequency was found to be an indicator of deposits precipitation with sufficient protection at above 20 ~C. An exponential increase of protectiveness with temperature was observed, which was quantified by linear polarization resistance technique. Observation by scanning electron microscope and X-ray diffraction analyses demonstrated that the critical temperature of calcium carbonate crystal form transition ranged from 15 to 20 ℃. Calcite formed below 15 ℃, while aragonite precipitated at above 20 ℃.展开更多
The influence of dissolved oxygen on calcareous deposits formed under galvanostatic polarization mode was studied.When the dissolved oxygen concentration was less than 7 mg L^(-1),the cathodic protection potential sho...The influence of dissolved oxygen on calcareous deposits formed under galvanostatic polarization mode was studied.When the dissolved oxygen concentration was less than 7 mg L^(-1),the cathodic protection potential showed a plateau at the initial polarization,and then quickly shifted negatively.While the dissolved oxygen was more than 9 mg L^(-1),the potential shifted negatively in a linear form.After 168 h of polarization,the final protection potential shifted negatively with the decreasing dissolved oxygen concentration.The deposition progress was monitored by electrochemical impedance spectroscopy,and only one single loop was found in Nyquist diagram,indicating deposits of ineffective protectiveness precipitation under the experimental conditions.The protection factor of deposits increased with the decreasing dissolved oxygen concentration which was detected by linear polarization resistance technique.The cathodic electrochemical reaction could change very shortly from oxygen reduction to hydrogen evolution after cathodic protection under very low dissolved oxygen concentration,such as 1 mg L^(-1),resulting in the hydrogen bubbling from the metallic surface and the decrease of deposits protection factor.Observation by scanning electron microscopy and X-ray diffraction analysis demonstrated that the deposits were mainly of calcite under the experimental conditions,and that dissolved oxygen had no effect on the crystalline types of calcium carbonate.展开更多
A galvanostatic glucose oxidase (GOD_x)/polypyrrole (Ppy) biosensor fabricated through a potential jumping process was reported.In spite of the instantaneous voltage jumping from 0.95 V to 1.7 V versus Ag/AgCl in the ...A galvanostatic glucose oxidase (GOD_x)/polypyrrole (Ppy) biosensor fabricated through a potential jumping process was reported.In spite of the instantaneous voltage jumping from 0.95 V to 1.7 V versus Ag/AgCl in the galvanostatic polymerization of pyrrole with commercial GOD_x,this GOD_x enzyme still could be successfully bundled with polypyrrole (Ppy).And,the results also confirmed that this glucose sensor not only possessed of better sensitivity to glucose than that fabricated from potentiometry or mild voltage elevating galvanometry for the similar preparing conditions but also exhibited two-week long-term stability.Finally,the kinetic data of Michalis constant (K_m) and Maximum current (I_m) for the optimized sensor were derived.The discovery this electro-modification process may disclose a novel method for fabricating the other enzyme biosensors.展开更多
The Mg corrosion mechanism was explored using galvanostatic polarisation curves,hydrogen evolution and weight loss.The data(a)were consistent with the existence of the uni-positive Mg+ion,(b)indicated that some hydrog...The Mg corrosion mechanism was explored using galvanostatic polarisation curves,hydrogen evolution and weight loss.The data(a)were consistent with the existence of the uni-positive Mg+ion,(b)indicated that some hydrogen dissolved in the WE43 metal,and(c)indicated that self corrosion was more important than the applied current density in causing weight loss.展开更多
Potential oscillations of a stainless steel electrode galvanostatically anodized have been observed in amixture of chromic and sulfuric acids. The potential regularly oscillated between 1.6 V vs. SCE (lower) and 2.1V(...Potential oscillations of a stainless steel electrode galvanostatically anodized have been observed in amixture of chromic and sulfuric acids. The potential regularly oscillated between 1.6 V vs. SCE (lower) and 2.1V(upper) with a certain frequency. The potential values are affected neither by the composition of chromic and sulfu-ric acids nor by the magnitude of applied current density although the potential frequency is very sensitive to theseparameters. This phenomenon is interpreted in terms of the repeated formation and disappearance of the saturatedlayer of dichromate ions on the electrode surface. Such scheme is consistent with the in situ FTIR spectroscopicresult that the concentration of Cr2O ions on the electrode surface increased with time during the polarization atthe lower potential but the change in concenetion of Cr2O ions was negligible at the higher potential.展开更多
Nano-fibrous polyaniline was synthesized on stainless steel electrode in 0.5mol·L-1 H2SO4 solution by pulse galvanostatic method. The effects of synthetic conditions of pulse galvanostatic method on the electroac...Nano-fibrous polyaniline was synthesized on stainless steel electrode in 0.5mol·L-1 H2SO4 solution by pulse galvanostatic method. The effects of synthetic conditions of pulse galvanostatic method on the electroactivity of polyaniline were investigated. The results show that the electroactivity of polyaniline film strongly depends on the synthetic conditions, such as the ratio of “on time” to “off time”(ton/toff), frequency, monomer concentration, temperature and mean current density. Different electroactivities of polyaniline are caused by different morphologies of polyaniline. The nano-fibrous polyaniline has higher electroactivity than polyaniline with other morphologies. Under the following conditions: mean current density of pulse galvanostatic method 13mA·cm-2, ton/toff 1, frequency 200Hz, monomer concentration 0.3mol·L-1 and temperature 20℃, nano-fibrous polyaniline film with the highest electroactivity can be obtained.展开更多
The correlation between the grain size of electrodeposited coatings and the current densities was modeled by considering galvanostatic conditions. In order to test the model by experimental results, nanocrystalline ...The correlation between the grain size of electrodeposited coatings and the current densities was modeled by considering galvanostatic conditions. In order to test the model by experimental results, nanocrystalline （NC） nickel samples were deposited at different current densities using a Watts bath. The grain size of the deposits was evaluated by X-ray diffraction （XRD） technique. Model predictions were validated by finding a curve being the best-fit to the experimental results which were gathered from literature for different NC coatings in addition to those data measured in this research for NC nickel coatings. According to our model, the variation of grain size with the reciprocal of the current density follows a power law. A good agreement between the experimental results and model predictions was observed which indicated that the derived analytical model is applicable for producting the nanocrystalline electrodeposits with the desired grain size by controling current density.展开更多
In optimizing fast charge capability,mitigating side reaction rate,and unveiling particle cracking tolerance for Li-ion batteries(LIBs),the galvanostatic charge–discharge(GCD)at different charge/discharge rates,the s...In optimizing fast charge capability,mitigating side reaction rate,and unveiling particle cracking tolerance for Li-ion batteries(LIBs),the galvanostatic charge–discharge(GCD)at different charge/discharge rates,the static electrochemical impedance spectroscopy(SEIS)under open circuit voltage(OCV)conditions,and the dynamic EIS(DEIS)under dynamic conditions are widely used to investigate charge transfer reactions in LIBs.In spite of great progresses achieved,it is still an open question how to decouple charge transfer reactions under dynamic conditions,especially under conditions of different charge/discharge rates and state of charges(SOCs).To address the above challenges,this work develops a unified framework to digitize,visualize,and finally decouple charge transfer reactions in LIBs under dynamic conditions.In detail:(i)a set of matrix-based numerical solutions to GCD,SEIS,and DEIS are deduced for LIBs;(ii)an open-source DEIS-Toolbox@LIB to digitize/visualize charge transfer reactions is developed;(iii)EIS under dynamic and OCV conditions are discriminated;and(iv)a dynamic decoupling of charge transfer reactions is achieved with respect to core parameters under dynamic conditions for LIBs.The developed framework serves to digitize/visualize/decouple charge transfer reactions under dynamic conditions,and then to unveil limiting factors of fast charge/discharge and triggering mechanisms of side reactions for batteries.展开更多
Mg-Li-Gd alloys were prepared by electrochemical codeposition from LiCl-KCl-MgCl 2 -Gd 2 O 3 melts on molybdenum electrode with constant current density at 823 and 973 K. The microstructure of the Mg-Li-Gd alloys was ...Mg-Li-Gd alloys were prepared by electrochemical codeposition from LiCl-KCl-MgCl 2 -Gd 2 O 3 melts on molybdenum electrode with constant current density at 823 and 973 K. The microstructure of the Mg-Li-Gd alloys was analyzed by X-ray diffraction （XRD）, optical microscopy （OM） and scanning electron microscopy （SEM）. The results show that magnesium and gadolinium deposit mainly in the first 30 min, and the alloy obtained contains 96.53% Mg, 0.27% Li and 3.20% Gd （mass fraction）. Then, the reduction of lithium ions occurs quickly. The composition of alloy can be adjusted by controlling electrolysis time or Gd 2 O 3 concentration in LiCl-KCl melts. With the addition of Gd into Mg-Li alloys, the corrosion resistance of the alloys is enhanced. XRD results suggest that Mg 3 Gd and Mg 2 Gd can be formed in Mg-Li-Gd alloys. The distribution of Gd element in Mg-Li-Gd alloys indicates that Gd element mainly distributes at the grain boundaries of Mg-Li-Gd alloys.展开更多
Mg-Al-Sn alloy is one of the new developed anode materials for seawater activated batteries. The potentiodynamic polarization, galvanostatic discharge and electrochemical impedance spectroscopy of Mg-6%Al-1%Sn and Mg-...Mg-Al-Sn alloy is one of the new developed anode materials for seawater activated batteries. The potentiodynamic polarization, galvanostatic discharge and electrochemical impedance spectroscopy of Mg-6%Al-1%Sn and Mg-6%Al-5%Sn(mass fraction) alloys in seawater were studied and compared with the commercial AZ31 and AP65 alloys. The results show that the Mg-6%Al-1%Sn alloy obtains the most negative discharge potential of average-1.611V with a electric current density of 100 mA/cm2. EIS studies reveal that the Mg-Al-Sn alloy/seawater interfacial electrochemical process is determined by an activation controlled reaction. The assembled prototype batteries with Mg-6%Al-1%Sn alloy as anodes and Ag Cl as cathodes exhibit a satisfactory integrated discharge properties.展开更多
The influence of Ga and In on the electrochemical properties of Mg anode materials were investigated by the polarization and galvanostatic curve tests. The microstructure and the corroded surface of the Mg-In-Ga alloy...The influence of Ga and In on the electrochemical properties of Mg anode materials were investigated by the polarization and galvanostatic curve tests. The microstructure and the corroded surface of the Mg-In-Ga alloys were observed by scanning electron microscopy （SEM）. The corrosion product of the Mg-0.8%In （mass fraction） and Mg-0.8%Ga-0.3%In alloy were determined by X-ray diffraction. The results show that no second phase exists in the Mg-xIn （x=0-0.8%） allloys. Intergranular compounds containing Ga and In elements occur in the Mg-0.8%In-xGa （x=0-0.8%） alloys. The addition of In into Mg as well as the addition of 0.05%-0.5%Ga into Mg-In alloy promotes the corrosion resistance. The addition of Ga into Mg-In alloys also promotes the electrochemical activity. The Mg-0.8%In-0.8%Ga alloy has the most negative mean potential,-1.682 V, which is more negative than -1.406 V in AZ91D. The corrosion type of the Mg-In-Ga alloys is general corrosion and the corrosion product is Mg（OH）2.展开更多
A multifunctional polymeric nanofilm of triazinedithiolsilane monosodium salt, which can resist corrosion and activatecopper surface concurrently, was prepared by galvanostatic technique and the following hydrolysis-c...A multifunctional polymeric nanofilm of triazinedithiolsilane monosodium salt, which can resist corrosion and activatecopper surface concurrently, was prepared by galvanostatic technique and the following hydrolysis-condensation approach.Electrochemical tests were carried out to evaluate the resistant ability of nanofilm. The changes of functional groups atop thenanofilms were monitored with Fourier transform infrared spectroscopy （FT-IR） and contact angles （CA） simultaneously. Thechemical composition and the morphology of the polymeric nanofilm were investigated by X-ray photoelectron spectroscopy （XPS）and scanning electron microscope （SEM）, respectively. The results reveal that the preferentially developed disulfide units protect thecopper during the whole preparation process, and the subsequently hydrolyzed nanofilms without/with heating shape into newinterface phases bearing the multifunctionality. This multifunctional interface （the polymeric nanofilm on copper surface） opens upthe possibilities for other OH-containing reagents to be anchored onto copper surface in demanding researches or industrialapplications.展开更多
We measured the anodic hydrogen evolution rates for various applied anodic current densities and estimated the corresponding cathodic hydrogen evolution rates.The estimated cathodic hydrogen evolution rates were less ...We measured the anodic hydrogen evolution rates for various applied anodic current densities and estimated the corresponding cathodic hydrogen evolution rates.The estimated cathodic hydrogen evolution rates were less than the measured anodic hydrogen evolution rates,contradicting the enhanced catalytic activity mechanism of Mg corrosion.In addition,this model was contradicted by the measured apparent Mg valence of 1.2±0.1.In contrast,the uni-positive Mg^(+)mechanism of Mg corrosion was supported by(i)the apparent Mg valence of 1.2±0.1,and(ii)the fact that the measured anodic hydrogen evolution rate increased with increasing weight loss rate.展开更多
The purpose of this paper was to investigate the possibility of treating C. I. Reactive Blue 19 wastewater by electrochemical oxidation via electrogenerated active chlorine, using metallic oxide coatings （dimensional...The purpose of this paper was to investigate the possibility of treating C. I. Reactive Blue 19 wastewater by electrochemical oxidation via electrogenerated active chlorine, using metallic oxide coatings （dimensional stable anode, DSA） as anode. The electrolysis for the simulated wastewater was conducted at a constant current. Absorbances at 592 nm and 255 nm were measured to follow the decolorization of the dye and the degradatin of its aromatic ring. After 4 h of electrolysis under the experimental conditions： current density of 15 A·m^-2, 0.2 mol·L^-1 NaCl, 0.1 mol·L^-1 Na2SO4, 0.1 mmol·L^-1 dye, initial pH=6.4 and T=30℃, 100% decolorization of the dye and about 45% degradation of its aromatic ring were achieved, while no obvious change of total organic carbon was observed. The experimental results suggest that the decolorization of the dye and degradation of its aromatic ring were directly affected by current density, temperature, concentrations of the dye and sodium chloride, while slightly affected by initial pH and sodium sulfate concentration; the decolorization of the dye and degradation of its aromatic ring followed pseudo-first-order kinetics; and indirect electrooxidation, using electrogenerated active chlorine, predominated in the electrochemical oxidation.展开更多
The electrochemical co-reduction of Ho(Ⅲ)and Mg(Ⅱ)ions was investigated on Mo electrode in eutectic LiCl–KCl salts at temperature of 773 K using various electrochemical techniques.Cyclic voltammogram(CV)and square ...The electrochemical co-reduction of Ho(Ⅲ)and Mg(Ⅱ)ions was investigated on Mo electrode in eutectic LiCl–KCl salts at temperature of 773 K using various electrochemical techniques.Cyclic voltammogram(CV)and square wave voltammogram exhibit three reduction peaks corresponding to the reduction of Ho(Ⅲ)on pre-deposited Mg electrode,whose potentials are more positive than that of Ho on Mo electrode because of the formation of Mg-Ho intermetallic compounds by co-reduction of Ho(Ⅲ)and Mg(Ⅱ)ions.Meanwhile,chronopotentiometry and open-circuit chronopotentiometry were used to explore the electrochemical formation of Mg–Ho intermetallics.Mg–Ho alloys were produced by galvanostatic electrolysis at the current of 1.5 A for different electrolysis durations.Ho_(5)Mg_(24),HoMg_(2) and HoMg intermetallic compounds were acquired and characterized by X-ray diffraction(XRD)and scanning electron microscopy(SEM)coupled with energy-dispersive spectroscopy(EDS).The results indicate that Mg–Ho intermetallic compounds,Ho_(5)Mg_(24),HoMg_(2) and HoMg,could be prepared by molten salts electrolysis.展开更多
Aqueous zinc-ion batteries,especially Zn-Mn02 battery,have attracted intensive attention owing to their unique features of high capacity,environmental friendliness,and safety.However,the problem of Mn dissolution hind...Aqueous zinc-ion batteries,especially Zn-Mn02 battery,have attracted intensive attention owing to their unique features of high capacity,environmental friendliness,and safety.However,the problem of Mn dissolution hinders the development of zinc-ion batteries with long-term usage and high-rate performance.In this work,a novel preparation method for the polyaniline(PANI)-coated composite aerogel of Mn02 and rGO(MnO2/rGO/PANI)electrode is reported.The obtained composite possesses high electrical conductivity,and also effectively suppresses the dissolution of Mn.The fabricated Mn02/rGO/PANI//Zn battery exhibits a high capacity of 241.1 mAh·g^-1 at 0.1 A·g^-1,and an excellent capacity retention of 82.7%after 600 charge/discharge cycles.In addition,the rapid diffusion coefficient of the Mn02/rGO/PANI electrode was further examined by galvanostatic intermittent titration technique.This work provides new insights into the development of high-performance Zn-Mn02 battery with a better understanding of its diffusion kinetics.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
The implementation of alternative harvest systems which are able to accelerate the kinetics of growth of plants, is extremely important to decrease the time of crop. In this sense, Electro-Hydroponic culture, i.e., th...The implementation of alternative harvest systems which are able to accelerate the kinetics of growth of plants, is extremely important to decrease the time of crop. In this sense, Electro-Hydroponic culture, i.e., the application of an electric field in the nutrient solution of the hydroponic culture emerges as an alternative and interesting harvest system. The objective of the present study was to investigate the effect of the electric field applying different intensities of direct current (DC) at the galvanostatic regime (50, 37.5, 25 and 12.5 mA) on the growth of lettuce (Lactuca sativa) plants in hydroponic culture. Fifty lettuce plants were used in a nutrient solution, from which 4 groups composed of ten lettuces each one, were subjected at 12.5, 25, 37.5 and 50 mA, respectively. A fifth group of ten lettuces was used as a reference test, i.e., without application of DC. The experiments were carried out during 16 days. The results reveal that the kinetics of growth of the lettuce is dependent on the applied current;actually it is observed an increase in the foliate area of the plants cultivated in the presence of DC than that obtained in the reference test. Furthermore, the plants subjected at 12.5 mA, revealed an increase in the foliate area of 65.3% and 73.2% in comparison with the reference test.展开更多
Lithium-sulfur(Li-S)batteries have attracted significant attention for their high specific capacity,non-toxic and harmless advantages.However,the shuttle effect limits their development.In this work,small-sized tin di...Lithium-sulfur(Li-S)batteries have attracted significant attention for their high specific capacity,non-toxic and harmless advantages.However,the shuttle effect limits their development.In this work,small-sized tin disulfide(SnS_(2))nanoparticles are embedded between interlayers of twodimensional porous carbon nanosheets(PCNs),forming a multi-functional nanocomposite(PCN-SnS_(2))as a cathode carrier for Li-S batteries.The graphitized carbon nanosheets improve the overall conductivity of the electrode,and the abundant pores not only facilitate ion transfer and electrolyte permeation,but also buffer the volume change during the charge and discharge process to ensure the integrity of the electrode material.More importantly,the physical confinement of PCN,as well as the strong chemical adsorption and catalytic reaction of small SnS_(2)nanoparticles,synergistically reduce the shuttle effect of polysulfides.The interaction between a porous layered structure and physical-chemical confinement gives the PCN-SnS_(2)-S electrode high electrochemical performance.Even at a high rate of 2 C,a discharge capacity of 650 mA h g^(-1)is maintained after 150 cycles,underscoring the positive results of SnS_(2)-based materials for Li-S batteries.The galvanostatic intermittent titration technique results further confirm that the PCN-SnS_(2)-S electrode has a high Li+transmission rate,which reduces the activation barrier and improves the electrochemical reaction kinetics.This work provides strong evidence that reducing the size of SnS_(2)nanostructures is beneficial for capturing and reacting with polysulfides to alleviate their shuttle effect in Li-S batteries.展开更多
Polyfluorene (PF) film has been successfully electropolymerized at lower potential (0.91 V vs.Ag/AgCl) in the mixed electrolyte of boron trifluoride diethyl etherate and trifluoroacetic acid.The PF film is characteriz...Polyfluorene (PF) film has been successfully electropolymerized at lower potential (0.91 V vs.Ag/AgCl) in the mixed electrolyte of boron trifluoride diethyl etherate and trifluoroacetic acid.The PF film is characterized to have about 10 repeat units and no presence of ketonic defect site.UV-vis and photoluminescent spectral studies indicate that the PF film is blue light emitting.From cyclic voltammetry and galvanostatic charge-discharge tests in 1 M lithium perchlorate/acetonitrile electrolyte,the polyfluorene/activated carbon electrode shows a specific capacitance of 227.1 F g-1 (per active layer mass) and reversible redox reaction at the potential of 1.4 V in a three electrode configuration.An asymmetric electrochemical capacitor based on this composite electrode and activated carbon electrode exhibits a specific energy of 14.7 Wh kg-1 (per active layer mass).These results indicate that electrochemically prepared polyfluorene could be used as energy storage component for electrochemical application.展开更多
基金financially supported by the National Science and Technology Major Project of China(No. 2011ZX05027-004-06)
文摘The influence of temperature on calcareous deposits formed under galvanostatic polarization mode was studied. The deposition was monitored by electrochemical impedance spectrum, and a supplementary loop in Nyquist diagram at high frequency was found to be an indicator of deposits precipitation with sufficient protection at above 20 ~C. An exponential increase of protectiveness with temperature was observed, which was quantified by linear polarization resistance technique. Observation by scanning electron microscope and X-ray diffraction analyses demonstrated that the critical temperature of calcium carbonate crystal form transition ranged from 15 to 20 ℃. Calcite formed below 15 ℃, while aragonite precipitated at above 20 ℃.
基金the financial support of this project by the National Basic Research Program of China(973 Project,No.2014CB643300)National Environmental Corrosion Platform(NECP)
文摘The influence of dissolved oxygen on calcareous deposits formed under galvanostatic polarization mode was studied.When the dissolved oxygen concentration was less than 7 mg L^(-1),the cathodic protection potential showed a plateau at the initial polarization,and then quickly shifted negatively.While the dissolved oxygen was more than 9 mg L^(-1),the potential shifted negatively in a linear form.After 168 h of polarization,the final protection potential shifted negatively with the decreasing dissolved oxygen concentration.The deposition progress was monitored by electrochemical impedance spectroscopy,and only one single loop was found in Nyquist diagram,indicating deposits of ineffective protectiveness precipitation under the experimental conditions.The protection factor of deposits increased with the decreasing dissolved oxygen concentration which was detected by linear polarization resistance technique.The cathodic electrochemical reaction could change very shortly from oxygen reduction to hydrogen evolution after cathodic protection under very low dissolved oxygen concentration,such as 1 mg L^(-1),resulting in the hydrogen bubbling from the metallic surface and the decrease of deposits protection factor.Observation by scanning electron microscopy and X-ray diffraction analysis demonstrated that the deposits were mainly of calcite under the experimental conditions,and that dissolved oxygen had no effect on the crystalline types of calcium carbonate.
文摘A galvanostatic glucose oxidase (GOD_x)/polypyrrole (Ppy) biosensor fabricated through a potential jumping process was reported.In spite of the instantaneous voltage jumping from 0.95 V to 1.7 V versus Ag/AgCl in the galvanostatic polymerization of pyrrole with commercial GOD_x,this GOD_x enzyme still could be successfully bundled with polypyrrole (Ppy).And,the results also confirmed that this glucose sensor not only possessed of better sensitivity to glucose than that fabricated from potentiometry or mild voltage elevating galvanometry for the similar preparing conditions but also exhibited two-week long-term stability.Finally,the kinetic data of Michalis constant (K_m) and Maximum current (I_m) for the optimized sensor were derived.The discovery this electro-modification process may disclose a novel method for fabricating the other enzyme biosensors.
文摘The Mg corrosion mechanism was explored using galvanostatic polarisation curves,hydrogen evolution and weight loss.The data(a)were consistent with the existence of the uni-positive Mg+ion,(b)indicated that some hydrogen dissolved in the WE43 metal,and(c)indicated that self corrosion was more important than the applied current density in causing weight loss.
文摘Potential oscillations of a stainless steel electrode galvanostatically anodized have been observed in amixture of chromic and sulfuric acids. The potential regularly oscillated between 1.6 V vs. SCE (lower) and 2.1V(upper) with a certain frequency. The potential values are affected neither by the composition of chromic and sulfu-ric acids nor by the magnitude of applied current density although the potential frequency is very sensitive to theseparameters. This phenomenon is interpreted in terms of the repeated formation and disappearance of the saturatedlayer of dichromate ions on the electrode surface. Such scheme is consistent with the in situ FTIR spectroscopicresult that the concentration of Cr2O ions on the electrode surface increased with time during the polarization atthe lower potential but the change in concenetion of Cr2O ions was negligible at the higher potential.
基金Project(50473022) supported by the National Natural Science Foundation project supported by the State Key Laboratoryof Chemo/Biosensing and Chemometrics of China
文摘Nano-fibrous polyaniline was synthesized on stainless steel electrode in 0.5mol·L-1 H2SO4 solution by pulse galvanostatic method. The effects of synthetic conditions of pulse galvanostatic method on the electroactivity of polyaniline were investigated. The results show that the electroactivity of polyaniline film strongly depends on the synthetic conditions, such as the ratio of “on time” to “off time”(ton/toff), frequency, monomer concentration, temperature and mean current density. Different electroactivities of polyaniline are caused by different morphologies of polyaniline. The nano-fibrous polyaniline has higher electroactivity than polyaniline with other morphologies. Under the following conditions: mean current density of pulse galvanostatic method 13mA·cm-2, ton/toff 1, frequency 200Hz, monomer concentration 0.3mol·L-1 and temperature 20℃, nano-fibrous polyaniline film with the highest electroactivity can be obtained.
文摘The correlation between the grain size of electrodeposited coatings and the current densities was modeled by considering galvanostatic conditions. In order to test the model by experimental results, nanocrystalline （NC） nickel samples were deposited at different current densities using a Watts bath. The grain size of the deposits was evaluated by X-ray diffraction （XRD） technique. Model predictions were validated by finding a curve being the best-fit to the experimental results which were gathered from literature for different NC coatings in addition to those data measured in this research for NC nickel coatings. According to our model, the variation of grain size with the reciprocal of the current density follows a power law. A good agreement between the experimental results and model predictions was observed which indicated that the derived analytical model is applicable for producting the nanocrystalline electrodeposits with the desired grain size by controling current density.
基金supported by the National Natural Science Foundation of China(22479092,22078190)。
文摘In optimizing fast charge capability,mitigating side reaction rate,and unveiling particle cracking tolerance for Li-ion batteries(LIBs),the galvanostatic charge–discharge(GCD)at different charge/discharge rates,the static electrochemical impedance spectroscopy(SEIS)under open circuit voltage(OCV)conditions,and the dynamic EIS(DEIS)under dynamic conditions are widely used to investigate charge transfer reactions in LIBs.In spite of great progresses achieved,it is still an open question how to decouple charge transfer reactions under dynamic conditions,especially under conditions of different charge/discharge rates and state of charges(SOCs).To address the above challenges,this work develops a unified framework to digitize,visualize,and finally decouple charge transfer reactions in LIBs under dynamic conditions.In detail:(i)a set of matrix-based numerical solutions to GCD,SEIS,and DEIS are deduced for LIBs;(ii)an open-source DEIS-Toolbox@LIB to digitize/visualize charge transfer reactions is developed;(iii)EIS under dynamic and OCV conditions are discriminated;and(iv)a dynamic decoupling of charge transfer reactions is achieved with respect to core parameters under dynamic conditions for LIBs.The developed framework serves to digitize/visualize/decouple charge transfer reactions under dynamic conditions,and then to unveil limiting factors of fast charge/discharge and triggering mechanisms of side reactions for batteries.
基金Project(2009AA050702)supported by the National High-tech Research and Development Program of ChinaProject(GC06A212)supported by the Scientific Technology Project of Heilongjiang Province,China+2 种基金Project(50871033)supported by the National Natural Science Foundation of ChinaProject(208181)supported by the Key Project of Ministry of Education,ChinaProject(HEUCF101002)supported by the Fundamental Research Funds for the Central Universities,China
文摘Mg-Li-Gd alloys were prepared by electrochemical codeposition from LiCl-KCl-MgCl 2 -Gd 2 O 3 melts on molybdenum electrode with constant current density at 823 and 973 K. The microstructure of the Mg-Li-Gd alloys was analyzed by X-ray diffraction （XRD）, optical microscopy （OM） and scanning electron microscopy （SEM）. The results show that magnesium and gadolinium deposit mainly in the first 30 min, and the alloy obtained contains 96.53% Mg, 0.27% Li and 3.20% Gd （mass fraction）. Then, the reduction of lithium ions occurs quickly. The composition of alloy can be adjusted by controlling electrolysis time or Gd 2 O 3 concentration in LiCl-KCl melts. With the addition of Gd into Mg-Li alloys, the corrosion resistance of the alloys is enhanced. XRD results suggest that Mg 3 Gd and Mg 2 Gd can be formed in Mg-Li-Gd alloys. The distribution of Gd element in Mg-Li-Gd alloys indicates that Gd element mainly distributes at the grain boundaries of Mg-Li-Gd alloys.
基金Project supported by the Fundamental Research Funds for the Central Universities of China
文摘Mg-Al-Sn alloy is one of the new developed anode materials for seawater activated batteries. The potentiodynamic polarization, galvanostatic discharge and electrochemical impedance spectroscopy of Mg-6%Al-1%Sn and Mg-6%Al-5%Sn(mass fraction) alloys in seawater were studied and compared with the commercial AZ31 and AP65 alloys. The results show that the Mg-6%Al-1%Sn alloy obtains the most negative discharge potential of average-1.611V with a electric current density of 100 mA/cm2. EIS studies reveal that the Mg-Al-Sn alloy/seawater interfacial electrochemical process is determined by an activation controlled reaction. The assembled prototype batteries with Mg-6%Al-1%Sn alloy as anodes and Ag Cl as cathodes exhibit a satisfactory integrated discharge properties.
基金Project(20110162120051)supported by Specialized Research Fund for the Doctor Program of Higher Education,ChinaProject(51101171)supported by the National Natural Science Foundation of China
文摘The influence of Ga and In on the electrochemical properties of Mg anode materials were investigated by the polarization and galvanostatic curve tests. The microstructure and the corroded surface of the Mg-In-Ga alloys were observed by scanning electron microscopy （SEM）. The corrosion product of the Mg-0.8%In （mass fraction） and Mg-0.8%Ga-0.3%In alloy were determined by X-ray diffraction. The results show that no second phase exists in the Mg-xIn （x=0-0.8%） allloys. Intergranular compounds containing Ga and In elements occur in the Mg-0.8%In-xGa （x=0-0.8%） alloys. The addition of In into Mg as well as the addition of 0.05%-0.5%Ga into Mg-In alloy promotes the corrosion resistance. The addition of Ga into Mg-In alloys also promotes the electrochemical activity. The Mg-0.8%In-0.8%Ga alloy has the most negative mean potential,-1.682 V, which is more negative than -1.406 V in AZ91D. The corrosion type of the Mg-In-Ga alloys is general corrosion and the corrosion product is Mg（OH）2.
基金Project(2013DFR40700)supported by International S&T Cooperation Program of ChinaProjects(21174034,51003019,51302280)supported by the National Natural Science Foundation of China
文摘A multifunctional polymeric nanofilm of triazinedithiolsilane monosodium salt, which can resist corrosion and activatecopper surface concurrently, was prepared by galvanostatic technique and the following hydrolysis-condensation approach.Electrochemical tests were carried out to evaluate the resistant ability of nanofilm. The changes of functional groups atop thenanofilms were monitored with Fourier transform infrared spectroscopy （FT-IR） and contact angles （CA） simultaneously. Thechemical composition and the morphology of the polymeric nanofilm were investigated by X-ray photoelectron spectroscopy （XPS）and scanning electron microscope （SEM）, respectively. The results reveal that the preferentially developed disulfide units protect thecopper during the whole preparation process, and the subsequently hydrolyzed nanofilms without/with heating shape into newinterface phases bearing the multifunctionality. This multifunctional interface （the polymeric nanofilm on copper surface） opens upthe possibilities for other OH-containing reagents to be anchored onto copper surface in demanding researches or industrialapplications.
基金the financial support for this research by the Australian Research Council(ARC)through the discovery grant DP170102557
文摘We measured the anodic hydrogen evolution rates for various applied anodic current densities and estimated the corresponding cathodic hydrogen evolution rates.The estimated cathodic hydrogen evolution rates were less than the measured anodic hydrogen evolution rates,contradicting the enhanced catalytic activity mechanism of Mg corrosion.In addition,this model was contradicted by the measured apparent Mg valence of 1.2±0.1.In contrast,the uni-positive Mg^(+)mechanism of Mg corrosion was supported by(i)the apparent Mg valence of 1.2±0.1,and(ii)the fact that the measured anodic hydrogen evolution rate increased with increasing weight loss rate.
文摘The purpose of this paper was to investigate the possibility of treating C. I. Reactive Blue 19 wastewater by electrochemical oxidation via electrogenerated active chlorine, using metallic oxide coatings （dimensional stable anode, DSA） as anode. The electrolysis for the simulated wastewater was conducted at a constant current. Absorbances at 592 nm and 255 nm were measured to follow the decolorization of the dye and the degradatin of its aromatic ring. After 4 h of electrolysis under the experimental conditions： current density of 15 A·m^-2, 0.2 mol·L^-1 NaCl, 0.1 mol·L^-1 Na2SO4, 0.1 mmol·L^-1 dye, initial pH=6.4 and T=30℃, 100% decolorization of the dye and about 45% degradation of its aromatic ring were achieved, while no obvious change of total organic carbon was observed. The experimental results suggest that the decolorization of the dye and degradation of its aromatic ring were directly affected by current density, temperature, concentrations of the dye and sodium chloride, while slightly affected by initial pH and sodium sulfate concentration; the decolorization of the dye and degradation of its aromatic ring followed pseudo-first-order kinetics; and indirect electrooxidation, using electrogenerated active chlorine, predominated in the electrochemical oxidation.
基金the National Natural Science Foundation of China(Nos.11575047,11675044,21790373,21876034 and 11875116)the Major Research Plan of the National Natural Science Foundation of China(Nos.91326113 and 91226201)the Fundamental Research Funds for the Central Universities(No.HEUCF201849)。
文摘The electrochemical co-reduction of Ho(Ⅲ)and Mg(Ⅱ)ions was investigated on Mo electrode in eutectic LiCl–KCl salts at temperature of 773 K using various electrochemical techniques.Cyclic voltammogram(CV)and square wave voltammogram exhibit three reduction peaks corresponding to the reduction of Ho(Ⅲ)on pre-deposited Mg electrode,whose potentials are more positive than that of Ho on Mo electrode because of the formation of Mg-Ho intermetallic compounds by co-reduction of Ho(Ⅲ)and Mg(Ⅱ)ions.Meanwhile,chronopotentiometry and open-circuit chronopotentiometry were used to explore the electrochemical formation of Mg–Ho intermetallics.Mg–Ho alloys were produced by galvanostatic electrolysis at the current of 1.5 A for different electrolysis durations.Ho_(5)Mg_(24),HoMg_(2) and HoMg intermetallic compounds were acquired and characterized by X-ray diffraction(XRD)and scanning electron microscopy(SEM)coupled with energy-dispersive spectroscopy(EDS).The results indicate that Mg–Ho intermetallic compounds,Ho_(5)Mg_(24),HoMg_(2) and HoMg,could be prepared by molten salts electrolysis.
基金supported by the National Natural Science Foundation of China(Nos.51602284 and 51702286)Natural Science Foundation of Zhejiang Province,China(Nos.LQ17B030002 and LR19E020003)General Scientific Research Project of the Department of Education of Zhejiang Province,China(No.Y201839638).
文摘Aqueous zinc-ion batteries,especially Zn-Mn02 battery,have attracted intensive attention owing to their unique features of high capacity,environmental friendliness,and safety.However,the problem of Mn dissolution hinders the development of zinc-ion batteries with long-term usage and high-rate performance.In this work,a novel preparation method for the polyaniline(PANI)-coated composite aerogel of Mn02 and rGO(MnO2/rGO/PANI)electrode is reported.The obtained composite possesses high electrical conductivity,and also effectively suppresses the dissolution of Mn.The fabricated Mn02/rGO/PANI//Zn battery exhibits a high capacity of 241.1 mAh·g^-1 at 0.1 A·g^-1,and an excellent capacity retention of 82.7%after 600 charge/discharge cycles.In addition,the rapid diffusion coefficient of the Mn02/rGO/PANI electrode was further examined by galvanostatic intermittent titration technique.This work provides new insights into the development of high-performance Zn-Mn02 battery with a better understanding of its diffusion kinetics.
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.
文摘The implementation of alternative harvest systems which are able to accelerate the kinetics of growth of plants, is extremely important to decrease the time of crop. In this sense, Electro-Hydroponic culture, i.e., the application of an electric field in the nutrient solution of the hydroponic culture emerges as an alternative and interesting harvest system. The objective of the present study was to investigate the effect of the electric field applying different intensities of direct current (DC) at the galvanostatic regime (50, 37.5, 25 and 12.5 mA) on the growth of lettuce (Lactuca sativa) plants in hydroponic culture. Fifty lettuce plants were used in a nutrient solution, from which 4 groups composed of ten lettuces each one, were subjected at 12.5, 25, 37.5 and 50 mA, respectively. A fifth group of ten lettuces was used as a reference test, i.e., without application of DC. The experiments were carried out during 16 days. The results reveal that the kinetics of growth of the lettuce is dependent on the applied current;actually it is observed an increase in the foliate area of the plants cultivated in the presence of DC than that obtained in the reference test. Furthermore, the plants subjected at 12.5 mA, revealed an increase in the foliate area of 65.3% and 73.2% in comparison with the reference test.
基金the National Key R&D Program of China(2016YFA0202602)the National Natural Science Foundation of China(U1663225)+3 种基金the Fundamental Research Funds for the Central Universities(2020-YB-009)the Academy of Scientific Research and Technology(6611,ASRT,Egypt)the 111 National project(B20002)from the Ministry of Science and Technology and the Ministry of Education,ChinaSinopec Ministry of Science and Technology Basic Prospective Research Project(217027-5 and 218025-9)。
文摘Lithium-sulfur(Li-S)batteries have attracted significant attention for their high specific capacity,non-toxic and harmless advantages.However,the shuttle effect limits their development.In this work,small-sized tin disulfide(SnS_(2))nanoparticles are embedded between interlayers of twodimensional porous carbon nanosheets(PCNs),forming a multi-functional nanocomposite(PCN-SnS_(2))as a cathode carrier for Li-S batteries.The graphitized carbon nanosheets improve the overall conductivity of the electrode,and the abundant pores not only facilitate ion transfer and electrolyte permeation,but also buffer the volume change during the charge and discharge process to ensure the integrity of the electrode material.More importantly,the physical confinement of PCN,as well as the strong chemical adsorption and catalytic reaction of small SnS_(2)nanoparticles,synergistically reduce the shuttle effect of polysulfides.The interaction between a porous layered structure and physical-chemical confinement gives the PCN-SnS_(2)-S electrode high electrochemical performance.Even at a high rate of 2 C,a discharge capacity of 650 mA h g^(-1)is maintained after 150 cycles,underscoring the positive results of SnS_(2)-based materials for Li-S batteries.The galvanostatic intermittent titration technique results further confirm that the PCN-SnS_(2)-S electrode has a high Li+transmission rate,which reduces the activation barrier and improves the electrochemical reaction kinetics.This work provides strong evidence that reducing the size of SnS_(2)nanostructures is beneficial for capturing and reacting with polysulfides to alleviate their shuttle effect in Li-S batteries.
基金supported by the National Natural Science Foundation of China (50903078)Specialized Research Fund for the Doctoral Program of Higher Education (New Teachers) (20090132120017)Promotive Research Fund for Excellent Young and Middle-aged Scientists of Shandong Province (BS2009CL036)
文摘Polyfluorene (PF) film has been successfully electropolymerized at lower potential (0.91 V vs.Ag/AgCl) in the mixed electrolyte of boron trifluoride diethyl etherate and trifluoroacetic acid.The PF film is characterized to have about 10 repeat units and no presence of ketonic defect site.UV-vis and photoluminescent spectral studies indicate that the PF film is blue light emitting.From cyclic voltammetry and galvanostatic charge-discharge tests in 1 M lithium perchlorate/acetonitrile electrolyte,the polyfluorene/activated carbon electrode shows a specific capacitance of 227.1 F g-1 (per active layer mass) and reversible redox reaction at the potential of 1.4 V in a three electrode configuration.An asymmetric electrochemical capacitor based on this composite electrode and activated carbon electrode exhibits a specific energy of 14.7 Wh kg-1 (per active layer mass).These results indicate that electrochemically prepared polyfluorene could be used as energy storage component for electrochemical application.
