Morphological and Structure-Property Analyses of Poly(arylene ether sulfone)-Based Random and Multiblock Copolymers for Fuel Cells

The commercialization of proton exchange membrane (PEM) fuel cells depends largely upon the development of PEMs whose properties are enhanced over current perfluorinated sulfonic acid PEMs. Understanding how a PEM's molecular weight and morphology affect its relevant performance properties is essential to this effort. Changes in molecular weight were found to have little effect on the phase separated morphologies, water uptake, and proton conductivities of random copolymers. Changes in block length, however, have a pronounced effect on multiblock copolymers, affecting surface and bulk morphologies, water uptake, proton conductivity, and hydrolytic stability, suggesting that multiblock copolymer PEM properties may be optimized by changes in morphology. A major goal of current proton exchange membrane fuel cell research involves developing high temperature membranes that can operate at ~120 °C and low humidites. Multiblock copolymers synthesized from 100% disulfonated poly(arylene ether sulfone) (BPSH100) and naphthalene polyimide (PI) oligomers may be an alternative. At block lengths of ~15 kg/mol they displayed no morphological changes up to 120 °C or even higher. Water desorption was observed to decrease with increasing block length. The copolymers exhibited little to no water loss during a 200 °C isotherm in contrast to random BPSH copolymers and Nafion. A BPSH100-PI multiblock copolymer with large block length appears to have morphological stability and retain water at temperatures exceeding 120 °C, suggesting its candidacy as a high temperature PEM. A growing number of alternative PEM research efforts involve multiblock copolymer chemistries, but little emphasis is placed on the methods used to couple the oligomers. Fluorinated linkage groups can help increase block efficiency during coupling, but their effect on a PEM is not well-known. The choice of linkage type, hexafluorobenzene (HFB) vs. decafluorobiphenyl (DFBP), appears to have small but observable influences on multiblock copolymers with disulfonated and unsulfonated poly(arylene ether sulfone) oligomers. DFBP linkages promote greater phase separation than HFB linkages, resulting in increased stiffness, decreased ductility, and increased proton conductivity at low humidities. DFBP linkages also promote more surface enrichment of fluorine, causing changes in surface morphology and slightly increased water desorption, but determining the impact on actual fuel cell performance requires further research.

Name thesis:degree_name

Ph. D.

Level thesis:degree_level

doctoral

Discipline thesis:degree_discipline

Macromolecular Science and Engineering

Department dc:contributor.department

Macromolecular Science and Engineering

Grantor dc:publisher

Virginia Tech

Year dc:date.issued

2007

Author dc:creator

• Badami, Anand Shreyans

Chair dc:contributor.committeechair

• McGrath, James E.

Committee members dc:contributor.committeemember

• Joseph, Eugene G.
• Wilkes, Garth L.
• Riffle, Judy S.
• Davis, Richey M.

• proton exchange membrane
• sulfonated polymers
• molecular weight
• block length
• high temperature
• linkage group

Statement dc:rights

• In Copyright

Licence dc:rights.uri

• http://rightsstatements.org/vocab/InC/1.0/

Dc Identifier Other

etd-11052007-130520

OAI identifier oai:identifier

oai:vtechworks.lib.vt.edu:10919/29469