Carbon nanotube supported platinum-palladium nanoparticles for formic acid oxidation

被引:112
作者
Winjobi, Olumide [1 ]
Zhang, Zhiyong [1 ]
Liang, Changhai [2 ]
Li, Wenzhen [1 ]
机构
[1] Michigan Technol Univ, Dept Chem Engn, Houghton, MI 49931 USA
[2] Dalian Univ Technol, State Key Lab Fine Chem, Dalian, Peoples R China
关键词
Fuel cell; Alloy catalyst; Palladium; Formic acid oxidation; Carbon nanotubes; LARGE-SCALE SYNTHESIS; CATHODE CATALYST; ELECTROCATALYTIC OXIDATION; PD NANOPARTICLES; ANODE CATALYSTS; ELECTROOXIDATION; FORMALDEHYDE; PERFORMANCE;
D O I
10.1016/j.electacta.2010.02.062
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Pt, Pd and PtxPdy alloy nanoparticles (Pt1Pd1, Pt1Pd3, atomic ratio of Pt to Pd is 1:1.1:3, respectively) supported on carbon nanotube (CNT) with high and uniform dispersion were prepared by a modified ethylene glycol method. Transmission electron microscopy images show that small Pt and PtxPdy nanoparticles are homogeneously dispersed on the outer walls of CNT, while Pd nanoparticles have some aggregations and comparatively larger particle size. The average particle sizes of Pt/CNT, Pt1Pd1/CNT, Pt1Pd3/CNT and Pd/CNT obtained from the Pt/Pd (2 2 0) diffraction peaks in the X-ray diffraction patterns are 2.0, 2.4, 3.1 and 5.4 nm, respectively. With increasing Pd amount of the catalysts, the mass activity of formic acid oxidation reaction (FAOR) on the CNT supported catalysts increases in both cyclic voltammetry (CV) and chronoamperometry (CA) tests, although the particle size gets larger (thus, the relative surface area gets smaller). The CV study indicates a 'direct oxidation pathway' of FAOR occurred on the Pd surface, while on the Pt surface, the FAOR goes through 'COads intermediate pathway'. Pd/CNT demonstrates 7 times better FAOR mass activity than Pt/CNT (2.3 mA/mgPd vs. 0.33 mA/mgPt) at an applied potential of 0.27 V (vs. RHE) in the CA test. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4217 / 4221
页数:5
相关论文
共 45 条
[1]   The electro-oxidation of formic acid on Pt-Pd single crystal bimetallic surfaces [J].
Arenz, M ;
Stamenkovic, V ;
Schmidt, TJ ;
Wandelt, K ;
Ross, PN ;
Markovic, NM .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2003, 5 (19) :4242-4251
[2]   Graphite nanofibers as an electrode for fuel cell applications [J].
Bessel, CA ;
Laubernds, K ;
Rodriguez, NM ;
Baker, RTK .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (06) :1115-1118
[3]  
CHE GL, 1999, NATURE, V298, P760
[4]   LARGE-SCALE SYNTHESIS OF CARBON NANOTUBES [J].
EBBESEN, TW ;
AJAYAN, PM .
NATURE, 1992, 358 (6383) :220-222
[5]   Electrocatalytic oxidation of formaldehyde on palladium nanoparticles supported on multi-walled carbon nanotubes [J].
Gao, Guo-Yu ;
Guo, Dao-Jun ;
Li, Hu-Lin .
JOURNAL OF POWER SOURCES, 2006, 162 (02) :1094-1098
[6]   HELICAL MICROTUBULES OF GRAPHITIC CARBON [J].
IIJIMA, S .
NATURE, 1991, 354 (6348) :56-58
[7]   Characterization and application of electrodeposited Pt, Pt/Pd, and Pd catalyst structures for direct formic acid micro fuel cells [J].
Jayashree, RS ;
Spendelow, JS ;
Yeom, J ;
Rastogi, C ;
Shannon, MA ;
Kenis, PJA .
ELECTROCHIMICA ACTA, 2005, 50 (24) :4674-4682
[8]   Oxygen Reduction Reaction on Carbon Supported Pt and Pd in Alkaline Solutions [J].
Jiang, L. ;
Hsu, A. ;
Chu, D. ;
Chen, R. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2009, 156 (03) :B370-B376
[9]   Ordered nanoporous arrays of carbon supporting high dispersions of platinum nanoparticles [J].
Joo, SH ;
Choi, SJ ;
Oh, I ;
Kwak, J ;
Liu, Z ;
Terasaki, O ;
Ryoo, R .
NATURE, 2001, 412 (6843) :169-172
[10]   The effect of experimental parameters on the synthesis of carbon nanotube/nanofiber supported platinum by polyol processing techniques [J].
Knupp, Seth L. ;
Li, Wenzhen ;
Paschos, Odysseas ;
Murray, Thomas M. ;
Snyder, Jeremy ;
Haldar, Pradeep .
CARBON, 2008, 46 (10) :1276-1284