Lyotropic Mesophases in Donor-Acceptor Polymers for Mobility

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for fabricating organic devices using lyotropic semiconducting polymers lack control over crystallinity and molecular packing, which are crucial for optimizing the performance of polymer-based electronic devices, particularly in achieving high carrier mobility and efficient charge transport.

Innovation Solution

Designing rigid donor-acceptor copolymers with soft side chains that facilitate the formation of lyotropic mesophases, allowing for improved polymer alignment and increased amphiphilicity, which enhances crystallinity and intermolecular interactions, leading to better charge transport properties.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If conventional fabrication methods are used for organic devices, then the process is simple and easy to manufacture, but control over crystallinity and molecular packing is lacking, resulting in suboptimal device performance

Engineering Contradiction:
Improvecontrol over crystallinity and molecular packingVSAvoidcomplexity of polymer design and processing
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The patent applies parameter changes by systematically varying polymer composition parameters (donor-acceptor ratios, side chain lengths, molecular weights) to achieve desired crystallinity and molecular packing. This allows precise control over device performance parameters while maintaining a systematic approach to optimization

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs composite materials by creating donor-acceptor copolymer systems where distinct molecular components (electron-donating and electron-accepting units) are combined to achieve synergistic effects. This composite approach enables independent optimization of electronic properties, crystallinity, and processability

Inventive Principle:
Principle #40Composite materials

2Reliability

If rigid donor-acceptor copolymers with soft side chains are designed to form lyotropic mesophases, then carrier mobility is significantly improved, but the device fabrication process becomes more complex

Engineering Contradiction:
Improvecarrier mobilityVSAvoidcomplexity of lyotropic mesophase formation process
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent applies local quality by designing polymers with distinct regional characteristics: rigid donor-acceptor backbone segments for high carrier mobility and soft side chains for solubility and mesophase formation. This spatial differentiation of material properties enables simultaneous optimization of electronic performance and processability

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent exploits phase transitions by utilizing lyotropic mesophase formation during solution processing. The transition from isotropic solution to ordered mesophase upon solvent evaporation or temperature change enables self-organization of polymer chains into configurations that enhance carrier mobility without requiring complex external alignment procedures

Inventive Principle:
Principle #36Phase transitions

3Reliability

If amphiphilicity is increased to enhance crystallinity and intermolecular interactions, then charge transport properties are improved, but the polymer design and solvent selection become more complex

Engineering Contradiction:
Improvecharge transport propertiesVSAvoidcomplexity of amphiphilic polymer design
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent applies segmentation by dividing the polymer structure into distinct functional segments: hydrophobic rigid backbone segments for charge transport and hydrophilic side chain segments for solubility. This segmentation creates inherent amphiphilicity that drives self-organization and enhances charge transport while providing clear design guidelines for polymer synthesis

Inventive Principle:
Principle #1Segmentation

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 approach results in significant improvements in carrier mobility, with transistors exhibiting up to 0.61 cm2V−1s−1 mobility and a three-fold increase in mobility compared to spin-coated devices, demonstrating the effectiveness of lyotropic mesophases in enhancing device performance.

Implementation Method 1

Formation and structure of lyotropic liquid crystalline mesophases in donor-acceptor semiconducting polymers

Methodology Applied
Scientific EffectLiquid crystalline mesophases: Liquid Crystals

Implementation Method 2

allowing for improved polymer alignment and increased amphiphilicity, which enhances crystallinity and intermolecular interactions

Methodology Applied
Scientific EffectSelf-assembly: Self-Assembly

Data Source

PatentUS10249821B2Formation and structure of lyotropic liquid crystalline mesophases in donor-acceptor semiconducting polymers
Publication Date: 2019.04.02 RGT UNIV OF CALIFORNIA
  • US10249821B2 patent drawing
  • US10249821B2 patent drawing
  • US10249821B2 patent drawing

AI summary

Design of side chains yielding highly amphiphilic conjugated polymers is proven to be an effective and general method to access lyotropic liquid crystalline mesophases, allowing greater control over crystalline morphology and improving transistor performance. The general strategy enables variations in structure and interactions that impact alignment and use of liquid crystalline alignment methods. Specifically, solvent-polymer interactions are harnessed to facilitate the formation of high quality polymer crystals in solution. Crystallinity developed in solution is then transferred to the solid state, and thin films of donor-acceptor copolymers cast from lyotropic solutions exhibit improved crystalline order in both the alkyl and π-stacking directions. Due to this improved crystallinity, transistors with active layers cast from lyotropic solutions exhibit a significant improvement in carrier mobility compared to those cast from isotropic solution. One or more embodiments of the present invention achieve a maximum carrier mobility of 0.61 cm2V−1s−1.