Elucidating local diffusion dynamics in nickel-rich layered oxide cathodes.

Elucidating Li-ion transport properties is essential for designing suitable methodologies to optimise electrochemical performance in Ni-rich cathodes for high energy density Li-ion batteries. Here, we report the local-scale Li-diffusion characteristics of a series of nickel-rich layered oxide cathodes, prepared microwave methods, using muon spin relaxation methods. Our results detail the effects of cation dopants, selected for structure stability, on transport properties in candidate nickel-rich chemistries.

Liquid-Phase Approach to Glass-Microfiber-Reinforced Sulfide Solid Electrolytes for All-Solid-State Batteries.

Deformable, fast-ion conducting sulfides enable the construction of bulk-type solid-state batteries that can compete with current Li-ion batteries in terms of energy density and scalability. One approach to optimizing the energy density of these cells is to minimize the size of the electrolyte layer by integrating the solid electrolyte in thin membranes. However, additive-free thin membranes, as well as many membranes based on preprepared scaffolds, are difficult to prepare or integrate in solid cells on a large scale.

Direct Observation of Dynamic Lithium Diffusion Behavior in Nickel-Rich, LiNiMnCoO (NMC811) Cathodes Using Muon Spectroscopy.

Ni-rich layered oxide cathode materials such as LiNiMnCoO (NMC811) are widely tipped as the next-generation cathodes for lithium-ion batteries. The NMC class offers high capacities but suffers an irreversible first cycle capacity loss, a result of slow Li diffusion kinetics at a low state of charge. Understanding the origin of these kinetic hindrances to Li mobility inside the cathode is vital to negate the first cycle capacity loss in future materials design.

In Situ Diffusion Measurements of a NASICON-Structured All-Solid-State Battery Using Muon Spin Relaxation.

In situ muon spin relaxation is demonstrated as an emerging technique that can provide a volume-averaged local probe of the ionic diffusion processes occurring within electrochemical energy storage devices as a function of state of charge. Herein, we present work on the conceptually interesting NASICON-type all-solid-state battery LiM(PO), using M = Ti in the cathode, M = Zr in the electrolyte, and a Li metal anode. The pristine materials are studied individually and found to possess low ionic hopping activation energies of ∼50-60 meV and competitive Li self-diffusion coefficients of ∼10-10 cm s at 336 K.

LiLaMO (M = W, Te) as a new series of lithium-rich double perovskites for all-solid-state lithium-ion batteries.

Solid-state batteries are a proposed route to safely achieving high energy densities, yet this architecture faces challenges arising from interfacial issues between the electrode and solid electrolyte. Here we develop a novel family of double perovskites, LiLaMO (M = W, Te), where an uncommon lithium-ion distribution enables macroscopic ion diffusion and tailored design of the composition allows us to switch functionality to either a negative electrode or a solid electrolyte. Introduction of tungsten allows reversible lithium-ion intercalation below 1 V, enabling application as an anode (initial specific capacity >200 mAh g with remarkably low volume change of ∼0.