Polyamic Acid Binder for Silicon Anode Battery Stability

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Solution Overview

Problem

Polyimide binders used in lithium ion secondary batteries face challenges in achieving both high charge-discharge efficiency and good cycle characteristics, particularly when silicon-based materials expand and contract significantly.

Innovation Solution

A binder composition comprising polyamic acid with repeating units based on aromatic tetracarboxylic acid dianhydride and alicyclic diamine, or alicyclic tetracarboxylic acid dianhydride and aromatic diamine, is used to enhance adhesivity and stability of the active material layer during charge-discharge cycles.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If polyimide binder is used to maintain mechanical strength during silicon-based material expansion and contraction, then cycle characteristics are improved, but charge-discharge efficiency deteriorates

Engineering Contradiction:
Improvecycle characteristicsVSAvoidcharge-discharge efficiency
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The invention changes the chemical composition parameters of the binder by incorporating specific functional groups (carboxyl groups with 0.1-10 mmol/g and hydroxyl groups with 0.1-10 mmol/g) into the polyimide structure. This modification allows the binder to achieve both mechanical strength for cycle stability and improved ionic conductivity for charge-discharge efficiency through chemical interactions with lithium ions.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention creates a composite binder system by combining polyimide base resin with functional additives containing carboxyl and hydroxyl groups. This composite structure integrates the mechanical strength of polyimide with the electrochemical activity of the functional groups, enabling simultaneous improvement of cycle characteristics and charge-discharge efficiency.

Inventive Principle:
Principle #40Composite materials

2Quantity of substance

If silicon-based material is used to increase energy density, then capacity is improved, but active material layer integrity deteriorates due to expansion and contraction

Engineering Contradiction:
Improveenergy densityVSAvoidactive material layer integrity
Core Design Contradiction:
Quantity of substanceVSStability of the object's composition

Solution Approach 1:

The invention applies beforehand cushioning by incorporating functional groups (carboxyl and hydroxyl) into the binder structure that can chemically interact with silicon-based material before expansion occurs. These groups form protective complexes with silicon particles, cushioning the mechanical stress during expansion and contraction cycles and preventing active material layer damage.

Inventive Principle:
Principle #11Beforehand cushioning (Prior cushioning)

Solution Approach 2:

The functional groups (carboxyl and hydroxyl) in the binder act as intermediaries between the silicon-based active material and the polyimide matrix. These intermediary groups facilitate stress distribution and maintain adhesion during volume changes, preventing direct mechanical damage to the active material layer while allowing high silicon content for energy density.

Inventive Principle:
Principle #24Intermediary (Mediator)

Data Source

PatentUS10707491B2Binder for secondary battery
Publication Date: 2020.07.07 NEC CORP
  • US10707491B2 patent drawing
  • US10707491B2 patent drawing
  • US10707491B2 patent drawing

AI summary

An object of the present invention is to provide a binder composition for a secondary battery for achieving improved charge-discharge efficiency and good cycle characteristics at the same time. The binder composition for a secondary battery according to the present invention is characterized in comprising a polyamic acid comprising a repeating unit consisting of a skeleton based on an aromatic tetracarboxylic acid dianhydride and a skeleton based on an alicyclic diamine represented by structural formula: NH2—(CH2)n—R2—(CH2)m—NH2, wherein R2 represents alicyclic group, and n and m each independently represent the number of repeating units selected from 1 to 5; and/or a polyamic acid comprising a repeating unit consisting of a skeleton based on an alicyclic tetracarboxylic acid dianhydride and a skeleton based on an aromatic diamine.