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NAMS 2002 Workshop - ICOM 2008

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Fuel Cells I – 3<br />

Monday July 14, 3:30 PM-4:00 PM, Honolulu/Kahuku<br />

Proton Conducting Graft Copolymer Electrolyte Membranes for Fuel Cells<br />

J. Koh, Yonsei University, Seoul, Korea<br />

J. Park, Yonsei University, Seoul, Korea<br />

D. Roh, Yonsei University, Seoul, Korea<br />

J. Kim (Speaker), Yonsei University, Seoul, Korea, jonghak@yonsei.ac.kr<br />

A series of proton conducting comb copolymer membranes consisting of<br />

poly(vinylidene fluoride- co-chlorotrifluoroethylene) backbone and poly (styrene<br />

sulfonic acid) side chains, i.e. P(VDF- co-CTFE)-g-PSSA were synthesized using<br />

atom transfer radical polymerization (ATRP). 1H NMR, FT-IR spectroscopy, wide<br />

angle X-ray scattering (WAXS) and transmission electron microscopy (TEM)<br />

results present the successful ‘grafting from’ method using ATRP and the welldefined<br />

microphase-separated structure of the polymer electrolyte membranes.<br />

All the properties of ion exchange capacity (IEC), water uptake and proton<br />

conductivity for the membranes continuously increased with increasing PSSA<br />

contents. The results of thermal gravimetric analysis (TGA) also showed that all<br />

the membranes were stable up to 300 o C. After terminated chlorine atoms were<br />

converted to end-functional azide groups (P (VDF-co-CTFE)-g-PSSA-N3), the<br />

polymer electrolyte membranes were crosslinked under UV irradiation. The<br />

crosslinked P(VDF-co-CTFE)-g- PSSA membrane with 73 wt% of PSSA content<br />

exhibited the reduced water uptake from 300 to 83 %, the increased tensile<br />

strength from 21.1 to 26.2 MPa and the slightly reduced proton conductivity from<br />

0.074 to 0.068 S/cm at room temperature compared to the uncrosslinked<br />

membrane.

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