An embodiment is directed to a solid state electrolyte-comprising Li or Li-ion battery cell, comprising an anode electrode, a cathode electrode with an areal capacity loading that exceeds around 3.5 mAh/cm.sup.2, an ionically conductive separator layer that electrically separates the anode and cathode electrodes, and one or more solid electrolytes ionically coupling the anode and the cathode, wherein at least one of the one or more solid electrolytes or at least one solid electrolyte precursor of the one or more solid electrolytes is infiltrated into the solid state Li or Li-ion battery cell as a liquid.

An embodiment is directed to a solid state electrolyte-comprising Li or Li-ion battery cell, comprising an anode electrode, a cathode electrode with an areal capacity loading that exceeds around 3.5 mAh/cm.sup.2, an ionically conductive separator layer that electrically separates the anode and cathode electrodes, and one or more solid electrolytes ionically coupling the anode and the cathode, wherein at least one of the one or more solid electrolytes or at least one solid electrolyte precursor of the one or more solid electrolytes is infiltrated into the solid state Li or Li-ion battery cell as a liquid.

A lithium metal oxide (LMO) cathode includes a current collector having a length defining a first end and a second end, a width, and a first side and a second side, LMO active material applied to the first side and the second side of the current collector such that the LMO active material applied to each respective side of the current collector has an inner face contiguous with the current collector and an outer face, and a plurality of channels extending widthwise across the cathode within the LMO active material applied to the first and second sides. The LMO active material on each current collector side can have a thickness of about 100 μm to about 400 μm. The channels on the same side of the current collector can be spaced apart by 0.1 mm to 10 mm. The channels can have widths of 10 μm to 60 μm.

A lithium metal oxide (LMO) cathode includes a current collector having a length defining a first end and a second end, a width, and a first side and a second side, LMO active material applied to the first side and the second side of the current collector such that the LMO active material applied to each respective side of the current collector has an inner face contiguous with the current collector and an outer face, and a plurality of channels extending widthwise across the cathode within the LMO active material applied to the first and second sides. The LMO active material on each current collector side can have a thickness of about 100 μm to about 400 μm. The channels on the same side of the current collector can be spaced apart by 0.1 mm to 10 mm. The channels can have widths of 10 μm to 60 μm.

A lithium cobalt-based oxide cathode active material powder having: —a primary phase comprising Li, Co, and O, and —a secondary phase comprising LiNaSO.sub.4, wherein the content of said LiNaSO.sub.4 secondary phase in said powder is of at least 0.4 wt. % and inferior or equal to 1.1 wt. % with respect to a total weight of the cathode active material powder, said cathode active material powder being characterized in that it has a S/Na atomic ratio superior or equal to 0.80 and inferior or equal to 1.20.

A lithium cobalt-based oxide cathode active material powder having: —a primary phase comprising Li, Co, and O, and —a secondary phase comprising LiNaSO.sub.4, wherein the content of said LiNaSO.sub.4 secondary phase in said powder is of at least 0.4 wt. % and inferior or equal to 1.1 wt. % with respect to a total weight of the cathode active material powder, said cathode active material powder being characterized in that it has a S/Na atomic ratio superior or equal to 0.80 and inferior or equal to 1.20.

A preparation method of a composite anode material of micrometer-sized carbon-coated silicon and carbon includes: subjecting micrometer-sized silicon particles to a chemical vapor deposition reaction under a gas atmosphere containing carbon to obtain carbon-coated first micrometer-sized silicon particles; dispersing the carbon-coated first micrometer-sized silicon particles in a first mixed solvent to obtain a dispersed solution; adding alkali into the dispersed solution and heating the dispersed solution to obtain carbon-coated second micrometer-sized silicon particles; dispersing the carbon-coated second micrometer-sized silicon particles and graphene oxide in a second mixed solvent that are subjected to a hydrothermal reaction to obtain a composite hydrogel of reduced graphene oxide, silicon, and carbon; and heating the hydrogel to obtain the composite anode material.

A preparation method of a composite anode material of micrometer-sized carbon-coated silicon and carbon includes: subjecting micrometer-sized silicon particles to a chemical vapor deposition reaction under a gas atmosphere containing carbon to obtain carbon-coated first micrometer-sized silicon particles; dispersing the carbon-coated first micrometer-sized silicon particles in a first mixed solvent to obtain a dispersed solution; adding alkali into the dispersed solution and heating the dispersed solution to obtain carbon-coated second micrometer-sized silicon particles; dispersing the carbon-coated second micrometer-sized silicon particles and graphene oxide in a second mixed solvent that are subjected to a hydrothermal reaction to obtain a composite hydrogel of reduced graphene oxide, silicon, and carbon; and heating the hydrogel to obtain the composite anode material.

A solid electrolyte includes a polymer and a lithium salt, a sodium salt or mixtures of these salts. The polymer has at least 50 mol % of recurring units of formula (I). A method is for the preparation of the electrolyte. Energy storage devices can include the electrolyte.

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A doped phosphorus-sulfur iodide solid electrolyte, a preparation method therefor, and use thereof. The chemical formula of said solid electrolyte is Li.sub.6-xM.sub.xP.sub.1-xS.sub.5I, in which 0<x<0.8, and M is tungsten and/or molybdenum. Said method comprises: 1) mixing a lithium source, a phosphorus source, an iodine source, a sulfur source, and an M source in an inert atmosphere, and then ball-milling same to obtain a solid electrolyte precursor; and 2) sintering the solid electrolyte precursor obtained in step 1) in an inert atmosphere or in vacuum to obtain the doped phosphorus-sulfur iodide solid electrolyte.