The present invention discloses an iron-based cathode material for a sodium-ion battery, which comprises a Na.sub.3Fe.sub.2(SO.sub.4).sub.3F material and a carbon-based material embedded into the bulk structure of Na.sub.3Fe.sub.2(SO.sub.4).sub.3F material. The weight percentage of the carbon-based material is ranked between 1% and 10%. The present invention also provides a method for preparing the above-mentioned iron-based cathode material for a sodium-ion battery, and a corresponding sodium-ion full battery using the Na.sub.3Fe.sub.2(SO.sub.4).sub.3F-based cathode material. The Na.sub.3Fe.sub.2(SO.sub.4).sub.3F cathode material ensures desired electrochemical sodium storage performance, involving high specific sodium storage capacity, improved cycle stability and superior rate performance in comparison with that of various pristine Na.sub.xFe.sub.y(SO.sub.4).sub.z materials. The actual operating potential of the reported sodium-ion full battery in the present invention is significantly higher than the output potential of existing commercial sodium-ion full batteries, and the increase in battery energy density is also achieved.

An all solid battery includes a multilayer chip in which each of a plurality of solid electrolyte layers including solid electrolyte and each of a plurality of internal electrodes including an electrode active material are alternately stacked, the multilayer chip having a rectangular parallelepiped shape, the plurality of internal electrodes being alternately exposed to two side faces of the multilayer chip other than two end faces of a stacking direction of the multilayer chip, and a pair of external electrodes that contacts the two side faces. At least one of the pair of external electrodes includes an electrode active material of which a pole is a same as that of an electrode active material of the internal electrode which contacts the one of the pair of external electrodes.

A method of applying a homogenous film coating to a constituent particle of component includes setting up a target element in a sputtering chamber. The method also includes arranging a receptacle in the sputtering chamber. The method additionally includes arranging the constituent particle on the receptacle. The method also includes bombarding the target element via energetic particles to eject material from the target element and deposit the material onto the constituent particle. The method further includes agitating the receptacle during the bombarding to apply the material to the constituent particle as the homogenous film coating. The method may be used to apply a homogenous thin film coating to a sulfur-infused constituent particle for a sulfur cathode in a lithium-sulfur battery.

A lithium-sulfur 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: active elemental sulfur, conductive carbon, and sulfide electrolyte, and the sulfide electrolyte is uniformly coated on at least one surface of the conductive carbon. A method of forming a composite cathode for a lithium-sulfur battery includes: synthesizing dispersed carbon fiber from cotton to form carbonized dispersed cotton fiber (CDCF) powder; in-situ coating of the CDCF with an electrolyte component to form a composite powder; and mixing active elemental sulfur powder with the composite powder to form the composite cathode.

A method utilizing microwave energy to incorporate sulfur onto carbon, prepare cathode material for lithium sulfur battery applications, and the compositions resulting therefrom is disclosed.

The disclosure provides a coated positive electrode active material particle including an active material having the general chemical formula A.sub.xM.sub.yE.sub.z(XO.sub.4).sub.q, wherein A is an alkali metal or an alkaline earth metal, M includes cobalt, E is a non-electrochemically active metal, a boron group element, or silicon or any alloys or combinations thereof, X is phosphorus or sulfur or a combination thereof, 0<x≤1, y>0, z≥0, q>0, and the relative values of x, y, z, and q are such that the general chemical formula is charge balanced. The disclosure provides a method of attritor-mixing the active material. The disclosure provides an alkali metal or alkaline earth metal rechargeable battery including an electrolyte including an ionic liquid and an alkali metal salt or alkaline earth metal salt. The battery includes a pressure application system that applies pressure to at least a portion of the electrode surfaces contacting the electrolyte.

An object is to improve the characteristics of a power storage device such as a charging and discharging rate or a charge and discharge capacity. The grain size of particles of a positive electrode active material is nano-sized so that a surface area per unit mass of the active material is increased. Specifically, the grain size is set to greater than or equal to 10 nm and less than or equal to 100 nm, preferably greater than or equal to 20 nm and less than or equal to 60 nm. Alternatively, the surface area per unit mass is set to 10 m.sup.2/g or more, preferably 20 m.sup.2/g or more, further, the crystallinity of the active material is increased by setting an XRD half width to greater than or equal to 0.12° and less than 0.17°, preferably greater than or equal to 0.13° and less than 0.16°.

An object is to improve the characteristics of a power storage device such as a charging and discharging rate or a charge and discharge capacity. The grain size of particles of a positive electrode active material is nano-sized so that a surface area per unit mass of the active material is increased. Specifically, the grain size is set to greater than or equal to 10 nm and less than or equal to 100 nm, preferably greater than or equal to 20 nm and less than or equal to 60 nm. Alternatively, the surface area per unit mass is set to 10 m.sup.2/g or more, preferably 20 m.sup.2/g or more, further, the crystallinity of the active material is increased by setting an XRD half width to greater than or equal to 0.12° and less than 0.17°, preferably greater than or equal to 0.13° and less than 0.16°.

An electrode structure and its method of manufacture are disclosed. The disclosed electrode structures may be manufactured by depositing a first release layer on a first carrier substrate. A first protective layer may be deposited on a surface of the first release layer and a first electroactive material layer may then be deposited on the first protective layer.

An electrode structure and its method of manufacture are disclosed. The disclosed electrode structures may be manufactured by depositing a first release layer on a first carrier substrate. A first protective layer may be deposited on a surface of the first release layer and a first electroactive material layer may then be deposited on the first protective layer.