TY - JOUR
T1 - Mesoporous ceria-silica/poly(arylene ether sulfone) composite membranes for durability of fuel cell electrolyte membrane
AU - Kim, Joonseok
AU - Chung, Kyeonghun
AU - Lee, Hyejin
AU - Bae, Byungchan
AU - Cho, Eun Bum
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Sulfonated poly(arylene ether sulfone) (sPES)/mesoporous ceria-silica electrolyte composite membranes were prepared using a solvent casting method. The composite membranes with two components were prepared well on glass dish using dimethyl sulfoxide (DMSO) as well as N,N-dimethyl acetamide (DMAc) solvents, at various concentrations from 2.5 up to 30 wt% of the mesoporous ceria-silica powder. The degree of sulfonation was 50% for sPES and the mesoporous ceria-silica material had a 2D hexagonal (p6mm) mesostructure with the Ce/Si ratio of 0.5 and the sulfur atoms of 3.1 mmol/g in sulfonic acid groups. The oxidation stability against hydroxyl radicals ([rad]OH) was investigated both with Fenton's test and the hydrogen peroxide exposure. Hydrogen peroxide vapor exposure experiments was developed to screen the oxidation stability in a short time under high temperature and low relative humidity conditions, which is more similar to actual fuel cell system. The composite membranes exhibited higher oxidation stability than a pristine sPES membrane. However, the proton conductivity decreased with the incorporation of mesoprous ceria-silica, which should be resolved through further study using combination of the polymer matrix with different structure and the modification of mesoporous ceria-silica.
AB - Sulfonated poly(arylene ether sulfone) (sPES)/mesoporous ceria-silica electrolyte composite membranes were prepared using a solvent casting method. The composite membranes with two components were prepared well on glass dish using dimethyl sulfoxide (DMSO) as well as N,N-dimethyl acetamide (DMAc) solvents, at various concentrations from 2.5 up to 30 wt% of the mesoporous ceria-silica powder. The degree of sulfonation was 50% for sPES and the mesoporous ceria-silica material had a 2D hexagonal (p6mm) mesostructure with the Ce/Si ratio of 0.5 and the sulfur atoms of 3.1 mmol/g in sulfonic acid groups. The oxidation stability against hydroxyl radicals ([rad]OH) was investigated both with Fenton's test and the hydrogen peroxide exposure. Hydrogen peroxide vapor exposure experiments was developed to screen the oxidation stability in a short time under high temperature and low relative humidity conditions, which is more similar to actual fuel cell system. The composite membranes exhibited higher oxidation stability than a pristine sPES membrane. However, the proton conductivity decreased with the incorporation of mesoprous ceria-silica, which should be resolved through further study using combination of the polymer matrix with different structure and the modification of mesoporous ceria-silica.
KW - Fuel cell electrolyte membrane
KW - Hydroxyl radical
KW - Mesoporous ceria-silica
KW - Oxidation stability
KW - Sulfonated poly(arylene ether sulfone)
UR - http://www.scopus.com/inward/record.url?scp=85027942386&partnerID=8YFLogxK
U2 - 10.1016/j.micromeso.2016.01.049
DO - 10.1016/j.micromeso.2016.01.049
M3 - Article
AN - SCOPUS:85027942386
SN - 1387-1811
VL - 236
SP - 292
EP - 300
JO - Microporous and Mesoporous Materials
JF - Microporous and Mesoporous Materials
ER -