Abstract: Methods and systems are provided for forming a cathode pre-lithiation layer for a lithium-ion battery. In one example, a slurry for forming the cathode pre-lithiation layer may include a solvent including a uniform dispersion of a nanoscale cathode pre-lithiation reagent. The slurry may be cast onto a porous cathode active material layer and dried and calendered to form the cathode pre-lithiation layer. In some examples, the slurry may have a viscosity of up to 5000 cP at a shear rate of 100 s?1. In this way, delamination and interfacial impedance between the cathode pre-lithiation layer and the porous cathode active material layer may be reduced relative to a higher viscosity cathode pre-lithiation layer having a larger scale cathode pre-lithiation reagent cast onto a non-porous or low-porosity cathode active material layer.

Abstract: A silicon anode comprising a hybrid binder at a blending ratio of 10-90 wt. % for use in a Li-ion battery is provided. The combination of a hybrid binder in the Si anode for use in a rechargeable Li-ion cell shows the unexpected result of extending the cycle life and a balancing effect between adhesion strength and first cycle efficiency.

Abstract: A pre-lithiated silicon anode comprising a PVDF binder at 5-12 wt. % for use in a Li-ion cell is provided. In particular instances, a conductive additive may be added at less than 5 wt. %. The Si anode with PVDF binder is pre-lithiated prior to cell assembly and following Si anode fabrication. The combination of pre-lithiation and PVDF in the Si anode for use in a rechargeable Li-ion cell shows the unexpected result of extending the cycle life.

Abstract: A silicon anode comprising a hybrid binder at a blending ratio of 10-90 wt. % for use in a Li-ion battery is provided. The combination of a hybrid binder in the Si anode for use in a rechargeable Li-ion cell shows the unexpected result of extending the cycle life and a balancing effect between adhesion strength and first cycle efficiency.

Abstract: A pre-lithiated silicon anode comprising a PVDF binder at 5-12 wt. % for use in a Li-ion cell is provided. In particular instances, a conductive additive may be added at less than 5 wt. %. The Si anode with PVDF binder is pre-lithiated prior to cell assembly and following Si anode fabrication. The combination of pre-lithiation and PVDF in the Si anode for use in a rechargeable Li-ion cell shows the unexpected result of extending the cycle life.

Abstract: A method of making lithium manganese oxide of spinel structure is disclosed. The method involves the step of prelithiating a manganese oxide by reacting it with lithium hydroxide or lithium salt and then reacting the prelithiated manganese oxide in a second step at elevated temperature to form a lithium manganese oxide spinel. In a specific embodiment manganese dioxide powder is reacted with lithium hydroxide to prelithiate the manganese dioxide and the prelithiated manganese dioxide is separated from the reaction mixture and heated and reacted with lithium carbonate at elevated temperature to convert it to lithium manganese oxide spinel. The spinel product may be used advantageously in secondary (rechargeable) batteries.

Abstract: The invention relates to the manufacture of manganese dioxide by a chemical process. The resulting manganese dioxide product takes the form of particles characterized by filament-like protrusions jutting out from its surface. The manganese dioxide particles having such surface features can be manufactured by reacting manganese sulfate with sodium peroxodisulfate in an aqueous solution. The process can be controlled to yield manganese dioxide of varying density and surface area. The manganese dioxide formed in the process can be deposited directly onto the surface of electrolytic manganese dioxide (EMD) or onto the surface of other particles. The manganese dioxide product is particularly suitable for use as a cathode active material in electrochemical cells.