Lithium-transporting solid electrolyte

Polyethylene oxide) associates in solution with certain electrolytes (48—52). For example, high molecular weight species of poly(ethylene oxide) readily dissolve in methanol that contains 0.5 wt % KI, although the resin does not remain in methanol solution at room temperature. This salting-in effect has been attributed to ion binding, which prevents coagulation in the nonsolvent. Complexes with electrolytes, in particular lithium salts, have received widespread attention on account of the potential for using these materials in a polymeric battery. The performance of solid electrolytes based on poly(ethylene oxide) in terms of ion transport and conductivity has been discussed (53—58). The use of complexes of poly(ethylene oxide) in analytical chemistry has also been reviewed (59). 

What makes the sodium-sulfur cell possible is a remarkable property of a compound called beta-alumina, which has the composition NaAlnOiy. Beta-alumina allows sodium ions to migrate through its structure very easily, but it blocks the passage of polysulfide ions. Therefore, it can function as a semipermeable medium like the membranes used in osmosis (see Section 11.5). Such an ion-conducting solid electrolyte is essential to prevent direct chemical reaction between sulfur and sodium. The lithium-sulfur battery operates on similar principles, and other solid electrolytes such as calcium fluoride, which permits ionic transport of fluoride ion, may find use in cells based on those elements. 

The last few years have witnessed a high level of activity pertaining to the research and development of all-solid, thin-film polymer electrolyte batteries most of these use lithium as the active anode material, polymer-based matrices as solid electrolytes, and insertion compounds as active cathode materials. High-performance prototypes of such batteries stand currently under research, whose trends are expected to include the development of amorphous polymers with very low glass-transition temperatures, mixed polymer electrolytes, and fast-ion conductors in which the cationic transport number approaches unity. 

Lu, R Harris, S. J. Lithium transport within the solid electrolyte interphase, Electrochem. 

To be able to understand how computational approaches can and should be used for electrochemical prediction we first of all need to have a correct description of the precise aims. We start from the very basic lithium-ion cell operation that ideally involves two well-defined and reversible reduction and oxidation redox) reactions - one at each electrode/electrolyte interface - coordinated with the outer transport of electrons and internal transport of lithium ions between the positive and negative electrodes. However, in practice many other chemical and physical phenomena take place simultaneously, such as anion diffusion in the electrolyte and additional redox processes at the interfaces due to reduction and/or oxidation of electrolyte components (Fig. 9.1). Control of these additional phenomena is crucial to ensure safe and stable ceU operation and to optimize the overall cell performance. In general, computations can thus be used (1) to predict wanted redox reactions, for example the reduction potential E ) of a film-forming additive intended for a protective solid electrolyte interface (SEI) and (2) to predict unwanted redox reactions, for example the oxidation potential (Eox) limit of electrolyte solvents or anions. As outlined above, the additional redox reactions involve components of the electrolyte, which thus is a prime aim of the modelling. The working agenda of different electrolyte materials in the cell -and often the unwanted reactions - are addressed to be able to mitigate the limitations posed in a rational way. 

The further development in the field of electrochemical power sources will be considerably influenced by the interaction of fundamental research (e.g. on electrocatalysis, solid state structure, transport phenomena, electrochemical kinetics and technology) and applied research, where progress will depend decisively on a successful cooperation in science between electrochemists, physicists, experts in materials, engineering, chemical engineering, electrical engineers a.o. Research work will probably concentrate on special power sources which are advantageously applied only in certain fields, as illustrated by the lithium solid electrolyte cell for pacemakers. 

Note that in lead secondary batteries, the electrolyte is considered to be active material, because it takes part in the electrochemical reactions. In lithium secondary batteries, however, the role of the electrolyte is to transport the hthium ions from one electrode to the other. In the electrolyte, the concentration of lithium ions therefore remains constant, even down to the consumption of hthium over time to reconstitute the interface layer between the electrolyte and the carbon of the electrodes. This interface layer is called the SEI (Solid-Electrolyte Interphase). It is a passivation layer, whose role is explained in section 4.1. 

The surface films discussed in this section reach a steady state when they are thick enough to stop electron transport. Hence, as the surface films become electrically insulating, the active electrodes reach passivation. In the case of monovalent ions such as lithium, the surface films formed in Li salt solutions (or on Li metal) can conduct Li-ions, and hence, behave in general as a solid electrolyte interphase (the SEI model ). See the basic equations 1-7 related to ion transport through surface films in section la above. The potentiodynamics of SEI electrodes such as Li or Li-C may be characterized by a Tafel-like behavior at a high electrical field and by an Ohmic behavior at the low electrical field. The non-uniform structure of the surface films leads to a non-uniform current distribution, and thereby, Li dissolution from Li electrodes may be characterized by cracks, and Li deposition may be dendritic. The morphology of these processes, directed by the surface films, is dealt with later in this chapter. When bivalent active metals are involved, their surface films cannot conduct the bivalent ions. Thereby, Mg or Ca deposition is impossible in most of the commonly used polar aprotic electrolyte solutions. Mg or Ca dissolution occurs at very high over potentials in which the surface films are broken. Hence, dissolution of multivalent active metals occurs via a breakdown and repair of the surface films. 

An electrically insulating but ion conducting ion-transport layer consisting of a solid electrolyte formulahon of polymers, liquid electrolytes, and lithium salts. 

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