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Development of highly phosphonated polymers for fuel cell membranes.

Jannasch, Patric LU orcid (2014) 226th Meeting of the Electrochemical Society
Abstract
Phosphonated polymers may show high intrinsic proton conductivities at low water contents provided that the local concentration of phosphonic acid groups is very high [1,2]. Moreover, the lower acidity of aryl- and alkylphosphonic acids in relation to sulfonic acids requires higher acid contents to reach high conductivities also at higher water contents. In this context, poly(vinylphosphonic acid) (PVPA) has emerged as an interesting component for fuel cell membranes because of its extremely high concentration of phosphonic acid, corresponding to 9.25 mmol –PO3H2 per g dry material. However, the high ionic content leads to complete water solubility as well as poor mechanical properties in the solid state. Consequently, it is necessary to... (More)
Phosphonated polymers may show high intrinsic proton conductivities at low water contents provided that the local concentration of phosphonic acid groups is very high [1,2]. Moreover, the lower acidity of aryl- and alkylphosphonic acids in relation to sulfonic acids requires higher acid contents to reach high conductivities also at higher water contents. In this context, poly(vinylphosphonic acid) (PVPA) has emerged as an interesting component for fuel cell membranes because of its extremely high concentration of phosphonic acid, corresponding to 9.25 mmol –PO3H2 per g dry material. However, the high ionic content leads to complete water solubility as well as poor mechanical properties in the solid state. Consequently, it is necessary to develop synthetic strategies to efficiently immobilize the PVPA in the membranes before practical use.



We have previously immobilized PVPA by preparing various block and graft copolymers with PVPA segments [3]. These copolymers where found to self-assemble and form robust membranes with nanostructured morphologies and high proton conductivities. Very recently we have pursued a number of novel synthetic strategies towards different highly phosphonated membranes. These approaches include phosphonated norbornene copolymers prepared via ring opening metathesis polymerization (ROMP) [4], multiblock copolymers selectively grafted with PVPA via anionic polymerization [5], as well as block and graft copolymers containing the more acidic poly(tetrafluorostyrenephosphonic acid) via atom transfer radical polymerization (ATRP) [6]. Challenges and selected results on the synthesis and properties of these copolymers and membranes will be presented and discussed along with future prospects. (Less)
Please use this url to cite or link to this publication:
author
organization
publishing date
type
Chapter in Book/Report/Conference proceeding
publication status
published
subject
host publication
ECS Meeting Abstracts
publisher
Electrochemical Society
conference name
226th Meeting of the Electrochemical Society
conference location
Cancun, Mexico
conference dates
2014-10-05 - 2014-10-09
language
English
LU publication?
yes
additional info
Invited lecture. Abstract 2014 MA2014-02 1062
id
9dcf7ba1-88c5-415f-9623-7d75229192ab (old id 4431998)
alternative location
http://ma.ecsdl.org/content/MA2014-02/21/1062.abstract?sid=db84cb6b-b319-442e-8ee4-c7d89e0fcc22
date added to LUP
2016-04-04 10:35:08
date last changed
2020-06-03 12:23:34
@inproceedings{9dcf7ba1-88c5-415f-9623-7d75229192ab,
  abstract     = {{Phosphonated polymers may show high intrinsic proton conductivities at low water contents provided that the local concentration of phosphonic acid groups is very high [1,2]. Moreover, the lower acidity of aryl- and alkylphosphonic acids in relation to sulfonic acids requires higher acid contents to reach high conductivities also at higher water contents. In this context, poly(vinylphosphonic acid) (PVPA) has emerged as an interesting component for fuel cell membranes because of its extremely high concentration of phosphonic acid, corresponding to 9.25 mmol –PO3H2 per g dry material. However, the high ionic content leads to complete water solubility as well as poor mechanical properties in the solid state. Consequently, it is necessary to develop synthetic strategies to efficiently immobilize the PVPA in the membranes before practical use.<br/><br>
<br/><br>
We have previously immobilized PVPA by preparing various block and graft copolymers with PVPA segments [3]. These copolymers where found to self-assemble and form robust membranes with nanostructured morphologies and high proton conductivities. Very recently we have pursued a number of novel synthetic strategies towards different highly phosphonated membranes. These approaches include phosphonated norbornene copolymers prepared via ring opening metathesis polymerization (ROMP) [4], multiblock copolymers selectively grafted with PVPA via anionic polymerization [5], as well as block and graft copolymers containing the more acidic poly(tetrafluorostyrenephosphonic acid) via atom transfer radical polymerization (ATRP) [6]. Challenges and selected results on the synthesis and properties of these copolymers and membranes will be presented and discussed along with future prospects.}},
  author       = {{Jannasch, Patric}},
  booktitle    = {{ECS Meeting Abstracts}},
  language     = {{eng}},
  publisher    = {{Electrochemical Society}},
  title        = {{Development of highly phosphonated polymers for fuel cell membranes.}},
  url          = {{http://ma.ecsdl.org/content/MA2014-02/21/1062.abstract?sid=db84cb6b-b319-442e-8ee4-c7d89e0fcc22}},
  year         = {{2014}},
}