TY - JOUR
T1 - Improvement in Direct Methanol Fuel Cell Performance by Treating the Anode at High Anodic Potential
AU - Joghee, Prabhuram
AU - Pylypenko, Svitlana
AU - Wood, Kevin
AU - Corpuz, April
AU - Bender, Guido
AU - Dinh, Huyen N.
AU - O'Hayre, Ryan
PY - 2014
Y1 - 2014
N2 - This work investigates the effect of a high anodic potential treatment protocol on the performance of a direct methanol fuel cell (DMFC). DMFC membrane electrode assemblies (MEAs) with PtRu/C (Hi-spec 5000) anode catalyst are subjected to anodic treatment (AT) at 0.8 V vs. DHE using potentiostatic method. Despite causing a slight decrease in the electrochemical surface area (ECSA) of the anode, associated with ruthenium dissolution, AT results in significant improvement in DMFC performance in the ohmic and mass transfer regions and increases the maximum power density by ∼15%. Furthermore, AT improves the long-term DMFC stability by reducing the degradation of the anode catalyst. From XPS investigation, it is hypothesized that the improved performance of AT-treated MEAs is related to an improved interface between the catalyst and Nafion ionomer. Among potential explanations, this improvement may be caused by incorporation of the ionomer within the secondary pores of PtRu/C agglomerates, which generates a percolating network of ionomer between PtRu/C agglomerates in the catalyst layer. Furthermore, the decreased concentration of hydrophobic CF2 groups may help to enhance the hydrophilicity of the catalyst layer, thereby increasing the accessibility of methanol and resulting in better performance in the high current density region.
AB - This work investigates the effect of a high anodic potential treatment protocol on the performance of a direct methanol fuel cell (DMFC). DMFC membrane electrode assemblies (MEAs) with PtRu/C (Hi-spec 5000) anode catalyst are subjected to anodic treatment (AT) at 0.8 V vs. DHE using potentiostatic method. Despite causing a slight decrease in the electrochemical surface area (ECSA) of the anode, associated with ruthenium dissolution, AT results in significant improvement in DMFC performance in the ohmic and mass transfer regions and increases the maximum power density by ∼15%. Furthermore, AT improves the long-term DMFC stability by reducing the degradation of the anode catalyst. From XPS investigation, it is hypothesized that the improved performance of AT-treated MEAs is related to an improved interface between the catalyst and Nafion ionomer. Among potential explanations, this improvement may be caused by incorporation of the ionomer within the secondary pores of PtRu/C agglomerates, which generates a percolating network of ionomer between PtRu/C agglomerates in the catalyst layer. Furthermore, the decreased concentration of hydrophobic CF2 groups may help to enhance the hydrophilicity of the catalyst layer, thereby increasing the accessibility of methanol and resulting in better performance in the high current density region.
KW - Anodic treatment
KW - CO stripping voltammetry
KW - Direct methanol fuel cell
KW - Long-term performance
KW - MOR polarization
KW - Reorganization of Nafion ionomer
UR - http://www.scopus.com/inward/record.url?scp=84880319334&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2013.06.105
DO - 10.1016/j.jpowsour.2013.06.105
M3 - Article
AN - SCOPUS:84880319334
SN - 0378-7753
VL - 245
SP - 37
EP - 47
JO - Journal of Power Sources
JF - Journal of Power Sources
ER -