TY - JOUR
T1 - Cell performance of polymer electrolyte fuel cell with urchin-like carbon supports
AU - Lu, Juei Dong
AU - Yang, Ming Chang
N1 - Funding Information:
The authors wish to acknowledge the financial support from the National Science Council in Taiwan under grant NSC-95-2120-M-006-009 . Special thank should go to Professor Hung-Shan Weng in the Department of Chemical Engineering for fundamental discussion on catalyst and Professor Hong-Ping Lin in the Department of Chemistry for providing the mesoporous carbon. An appreciation also should go to Ms. Mei-Her Chen for her technical helps.
PY - 2011/10/15
Y1 - 2011/10/15
N2 - Urchin-like structured carbon comprising carbon nanotubes grown on Fe catalyst-seeded mesoporous carbon have shown promising results as catalyst supports for use in direct methanol fuel cells (DMFCs) and proton exchange membrane fuel cells (PEMFCs). The Fe catalyst is prepared on the mesoporous carbon by immersion process followed by a high temperature reduction. The growth of carbon nanotubes then progress, for a predetermined time, through the thermal decomposition of acetylene at 800 °C. The resulting structure, comprising intimately connected mesoporous carbon and carbon nanotubes, is shown to offer performance advantages as a catalytic support for DMFCs and PEMFCs. When the hot-pressing pressure is fixed 20 kg cm-2 to fabricate a membrane electrode assembly (MEA) with urchin-like carbon supports, the CNT growth time is found to be 60 min for a highest maximum power density in both DMFCs and PEMFCs. The maximum power densities are 43 and 79% higher than those with purely mesoporous carbon in DMFCs and PEMFCs, respectively. In a direct comparison with commercial E-TEK catalyst, the urchin-like catalyst shows higher maximum power densities, in DMFC and PEMFC, by approximately 17 and 31%, respectively.
AB - Urchin-like structured carbon comprising carbon nanotubes grown on Fe catalyst-seeded mesoporous carbon have shown promising results as catalyst supports for use in direct methanol fuel cells (DMFCs) and proton exchange membrane fuel cells (PEMFCs). The Fe catalyst is prepared on the mesoporous carbon by immersion process followed by a high temperature reduction. The growth of carbon nanotubes then progress, for a predetermined time, through the thermal decomposition of acetylene at 800 °C. The resulting structure, comprising intimately connected mesoporous carbon and carbon nanotubes, is shown to offer performance advantages as a catalytic support for DMFCs and PEMFCs. When the hot-pressing pressure is fixed 20 kg cm-2 to fabricate a membrane electrode assembly (MEA) with urchin-like carbon supports, the CNT growth time is found to be 60 min for a highest maximum power density in both DMFCs and PEMFCs. The maximum power densities are 43 and 79% higher than those with purely mesoporous carbon in DMFCs and PEMFCs, respectively. In a direct comparison with commercial E-TEK catalyst, the urchin-like catalyst shows higher maximum power densities, in DMFC and PEMFC, by approximately 17 and 31%, respectively.
UR - https://www.scopus.com/pages/publications/79961031632
UR - https://www.scopus.com/pages/publications/79961031632#tab=citedBy
U2 - 10.1016/j.jpowsour.2011.06.041
DO - 10.1016/j.jpowsour.2011.06.041
M3 - Article
AN - SCOPUS:79961031632
SN - 0378-7753
VL - 196
SP - 8519
EP - 8524
JO - Journal of Power Sources
JF - Journal of Power Sources
IS - 20
ER -