Abstract:
A battery includes a substrate; a composite cathode disposed on the substrate; a solid-state electrolyte disposed on the composite cathode; and a lithium anode disposed on the solid-state electrolyte, such that the composite cathode comprises a gel polymer electrolyte layer and a porous cathode active material layer. A method of forming a cathode for a solid-state battery includes mixing an active cathode material, at least one of a conductive carbon component and an electronic conductive component, and a polymer binder to form a slurry; immersing the slurry in an alcohol reagent to form a porous disc structure by phase conversion; and immersing the porous disc structure in a liquid electrolyte to form the cathode.
Abstract:
Disclosed herein are graphene coatings characterized by a porous, three-dimensional, spherical structure having a hollow core, along with methods for forming such graphene coatings on glasses, glass-ceramics, ceramics, and crystalline materials. Such coatings can be further coated with organic or inorganic layers and are useful in chemical and electronic applications.
Abstract:
A cathode for a lithium-sulfur battery includes a sulfur-based composite layer having a porosity in a range of 60% to 99%; and a conductive polymer disposed atop the composite layer and within pores of the composite layer. Moreover, a method of forming a cathode for a lithium-sulfur battery includes providing a substrate; disposing a sulfur-based slurry layer on the substrate; freeze-drying the slurry layer to form a sulfur-based composite layer having a porosity in a range of 60% to 99%; and disposing a conductive polymer atop the composite layer and within pores of the composite layer.
Abstract:
Disclosed herein are graphene coatings characterized by a porous, three-dimensional, spherical structure having a hollow core, along with methods for forming such graphene coatings on glasses, glass-ceramics, ceramics, and crystalline materials. Such coatings can be further coated with organic or inorganic layers and are useful in chemical and electronic applications.
Abstract:
A solid electrolyte for a negative electrode of a secondary battery includes a first solid electrolyte having a first surface and a second solid electrolyte on the first solid electrolyte and having a second surface. The first solid electrolyte and the second solid electrolyte each have an ionic conductivity effective for a deposition metal, and the first surface and the second surface are different in composition, structure, or both. An electrode assembly and an electrochemical cell including the solid electrolyte and method for the manufacture thereof are also described.
Abstract:
Electrolyte for a solid-state battery includes a body having grains of inorganic material sintered to one another, where the grains include lithium. The body is thin, has little porosity by volume, and has high ionic conductivity.
Abstract:
Disclosed herein are methods for forming a graphene film on a substrate, the methods comprising depositing graphene on a surface of the substrate by a first vapor deposition step to form a discontinuous graphene crystal layer; depositing a graphene oxide layer on the discontinuous graphene crystal layer to form a composite layer; and depositing graphene on the composite layer by a second vapor deposition step, wherein the graphene oxide layer is substantially reduced to a graphene layer during the second vapor deposition step. Transparent coated substrates comprising such graphene films are also disclosed herein, wherein the graphene films have a resistance of less than about 10 KΩ/sq.
Abstract:
A gallium doped garnet composition of the formula: Li7-3yLa3Zr2GayO12 where y is from 0.4 to 2.0, and as defined herein. Also disclosed is a method for making a dense Li-ion conductive cubic garnet membrane, comprising one of two alternative lower temperature routes, as defined herein.
Abstract:
A catalyst-free CVD method for forming graphene. The method involves placing a substrate within a reaction chamber, heating the substrate to a temperature between 600° C. and 1100° C., and introducing a carbon precursor into the chamber to form a graphene layer on a surface of the substrate. The method does not use plasma or a metal catalyst to form the graphene.
Abstract:
Absorbent structures for CO2 capture include a honeycomb substrate having partition walls that extend through the honeycomb substrate. The partition walls have channel surfaces that define a plurality of individual channels including a plurality of reaction channels and a plurality of heat-exchange channels. The reaction channels and the heat-exchange channels are arranged such that individual reaction channels are in thermal communication with individual heat-exchange channels. Surfaces of the reaction channels surfaces include a sorbent material, and surfaces of the heat-exchange channels include a coating layer. The coating layer includes a water-impermeable layer formed from a polymer material. The polymer material of the water-impermeable layer does not substantially penetrate into the sorbent material of the partition walls or of the reaction-channel surfaces. Methods for forming the absorbent structures include coating the surfaces of the heat-exchange channels with the polymer material using a liquid composition such as an aqueous polymer emulsion.