Carbon-dispersed Pt-Rh nanoparticles for ethanol electro-oxidation. Effect of the crystallite size and of temperature

被引:65
作者
Lima, F. H. B. [1 ]
Profeti, D. [1 ]
Lizcano-Valbuena, W. H. [1 ]
Ticianelli, E. A. [1 ]
Gonzalez, E. R. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
ethanol electro-oxidation; C-C bond activation; platinum-rhodium alloy; in situ FTIR; on-line DEMS;
D O I
10.1016/j.jelechem.2008.01.024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This work presents results of studies of carbon-dispersed Pt-Rh (1:1) nanoparticles as electrocatalysts for the ethanol electro-oxidation. The influences of the crystallite size and the cell temperature on the yields of CO2, acetaldehyde and acetic acid are investigated. Metal nanoparticles were prepared by two different routes: (1) impregnation on carbon powder followed by thermal reduction on hydrogen atmosphere and (2) chemical reduction of the precursor salts. The surface active area and the electrochemical activity of the electrocatalysts were estimated by CO stripping and cyclic voltammetry in the absence and in the presence of ethanol, respectively. Reaction intermediates and products were analyzed by in situ Fourier Transform Infra-Red Spectroscopy (FTIR) and Differential Electrochemical Mass Spectrometry (DEMS). The electrochemical stripping of CO and the electrochemical ethanol oxidation were slightly faster on the Pt-Rh electrocatalysts compared to Pt/C. Also, in situ FTIR spectra and DEMS measurements evidenced that the CO2/acetaldehyde and the CO2/acetic acid ratios are higher for the Pt-Rh/C materials in relation to Pt/C. This was ascribed to the activation of the C-C bond breaking by Rh, this being more prominent for the materials with smaller crystallite sizes. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:121 / 129
页数:9
相关论文
共 33 条
[1]   Mechanism of stationary bulk CO oxidation on Pt(111) electrodes [J].
Batista, EA ;
Iwasita, T ;
Vielstich, W .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (38) :14216-14222
[2]   Effect of alcohol concentration and electrode composition on the ethanol electrochemical oxidation [J].
Bergamaski, K ;
Gomes, JF ;
Goi, BE ;
Nart, FC .
ECLETICA QUIMICA, 2003, 28 (02) :87-92
[3]  
BITTINSCATTANEO B, 1991, ELECTROANALYTICAL CH, V17, P181
[4]   The influence of PtRu atomic composition on the yields of ethanol oxidation: A study by in situ FTIR spectroscopy [J].
Camara, GA ;
de Lima, RB ;
Iwasita, T .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2005, 585 (01) :128-131
[5]   Parallel pathways of ethanol oxidation: The effect of ethanol concentration [J].
Camara, GA ;
Iwasita, T .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2005, 578 (02) :315-321
[6]   Correlation of electrochemical and physical properties of PtRu alloy electrocatalysts for PEM fuel cells [J].
Camara, GA ;
Giz, MJ ;
Paganin, VA ;
Ticianelli, EA .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2002, 537 (1-2) :21-29
[7]   Electro-oxidation of ethanol on Pt, Rh, and PtRh electrodes. A study using DEMS and in-situ FTIR techniques [J].
de Souza, JPI ;
Queiroz, SL ;
Bergamaski, K ;
Gonzalez, ER ;
Nart, FC .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (38) :9825-9830
[8]   CO ELECTROOXIDATION ON WELL-CHARACTERIZED PT-RU ALLOYS [J].
GASTEIGER, HA ;
MARKOVIC, N ;
ROSS, PN ;
CAIRNS, EJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (02) :617-625
[9]   Electronic structure and catalysis on metal surfaces [J].
Greeley, J ;
Norskov, JK ;
Mavrikakis, M .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 2002, 53 :319-348
[10]  
Gupta SS, 2006, J ELECTROANAL CHEM, V594, P65