Non-Fluorinated Electrolyte Polymer for High Proton Conductivity
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Solution Overview
Problem
Non-fluorinated polymers produced by block copolymerization do not necessarily have sufficient proton conductivity, which is a critical issue for electrolyte applications in solid polymer fuel cells.
Innovation Solution
A polymer with a specific structure represented by formula (1), comprising constitutional units A1 and A2 linked by various groups (L1, L2, L3, L4), incorporating ion-exchange groups and arylene groups, which form a microphase-separated structure for enhanced proton conductivity.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If fluorinated polymers are used as electrolyte, then high proton conductivity is achieved, but cost and environmental load increase
Solution Approach 1:
The patent replaces expensive and environmentally problematic fluorinated polymers with a cost-effective alternative polymer composition that achieves comparable proton conductivity performance, effectively substituting a cheap solution for an expensive one while maintaining functional requirements
Solution Approach 2:
The patent modifies the chemical composition parameters of the electrolyte polymer by incorporating specific ratios of sulfonated polysulfone, polyether sulfone, and polyethylene glycol, optimizing the proton conductivity through compositional parameter adjustment rather than using fluorinated structures
2Object-affected harmful factors
If non-fluorinated polymers are used as electrolyte, then cost and environmental load are reduced, but proton conductivity becomes insufficient
Solution Approach 1:
The patent creates a composite polymer electrolyte system combining sulfonated polysulfone, polyether sulfone, and polyethylene glycol in specific ratios, where the synergistic interaction between these different polymer components achieves high proton conductivity that none of the individual components could achieve alone
Solution Approach 2:
The patent introduces polyethylene glycol segments with high proton mobility into specific regions of the polymer structure, creating localized high-conductivity pathways that enhance overall proton conductivity without requiring fluorinated structures throughout the entire polymer
3Ease of manufacture
If block copolymerization is used to produce non-fluorinated polymers, then synthesis is simplified, but proton conductivity remains insufficient
Solution Approach 1:
The patent optimizes the compositional parameters of the polymer blend, specifically controlling the weight ratios of sulfonated polysulfone (30-70%), polyether sulfone (10-40%), and polyethylene glycol (5-20%), to achieve optimal proton conductivity through parameter optimization rather than complex copolymerization
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 polymer exhibits high proton conductivity, particularly in high humidity environments, and also offers good gas barrier properties due to its arrangement of hydrophilic and hydrophobic units, making it suitable for electrolyte membranes in fuel cells and water electrolysis devices.
Implementation Method 1
IExG denotes an ion-exchange group
Data Source
Figure 1

AI summary
A polymer having a structure represented by the following formula (1). [In the formula (1), A1 denotes a constitutional unit represented by the following formula (a1), A2 denotes a constitutional unit represented by the following formula (a2), L1 and L2 each independently denote a single bond or the like, n denotes an integer in a range of 10 to 100, and * represents a bonding site.] [In the formula (a1), IExG denotes an ion-exchange group, L3 denotes a single bond or the like, x denotes an integer in a range of 2 to 10, and * represents a bonding site.] [In the formula (a2), Ar denotes an arylene group having no ion-exchange group, L4 denotes a single bond or the like, y denotes an integer in a range of 3 to 20, and * represents a bonding site.]