Activity of carbon-supported platinum nanoparticles toward methanol oxidation reaction:: Role of metal precursor and a new surfactant, tert-octanethiol

被引:88
作者
Sen, Fatih
Gokagac, Gulsun [1 ]
机构
[1] Middle E Tech Univ, Dept Chem, TR-06531 Ankara, Turkey
[2] Yuzuncu Yil Univ, TR-65080 Van, Turkey
关键词
D O I
10.1021/jp065809y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two groups of carbon-supported platinum nanoparticle catalysts have been prepared. In group 1, catalysts I and 11 were prepared using PtCl4 and H2PtCI6 as starting materials and 1-hexanethiol, HSCH2CH2CH2CH2CH2CH3, as a surfactant. For group 11, the same platinum complexes were used as starting materials (catalyst III from PtCl4, catalyst IV from H2PtCl6) and tert-octanethiol, HSC(CH3)(2)CH2CH2CH2CH2CH3, was used as a surfactant for the first time. It has been found that the group II catalysts are between similar to 2 and similar to 3.3 times more active toward methanol oxidation reaction compared to other prepared and commercial catalysts. Transmission electron microscopy shows that the platinum nanoparticles are homogeneously dispersed on the carbon support and exhibit a narrow size distribution; the average particle size was found to be 2 +/- 0.4 and 3 +/- 0.4 nm in diameter for group I and group II catalysts, respectively. X-ray diffractogram analysis indicates that the platinum nanoparticles have a face centered cubic structure consistent with that of platinum metal itself., X-ray photoelectron spectra of the catalysts indicate two different types of platinum with the Pt 4f(7/2) binding energies of 71.1, 74.4 eV; 71.3, 74.3 eV; 71.0, 74.4 eV; and 71.5, 74.5 eV for catalysts I-IV, respectively. These have been identified as Pt(0O) and Pt(IV), which could be platinum oxide or hydroxide. By looking at the oxidation state data, we found that catalysts I-IV consist of 71% Pt(0) and 29% Pt(IV); 83% Pt(0) and 17% Pt(IV); 76% Pt(0) and 24% Pt(IV); and 65% Pt(0) and 35% Pt(IV), respectively.
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页码:1467 / 1473
页数:7
相关论文
共 36 条
[1]   Electrochemical analysis of high temperature methanol electro-oxidation at Pt-decorated Ru catalysts [J].
Aricò, AS ;
Baglio, V ;
Di Blasi, A ;
Modica, E ;
Monforte, G ;
Antonucci, V .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2005, 576 (01) :161-169
[2]   Effect of Pt-Ru alloy composition on high-temperature methanol electro-oxidation [J].
Aricò, AS ;
Antonucci, PL ;
Modica, E ;
Baglio, V ;
Kim, H ;
Antonucci, V .
ELECTROCHIMICA ACTA, 2002, 47 (22-23) :3723-3732
[3]   ELECTROCATALYTIC OXIDATION OF METHANOL ON PLATINUM-BASED BINARY ELECTRODES [J].
BEDEN, B ;
KADIRGAN, F ;
LAMY, C ;
LEGER, JM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1981, 127 (1-3) :75-85
[4]   SYNTHESIS OF THIOL-DERIVATIZED GOLD NANOPARTICLES IN A 2-PHASE LIQUID-LIQUID SYSTEM [J].
BRUST, M ;
WALKER, M ;
BETHELL, D ;
SCHIFFRIN, DJ ;
WHYMAN, R .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1994, (07) :801-802
[5]   X-ray photoelectron spectroscopy sulfur 2p study of organic thiol and disulfide binding interactions with gold surfaces [J].
Castner, DG ;
Hinds, K ;
Grainger, DW .
LANGMUIR, 1996, 12 (21) :5083-5086
[6]  
CELIK CMS, 2004, THESIS MIDDLE E TU A
[7]   Preparation of carbon-supported PtRu nanoparticles for direct methanol fuel cell applications - a comparative study [J].
Deivaraj, TC ;
Lee, JY .
JOURNAL OF POWER SOURCES, 2005, 142 (1-2) :43-49
[8]   Synthesis and catalytic properties of soluble platinum nanoparticles protected by a thiol monolayer [J].
Eklund, SE ;
Cliffel, DE .
LANGMUIR, 2004, 20 (14) :6012-6018
[9]   Thiol-terminated Di-, Tri-, and tetraethylene oxide functionalized gold nanoparticles: A water-soluble, charge-neutral cluster [J].
Foos, EE ;
Snow, AW ;
Twigg, ME ;
Ancona, MG .
CHEMISTRY OF MATERIALS, 2002, 14 (05) :2401-2408
[10]   Behaviour of bimetallic Pt-Pd carbon-supported catalysts in methanol electrooxidation [J].
Gökagaç, G ;
Léger, JM ;
Hahn, F .
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, 2003, 58 (05) :423-432