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Electrodeposited Pt and Pt-Sn nanoparticles on Ti as anodes for direct methanol fuel cells 被引量:3

Electrodeposited Pt and Pt-Sn nanoparticles on Ti as anodes for direct methanol fuel cells
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摘要 Electro-oxidation of methanol was studied on titanium supported nanocrystallite Pt and Ptx-Sny catalysts prepared by electrodeposition techniques. Their electro-catalytic activities were studied in 0.5 mol/L H2SO4 and compared to those of a smooth Pt, Pt/Pt and Pt-Sn/Pt electrodes. Platinum was deposited on Ti by galvanostatic and potentiostatic techniques. X-ray diffractometer (XRD) and energy dispersive X-ray (EDX) techniques were applied in order to investigate the chemical composition and the phase structure of the modified electrodes. Scanning electron microscopy (SEM) was used to characterize the surface morphology and to correlate the results obtained from the two electrochemical deposition methods. Results show that modified Pt/Ti electrodes prepared by the two methods have comparable performance and enhanced catalytic activity towards methanol electro-oxidation compared to Pt/Pt and smooth Pt electrodes. Steady state Tafel plots experiments show a higher rate of methanol oxidation on a Pt/Ti catalyst than that on a smooth Pt. Introduction of a small amount of Sn deposited with Pt improves the catalytic activity and the stability of prepared electrode with time as indicated from the cyclic votlammetry and the chronoamperometric experiments. The effect of variations in the composition for binary catalysts of the type Ptx-Sny/Ti towards the methanol oxidation reaction is reported. Consequently, the Ptx-Sny/Ti (x∶y (8∶1), molar ratio) catalyst is a very promising one for methanol oxidation. Electro-oxidation of methanol was studied on titanium supported nanocrystallite Pt and Ptx-Sny catalysts prepared by electrodeposition techniques. Their electro-catalytic activities were studied in 0.5 mol/L H2 SO4 and compared to those of a smooth Pt, Pt/Pt and Pt-Sn/Pt electrodes. Platinum was deposited on Ti by galvanostatic and potentiostatic techniques. X-ray diffractometer (XRD) and energy dispersive X-ray (EDX) techniques were applied in order to investigate the chemical composition and the phase structure of the modified electrodes. Scanning electron microscopy (SEM) was used to characterize the surface morphology and to correlate the results obtained from the two electrochemical deposition methods. Results show that modified Pt/Ti electrodes prepared by the two methods have comparable performance and enhanced catalytic activity towards methanol electro-oxidation compared to Pt/Pt and smooth Pt electrodes. Steady state Tafel plots experiments show a higher rate of methanol oxidation on a Pt/Ti catalyst than that on a smooth Pt. Introduction of a small amount of Sn deposited with Pt improves the catalytic activity and the stability of prepared electrode with time as indicated from the cyclic votlammetry and the chronoamperometric experiments. The effect of variations in the composition for binary catalysts of the type Ptx-Sny/Ti towards the methanol oxidation reaction is reported. Consequently, the Ptx-Sny/Ti (x:y (8: 1), molar ratio) catalyst is a very promising one for methanol oxidation.
出处 《燃料化学学报》 EI CAS CSCD 北大核心 2009年第3期346-354,共9页 Journal of Fuel Chemistry and Technology
关键词 电化学 甲醇 电沉积 PT electrodeposition methanol electro-oxidation fuel cells electro-catalysis.
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  • 1Wang J,Wasmus S,Savinell R F.J Electrochem Soc,1995,142(12):4218.
  • 2Hable C T,Wrighton M S.Langmuir,1993,9(11):3284.
  • 3Arico A S,Creti P,Antonucci P L,Antonucci V.Electrochem Solid-State Lett,1998,1(2):66.
  • 4Lamy C,Belgsir E M,Leger J-M.J Appl Electrochem,2001,31(7):799.
  • 5Lamy C,Lima A,LeRhun V,Delime F,Coutanceau C,Leger J-M.J Power Sources,2002,105(2):283.
  • 6Wei Z B,Wang S L,Yi B L,Liu J G,Chen L K,Zhou W J,Li W Z,Xin Q.J Power Sources,2002,106(1-2):364.
  • 7Radmilovic V,Gasteiger H A,Ross P N Jr.J Catal,1995,154(1):98.
  • 8Baronetti G T,de Miguel S R,Scelza O A,Castro A A.Appl Catal,1986,24(1-2):109.
  • 9Breiter M W.J Electroanal Chem,1969,23(2):173.
  • 10Gurau B,Viswanathan R,Liu R,Lafrenz T J,Ley K L,Smotkin E S,Reddington E,Sapienza A,Chan B C,Mallouk T E,Sarangapani S.J Phys Chem B,1998,102(49):9997.

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