The present invention relates to an oxyhalide electrochemical cell comprising an anode of a Group IA metal and a cathode of a composite material prepared from a first electrochemically active carbonaceous material and a second electrochemically non-active carbonaceous material. The cathode material of the present invention provides increased discharge capacity compared to traditional lithium oxyhalide cells. In addition, the cathode material of the present invention is chemically stable which makes it particularly useful for applications that require increased rate capability in extreme environmental conditions such as those found in oil and gas exploration.

Set forth herein are electrolyte compositions that include both organic and inorganic constituent components and which are suitable for use in rechargeable batteries. Also set forth herein are methods and systems for making and using these composite electrolytes.

Method for producing a positive electrode for a solid-state lithium microbattery comprising the following successive steps: supplying of a substrate made of ceramic, glass or silicon, locally covered with a metal layer, depositing of a cathodic layer made of a positive electrode material, for example made of mixed lithium oxide, the cathodic layer having a thickness greater than 1 μm, a first portion of the cathodic layer covering the substrate and a second portion of the cathodic layer covering the metal layer, intended to form the positive electrode, carrying out of a heat treatment at a temperature greater than or equal to 400° C., on the cathodic layer, in such a way as to crystallise the second portion of the cathodic layer in order to form a positive electrode, and in such a way as to delaminate the first portion of the cathodic layer.

Set forth herein are electrolyte compositions that include both organic and inorganic constituent components and which are suitable for use in rechargeable batteries. Also set forth herein are methods and systems for making and using these composite electrolytes.

The present disclosure relates to a lithium ion-conducting glass ceramic which comprises a residual glass phase that is also ion-conducting, a process for the production thereof as well as its use in a battery. The glass ceramic according to the present disclosure comprises a main crystal phase which is isostructural to the NaSICon crystal phase, wherein the composition can be described with the following formula: Li.sub.1+x−yM.sub.y.sup.5+M.sub.x.sup.3+M.sub.2−x−y.sup.4+(PO.sub.4).sub.3, wherein x is greater than 0 and at most 1, as well as greater than y. Y may take values of between 0 and 1. Here, the following boundary condition has to be fulfilled: (1+x−y)>1. Here, M represents a cation with the valence of +3, +4 or +5. M.sup.3+ is selected from Al, Y, Sc or B, wherein at least Al as trivalent cation is present. Independently thereof, M.sup.4+ is selected from Ti, Si or Zr, wherein at least Ti as tetravalent cation is present. Independently thereof, M.sup.5+ is selected from Nb, Ta or La.

An all-solid-state secondary battery has a positive electrode collector, a positive electrode active material layer, a negative electrode active material layer, a negative electrode collector, and a solid electrolyte. The solid electrolyte has an interlayer solid electrolyte located between the positive electrode active material layer and the negative electrode active material layer, and the all-solid-state secondary battery further includes a trapping layer that traps a metal of which at least one of the positive electrode collector and the negative electrode collector is formed.

A current collector layer for an all-solid-state battery is provided with which a good electron path can be easily formed and rate characteristic can be improved. A current collector layer 5 for an all-solid-state battery 1, the current collector layer 5 including: a carbon material; and a solid electrolyte, the all-solid-state battery 1 including a group 1 or 2 ion conductive solid electrolyte layer 2, the carbon material being mixed with Si at a weight ratio of 1:1 to produce a mixture, the mixture having an X-ray diffraction spectrum having a ratio of a peak height a to a peak height b, a/b, of 0.2 or more and 10.0 or less as being measured, the peak height a being highest in a range of 2θ of 24° or more and less than 28°, and the peak height b being highest in a range of 2θ of 28° or more and less than 30°.

The present disclosure relates to a lithium ion-conducting glass ceramic which comprises a residual glass phase that is also ion-conducting, a process for the production thereof as well as its use in a battery. The glass ceramic according to the present disclosure comprises a main crystal phase which is isostructural to the NaSICon crystal phase, wherein the composition can be described with the following formula: Li.sub.1+x−yM.sub.y.sup.5+M.sub.x.sup.3+M.sub.2−x−y.sup.4+(PO.sub.4).sub.3′, wherein x is greater than 0 and at most 1, as well as greater than y. Y may take values of between 0 and 1. Here, the following boundary condition has to be fulfilled: (1+x−y)>1. Here, M represents a cation with the valence of +3, +4 or +5. M.sup.3+ is selected from Al, Y, Sc or B, wherein at least Al as trivalent cation is present. Independently thereof, M.sup.4+ is selected from Ti, Si or Zr, wherein at least Ti as tetravalent cation is present. Independently thereof, M.sup.5+ is selected from Nb or Ta.

A voltage source includes two electrically conductive terminals (101, 102) with an electrolyte (103) between them. Said electrolyte (103) is a mixture in which the main component is ash produced in a power plant or an incineration plant.

Ceramic-polymer film includes a polymer matrix, plasticizers, a lithium salt, and a ceramic nanoparticle, LLZO: Al.sub.xLi.sub.7-xLa.sub.3Zr.sub.1.75Ta.sub.0.25O.sub.12 where x ranges from 0 to 0.85. The nanoparticles have diameters that range from 20 to 2000 nm and the film has an ionic conductivity of greater than 1×10.sup.−4 S/cm (−20° C. to 10° C.) and larger than 1×10.sup.−3 S/cm (≥20° C.). Using a combination of selected plasticizers to tune the ionic transport temperature dependence enables the battery based on the ceramic-polymer film to be operable in a wide temperature window (−40° C. to 90° C.). Large size nanocomposite film (area ≥8 cm×6 cm) can be formed on a substrate and the concentration of LLZO nanoparticles decreases in the direction of the substrate to form a concentration gradient over the thickness of the film. This large size film can be employed as a non-flammable, solid-state electrolyte for lithium electrochemical pouch cell and further assembled into battery packs.