The Study of the Binder Poly(acrylic acid) and Its Role in Concomitant Solid-Electrolyte Interphase Formation on Si Anodes.

We use neutron reflectometry to study how the polymeric binder, poly(acrylic acid) (PAA), affects the in situ formation and chemical composition of the solid-electrolyte interphase (SEI) formation on a silicon anode at various states of charge. The reflectivity is correlated with electrochemical quartz crystal microbalance to better understand the viscoelastic effects of the polymer during cycling. The use of model thin films allows for a well-controlled interface between the amorphous Si surface and the PAA layer. If the PAA perfectly coats the Si surface and standard processing conditions are used, the binder will prevent the lithiation of the anode. The PAA suppresses the growth of a new layer formed at early states of discharge (open circuit voltage to 0.8 V vs Li/Li+), protecting the surface of the anode. At 0.15 V, the SEI layer underneath the PAA changes in chemical composition as indicated by an increase in the scattering length density and thickness as the layer incorporates components from the electrolyte, most likely the salt. At lithiated and delithiated states, the SEI layer changes in chemical composition and grows in thickness with delithiation and shrinks during lithiation.

A high temperature gas flow environment for neutron total scattering studies of complex materials.

We present the design and capabilities of a high temperature gas flow environment for neutron diffraction and pair distribution function studies available at the Nanoscale Ordered Materials Diffractometer instrument at the Spallation Neutron Source. Design considerations for successful total scattering studies are discussed, and guidance for planning experiments, preparing samples, and correcting and reducing data is defined. The new capabilities are demonstrated with an in situ decomposition study of a battery electrode material under inert gas flow and an in operando carbonation/decarbonation experiment under reactive gas flow. This capability will aid in identifying and quantifying the atomistic configurations of chemically reactive species and their influence on underlying crystal structures. Furthermore, studies of reaction kinetics and growth pathways in a wide variety of functional materials can be performed across a range of length scales spanning the atomic to the nanoscale.

Transport, phase reactions, and hysteresis of iron fluoride and oxyfluoride conversion electrode materials for lithium batteries.

Potentiostatic intermittent titration technique (PITT) was applied to FeF2, FeF3, and FeO0.67F1.33 to gain insight into the transport-related aspects of the conversion reaction by quantitative analysis of Li(+) diffusion and hysteresis. PITT derived diffusion coefficient measurements were benchmarked relative to values extracted by electrochemical impedance spectroscopy (EIS). A reverse-step PITT methodology was used to evaluate true hysteresis by eliminating nucleation induced overpotentials. This method evaluates the minimum potential hysteresis and allowed an accurate representation of the potential required to move conversion reactions forward at C/1000 rates in both lithiation and delithiation. The high resolution PITT data were also used to gain further insight into reaction mechanisms involved in the reversible conversion reactions. Physical evidence, based on pair distribution function (PDF) structural analysis, and electrochemical evidence are presented regarding a new step in the reaction during the rutile FeF2 reconversion reaction.