TY - JOUR
T1 - Surface modification of commercial PtRu nanoparticles for methanol electro-oxidation
AU - Kuo, Che Wei
AU - Lu, I. Te
AU - Chang, Li Chung
AU - Hsieh, Yu Chi
AU - Tseng, Yuan-Chieh
AU - Wu, Pu-Wei
AU - Lee, Jyh Fu
PY - 2013/5/6
Y1 - 2013/5/6
N2 - The surfaces of commercially available PtRu nanoparticles (PtRu/C) have been successfully modified via a displacement reaction between the Ru atoms on the PtRu/C and the Pt ions in an aqueous hexachloroplatinic acid solution. The concentration of the hexachloroplatinic acid solution was deliberately formulated to allow for the formation of sub-monolayered Pt (Pt(1/16)) and monolayered Pt (Pt(1/8)) on the surface of PtRu/C. Material characterization, including X-ray diffraction patterns and transmission electron microscopy images, showed that the PtRu phases of the samples were identical but that the particle sizes increased slightly after the surface modification. Data from inductively coupled plasma mass spectrometry confirmed the deposition of Pt with negligible loss of Ru. X-ray absorption spectroscopy showed Pt-enriched surfaces, and the surface Pt content decreased in the order Pt(1/8) > Pt(1/16) > PtRu/C. Cyclic voltammetry and chronoamperometry were conducted for methanol electro-oxidation, and our results indicated impressive catalytic ability and carbon monoxide tolerance for Pt(1/16), followed by Pt(1/8) and PtRu/C. The mass activities of Pt(1/16) and Pt(1/8) increased 223% and 135% over that of PtRu/C. We attributed the observed improvements to the reduced amount of Ru on the PtRu surface, which resulted in an optimized PtRu ratio with enhanced catalytic ability.
AB - The surfaces of commercially available PtRu nanoparticles (PtRu/C) have been successfully modified via a displacement reaction between the Ru atoms on the PtRu/C and the Pt ions in an aqueous hexachloroplatinic acid solution. The concentration of the hexachloroplatinic acid solution was deliberately formulated to allow for the formation of sub-monolayered Pt (Pt(1/16)) and monolayered Pt (Pt(1/8)) on the surface of PtRu/C. Material characterization, including X-ray diffraction patterns and transmission electron microscopy images, showed that the PtRu phases of the samples were identical but that the particle sizes increased slightly after the surface modification. Data from inductively coupled plasma mass spectrometry confirmed the deposition of Pt with negligible loss of Ru. X-ray absorption spectroscopy showed Pt-enriched surfaces, and the surface Pt content decreased in the order Pt(1/8) > Pt(1/16) > PtRu/C. Cyclic voltammetry and chronoamperometry were conducted for methanol electro-oxidation, and our results indicated impressive catalytic ability and carbon monoxide tolerance for Pt(1/16), followed by Pt(1/8) and PtRu/C. The mass activities of Pt(1/16) and Pt(1/8) increased 223% and 135% over that of PtRu/C. We attributed the observed improvements to the reduced amount of Ru on the PtRu surface, which resulted in an optimized PtRu ratio with enhanced catalytic ability.
KW - Displacement reaction
KW - Methanol electro-oxidation
KW - Platinum
KW - Ruthenium
KW - X-ray absorption spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=84876939517&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2013.04.001
DO - 10.1016/j.jpowsour.2013.04.001
M3 - Article
AN - SCOPUS:84876939517
VL - 240
SP - 122
EP - 130
JO - Journal of Power Sources
JF - Journal of Power Sources
SN - 0378-7753
ER -