Interaction of Mechanical and Electrochemical Factors duringCorrosion Fatigue of Fe-26Cr-1Mo Stainless Steel in 1M H_2SO_4 Solution

The cyclic plastic straining electrode technique has been used to investigate the transient electrochemical behaviour of Fe-26Cr1Mo stainless steel in 1M H2SO4 solution at a passive potential.The influence of plastic strain amplitude and plastic strain rate on the dissolution current response was analysed. The experimental results showed that the transient current was dependent on the competitive process of the surface film rupture and repassivation of the new surface. The high plastic strain amplitude and the high plastic strain rate caused a change of electrochemical activity of specimen surface. In the condition of low strain amplitude and strain rate, the characteristics of current response was mainly relative tp the process of new surface repassivation.The competition kinetics has been analysed through the comparison of plastic strain rate and repassivating rate

Probing component contributions and internal polarization in silicon-graphite composite anode for lithium-ion batteries with an electrochemical-mechanical model

Silicon–graphite(Si–Gr)composite anodes are attractive alternatives to replace Gr anodes for lithium-ion batteries(LIBs)owing to their relatively high capacity and mild volume change.However,it is difficult to understand electrochemical interactions of Si and Gr in Si–Gr composite anodes and internal polarization of LIBs with regular experiment methods.Herein,we establish an electrochemical-mechanical coupled model to study the effect of rate and Si content on the electrochemical and stress behavior in a Si–Gr composite anode.The results show that the composites of Si and Gr not only improve the lithiation kinetics of Gr but also alleviate the voltage hysteresis of Si and decrease the risk of lithium plating in the negative electrode.What's more,the Si content is a tradeoff between electrode capacity and electrode volume variation.Further,various internal polarization contributions of cells using Si–Gr composite anodes are quantified by the voltage decomposition method.The results indicate that the electrochemical polarization of electrode materials and the electrolyte ohmic over-potential are dominant factors in the rate performance of cells,which provides theoretical guidance for improving the rate performance of LIBs using Si–Gr composite anodes.