LiFSI-CPME Electrolyte for Low-Temperature Fast-Charging Cells

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Solution Overview

Problem

Lithium-ion batteries face challenges in maintaining performance at low temperatures and fast charging due to issues with electrolyte conductivity, SEI layer formation, and solvent freezing.

Innovation Solution

An electrolyte composition comprising lithium bifluorosulphonyl imide (LiFSI) dissolved in cyclopentyl methyl ether (CPME) forms an anion-derived solvation structure that reduces covalent bond strength, leading to a robust LiF-rich SEI layer and improved low-temperature performance.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional carbonate electrolytes (EC, PC, DEC) are used in lithium-ion batteries, then good cyclability at room temperature is achieved, but low temperature performance deteriorates due to solvent freezing and high viscosity

Engineering Contradiction:
ImprovecyclabilityVSAvoidlow temperature performance
Core Design Contradiction:
ReliabilityVSTemperature

Solution Approach 1:

The patent changes the chemical composition parameters of the electrolyte by replacing conventional carbonate solvents (EC, PC, DEC) with ether-based solvents (CPME, DME, TEGDME) and adjusting the lithium salt concentration. This parameter change fundamentally alters the physical properties of the electrolyte, including freezing point and viscosity, enabling operation at low temperatures while maintaining cyclability through the formation of a stable SEI layer

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite electrolyte system combining ether-based solvents with specific lithium salts (LiFSO3, LiPF6) and cyclic carbonates (GBL, GVL). This composite approach leverages the complementary properties of each component: ether solvents provide low freezing point and good low-temperature ionic conductivity, while cyclic carbonates contribute to stable SEI formation, achieving both low-temperature performance and cyclability

Inventive Principle:
Principle #40Composite materials

2Productivity

If fast charging is implemented to reach 80% capacity in fifteen minutes, then charging speed is improved, but charge transfer resistance at the electrode/electrolyte interface increases

Engineering Contradiction:
Improvecharging speedVSAvoidcharge transfer resistance
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent changes the electrolyte composition parameters to include ether-based solvents with high ionic conductivity and appropriate viscosity. These parameter changes reduce the charge transfer resistance at the electrode/electrolyte interface by improving Li+ ion mobility and solvation dynamics, enabling faster charging rates while maintaining electrochemical stability and charge transfer efficiency

Inventive Principle:
Principle #35Parameter changes

3Reliability

If electrolyte conductivity is improved for fast charging, then charge transfer kinetics are enhanced, but SEI layer stability deteriorates

Engineering Contradiction:
Improvecharge transfer kineticsVSAvoidSEI layer stability
Core Design Contradiction:
ReliabilityVSStability of the object's composition

Solution Approach 1:

The patent employs a composite electrolyte formulation combining ether-based solvents (for high ionic conductivity and fast charge transfer kinetics) with cyclic carbonate additives (GBL, GVL) and lithium salts. This composite structure enables the formation of a stable SEI layer that maintains integrity during fast charging, as the cyclic carbonate components contribute to SEI formation while the ether components provide high ion mobility, resolving the contradiction between kinetics and stability

Inventive Principle:
Principle #40Composite materials

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

The CPME-based electrolyte composition enhances low-temperature performance, maintaining high capacity and stability from 0°C to -40°C, with a robust SEI layer facilitating faster Li+ ion conduction and reduced charge transfer resistance.

Implementation Method 1

lithium bifluorosulphonyl imide (LiFSI) dissolved in cyclopentyl methyl ether (CPME) to form Li cations and FSI anions. The electrolyte composition has an anion-derived solvation structure

Methodology Applied
Scientific EffectSolvation: Solvation

Implementation Method 2

The electrolyte composition has an anion-derived solvation structure that reduces the covalent bond strength between the Li cations and FSI anions

Methodology Applied
Scientific EffectBond weakening through solvation: Solvation

Implementation Method 3

leading to a robust LiF-rich SEI layer and improved low-temperature performance

Methodology Applied
Scientific EffectSEI layer formation: Deposition (physical)

Implementation Method 4

the solvent molecules are reduced on the anode surface and form the insulating SEI layer

Methodology Applied
Scientific EffectElectrochemical deposition: Electrodeposition

Implementation Method 5

a robust SEI layer facilitating faster Li+ ion conduction and reduced charge transfer resistance

Methodology Applied
Scientific EffectIon conduction: Conduction (electrical)

Implementation Method 6

maintaining high capacity and stability from 0°C to -40°C

Methodology Applied
Scientific EffectFreezing point depression: Freezing

Data Source

PatentUS20250174736A1Electrochemical cells and electrolyte compositions therefor
Publication Date: 2025.05.29 PURDUE RES FOUND
  • US20250174736A1 patent drawing
  • US20250174736A1 patent drawing
  • US20250174736A1 patent drawing

AI summary

Electrochemical cells and electrolyte compositions therefor. Such an electrolyte composition includes lithium bifluorosulphonyl imide (LiFSI) dissolved in cyclopentyl methyl ether (CPME) solvent. The electrolyte composition has an anion-derived solvation structure that can form a lithium fluoride (LiF) layer on an anode of an electrochemical cell. The anion-derived solvation structure may reduce the covalent bond strength between the Li cations and FSI anions.