Positive electrode material of metal halide battery and preparation method thereof
A metal halide, alkali metal halide technology, applied in battery electrodes, secondary batteries, circuits, etc., can solve the problem of abnormal growth of electroactive metal particles, alkali metal halide, the actual utilization rate of electroactive metal element is not improved, Solve the problems of low utilization rate of electroactive metal element, and achieve the effect of solving low cycle life and stability, improving effective utilization rate and good battery stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0025] In this embodiment, the preparation of positive electrode material is as follows:
[0026] (1) Mix ultrafine Ni and NaCl according to the molar ratio of 0.6, grind in alcohol, then add an appropriate amount of binder PVA or PVP, and pore-forming agent ammonium carbonate or ammonium bicarbonate, spray granulation, under 2mpa-5mpa After the preforming of the tablet, it is placed in a hydrogen atmosphere and calcined at a rate of 100°C / h to 700°C, and kept for 1h to obtain NaCl-Ni powder.
[0027] (2) Grinding the graphene to a particle size of 10 micrometers to 100 micrometers, and then keeping the temperature at 150° C. for 6 hours in a closed container with an inert atmosphere to obtain conductive ceramic powder.
[0028] (3) Physically mix NaCl-Ni powder, conductive ceramic powder and other additives by ball milling, wherein the mass ratio of NaCl-Ni powder to conductive ceramic powder is 10:1, so that the conductive ceramic powder is dispersed in the NaCl-Ni powder, ...
Embodiment 2
[0031] (1) Mix ultrafine NiO and NaCl according to the molar ratio of 1.05, grind them in alcohol, then add an appropriate amount of binder PVA or PVP, pore-forming agent ammonium carbonate or ammonium bicarbonate, spray granulation, and press down at 2mpa-5mpa After the sheet is preformed, it is placed in a hydrogen atmosphere and calcined at a rate of 100°C / h to 700°C, and kept for 1h to obtain NaCl-Ni powder.
[0032] (2) The porous two-dimensional sheet-like conductive ceramic Ti 2 C is ground to a particle size of 10 microns to 100 microns, and then kept at a constant temperature of 150° C. for 6 hours in a closed container with an inert atmosphere to obtain conductive ceramic powder.
[0033] (3) Physically mix NaCl-Ni powder, conductive ceramic powder and other additives by ball milling, wherein the mass ratio of NaCl-Ni powder to conductive ceramic powder is 5:1, so that the conductive ceramic powder is dispersed in the NaCl-Ni powder, Obtain positive electrode powder...
Embodiment 3
[0036](1) Mix superfine nickel oxalate and NaCl according to the molar ratio of 1.2, grind in alcohol, then add an appropriate amount of binder PVA or PVP, and pore-forming agent ammonium carbonate or ammonium bicarbonate, spray granulation, at 2mpa-5mpa After the lower tablet is preformed, it is placed in a hydrogen atmosphere and calcined at a rate of 100°C / h to 700°C, and kept for 1h to obtain NaCl-Ni powder.
[0037] (2) Combining graphene with porous two-dimensional sheet-like conductive ceramic Ti 2 C is ground to a particle size of 10 microns to 100 microns, and then kept at a constant temperature of 150° C. for 6 hours in a closed container with an inert atmosphere to obtain conductive ceramic powder.
[0038] (3) Physically mix NaCl-Ni powder, conductive ceramic powder and other additives by ball milling, wherein the mass ratio of NaCl-Ni powder to conductive ceramic powder is 15:1, so that the conductive ceramic powder is dispersed in the NaCl-Ni powder, Obtain posi...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com