High Area NiMo-RuO_2 Composite Coating as Hydrogen Electrode

The preparation method of NiMo-RuO2 composite coating, micrographic surface feature and roughness factor of the coating, influence of content of RuO, on electrocatalytic activity, steady-state polarization curves and electrochemical parameters, and stability of the electrode in 30% KOH contaning 10×10-6Fe3+ were repored. Experement results showed the NiMo-RuO2 electrode has more excellent elec-trocatalytic activity and stability than NiMo electrode.

BASIC EQUATIONS FOR THERMO－ELECTROCHEMISTRYAND THE ENTROPY CHANGE OF THE STANDARDHYDROGEN ELECTRODE REACTION

A set of thermo-electrochemical (TEC) equations for the cell and half-cell reactions has been derived. Is is shown that the difference between the enthalpy change determined by TEC technology and the one calculated with the current thermodynamic data of ions of any half-cell reaction in electochemical systems is coastant. The absolute entrupy change of the standard hydrogen electrode reaction was determined to be 85.2 J.K-1 .mol-1 at room temperature:

High-temperature electrochemical performance and phase composition of Ti_(0.7) Zr_(0.5) V_(0.2) Mn_(1.8-x)Ni_x hydrogen storage electrode alloys

The rapid development of electric vehicles demands the development of high performance nickel metal hydride battery that is able to endure high temperature. The discharge properties of Ti 0.7 Zr 0.5 V 0.2 Mn 1.8- x Ni x ( x =0.4, 0.8, 1.1, 1.4, 1.7)hydrogen storage alloys was investigated and its phase composition was analyzed using X ray diffraction. The results show that the cycling life was improved as the content of nickel increases. When x =0.4, 0.8, 1.1 and 1.4, the main phase is MgZn 2 type C14 Laves phase and the second one is cubic TiNi phase. When x =1.7, the Laves phase structure disappears. EDAS analysis shows that the increase of nickel content is effective in suppressing the dissolution of vanadium component in alloys. [

Electrocatalytic Activity of Ni/C Electrodes Prepared by Metal Vapor Synthesis For Hydrogen Evolution in Alkaline Solution

The metal vapor synthesis (MVS) methed was used to prepare activatedcarbon supported nickel electrode. The electrocatalytic activity of the electrode forhydrogen evolution reaction(HGR) in alkaline solution was studied. Cathodicpolarization curves showed the electrocatalytic activity of Ni/C electrode prepared byMVS method was higher than that of the one prepared by conventional method.

Study on hydrogen diffusion behavior in MlNi_(3.75) Co_(0.65) Mn_(0.4) Al_(0.2) alloy electrode by chronoamperometry

Hydrogen diffusion coefficients in MlNi 3.75 Co 0.65 Mn 0.4 Al 0.2 alloy electrode as a function of state of charge (SOC) or temperature were determined by chronoamperometry. It is found that hydrogen diffusion coefficient decreases with the increase of SOC or the decrease of temperature. The activation energy for hydrogen diffusion in the alloy electrode with 50%SOC is evaluated to be 19.9?kJ/mol.

Surface Modification of AB_2 and AB_5 Hydrogen Storage Alloy Electrodes by the Hot-Charging Treatment

The effect of the hot-charging treatment on the performance of AB2 and AB5 hydrogen storage alloy electrodes was investigated. The result showed that the treatment can markedly improve the voltage plateau ratio (VPR), the high rate discharge ability (HRDA), the diffusion coefficient of hydrogen DH and the discharge capacity of the AB2 hydrogen storage alloy electrode. The SEM analysis showed that the hot-charging treatment brings about a Ni-rich surface due to the dissolution of Zr oxides. It is also very helpful for the improvement of the kinetic properties of AB2 hydrogen storage alloy electrode because the microcracking of the surface results in fresh surface. This can be the basic modification treatment for NiMH battery used in electric vehicles (EVs) in the future. But for AB5 type alloys, the treatment has the disadvantage of impairing the comprehensive electrochemical properties, because the surface of the alloy may be corroded during the treatment. The mechanism of the surface modification of the electrode is also proposed.

AC IMPEDANCE STUDY OF HYDROGEN STORAGE ELECTRODES

The impedance diagram of hdrogen storage electrodes(AH electrodes )displayed twosemicircles.Thelow frequency one is affected by cycle number and composition of MH electrodes.

Effect of Rapid Quenching on Microstructures and Electrochemical Performances of La_2Mg(Ni_(0.85)Co_(0.15))_9M_(0.1)(M=B, Cr) Hydrogen Storage Alloys

The La-Mg-Ni-system （PuNi3-type） La2Mg （Ni0.85 Co0.15 ）9M0.1 （ M = B, Cr） hydrogen storage etectrode alloys were prepared by casting and rapid quenching. The electrochemical performances and microstructures of the as-cast and quenched alloys were determined and measured. The effects of rapid quenching on the microstructures and electrochemical properties of the alloys were investigated in detail. The obtained results show that the alloys are composed of the （La, Mg） Ni3 phase （PuNi3-type structure） and the LaNi5 phase, as well as the small amount of the LaNi2 phase. A trace of the Ni2B phase exists in the as-cast alloy containing boron, and the Ni2B phase in the alloy nearly disappears after rapid quenching. The relative amount of each phase in the alloys depends on the quenching rate. The rapid quenching technique can greatly improve the electrochemical performance of the alloy, and the effect of rapid quenching on the activation performances of the alloys is minor. Rapid quenching enhances the cycle stability of the alloy, and the cycle life of the alloy increases with the increase of the quenching rate.

Progress on direct assembly approach for in situ fabrication of electrodes of reversible solid oxide cells

Reversible solid oxide cells(SOCs)are very efficient and clean for storage and regeneration of renewable electrical energy by switching between electrolysis and fuel cell modes.One of the most critical factors governing the efficiency and durability of SOCs technology is the stability of the interface between oxygen electrode and electrolyte,which is conventionally formed by sintering at a high temperature of~1000–1250℃,and which suffers from delamination problem,particularly for reversibly operated SOCs.On the other hand,our recent studies have shown that the electrode/electrolyte interface can be in situ formed by a direct assembly approach under the electrochemical polarization conditions at 800℃and lower.The direct assembly approach provides opportunities for significantly simplifying the cell fabrication procedures without the doped ceria barrier layer,enabling the utilization of a variety of high-performance oxygen electrode materials on barrier layer–free yttria-stabilized zirconia(YSZ)electrolyte.Most importantly,the in situ polarization induced interface shows a promising potential as highly active and durable interface for reversible SOCs.The objective of this progress report is to take an overview of the origin and research progress of in situ fabrication of oxygen electrodes based on the direct assembly approach.The prospect of direct assembly approach in the development of effective SOCs and in the fundamental studies of electrode/electrolyte interface reactions is discussed.

Electocbemical Process of Ti-Ni Alloy Electrodes by Cyclic Voltammetry

The electrochemical process of Ti-Ni alloy electrode was studied by using cyclic voltammetry. The hydrogen-absorbing electrode could be approximately regarded as a reversible hydrogen elecrede. The con- trolling steps of the discharging process varying with the anodic overpotentials were investigated and the effect ofelecrode constituent modification or Zr adulteation on the electrochemical behavior was also studied.

Study on Structure and Electrochemical Properties of La_( 0.7)Mg_(0.3)Ni_ (2.98)Co_ (0.52) Hydrogen Storage Alloy

A hydrogen storage electrode alloy La_ 0.7Mg_ 0.3Ni_ 2.98Co_ 0.52 was obtained by electromagnetism inductive melting of alloys such as La, Mg, Ni and Co. XRD analyses indicate that the microstructure of the prepared alloy was composed of LaNi_5 phase as matrix and another unknown phase as secondary phase. In this experiment, the highest discharge capacity of alloy is 378 mAh·g -1 at 293 K, which is 20% higher than the discharge capacity of LaNi_5-type alloys. The alloy was activated after two cycles and the discharge potential is high and stable, and more than 90% of the discharge time is in a voltage higher than 1.2 V. However, the cycle stability is poor as practical application, to improve the cycle life of the alloy becomes the key factor. Moreover, the loose structure of the alloy is maybe one reason that makes the cycle stability capacity of the alloy decrease by SEM.

Crystal structure and some dynamic performances of Ti_(0.25)V_(0.34)Dy_(0.01)Cr_(0.1)Ni_(0.3) hydrogen storage electrode

Crystal structure and some dynamic performances of Zi0.25V0.34Dy0.01Cr0.1Ni0.3 hydrogen storage electrode alloy have been investigated by XRD, FESEM-EDS, TEM and EIS measurements. The result shows that the alloy is mainly composed of V-based solid solution phase with body-centered-cubic structure and mono-crystal Ni3Ti phase with hexagonal structure （Space grope： P63/ mmc）, and it was first observed as TiNi-based secondary phase. The higher charge transfer resistance, higher apparent activation energy and lower hydrogen diffusion coefficient are reasons for the poor electrochemical activity of the dehydriding kinetics of Ti- V-Cr-Ni hydride alloy.

Microstructure and Electrochemical Characteristics of Melt-Spinning Alloy Ml(NiCoMnAl)_5

The microstructure and electrochemical characteristics of Ml(NiCoMnAl) 5 alloys prepared by both the melt spinning method and the conventional induction melting were investigated and compared. SEM and XRD studies show that the microstructure of melt spinning alloys is columnar structure. With increasing melt spinning rate, the crystal grains become finer and preferentially grow along (111)[111] direction. The melt spinning and cast alloys belong to CaCu 5 type hexagonal crystal structure. The electrochemical measurements show that the initial capacities of melt spinning alloy electrodes are all above 210 mAh·g -1 with good activation behavior, reaching their maximum capacities after two charge discharge cycles. The maximum capacity (294 mAh·g -1 ) of melt spinning (10 m·s -1 ) alloy electrodes is as the same as that of as cast alloy electrode, and stability of charge discharge cycles of all melt spinning alloy electrodes is better than that of the as cast alloy electrodes. When charged at 600 mA·g -1 , the capacity of melt spinning (10 m·s -1 ) alloy electrode could reach 65% of its maximum capacity about 45 min with high rate discharge capability; but with the cycle number increasing, the stability of its capacity is less than that electrodes of melt spinning rate.

Effect of substitution of aluminum for nickel on electrochemical properties of La_(0.75)Mg_(0.25)Ni_(3.5–x)Co_(0.2)Al_x hydrogen storage alloys

La0.75Mg0.25Ni3.5–xCo0.2Alx （x=0–0.09） hydrogen storage alloys were prepared by induction melting and effect of Al substitution for Ni on phase constitution and electrochemical property was investigated.With the substitution of Al for Ni,LaNi5 and LaNi2 phases occurred and （La,Mg）2（Ni,Co,Al）7 phase with hexagonal Ce2Ni7-type structure replaced （La,Mg）2（Ni,Co）7 phase.The cell volumes of LaNi5 and （La,Mg）2（Ni,Co,Al）7 main phases increased with increasing Al content.Some electrochemical properties and kinetic parameters of the alloys,including discharge capacity,high rate discharge ability （HRD）,loss angle （ψ）,exchange current density （I0） and limiting current density （IL）,decreased with increasing amount of substitution of Al for Ni.Substitution of Al for Ni could be favorable for positive shift in corrosion potential of the alloy electrode,and prolonged cyclic lifetime of La0.75Mg0.25Ni3.5–xCo0.2Alx （x=0–0.09） alloy electrodes.

Effect of Hardfaced Interlayer Thickness and Low Hydrogen Ferritic Capping on Ballistic Performance of Shielded Metal Arc Welded Armour Steel Joints

Armour grade quenched and tempered steel closely confirming to AISI 4340 is well known for its superior ballistic performance and hence used in the fabrication of combat vehicles. The traditional fillers like austenitic stain- less steel showed poor ballistic performance of these welded joints as compared to the base metal. Attempts have been made to deposit hardfaced interlayer between austenitic stainless steel weld metals. Though this method, mar-- ginal improvements in ballistic performance can be yielded, and cracks were observed in between base metal and hardfaced layer. Thickness of the hardfaced interlayer plays a vital role for the effective ballistic performance. Thus, an attempt has been made to investigate the effect of hardfaced interlayer thickness on ballistic performance of ar- mour steel welds. The results of effect of buttering, low hydrogen ferritic （LHF） filler and three different hardfaced layer thicknesses （4, 5.5 and 7 ram） on ballistid performance of shielded metal arc welded armour steel joints were given.

Self-supported ternary Co0.5Mn0.5P/carbon cloth （CC） as a high-performance hydrogen evolution electrocatalyst

Scalable production of earth-abundant, easy-to-prepare, and cost-effective electrocatalysts for the hydrogen evolution reaction （HER） is essential for sustainable energy-based systems. Herein, we systematically studied the electrocatalytic HER performance of a self-supported ternary Co0.5Mn0.5P/carbon cloth （CC） nanomaterial prepared using a hydrothermal reaction and phosphorizafion process. Electrochemical tests demonstrated that the ternary Co0.5Mn0.5P/CC nanomaterial could be a highly active electrocatalyst in acidic media, with overpotentials of only 41 and 89 mV, affording current densities of 10 and 100 mA.cm-2, respectively, and a Tafel slope of 41.7 mV.dec-1. Furthermore, the electrocatalyst exhibited superior stability, with 3,000 cycles of cyclic voltammetry from -0.2 to 0.2 V at a scan rate of 100 mV.s-1 and 40 h of static polarization at a fixed overpotential of large-scale hydrogen production. 83 mV, indicating its potential for