Comparison of Lithium Diffusion Coefficient Measurements in Tellurium Electrodes via Different Electrochemical Techniques

Both thin (55 μ m) composite and thick (350 μ m) all active material battery porous electrodes were prepared for estimating the diffusion coefficient of Li + ( D Li + ) in tellurium (Te) during electrochemical lithiation. Galvanostatic intermittent titration technique (GITT), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) were applied to quantify the chemical lithium solid-state diffusion coefficient within the Te active material in the electrodes. Multiple methods of GITT and EIS were assessed. For the composite Te electrodes, the D Li + was on the order of 10 −11 cm 2 s −1 from both CV and GITT methods, but 10 −9 cm 2 s −1 from EIS. For the thick tellurium electrodes, both GITT and EIS resulted in lithium diffusion coefficient estimates in the range of 10 −11 –10 −12 cm 2 s −1 . The general trend across all methods that quantified the diffusion coefficient as a function of lithiation of tellurium was that the D Li + decreased rapidly when the Te material was initially lithiated. The D Li + at the phase transition voltage plateau (∼1.7 V, vs Li/Li + , where both Te and Li 2 Te were expected) had the lowest D Li + , while the D Li + both before and after the plateau was generally higher. Among all the electrochemical measurements of D Li + , the modified GITT method with modelling the relaxation region resulted in relatively low scatter in the data, provided values as a function of lithiation, and was well suited to thick electrodes with a flat discharge plateau as was the case herein.