The present disclosure provides an electrochemical energy storage device, which comprises a cell, an electrolyte and a package. The electrochemical energy storage device further comprises a binding material positioned between the cell and the package. The binding material comprises an adhesive layer and a covering layer. The adhesive layer is directly or indirectly adhered and positioned on an outer surface of the cell, and a surface of the adhesive layer which is far away from the cell is an adhesive surface; the covering layer is positioned on the adhesive surface of the adhesive layer, the covering layer is dissolved or swollen into the electrolyte in whole or in part so as to expose the adhesive surface of the adhesive layer, therefore the adhesive layer can make the cell adhered with the package. The covering layer is a polar molecule, the polar molecule comprises one or more selected from the group consisting of —F, —CO—NH—, —NH—CO—NH—, and —NH—CO—O—. The electrochemical energy storage device of the present disclosure may not only fixedly connect the cell to the package so as to resolve the problems during the drop test, but also may resolve the problem that the cell is difficult to put into the package because the two surfaces of the binding material are both adhesive, the electrochemical energy storage device also has an excellent cycle performance and an excellent charge-discharge performance under a high rate.

A rechargeable electrochemical battery cell with a housing, a positive electrode, a negative electrode and an electrolyte which contains SO.sub.2 and a conducting salt of the active metal of the cell, whereby at least one of the electrodes contains a binder chosen from the group: Binder A, which consists of a polymer, which is made of monomeric structural units of a conjugated carboxylic acid or of the alkali salt, earth alkali salt or ammonium salt of this conjugated carboxylic acid or a combination thereof or binder B which consists of a polymer based on monomeric styrene structural units or butadiene structural units or a mixture of binder A and B.

A rechargeable electrochemical battery cell with a housing, a positive electrode, a negative electrode and an electrolyte which contains SO.sub.2 and a conducting salt of the active metal of the cell, whereby at least one of the electrodes contains a binder chosen from the group: Binder A, which consists of a polymer, which is made of monomeric structural units of a conjugated carboxylic acid or of the alkali salt, earth alkali salt or ammonium salt of this conjugated carboxylic acid or a combination thereof or binder B which consists of a polymer based on monomeric styrene structural units or butadiene structural units or a mixture of binder A and B.

Square section liquid metal batteries (LMBs) with a grid device to suppress instabilities of fluids. The LMBs include a shell, negative current collector, negative material, metallic nets/plates, grid device, electrolyte, positive material, rectangular holes on partitions of grid device, and positive current collector. The positive material, electrolyte, and negative material are filled in the shell and automatically stratified from bottom to top according to the density from large to small. The negative current collector is linked with negative material, and the positive current collector is linked with positive material. The grid device is composed of partitions which cross each other and pass through the negative material, the electrolyte vertically in sequence, and extend inside the positive material. There are rectangular holes opened on the grid device, and the vertical height of each rectangular hole is larger than the biggest displacement of electrolyte during charging and discharging processes.

Square section liquid metal batteries (LMBs) with a grid device to suppress instabilities of fluids. The LMBs include a shell, negative current collector, negative material, metallic nets/plates, grid device, electrolyte, positive material, rectangular holes on partitions of grid device, and positive current collector. The positive material, electrolyte, and negative material are filled in the shell and automatically stratified from bottom to top according to the density from large to small. The negative current collector is linked with negative material, and the positive current collector is linked with positive material. The grid device is composed of partitions which cross each other and pass through the negative material, the electrolyte vertically in sequence, and extend inside the positive material. There are rectangular holes opened on the grid device, and the vertical height of each rectangular hole is larger than the biggest displacement of electrolyte during charging and discharging processes.

A device such as, for example, an energy storage device or a micro-resistor, is disclosed which includes a silicon based electrode in which decreased interfacial resistance/impedance throughout the charge-mobile region of the device is provided. The decreased interfacial resistance/impedance is provided by forming an interfacial additive composite layer composed of a molten lithium containing salt layer and a layer of a Li-salt containing conductive polymeric adhesive material between the silicon based electrode and a solid polymer electrolyte layer. The presence of such an interfacial additive composite layer increases the ion and electron mobile dependent performances at the silicon based electrode interface due to significant decrease in the resistance/impedance that is observed at the respective interface as well as the impedance observed in the bulk of the device.

A device such as, for example, an energy storage device or a micro-resistor, is disclosed which includes a silicon based electrode in which decreased interfacial resistance/impedance throughout the charge-mobile region of the device is provided. The decreased interfacial resistance/impedance is provided by forming an interfacial additive composite layer composed of a molten lithium containing salt layer and a layer of a Li-salt containing conductive polymeric adhesive material between the silicon based electrode and a solid polymer electrolyte layer. The presence of such an interfacial additive composite layer increases the ion and electron mobile dependent performances at the silicon based electrode interface due to significant decrease in the resistance/impedance that is observed at the respective interface as well as the impedance observed in the bulk of the device.

Provided herein are energy storage devices. In some cases, the energy storage devices are capable of being transported on a vehicle and storing a large amount of energy. An energy storage device is provided comprising at least one liquid metal electrode, an energy storage capacity of at least about 1 MWh and a response time less than or equal to about 100 milliseconds (ms).

An electrolyte for a secondary battery and a lithium secondary battery including the same are disclosed herein. In some embodiments, an electrolyte includes a first electrolyte solution represented by Formula 1 and a second electrolyte solution represented by Formula 2

M.sup.1N.sup.1X.sup.1-n(SO.sub.2)  [Formula 1]

M.sup.2N.sup.2X.sup.2-m(SO.sub.2)  [Formula 2]

wherein M.sup.1 and M.sup.2 are different from each other and each independently an alkali metal, N.sup.1 and N.sup.2 are each independently at least one metal selected from the group consisting of an alkali metal, a transition metal, and a post-transition metal, X.sup.1 and X.sup.2 are each independently a halogen element, and n and m are each independently an integer of 1 to 4.

An all-inorganic electrolyte formulation for use in a lithium-ion battery system comprising at least one of each a phosphoranimine, a phosphazene, a monomeric organophosphate and a supporting lithium salt. The electrolyte preferably has a melting point below 0° C., and a vapor pressure of combustible components at 60.6° C. sufficiently low to not produce a combustible mixture in air, e.g., less than 40 mmHg at 30° C. The phosphoranimine, phosphazene, and monomeric phosphorus compound preferably do not have any direct halogen-phosphorus bonds. A solid electrolyte interface layer formed by the electrolyte with an electrode is preferably thermally stable ≥80° C.