Unravelling the electrochemical impedance spectroscopy of silicon half cells with commercial loading

Silicon (Si) is an important anode material for lithium ion batteries (LIBs), and increasing the loading of Si electrodes is an important step towards commercialization. However, half cells commonly used for Si studies are limited by polarization of the lithium (Li) counter electrode, especially at high Si loading. To study the interplay between Si and Li electrodes, a set of electrochemical impedance spectroscopy (EIS) spectra are generated using cycled Si half cells at four different potentials in the charge–discharge profile, and then repeated using symmetric Si/Si and Li/Li cells assembled from half cells cycled to equivalent stages in the cycle. Distribution of relaxation times (DRT) analysis is used to design equivalent circuits (ECs) for both Si/Si and Li/Li symmetric cells incorporating both electrolyte and electrode-related diffusion, and these are applied to the half cells. The results demonstrate that the behaviour of half cells is dominated by the solid electrolyte interphase (SEI) impedances at the Li counter electrode at the low and high potentials where the Li+ mobility signal in Si is limited, while the Si electrode is dominant at intermediate potentials where the signal from mobile Li+ is strong. EIS studies of Si half cells should therefore be performed at intermediate potentials, or as symmetric cells.publishedVersio

Enabling Increased Delithiation Rates in Silicon-Based Anodes through Alloying with Phosphorus

The capability of battery materials to deliver not only high lithium storage capacity, but also the ability to operate at high charge/discharge rates is an essential property for development of new batteries. In the present work, the influence on the charge/discharge rate behaviour of substoichiometric concentrations of phosphorus (P) in silicon (Si) nanoparticles was studied. The results revealed an increase in rate capability as a function of the P concentration between 0 and 5.2 at %, particularly during delithiation. The stoichiometry of the nanoparticles was found to strongly affect the formation of the Li3.5Si phase during lithiation. Cyclic stability experiments demonstrated an initial increase in capacity for the SiPx materials. Galvanostatic intermittent titration technique and electrochemical impedance spectroscopy demonstrated the increased lithium diffusivity with inclusion of P. Density functional theory and ab initio molecular dynamics were deployed to provide a rationale for the electrochemical behaviour of SiPx.publishedVersio

Enabling Increased Delithiation Rates in Silicon-Based Anodes through Alloying with Phosphorus

The capability of battery materials to deliver not only high lithium storage capacity, but also the ability to operate at high charge/discharge rates is an essential property for development of new batteries. In the present work, the influence on the charge/discharge rate behaviour of substoichiometric concentrations of phosphorus (P) in silicon (Si) nanoparticles was studied. The results revealed an increase in rate capability as a function of the P concentration between 0 and 5.2 at %, particularly during delithiation. The stoichiometry of the nanoparticles was found to strongly affect the formation of the Li3.5Si phase during lithiation. Cyclic stability experiments demonstrated an initial increase in capacity for the SiPx materials. Galvanostatic intermittent titration technique and electrochemical impedance spectroscopy demonstrated the increased lithium diffusivity with inclusion of P. Density functional theory and ab initio molecular dynamics were deployed to provide a rationale for the electrochemical behaviour of SiPx.publishedVersio