Effects of anode slime removing by Fe^(2+)dissolution method on electrochemical properties of Pb−0.6%Ag anode and zinc electrowinning

Fe^(2+)dissolution method and manual method were used to remove the anode slime and their effects on properties of cast Pb−0.6wt.%Ag anode and zinc electrowinning were compared.The results reveal that the Fe^(2+)dissolution method can avoid mechanical damage to the oxide film layer on the anode surface,which cannot be achieved by traditional manual method.This can lower the anode corrosion rate by 57.14%,thus reducing Pb contamination in electrolyte and zinc products.Meanwhile,compared with manual method,Fe^(2+)dissolution method can significantly improve the electrocatalytic activity of the anode and lower the initial power consumption of zinc electrowinning to 2720 kW·h/t after removing anode slime.

Tailoring the microstructure of Mg-Al-Sn-RE alloy via friction stir processing and the impact on its electrochemical discharge behaviour as the anode for Mg-air battery

Constructing the magnesium alloy with fine grains,low density of dislocations,and weak crystal orientation is of crucial importance to enhance its comprehensive performance as the anode for Mg-air battery.However,this unique microstructure can hardly be achieved with conventional plastic deformation such as rolling or extrusion.Herein,we tailor the microstructure of Mg-Al-Sn-RE alloy by using the friction stir processing,which obviously refines the grains without increasing dislocation density or strengthening crystal orientation.The Mg-air battery with the processed Mg-Al-Sn-RE alloy as the anode exhibits higher discharge voltages and capacities than that employing the untreated anode.Furthermore,the impact of friction stir processing on the electrochemical discharge behaviour of Mg-Al-Sn-RE anode and the corresponding mechanism are also analysed according to microstructure characterization and electrochemical response.

Nanotube array-like WO_3/W photoanode fabricated by electrochemical anodization for photoelectrocatalytic overall water splitting

Photoactive WO3is attractive as a photocatalyst for green energy evolution through water splitting.In the present work,an electrochemical anodic oxidation method was used to fabricate a photo‐responsive nanotube array‐like WO3/W(NA‐WO3/W)photoanode from W foil as a precursor.Compared with a reference commercial WO3/W electrode,the NA‐WO3/W photoanode exhibited enhanced and stable photoelectrocatalytic(PEC)activity for visible‐light‐driven water splitting with a typical H2/O2stoichiometric ratio of2:1and quantum efficiency of approximately5.23%under visible‐light irradiation from a light‐emitting diode(λ=420nm,15mW/cm2).The greatly enhanced PEC performance of the NA‐WO3/Wphotoanode was attributed to its fast electron–hole separation rate,which resulted from the one‐dimensional nanotube array‐like structure,high crystallinity of monoclinic WO3,and strong interaction between WO3and W foil.This work paves the way to a facile route to prepare highly active photoelectrodes for solar light transfer to chemical energy.

Influence of Ga and Bi on electrochemical performance of Al-Zn-Sn sacrificial anodes

The influence of Ga and Bi on the microstructure and electrochemical performance of Al-7Zn-0.1Sn （mass fraction,%） sacrificial anodes was investigated by means of optical microscopy （OM）,scanning electron microscopy/energy dispersive X-ray analysis （SEM/EDAX） and electrochemical measurements.It was found that the coarse dendrites structure transformed into the equiaxed grains as well as a small amount of dendrite grains after adding Ga and Bi into Al-Zn-Sn alloys.A high current efficiency of 97% and even corrosion morphology were obtained for Al-7Zn-0.1Sn-0.015Ga-0.1Bi alloy.The results indicate that the proper amount of Ga and Bi is effective on improving the microstructure and electrochemical performance of Al-Zn-Sn alloy.

Electrochemical properties of magnesium alloy anodes discharged in seawater

Magnesium alloys can be developed as anode materials for seawater activated batteries. The electrochemical properties of AZ31, AP65 and Mg-3%Ga-2%Hg alloy anodes discharged in seawater were studied. The potentiodynamic polarization shows that the Mg-3%Ga-2%Hg alloy provides more negative corrosion potentials than AZ31 or AP65 alloy. The galvanostatic discharge results show that the Mg-3%Ga-2%Hg alloy exhibits good electrochemical properties as anodes in seawater. And the EIS studies reveal that the magnesium alloy anode/seawater interfacial process is determined by an activation controlled reaction. The Mg3Hg and Mg21Ga5Hg3 phases in Mg-3%Ga-2%Hg alloy improve its electrochemical properties better than the Mg17（Al,Zn）12 phase in AZ31 and Mg（Pb） solid solution phase in AP65 alloys.

Effect of citric acid on microstructure and electrochemical characteristics of high voltage anodized alumina film formed on etched Al Foils

Aluminum capacitor foils with a tunnel etch structure were reacted with boiling water and then anodized at 530 V in boric acid solution or boric acid＋citric acid mixed solution.The microstructure and crystallinity of the resulting anodized film were examined by TEM and XRD.The special capacitance,resistance and withstanding voltage of the film were explored with electrochemical impedance spectroscopy（EIS）,LCR meter and small-current charging.The results show that the high voltage anodized oxide film consists of an inner layer with high crystallinity and an outer layer with low crystallinity.However,the crystallinity of the film formed in boric acid＋citric acid mixed solution is higher than that of the film formed in only boric acid solution,leading to an increase in film＇s field strength and special capacitance.Meanwhile,there are more defects from phase transformation in the out layer of the film formed in boric acid＋citric acid mixed solution than in that of film formed in only boric acid solution,leading to a decrease in film＇s resistance and withstanding voltage.

Influence of Ga and In on microstructure and electrochemical properties of Mg anodes

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.

Effects of gallium on electrochemical discharge behavior of Al-Mg-Sn-In alloy anode for air cell or water-activated cell

In order to evaluate the electrochemical properties of aluminum alloy anode under high current densities in alkaline electrolyte, the galvanostatic discharge, potentiodynamic polarization and hydrogen evolution tests of three experimental Al?Mg?Sn?In?(Ga) alloys were performed. The results show that the alloying element gallium improves the working potentials of experimental Al?Mg?Sn?In alloys under different discharge current densities. The average working potentials of the alloys containing gallium can reach?1.3 V under current density ranging from 650 to 900 mA/cm2, while those of alloy without Ga are only?1.0 V. Such phenomenon is attributed to the solid solution which can form amalgam with aluminum matrix. Such an amalgam can form the hydrolyzed species during the discharge process and lead to the corrosion infiltrating into aluminum matrix.

Effect of MnO_4^- and silver content on electrochemical behaviour of Pb-Ag alloy anodes during potential decay periods

The effect of MnO4- and silver content on electrochemical behaviour of five commercial Pb-Ag alloy anodes was studied in acid zinc sulphate electrolyte with and without MnO4- ions at 38 °C during potential decay periods. When the anodes were immersed into acid zinc sulphate electrolyte without MnO4- ions, the Pb-0.72%Ag anode entered complete passivation state in the shortest time among the five anodes, followed by anodes Pb-0.67%Ag, Pb-0.60%Ag, Pb-0.58%Ag and Pb-0.29%Ag-0.1%Ca by measurement of open circuit potential. During immersion of the anodes, MnO4 ions accelerated the passivation and increased the corrosion current density of the anodes. After immersion in zinc electrolyte with MnO4-, the anode Pb-0.72%Ag had the best corrosion resistance, followed by anodes Pb-0.67%Ag, Pb-0.60%Ag, then the close anodes Pb-0.58%Ag and Pb-0.29%Ag-0.1%Ca by the electrochemical impedance spectroscopy （EIS） analysis.

Effect of germanium on electrochemical performance of chain-like Co-P anode material for Ni/Co rechargeable batteries

Co-P （4.9% P） powders with a chain-like morphology were prepared by a novel chemical reduction method. The Co-P and germanium powders were mixed at various mass ratios to form Co-P composite electrodes. Charge and discharge test and electrochemical impedance spectroscopy （EIS） were carried out to investigate the electrochemical performance, which can be significantly improved by the addition of germanium. For instance, when the mass ratio of Co-P powders to germanium is 5：1, the sample electrode shows a reversible discharge capacity of 350.3 mA·h/g and a high capacity retention rate of 95.9% after 50 cycles. The results of cyclic voltammmetry （CV） show the reaction mechanism of Co/Co（OH）2 within Co-P composite electrodes and EIS indicates that this electrode shows a low charge-transfer resistance, facilitating the oxidation of Co to Co（OH）2.

Effects of Hg and Ga on microstructures and electrochemical corrosion behaviors of Mg anode alloys

The effects of Hg and Ga on the electrochemical corrosion behaviors of the Mg-2%Hg, Mg-2%Ga and Mg-2%Hg-2%Ga (mass fraction) alloys were investigated by measurements of polarization curves, galvanostatic tests and measurements of electrochemical impedance spectroscopy. Scanning electron microscopy, X-ray diffractometry and energy dispersive spectrometry were employed to characterize the microstructures and the corroded surface of the above alloys. The results demonstrate that the microstructure of the Mg-2%Ga alloy is solid solution and the Mg-2%Hg and Mg-2%Hg-2%Ga alloys have white second-phases at the grain boundaries. The Mg-2%Ga alloy has the worst electrochemical activity and the best corrosion resistance, showing a mean potential of -1.48 V and a corrosion current density of 0.15 mA/cm2. The Mg-2%Hg-2%Ga alloy has the best electrochemical activity and the worst corrosion resistance, showing a mean potential of -1.848 V and a corrosion current density of 2.136 mA/cm2. The activation mechanism of the Mg-Hg-Ga alloy is dissolution-deposition of the Hg and Ga atoms.

Electrochemical behavior of mesh and plate oxide coated anodes during zinc electrowinning

The catalytic performance of two oxides coated anodes （OCSs） meshes and one OCA plate was investigated in a zinc electrowinning electrolyte at 38 ℃. Their electrochemical behaviors were compared with that of a conventional Pb-0.7%Ag alloy anode. Electrochemical measurements such as cyclic voltammetric, galvanostatic, potentiodynamic, open-circuit potential （OCP） and in situ electrochemical noise measurements were considered. After 2 h of OCP test, the linear polarization shows that the corrosion current density of the Ti/（IrO2-Ta2O5） mesh electrode is the lowest （3.37μA/cm^2） among the three OCAs and shows excellent performance. Additionally, after 24 h of galvanostatic polarization at 50 mA/cm^2and 38 ℃, the Ti/MnO2mesh anode has the highest potential （1.799 V）, followed by the Ti/（IrO2-Ta2O5） plate （1.775 V） and Ti/（IrO2-Ta2O5） mesh （1.705 V） anodes. After 24 h of galvanostatic polarization followed by 16 h of decay, the linear polarization method confirms the sequence obtained after 2 h of OCP test, and the Ti/（IrO2-Ta2O5） mesh attains the lowest corrosion current density. The Ti/（IrO2-Ta2O5） mesh anode also shows better performance after 24 h of galvanostatic polarization with the overpotential lower than that of the conventional Pb-Ag anode by about 245 mV.

Influence of Mg and Ti on the microstructure and electrochemical performance of aluminum alloy sacrificial anodes

The experiments focused on the influence of magnesium and titanium as additional alloying elements on the microstructure and electro-chemical behavior of Al-Zn-In sacrificial anodes. The electrochemical behavior of the aluminum sacrificial anode with 3 wt.% sodium chloride solution was studied by electrochemical impedance spectroscopy (EIS) tests. It was found that a microstructure with few precipitates and refined grains could be achieved by adding 1 wt.% Mg and 0.05 wt.% Ti to the Al-Zn-In alloy,resulting...

Effect of modified elastomeric binders on the electrochemical properties of silicon anodes for lithium-ion batteries

Silicon has been investigated intensively as a promising anode material for rechargeable lithium-ion batteries. The choice of a binder is very important to solve the problem of the large capacity fade observed along cycling. The effect of modified elastomeric binders on the electrochemical performance of crystalline nano-silicon powders was studied. Compared with the conventional binder （polyvinylidene fluoride （PVDF））, Si electrodes using the elastomeric styrene butadiene rubber （SBR） and sodium carboxymethyl cellulose （SCMC） com- bined binder show an improved cycling performance. The reversible capacity of the Si electrode with the SCMC/SBR binder is as high as 2221 mA.h/g for 30 cycles in a voltage window between 0.005 and 2 V. The structure changes from SEM images of the silicon electrodes with different binders were used to explore the property improvement.

Effect of grain size on the electrochemical behavior of pure magnesium anode

Three kinds of pure magnesium anode materials with different grain sizes were prepared by extrusion at different temperatures.The grain size of each sample was calculated,then the effect of grain size on the electrochemical properties of pure magnesium anode was investigated by chemical immersion hydrogen test,potentiodynamic polarization scanning,constant current discharge and electrochemical impedance spectroscopy.As the extrusion temperature increases from 180℃ to 250℃,the average grain size of pure magnesium increases from 20m to 30m,and the pure magnesium extruded at 250℃ has the best electrochemical performance as magnesium anode,with the discharge potential of−1.571 V(vs.SCE).Plastic deformation process is a convenient method that can change the microstructure and improve the electrochemical behavior of magnesium anode.

Effect of yttrium and calcium additions on electrochemical behaviors and discharge performance of AZ80 anodes for Mg-air battery

The effects of yttrium(Y)and yttrium+calcium(Y+Ca)additions on the electrochemical properties and discharge performance of the as-extruded Mg−8Al−0.5Zn−0.2Mn(AZ80)anodes for Mg−air batteries were investigated.The results show that the addition of 0.2 wt.%Y increased the corrosion resistance and discharge activity of AZ80 anode.This was attributed to the fine and sphericalβ-Mg_17)Al_(12) phases dispersing evenly in AZ80+0.2Y alloy,which suppressed the localized corrosion and severe“chunk effect”,and facilitated the rapid activation ofα-Mg.Combinative addition of 0.2 wt.%Y and 0.15 wt.%Ca generated grain refinement and a reduction of theβ-Mg_17)Al_(12) phase,resulting in a further enhancement in discharge voltage.However,the incorporation of Ca in Mg_17)Al_(12) and Al_(2)Y compounds compromised the corrosion resistance and anodic efficiency of AZ80+0.2Y+0.15Ca anode.Consequently,AZ80+0.2Y anode exhibited excellent overall discharge performance,with the peak discharge capacity and anodic efficiency of 1525 mA·h·g^(−1) and 67%at 80 mA/cm^(2),13%and 14%higher than those of AZ80 anode,respectively.

Discharge properties and electrochemical behaviors of AZ80-La-Gd magnesium anode for Mg-air battery

In this work,the discharge properties and electrochemical behaviors of as-cast AZ80-La-Gd anode for Mg-air battery have been investigated and compared with the AZ80 anode.The microstructure evolution,electrochemical behaviors and surface morphologies after discharge have been discussed to connect the discharge properties.The results indicate that the modified AZ80-La-Gd is an outstanding candidate for anode for Mg-air batter,which has high cell voltage,stable discharge curves,good specific capacity and energy,and good anodic efficiency.It exhibits the best anodic efficiency,specific capacity and energy of 76.45%,1703.6 mAh·g^(-1)and 2186.3 mWh·g^(-1),respectively,which are20.24%,18.92%and 25.71%higher than values for AZ80 anode.Such excellent discharge performance is attributed to the Al-RE particles.They refine the Mg_(17)Al_(12)phase and therefore improve the self-corrosion resistance and desorption ability of AZ80 anode.

Influence of CsNO_3 as electrolyte additive on electrochemical property of lithium anode in rechargeable battery

Lithium metal is one of the most promising anode materials for rechargeable battery with high energy density,but its practical use is still hindered by two main problems,namely,lithium dendrite growth and low Coulombic efficiency.To address the issues,cesium nitrate(CsNO3)is selected as the additive to modify the electrolyte for lithium secondary battery.Here we report electrochemical performance of lithium secondary battery with different concentration of CsNO3 as electrolyte additive.The study result demonstrates that Coulombic efficiency of Li–Cu cells and the lifetime of symmetric lithium cells contained CsNO3 additive are improved greatly.Li–Cu cell with 0.05 mol/L CsNO3 and 0.15 mol/L LiNO3 as electrolyte additive presents the best electrochemical performance,having the highest Coulombic efficiency of around 97%and the lowest interfacial resistance.With increasing the concentration of CsNO3 as electrolyte additive,the electrochemical performance of cells becomes poor.Meanwhile,the morphology of lithium deposited films with CsNO3-modified electrolyte become smoother and more uniform compared with the basic electrolyte.

Improved Electrochemical Performance of Mg-doped ZnO Thin Film as Anode Material for Lithium Ion Batteries

Zn1-xMgxO （x = 0, 0.18） thin films were fabricated on the copper substrates by radiofrequency magnetron sputtering using the high pure argon as a sputtering gas. The Zn1-xMgxO films were characterized by X-ray powder diffraction （XRD）, scanning electron microscope （SEM） and galvanostatic tests. The electrochemical test showed an improved electrochemical performance of Zn0.82EMg0.18O thin film as an anode material for lithium ion batteries.

Effect of rolling processing on microstructure and electrochemical properties of high active aluminum alloy anode

The effect of rolling processing on the microstructure,electrochemical property and anti-corrosion property of Al-Mg-Sn-Bi-Ga-In alloy anode in alkaline solution(80℃,Na2SnO3+5 mol/L NaOH)was analyzed by the chronopotentiometry (E-T curves),hydrogen collection tests and modern microstructure analysis.The results show that when the rolling temperature is 370℃,the electrochemical activity of Al anode decreases gradually with the increase of pass deformation in rolling,while the anti-corrosion property is improved in the beginning and then declined rapidly.When the pass deformation of rolling is 40%,the Al anode has good electrochemical activity as good as the anti-corrosion property and with the increase of rolling temperature,both electrochemical activity and anti-corrosion property of Al anode increase first and then decrease.When the rolling temperature is 420 ℃,the aluminum alloy anode has the most negative electrode potential of about-1.521 V(vs Hg/HgO)and the lowest hydrogen evolution rate of 0.171 6 mL/(min·cm2).The optimum comprehensive performance of Al alloy anode is obtained.