Carbon-Supported CoSe2 Nanoparticles for Oxygen Reduction Reaction in Acid Medium

被引:89
作者
Feng, Y. J. [1 ]
He, T. [1 ,2 ]
Alonso-Vante, N. [1 ]
机构
[1] Univ Poitiers, Lab Electrocatalysis, CNRS, UMR 6503, F-86022 Poitiers, France
[2] Honda Res Inst USA Inc, Columbus, OH 43212 USA
关键词
Acid Medium; CoSe2; Nanoparticles; Methanol Tolerance; Non-precious Metal; Oxygen Reduction Reaction (ORR); PEM FUEL-CELLS; TRANSITION-METAL CHALCOGENIDES; MODEL CATALYSTS; HEAT-TREATMENT; THIN-FILMS; ELECTROCATALYSTS; PLATINUM; ELECTROREDUCTION; NANOCRYSTALS; RUTHENIUM;
D O I
10.1002/fuce.200900038
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Carbon-supported CoSe2 nanoparticles, as non-precious metal cathodic catalyst, were prepared via the in situ surfactant-free method with the conventional heating. Structural and electrochemical properties of the obtained 20 wt.-% CoSe2/C nanoparticles were investigated by means of powder X-ray diffraction (PXRD), differential thermal gravimetric analysis (DTA-DTG) and rotating disc electrode (RDE) techniques. CoSe2 nanoparticles have two kinds of crystal structure after heat treatment under nitrogen at different temperature: orthorhombic at 250 and 300 degrees C; cubic at 400 and 430 degrees C. The latter structure has higher oxygen reduction activity than the former in 0.5 M H2SO4 center dot CoSe2/C nanoparticles after heat treatment from 250 to 430 degrees C, have an onset potential from 0.78 to 0.81 V versus the reference hydrogen electrode (RHE) in O-2-saturated 0.5 M H2SO4 at 25 degrees C. 20 wt.-% CoSe2/C nanoparticles, after heat treatment at 300 degrees C, promote ca. 3.5 electrons, per oxygen molecule, transferred during the oxygen reduction process. They have an oxidation wave centred at 0.96 V versus RHE and display higher methanol tolerance as compared to 20 wt.-% Pt/C (E-TEK).
引用
收藏
页码:77 / 83
页数:7
相关论文
共 41 条
[11]   Compounds FeSe2, CoSe2 and NiSe2 [J].
de Jong, WF ;
Willems, HWV .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1928, 170 (03) :241-245
[12]  
Feng Y., 2008, ECS T, V11, P67, DOI DOI 10.1149/1.2953508
[13]   Nonprecious metal catalysts for the molecular oxygen-reduction reaction [J].
Feng, Yongjun ;
Alonso-Vante, Nicolas .
PHYSICA STATUS SOLIDI B-BASIC SOLID STATE PHYSICS, 2008, 245 (09) :1792-1806
[14]   In situ free-surfactant synthesis and ORR-Electrochemistry of carbon-supported Co3S4 and CoSe2 nanoparticles [J].
Feng, Yongjun ;
He, Ting ;
Alonso-Vante, Nicolas .
CHEMISTRY OF MATERIALS, 2008, 20 (01) :26-28
[15]   Oxygen reduction reaction on carbon-supported CoSe2 nanoparticles in an acidic medium [J].
Feng, Yongjun ;
He, Ting ;
Alonso-Vante, Nicolas .
ELECTROCHIMICA ACTA, 2009, 54 (22) :5252-5256
[16]   Pd-Ti and Pd-Co-Au electrocatalysts as a replacement for platinum for oxygen reduction in proton exchange membrane fuel cells [J].
Fernández, JL ;
Raghuveer, V ;
Manthiram, A ;
Bard, AJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (38) :13100-13101
[17]  
FISCHER C, 1995, J APPL ELECTROCHEM, V25, P1004
[18]   Activity benchmarks and requirements for Pt, Pt-alloy, and non-Pt oxygen reduction catalysts for PEMFCs [J].
Gasteiger, HA ;
Kocha, SS ;
Sompalli, B ;
Wagner, FT .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2005, 56 (1-2) :9-35
[19]   Just a Dream-or Future Reality? [J].
Gasteiger, Hubert A. ;
Markovic, Nenad M. .
SCIENCE, 2009, 324 (5923) :48-49
[20]   PREPARATION OF NEW SELENIUM-RICH SELENIDES, CRSE3, MOSE-APPROXIMATE-TO-5, WSE-APPROXIMATE-TO-6-7, AND RESE-APPROXIMATE-TO-6-7 AND KNOWN SELENIDES, BY THE REACTION OF METAL-CARBONYLS WITH SELENIUM [J].
HIBBLE, SJ ;
RICE, DA ;
ALMOND, MJ ;
MOHAMMAD, KAH ;
PEARSE, SP ;
SAGAR, JR .
JOURNAL OF MATERIALS CHEMISTRY, 1992, 2 (12) :1237-1240