Solid-state electrolytes are attracting increasing interest for electrochemical energy storage technologies. In this Review, we provide a background overview and discuss the state of the art, ion-transport mechanisms and fundamental properties of solid-state electrolyte materials of interest for energy storage applications. We focus on recent advances in various classes of battery chemistries and systems that are enabled by solid electrolytes, including all-solid-state lithium-ion batteries and emerging solid-electrolyte lithium batteries that feature cathodes with liquid or gaseous active materials (for example, lithium–air, lithium–sulfur and lithium–bromine systems). A low-cost, safe, aqueous electrochemical energy storage concept with a ‘mediator-ion’ solid electrolyte is also discussed. Advanced battery systems based on solid electrolytes would revitalize the rechargeable battery field because of their safety, excellent stability, long cycle lives and low cost. However, great effort will be needed to implement solid-electrolyte batteries as viable energy storage systems. In this context, we discuss the main issues that must be addressed, such as achieving acceptable ionic conductivity, electrochemical stability and mechanical properties of the solid electrolytes, as well as a compatible electrolyte/electrode interface. This Review details recent advances in battery chemistries and systems enabled by solid electrolytes, including all-solid-state lithium-ion, lithium–air, lithium–sulfur and lithium–bromine batteries, as well as an aqueous battery concept with a mediator-ion solid electrolyte.

Lithium battery chemistries enabled by solid-state electrolytes

The open literature concerning chemical and mechanistic aspects of the selective catalytic reduction of NO by ammonia (SCR process) on metal oxide catalysts is reviewed. Catalytic systems based on supported V2O5 (including the industrial TiO2-supported V2O5–WO3 and/or V2O5–MoO3 catalysts) and catalysts containing Fe2O3, CuO, MnOx and CrOx are considered. The results of spectroscopic studies of the adsorbed surface species, adsorption–desorption measurements, flow reactor and kinetic experiments are analyzed. The proposed reaction mechanisms are described and critically discussed. Points of convergence and of disagreement are underlined.

Chemical and mechanistic aspects of the selective catalytic reduction of NOx by ammonia over oxide catalysts: A review

The physical characteristics of sulfur aerosols

Owing to almost unmatched volumetric energy density, Li-ion batteries have dominated the portable electronics industry and solid state electrochemical literature for the past 20 years. Not only will that continue, but they are also now powering plug-in hybrid electric vehicles and electric vehicles. In light of possible concerns over rising lithium costs in the future, Na and Na-ion batteries have re-emerged as candidates for medium and large-scale stationary energy storage, especially as a result of heightened interest in renewable energy sources that provide intermittent power which needs to be load-levelled. The sodium-ion battery field presents many solid state materials design challenges, and rising to that call in the past couple of years, several reports of new sodium-ion technologies and electrode materials have surfaced. These range from high-temperature air electrodes to new layered oxides, polyanion-based materials, carbons and other insertion materials for sodium-ion batteries, many of which hold promise for future sodium-based energy storage applications. In this article, the challenges of current high-temperature sodium technologies including Na-S and Na-NiCl2 and new molten sodium technology, Na-O2 are summarized. Recent advancements in positive and negative electrode materials suitable for Na-ion and hybrid Na/Li-ion cells are reviewed, along with the prospects for future developments.

Sodium and sodium-ion energy storage batteries

Prussian blue: a new framework of electrode materials for sodium batteries

Studies of surface reactions of nitric oxide by nitrogen-15 isotope labeling. I. Reaction between nitric oxide and ammonia over supported platinum at 200-250.deg.

Joseph T. Kummer

Papers

Studies of surface reactions of nitric oxide by nitrogen-15 isotope labeling. I. Reaction between nitric oxide and ammonia over supported platinum at 200-250.deg.

Selective catalytic reaction of hydrogen with nitric oxide in the presence of oxygen

Battery having a molten alkali metal anode and a molten sulfur cathode

A Sodium-Sulfur Secondary Battery

Thermo-electric generator