Cathode Particle Co-precipitation for Density Control

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Solution Overview

Problem

Current cathode materials for lithium-ion batteries, such as NMC and NCA, face challenges in achieving high energy density, safety, long cycle life, low toxicity, and reduced production costs, with complex kinetics in reactive crystallization making it difficult to control particle number density during preparation.

Innovation Solution

A method involving co-precipitation in a semi-batch process with a defined precipitation zone, using parallel mixed vessels with controlled agitation and gas blanketing, and precise management of cation and anion streams to create compositional variation and adjust tap density of cathode particles.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If additional transition metals (Mn, Co, Al) substitute Ni in layered LiNiO2 to produce NMC or NCA materials, then safety and cycle life are improved, but available energy storage decreases

Engineering Contradiction:
Improvesafety and cycle lifeVSAvoidavailable energy storage
Core Design Contradiction:
ReliabilityVSQuantity of substance

Solution Approach 1:

The patent applies compositional grading within the particle structure, creating Ni-rich cores for high energy density and Mn/Al-rich surfaces for enhanced safety and stability. This local variation in composition allows different regions of the same particle to optimize for different properties, resolving the contradiction between energy storage and safety.

Inventive Principle:
Principle #3Local quality

2Manufacturing precision

If particle number density is not controlled during reactive crystallization, then particle growth behavior becomes unpredictable, but controlling particle number density is challenging due to complex precipitation kinetics involving metal chelators

Engineering Contradiction:
Improveparticle number density controlVSAvoidprocess complexity
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The patent performs preliminary action by controlling particle number density during the precipitation step before reactive crystallization occurs. By establishing the desired particle number density early in the process through controlled coprecipitation conditions, the subsequent reactive crystallization proceeds predictably without requiring complex real-time control mechanisms.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent implements feedback control by monitoring and adjusting process parameters during precipitation to maintain target particle number density. The method uses measured particle properties to adjust feeding rates and other parameters, ensuring consistent particle number density despite the complex kinetics involving multiple metal ions and chelators.

Inventive Principle:
Principle #23Feedback

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

This method effectively controls the number density distribution and tap density of cathode particles, enhancing their performance and stability, with significant improvements in particle size and density distribution, leading to improved battery performance and cost-effectiveness.

Implementation Method 1

the cathode particles are prepared under a co-precipitation reaction

Methodology Applied
Scientific EffectCoprecipitation: Coprecipitation

Implementation Method 2

The precipitation zone is evacuated and filled with He, N2 or Ar gas, for example blanketed or bubbled thereby

Methodology Applied
Scientific EffectGas blanketing:

Data Source

PatentUS11322738B2Method for preparing cathode particles and cathode active materials having same
Publication Date: 2022.05.03 MICROVAST ADVANCED MATERIALS INC
  • US11322738B2 patent drawing
  • US11322738B2 patent drawing
  • US11322738B2 patent drawing

AI summary

The invention relates to a method for preparing cathode particles under a co-precipitation reaction by feeding NaOH and metal sulfate solution into different vessels. The invention further provides a cathode active material having the cathode particles. By the method of the invention, the number density distribution of prepared particles is much smaller than feeding NaOH and metal sulfate together into same vessel.