TY - JOUR
T1 - Platinum Iron Intermetallic Nanoparticles Supported on Carbon Formed In Situ by High-Pressure Pyrolysis for Efficient Oxygen Reduction
AU - Hu, Yang
AU - Jensen, Jens Oluf
AU - Zhang, Wei
AU - Cleemann, Lars Nilausen
AU - Pan, Chao
AU - Li, Qingfeng
PY - 2016
Y1 - 2016
N2 - Carbon-supported PtFe alloy catalysts are synthesized by the one-step, high-temperature pyrolysis of Pt, Fe, and C precursors. As a result of the high temperature, the formed PtFe nanoparticles possess highly ordered, face-centered tetragonal, intermetallic structures with a mean size of ≈11.8 nm. At 0.9 V versus the reversible hydrogen electrode, the PtFe nanoparticles show a 6.8 times higher specific activity than the reference Pt/C catalyst towards the oxygen reduction reaction (ORR) as well as excellent stability, most likely because of the durable intermetallic structure and the preleaching treatment of the catalyst. During these preliminary syntheses, we found that a portion of the PtFe nanoparticles is buried in the in situ formed carbon phase, which limits Pt utilization in the catalyst and results in a mass-specific activity equivalent to the commercial Pt/C catalyst. Moreover, the possible presence of other active sites, for example, FeNx, CNx, and carbon-encapsulated metal nanoparticles, and their contribution to the ORR performance of the catalyst are also investigated.
AB - Carbon-supported PtFe alloy catalysts are synthesized by the one-step, high-temperature pyrolysis of Pt, Fe, and C precursors. As a result of the high temperature, the formed PtFe nanoparticles possess highly ordered, face-centered tetragonal, intermetallic structures with a mean size of ≈11.8 nm. At 0.9 V versus the reversible hydrogen electrode, the PtFe nanoparticles show a 6.8 times higher specific activity than the reference Pt/C catalyst towards the oxygen reduction reaction (ORR) as well as excellent stability, most likely because of the durable intermetallic structure and the preleaching treatment of the catalyst. During these preliminary syntheses, we found that a portion of the PtFe nanoparticles is buried in the in situ formed carbon phase, which limits Pt utilization in the catalyst and results in a mass-specific activity equivalent to the commercial Pt/C catalyst. Moreover, the possible presence of other active sites, for example, FeNx, CNx, and carbon-encapsulated metal nanoparticles, and their contribution to the ORR performance of the catalyst are also investigated.
KW - Alloys
KW - Electrochemistry
KW - Fuel cells
KW - Reduction
KW - Platinum
U2 - 10.1002/cctc.201600748
DO - 10.1002/cctc.201600748
M3 - Journal article
SN - 1867-3880
VL - 8
SP - 3131
EP - 3136
JO - ChemCatChem
JF - ChemCatChem
IS - 19
ER -