Breathing and oscillating growth of solid-electrolyte-interphase upon electrochemical cycling.

We report the first direct experimental evidence of the dynamic behavior of the solid-electrolyte-interphase (SEI) on copper electrodes upon electrochemical cycling. Synchrotron-based soft X-ray absorption spectroscopy (sXAS) and time-of-flight secondary ion mass spectrometry (TOF-SIMS) consistently show that both the chemical composition and the thickness of the SEI change with electrochemical potential throughout the slow formation process. In particular, sXAS results show that the nascent carbonate species in SEI show redox reversibility and decompose during the delithiation (oxidation) process, which leads to a significant shrinking of the SEI thickness as confirmed by TOF-SIMS. Meanwhile, the carbonates also matures and become more and more inactive at every lithiation (reduction) process. These experimental observations reveal unambiguously that SEI formation is much more complicated than a simple and monotonous deposition of electrolyte decomposition product; instead, it could be an oscillating process with a breathing growth.

Fundamental interplay between anionic/cationic redox governing the kinetics and thermodynamics of lithium-rich cathodes.

Reversible anionic redox has rejuvenated the search for high-capacity lithium-ion battery cathodes. Real-world success necessitates the holistic mastering of this electrochemistry's kinetics, thermodynamics, and stability. Here we prove oxygen redox reactivity in the archetypical lithium- and manganese-rich layered cathodes through bulk-sensitive synchrotron-based spectroscopies, and elucidate their complete anionic/cationic charge-compensation mechanism. Furthermore, via various electroanalytical methods, we answer how the anionic/cationic interplay governs application-wise important issues-namely sluggish kinetics, large hysteresis, and voltage fade-that afflict these promising cathodes despite widespread industrial and academic efforts. We find that cationic redox is kinetically fast and without hysteresis unlike sluggish anions, which furthermore show different oxidation vs. reduction potentials. Additionally, more time spent with fully oxidized oxygen promotes voltage fade. These fundamental insights about anionic redox are indispensable for improving lithium-rich cathodes. Moreover, our methodology provides guidelines for assessing the merits of existing and future anionic redox-based high-energy cathodes, which are being discovered rapidly.

Mesoscopic modeling of Li insertion in phase-separating electrode materials: application to lithium iron phosphate.

A simple mesoscopic model is presented which accounts for the inhomogeneity of physical properties and bi-stable nature of phase-change insertion materials used in battery electrodes. The model does not include any geometric detail of the active material and discretizes the total active material domain into meso-scale units featuring basic thermodynamic (non-monotonic equilibrium potential as a function of Li content) and kinetic (insertion-de-insertion resistance) properties. With only these two factors incorporated, the model is able to simultaneously capture unique phenomena including the memory effect observed in lithium iron phosphate electrodes. The analysis offers a new physical insight into modeling of phase-change active materials which are of special interest for use in high power Li-ion batteries.

Structural, transport, and electrochemical investigation of novel AMSO4F (A = Na, Li; M = Fe, Co, Ni, Mn) metal fluorosulphates prepared using low temperature synthesis routes.

We have recently reported a promising 3.6 V metal fluorosulphate (LiFeSO(4)F) electrode, capable of high capacity, rate capability, and cycling stability. In the current work, we extend the fluorosulphate chemistry from lithium to sodium-based systems. In this venture, we have reported the synthesis and crystal structure of NaMSO(4)F candidates for the first time. As opposed to the triclinic-based LiMSO(4)F phases, the NaMSO(4)F phases adopt a monoclinic structure. We further report the degree and possibility of forming Na(Fe(1-x)M(x))SO(4)F and (Na(1-x)Li(x))MSO(4)F (M = Fe, Co, Ni) solid-solution phases for the first time. Relying on the underlying topochemical reaction, we have successfully synthesized the NaMSO(4)F, Na(Fe(1-x)M(x))SO(4)F, and (Na(1-x)Li(x))MSO(4)F products at a low temperature of 300 degrees C using both ionothermal and solid-state syntheses. The crystal structure, thermal stability, ionic conductivity, and reactivity of these new phases toward Li and Na have been investigated. Among them, NaFeSO(4)F is the only one to present some redox activity (Fe(2+)/Fe(3+)) toward Li at 3.6 V. Additionally, this phase shows a pressed-pellet ionic conductivity of 10(-7) S x cm(-1). These findings further illustrate the richness of the fluorosulphate crystal chemistry, which has just been recently unveiled.