Patent classifications
H01M10/36
CATHODE MATERIAL
The present invention relates to a range of halide organic salts and their use in a cathode of an electrical cell and in batteries. Elemental halides have attracted intense interest as promising electrodes for energy storage. However, they suffer from a number of inherent physicochemical drawbacks, including the volatility of iodine, the corrosiveness of liquid bromine. The salts of the present invention may serve as a cathode matched with a zinc anode avoiding these issues.
METHOD FOR PREPARING 3D CARBONITRIDE COATED VSE2 COMPOSITE (3D-VSe2@CN)
The disclosure relates to a method for preparing a 3D sponge structured carbonitride coated VSe.sub.2 composite (3D-VSe.sub.2@CN), belonging to the technical fields of electrode materials and preparation of batteries. In the disclosure, carbon, nitrogen and VSe.sub.2 are composited by using NaCl as a template so as to construct a 3D sponge structured carbonitride coated VSe.sub.2 composite. The 3D sponge structure can increase the structure stability of the material in the cyclic process, and the carbocanitride can increase the electron conductivity and activity sites of the material, so as to allow easier diffusion of potassium ions. Meanwhile, the stable structure can cause the clustering of VSe.sub.2 all the time. Thus, the prepared composite has good and stable rate capability and cycle stability. The process method is simple, low in cost, environmental-friendly, and suitable for large-scale industrial production.
METHOD FOR PREPARING 3D CARBONITRIDE COATED VSE2 COMPOSITE (3D-VSe2@CN)
The disclosure relates to a method for preparing a 3D sponge structured carbonitride coated VSe.sub.2 composite (3D-VSe.sub.2@CN), belonging to the technical fields of electrode materials and preparation of batteries. In the disclosure, carbon, nitrogen and VSe.sub.2 are composited by using NaCl as a template so as to construct a 3D sponge structured carbonitride coated VSe.sub.2 composite. The 3D sponge structure can increase the structure stability of the material in the cyclic process, and the carbocanitride can increase the electron conductivity and activity sites of the material, so as to allow easier diffusion of potassium ions. Meanwhile, the stable structure can cause the clustering of VSe.sub.2 all the time. Thus, the prepared composite has good and stable rate capability and cycle stability. The process method is simple, low in cost, environmental-friendly, and suitable for large-scale industrial production.
Multivalent metal ion battery having a cathode of recompressed graphite worms and manufacturing method
Provided is a multivalent metal-ion battery comprising an anode, a cathode, a porous separator electronically separating the anode and the cathode, and an electrolyte in ionic contact with the anode and the cathode to support reversible deposition and dissolution of a multivalent metal, selected from Ni, Zn, Be, Mg, Ca, Ba, La, Ti, Ta, Zr, Nb, Mn, V, Co, Fe, Cd, Cr, Ga, In, or a combination thereof, at the anode, wherein the anode contains the multivalent metal or its alloy as an anode active material and the cathode comprises a cathode layer of an exfoliated graphite or carbon material recompressed to form an active layer that is oriented in such a manner that the active layer has a graphite edge plane in direct contact with the electrolyte and facing or contacting the separator.
Multivalent metal ion battery having a cathode of recompressed graphite worms and manufacturing method
Provided is a multivalent metal-ion battery comprising an anode, a cathode, a porous separator electronically separating the anode and the cathode, and an electrolyte in ionic contact with the anode and the cathode to support reversible deposition and dissolution of a multivalent metal, selected from Ni, Zn, Be, Mg, Ca, Ba, La, Ti, Ta, Zr, Nb, Mn, V, Co, Fe, Cd, Cr, Ga, In, or a combination thereof, at the anode, wherein the anode contains the multivalent metal or its alloy as an anode active material and the cathode comprises a cathode layer of an exfoliated graphite or carbon material recompressed to form an active layer that is oriented in such a manner that the active layer has a graphite edge plane in direct contact with the electrolyte and facing or contacting the separator.
Molecular crowding type electrolyte and battery comprising the same
The disclosure relates to a molecular crowding type electrolyte that comprises at least one type of water-miscible/soluble polymer which acts as molecular crowding agent, a salt and a water. The disclosure also relates to a battery comprising the molecular crowding type electrolyte, and a method of using the molecular crowding electrolyte in electrochemical system such as battery that comprises an anode, a cathode and the molecular crowding type electrolyte.
Molecular crowding type electrolyte and battery comprising the same
The disclosure relates to a molecular crowding type electrolyte that comprises at least one type of water-miscible/soluble polymer which acts as molecular crowding agent, a salt and a water. The disclosure also relates to a battery comprising the molecular crowding type electrolyte, and a method of using the molecular crowding electrolyte in electrochemical system such as battery that comprises an anode, a cathode and the molecular crowding type electrolyte.
FLEXIBLE MULTIFUNCTIONAL CROSS-LINKING ADHESIVE, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF
A flexible multifunctional cross-linking adhesive, a preparation method therefor and an application thereof. The adhesive uses guar gum and carboxyl styrene butadiene rubber as raw materials, and is formed by intermolecular cross-linking between hydroxyl groups rich in the guar gum and carboxyl groups contained in the carboxyl styrene butadiene rubber to form a flexible multifunctional cross-linked network. Compared to the prior art, the water-based adhesive is a flexible cross-linking adhesive that has a strong bonding force, high mechanical strength, and no cracking due to tensile deformation, and is insoluble in a battery electrolyte. The adhesive may effectively accommodate the volume effect of a sulfur positive electrode and keep the positive electrode structure intact during a cycling operation. At the same time, the adhesive has significant advantages such as environmental friendliness and being low cost. The compacted sulfur positive electrode has a simple preparation process and has relatively large application prospects.
FLEXIBLE MULTIFUNCTIONAL CROSS-LINKING ADHESIVE, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF
A flexible multifunctional cross-linking adhesive, a preparation method therefor and an application thereof. The adhesive uses guar gum and carboxyl styrene butadiene rubber as raw materials, and is formed by intermolecular cross-linking between hydroxyl groups rich in the guar gum and carboxyl groups contained in the carboxyl styrene butadiene rubber to form a flexible multifunctional cross-linked network. Compared to the prior art, the water-based adhesive is a flexible cross-linking adhesive that has a strong bonding force, high mechanical strength, and no cracking due to tensile deformation, and is insoluble in a battery electrolyte. The adhesive may effectively accommodate the volume effect of a sulfur positive electrode and keep the positive electrode structure intact during a cycling operation. At the same time, the adhesive has significant advantages such as environmental friendliness and being low cost. The compacted sulfur positive electrode has a simple preparation process and has relatively large application prospects.
SECONDARY BATTERY
A secondary battery according to the present invention comprises a positive electrode, a negative electrode and an electrolyte solution; the electrolyte solution contains a lithium salt and a solvent containing water; the negative electrode comprises a negative electrode active material that contains a carbon material; with respect to the carbon material, the peak intensity ratio (D/G value) of the D band to the G band in a Raman spectrum as obtained by Raman spectroscopy is from 0.05 to 0.7; a coating film is formed on the surface of the carbon material; and with respect to the coating film, if P1 is the peak intensity of the 1s electron orbital of an F atom at around the binding energy of 685 eV and P2 is the peak intensity of the 1s electron orbital of an O atom at around the binding energy of 532 eV in an XPS spectrum as determined by X-ray photoelectron spectroscopy, the ratio of the peak intensity P1 to the peak intensity P2, namely the value of P1/P2 is from 1.0 to 3.0.