A preparation method of SnO.sub.2@Sn coated reduced graphene oxide composite material. By compounding reduced graphene oxide and SnO.sub.2, SnO.sub.2 undergoes conversion and alloying reactions to form Sn nanoparticles, and the three components have a synergistic effect and good reversibility. Nano SnO.sub.2@Sn particles are uniformly distributed on the ultrathin RGO nanosheets. RGO can effectively alleviate volume expansion caused by SnO.sub.2 and prevent SnO.sub.2@Sn nanoparticles from agglomeration during cycle. The adhesion of SnO.sub.2@Sn on RGO can also effectively reduce the repacking of RGO nanosheets, so that the composite material maintains a large surface area during the charge-discharge process, providing sufficient space for the storage of potassium ions. Therefore, the prepared SnO.sub.2@Sn coated reduced graphene oxide composite material (SnO.sub.2 @Sn@RGO) has excellent electrochemical performance, exhibits excellent cycle performance, rate capability and long-term cycle stability, and has a very ideal first coulomb efficient.

A battery comprising an acidified metal oxide (“AMO”) material, preferably in monodisperse nanoparticulate form 20 nm or less in size, having a pH<7 when suspended in a 5 wt % aqueous solution and a Hammett function H.sub.0>−12, at least on its surface.

A predoping material is used for an alkali metal ion electric storage device and is represented by Formula (1):
RSM)n  (1)
where M represents lithium or sodium; n represents an integer of 2 to 6; and R represents an aliphatic hydrocarbon, optionally substituted aromatic hydrocarbon, or optionally substituted heterocycle having 1 to 10 carbon atoms).

According to the present disclosure, it is possible to appropriately prevent a shortage of a nonaqueous electrolyte solution in an electrode body and keep battery performance of a nonaqueous electrolyte secondary battery at a favorable state. A nonaqueous electrolyte secondary battery disclosed herein includes an electrode body and a nonaqueous electrolyte solution. The electrode body includes an electrolyte solution passage that is a flow passage through which the nonaqueous electrolyte solution flows between the inside and the outside of the electrode body. When a region of a negative-electrode composite material layer that is in contact with the electrolyte solution passage is referred to as a damming portion and a region that is located on the center side relative to the damming portion is referred to as a liquid retaining portion, the damming portion contains a negative electrode active material of which an electrical potential relative to a positive electrode active material is high and a ratio of expansion or contraction due to an increase or decrease in SOC is high, when compared to a negative electrode active material contained in the liquid retaining portion. With this configuration, the electrolyte solution passage can be closed by the damming portion in a charge state where the damming portion expands, and therefore leakage of the nonaqueous electrolyte solution can be suppressed.

An anode including a plurality of active material particles, a first polymer binder that undergoes a cyclization reaction when heated and a second polymer binder, wherein the first polymer binder is a different type of polymer binder from the first polymer binder; an electrochemical energy storage device containing the anode; and a method of making the anode are disclosed.

Embodiments of the present disclosure generally relate to electrode coatings and methods of coating electrodes. In an embodiment, a method of depositing a structure on a lithium ion battery (LIB) anode is provided. The method includes accelerating particles in a working gas through a convergent-divergent nozzle to a process velocity that is from a critical velocity of the particles to an erosion velocity of the LIB anode, the particles comprising a metal and/or a Group III-VI element; heating or cooling the particles in the working gas at a softening temperature; ejecting the particles in the working gas from a nozzle outlet of the convergent-divergent nozzle, the particles ejected at the process velocity, wherein at least a portion of the particles are in solid phase when ejected from the convergent-divergent nozzle; and depositing a first structure on the LIB anode, the first structure comprising the metal and/or the Group III-VI element.

A rechargeable lithium battery is provided. The battery includes an anode comprising a polymer-matrix electrolyte (PME) and an anode active material, a cathode comprising a PME and a cathode active material and a PME comprising an electrolyte polymer, a lithium salt and an electrolyte solvent. The PME is positioned between the anode and the cathode and directly contacts the anode and cathode to form a battery cell. The polymer-matrix electrolyte interpenetrates into the adjacent anode and cathode to form an integral structure.

A negative electrode active material for an electric device includes an alloy containing Si in a range from 23% to 64% exclusive, Sn in a range from 4% to 58% inclusive, Zn in a range from 0% to 65% exclusive, and inevitable impurities as a residue. The negative electrode active material can be obtained with a multi DC magnetron sputtering apparatus by use of, for example, silicon, tin and zinc as targets. An electric device such as a lithium ion secondary battery employing the negative electrode active material can improve cycle life of the battery and ensure a high capacity and high cycle durability.

Disclosed is a metal-air fuel cell based on a solid oxide electrolyte employing metal nanoparticles as fuel. The metal-air fuel cell includes an anode, a cathode, a solid oxide electrolyte and a metal fuel, wherein the metal fuel comprises metal nanoparticles having an average particle diameter ranging from 1 nm to 100 nm. The metal nanoparticles have a low melting point and provide high reactivity. Thus, the metal-air fuel cell forms a metal molten phase at a relatively low temperature thereby improving contactability and has improved reactivity to promote oxidation, thereby enabling highly efficient power generation.

Described herein are improved composite anodes and lithium-ion batteries made therefrom. Further described are methods of making and using the improved anodes and batteries. In general, the anodes include a porous composite having a plurality of agglomerated nanocomposites. At least one of the plurality of agglomerated nanocomposites is formed from a dendritic particle, which is a three-dimensional, randomly-ordered assembly of nanoparticles of an electrically conducting material and a plurality of discrete non-porous nanoparticles of a non-carbon Group 4A element or mixture thereof disposed on a surface of the dendritic particle. At least one nanocomposite of the plurality of agglomerated nanocomposites has at least a portion of its dendritic particle in electrical communication with at least a portion of a dendritic particle of an adjacent nanocomposite in the plurality of agglomerated nanocomposites.