TY - JOUR
T1 - Combinatorial discovery of new methanol-tolerant non-noble metal cathode electrocatalysts for direct methanol fuel cells
AU - Yu, Jong Sung
AU - Kim, Min Sik
AU - Kim, Jung Ho
PY - 2010/12/14
Y1 - 2010/12/14
N2 - Combinatorial synthesis and screening were used to identify methanol-tolerant non-platinum cathode electrocatalysts for use in direct methanol fuel cells (DMFCs). Oxygen reduction consumes protons at the surface of DMFC cathode catalysts. In combinatorial screening, this pH change allows one to differentiate active catalysts using fluorescent acid-base indicators. Combinatorial libraries of carbon-supported catalyst compositions containing Ru, Mo, W, Sn, and Se were screened. Ternary and quaternary compositions containing Ru, Sn, Mo, Se were more active than the "standard" Alonso-Vante catalyst, Ru3Mo0.08Se2, when tested in liquid-feed DMFCs. Physical characterization of the most active catalysts by powder X-ray diffraction, gas adsorption, and X-ray photoelectron spectroscopy revealed that the predominant crystalline phase was hexagonal close-packed (hcp) ruthenium, and showed a surface mostly covered with oxide. The best new catalyst, Ru7.0Sn1.0Se1.0, was significantly more active than Ru3Se2Mo0.08, even though the latter contained smaller particles.
AB - Combinatorial synthesis and screening were used to identify methanol-tolerant non-platinum cathode electrocatalysts for use in direct methanol fuel cells (DMFCs). Oxygen reduction consumes protons at the surface of DMFC cathode catalysts. In combinatorial screening, this pH change allows one to differentiate active catalysts using fluorescent acid-base indicators. Combinatorial libraries of carbon-supported catalyst compositions containing Ru, Mo, W, Sn, and Se were screened. Ternary and quaternary compositions containing Ru, Sn, Mo, Se were more active than the "standard" Alonso-Vante catalyst, Ru3Mo0.08Se2, when tested in liquid-feed DMFCs. Physical characterization of the most active catalysts by powder X-ray diffraction, gas adsorption, and X-ray photoelectron spectroscopy revealed that the predominant crystalline phase was hexagonal close-packed (hcp) ruthenium, and showed a surface mostly covered with oxide. The best new catalyst, Ru7.0Sn1.0Se1.0, was significantly more active than Ru3Se2Mo0.08, even though the latter contained smaller particles.
UR - https://www.scopus.com/pages/publications/78349261899
U2 - 10.1039/c0cp00767f
DO - 10.1039/c0cp00767f
M3 - Article
AN - SCOPUS:78349261899
SN - 1463-9076
VL - 12
SP - 15274
EP - 15281
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 46
ER -