In situ infrared (FTIR) study of the mechanism of the borohydride oxidation reaction

被引:79
作者
Concha, B. Molina [1 ]
Chatenet, M. [1 ]
Maillard, F. [1 ]
Ticianelli, E. A. [2 ]
Lima, F. H. B. [2 ]
de Lima, R. B. [3 ]
机构
[1] Univ Grenoble, CNRS, LEPMI, UMR 5631, F-38402 St Martin Dheres, France
[2] Univ Sao Paulo, Inst Quim, BR-13560970 Sao Carlos, SP, Brazil
[3] Univ Fed Maranhao, Ctr Tecnol, Dept Quim, BR-65085580 Sao Luis, MA, Brazil
关键词
PT-AG ELECTRODES; SODIUM-BOROHYDRIDE; BORON ATOMS; PART I; SPECTRA; GOLD; SPECTROSCOPY; BORANE; BO2; ELECTROCATALYSTS;
D O I
10.1039/c003652h
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
Early reports stated that Au was a catalyst of choice for the BOR because it would yield a near complete faradaic efficiency. However, it has recently been suggested that gold could yield to some extent the heterogeneous hydrolysis of BH4-,therefore lowering the electron count per BH4-, especially at low potential. Actually, the blur will exist regarding the BOR mechanism on Au as long as no physical proof regarding the reaction intermediates is not put forward. In that frame, in situ physical techniques like FTIR exhibit some interest to study the BOR. Consequently, in situ infrared reflectance spectroscopy measurements (SPAIRS technique) have been performed in 1 M NaOH/1 M NaBH4 on a gold electrode with the aim to detect the intermediate species. We monitored several bands in B-H ((nu) over bar similar to 1180,1080 and 972 cm(-1)) and B-O bond regions ((nu) over bar =1325 and similar to 1425cm(-1)), which appear sequentially as a function of the electrode polarization. These absorption bands are assigned to BH3, BH2 and BO2- species. At the light of the experimental results, possible initial elementary steps of the BOR on gold electrode have been proposed and discussed according to the relevant literature data.
引用
收藏
页码:11507 / 11516
页数:10
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