Adsorption of phospbate species on Pt(111) and Pt(100) as studied by in situ FTIR spectroscopy

被引:54
|
作者
Weber, M
Nart, FC
deMoraes, IR
Iwasita, T
机构
[1] UNIV SAO PAULO,INST QUIM,BR-13360970 SAO CARLOS,SP,BRAZIL
[2] UNIV MUNICH,INST PHYS,D-85521 MUNICH,GERMANY
来源
JOURNAL OF PHYSICAL CHEMISTRY | 1996年 / 100卷 / 51期
关键词
D O I
10.1021/jp960952k
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
In situ FTIR results on the adsorption of phosphate species on Pt(111) and Pt(100) single crystal surfaces are presented and discussed. In weak acid solutions (fluoride electrolyte pH = 2.8), the adsorption of phosphate species on Pt(111) starts at about 0.4 V vs Pd/H-2 and the maximum adsorption occurs at about 0.6 V. At low potentials, two spectral features due to adsorbed H2PO4- are observed at 1110 and 1000 cm(-1). With increasing potentials these two original bands are replaced by a new band located between 1150 and 1180 cm(-1), which is assigned to adsorbed HPO42- species. In strongly acidic solution (pH = 0.23), undissociated H3PO4 molecules are adsorbed at low potentials. This species is characterized by a band between 1035 and 1050 cm(-1). With increasing adsorption potential adsorbed H3PO4 dissociates, generating H2PO4-. For both solution pHs the deprotonation of adsorbed species is observed after the maximum of the anomalous voltammetric wave of the Pt(111) electrode. On Pt(100) and Pt(111) the adsorption of phosphate species shows almost identical behavior in mildly acidic solutions. Transformation from H2PO4- to HPO42- occurs on both single crystal surfaces at the same potentials.
引用
收藏
页码:19933 / 19938
页数:6
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