TY - JOUR
T1 - Preparation of a CO-tolerant PtRuxSny/C electrocatalyst with an optimal Ru/Sn ratio by selective Sn-deposition on the surfaces of Pt and Ru
AU - Yoo, Jong Suk
AU - Kim, Hyun Tae
AU - Joh, Han Ik
AU - Kim, Heeyeon
AU - Moon, Sang Heup
PY - 2011/2
Y1 - 2011/2
N2 - A CO-tolerant PtRuxSny/C electrocatalyst, with an optimal x/y ratio of 0.8/0.2, was prepared by selectively depositing Sn on the metallic surface of PtRu0.8/C for use as the anode in a polymer electrolyte membrane fuel cell. The CO tolerance of the catalyst was greater when Sn was added by chemical vapor deposition (CVD) than by a conventional precipitation method because most of the Sn added by CVD was located in the vicinity of Pt and Ru surfaces, on which CO molecules were strongly adsorbed. Accordingly, the bi-functional mechanism of CO oxidation, which involved the migration of oxygenated species from the Sn to the adsorbed CO, was expected to be promoted to greater extents in the catalysts prepared by Sn-CVD than those prepared by Sn-precipitation. On the other hand, the ligand-effect mechanism of CO oxidation, which was facilitated by the Pt-Ru alloy formation, was not much affected by the added Sn because the Pt-Ru alloy remained unchanged, particularly when y ≤ 0.2. Among PtRuxSny/C catalysts prepared by Sn-CVD, one prepared by partially substituting Sn for Ru in the PtRu1.0/C catalyst, e.g., PtRu0.8Sn0.2/C, showed higher CO tolerance than one prepared by simply adding Sn to the PtRu1.0/C catalyst, e.g., PtRu1.0Sn0.2/C, which demonstrated the importance of an optimum x/y ratio in the design of the ternary PtRuxSny/C catalysts.
AB - A CO-tolerant PtRuxSny/C electrocatalyst, with an optimal x/y ratio of 0.8/0.2, was prepared by selectively depositing Sn on the metallic surface of PtRu0.8/C for use as the anode in a polymer electrolyte membrane fuel cell. The CO tolerance of the catalyst was greater when Sn was added by chemical vapor deposition (CVD) than by a conventional precipitation method because most of the Sn added by CVD was located in the vicinity of Pt and Ru surfaces, on which CO molecules were strongly adsorbed. Accordingly, the bi-functional mechanism of CO oxidation, which involved the migration of oxygenated species from the Sn to the adsorbed CO, was expected to be promoted to greater extents in the catalysts prepared by Sn-CVD than those prepared by Sn-precipitation. On the other hand, the ligand-effect mechanism of CO oxidation, which was facilitated by the Pt-Ru alloy formation, was not much affected by the added Sn because the Pt-Ru alloy remained unchanged, particularly when y ≤ 0.2. Among PtRuxSny/C catalysts prepared by Sn-CVD, one prepared by partially substituting Sn for Ru in the PtRu1.0/C catalyst, e.g., PtRu0.8Sn0.2/C, showed higher CO tolerance than one prepared by simply adding Sn to the PtRu1.0/C catalyst, e.g., PtRu1.0Sn0.2/C, which demonstrated the importance of an optimum x/y ratio in the design of the ternary PtRuxSny/C catalysts.
KW - CO tolerance
KW - CVD
KW - Fuel cell
KW - Pt
KW - Ru
KW - Sn
UR - http://www.scopus.com/inward/record.url?scp=79551635440&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2010.11.061
DO - 10.1016/j.ijhydene.2010.11.061
M3 - Article
AN - SCOPUS:79551635440
SN - 0360-3199
VL - 36
SP - 1930
EP - 1938
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 3
ER -