Provided is a three-phase system V.sub.2O.sub.3/VN/Mo.sub.2C nanoelectrode material, and a preparation method and application thereof. The nanoelectrode material comprises V.sub.2O.sub.3 particles, VN particles, and Mo.sub.2C particles. The V.sub.2O.sub.3 particles, VN particles, and Mo.sub.2C particles are interlaced in lattice stripes and are uniformly distributed. The mass ratio of the V.sub.2O.sub.3, VN and Mo.sub.2C is (1 to 4):(10 to 40):(4 to 16). The above-mentioned three kinds of nanoparticles are intertwined to form more incoherent interface area. The increase in the area of the incoherent interface area will cause more defects, so that more active sites are provided, and the hydrogen production performance is improved.

Provided is a three-phase system V.sub.2O.sub.3/VN/Mo.sub.2C nanoelectrode material, and a preparation method and application thereof. The nanoelectrode material comprises V.sub.2O.sub.3 particles, VN particles, and Mo.sub.2C particles. The V.sub.2O.sub.3 particles, VN particles, and Mo.sub.2C particles are interlaced in lattice stripes and are uniformly distributed. The mass ratio of the V.sub.2O.sub.3, VN and Mo.sub.2C is (1 to 4):(10 to 40):(4 to 16). The above-mentioned three kinds of nanoparticles are intertwined to form more incoherent interface area. The increase in the area of the incoherent interface area will cause more defects, so that more active sites are provided, and the hydrogen production performance is improved.

The present invention discloses a polymer-metal compound composite ink, a preparation method and application thereof. The composite ink comprises: at least one polymer; at least one metal compound material, the metal compound material being selected from polyoxometalate compounds and nanocrystalline metal oxides; at least one solvent which is used for forming a disperse system in the form of a uniform fluid together with the remaining components in the composite ink. The present invention also discloses a method for preparing the composite ink. The composite ink of the present invention is easily available in raw material, easy to prepare and low in cost, and can be manufactured into a composite thin film by spin-coating, printing or in other ways. The composite thin film, as an electrode modification layer, can be applied to photoelectric devices such as solar cells or light-emitting diodes, so as to improve the contact performance between an electrode and an organic active layer and thus enhance the performance and yield of photoelectric devices.

A battery includes a case having a feedthrough port, a feedthrough assembly disposed in the feedthrough port, and a cell stack disposed within the case. The feedthrough port includes an inner conductor and an insulator core separating the inner conductor from the case. The cell stack includes an anode, a cathode, and a separator insulating the anode from the cathode, wherein the anode and cathode are offset from one another. An insulating boot surrounding the cell stack insulates the cell stack from the case. The insulating boot has an opening configured to receive therein the feedthrough assembly, which may include overmolded insulation. The interior surfaces and interior walls of the battery case may be thermal spray-coated with a dielectric material to prevent lithium dendrite formation between cathode and anode surfaces.

Methods and systems for removing impurities from electrolyte solutions having three or more valence states. In some embodiments, a method includes electrochemically reducing an electrolyte solution to lower its valence state to a level that causes impurities to precipitate out of the electrolyte solution and then filtering the precipitate(s) out of the electrolyte solution. In embodiments in which the electrolyte solution is desired to be at a valence state higher than the precipitation valence state, a method of the disclosure includes oxidizing the purified electrolyte solution to the target valence.

Methods and systems for removing impurities from electrolyte solutions having three or more valence states. In some embodiments, a method includes electrochemically reducing an electrolyte solution to lower its valence state to a level that causes impurities to precipitate out of the electrolyte solution and then filtering the precipitate(s) out of the electrolyte solution. In embodiments in which the electrolyte solution is desired to be at a valence state higher than the precipitation valence state, a method of the disclosure includes oxidizing the purified electrolyte solution to the target valence.

The disclosure pertains to methods for the preparation of crystalline monoclinic VO2 as well as to materials and articles. In a described method, amorphous VO2 is annealed in an oxygen-containing atmosphere to give crystalline monoclinic VO2.

The disclosure pertains to methods for the preparation of crystalline monoclinic VO2 as well as to materials and articles. In a described method, amorphous VO2 is annealed in an oxygen-containing atmosphere to give crystalline monoclinic VO2.

The present invention may provide a nano-sized composite having excellent electrical conductivity and specific surface area. The present invention may provide a method of producing the above-described composite through a simple process without an ultracentrifugation process or a flash annealing step. The present invention may provide an energy storage device having high power performance and having excellent specific capacity characteristics not only at low current density but also at high current density.

The present invention may provide a nano-sized composite having excellent electrical conductivity and specific surface area. The present invention may provide a method of producing the above-described composite through a simple process without an ultracentrifugation process or a flash annealing step. The present invention may provide an energy storage device having high power performance and having excellent specific capacity characteristics not only at low current density but also at high current density.