Adsorption of phosphate species on poly-oriented Pt and Pt(111) electrodes over a wide range of pH

被引:116
作者
Gisbert, Ruben [1 ]
Garcia, Gonzalo [1 ]
Koper, Marc T. M. [1 ]
机构
[1] Leiden Univ, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
关键词
Platinum; Phosphate adsorption; pH dependence; Pt(111); Phosphate buffers; SINGLE-CRYSTAL ELECTRODES; BUFFERED SOLUTIONS; ALKALINE MEDIA; PLATINUM; ANION; (BI)SULPHATE; OXIDATION; GOETHITE; HYDROGEN; SURFACES;
D O I
10.1016/j.electacta.2010.04.009
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The adsorption of phosphate anions from phosphate solutions at poly-oriented and single-crystal platinum electrodes primarily Pt(1 1 1) was studied over a wide range of pH by cyclic voltammetry The features observed at the poly-oriented Pt electrode in phosphate solution may be related to the different crystalline facets the (1 1 1) orientation presenting the most significant behavior in terms of phosphate adsorption On the reversible hydrogen electrode (RHE) scale the phosphate adsorption strength decreases with increasing alkalinity of the solution Qualitatively three different pH regions can be distinguished At pH <6 only a broad reversible peak is observed corresponding to the adsorption of H2PO4- and further deprotonation to adsorbed HPO4- For 6 < pH < 11 a butterfly feature followed by one or two anodic peaks (depending on scan rate) is observed ascribed to the adsorption of HPO4- followed by its subsequent deprotonation to adsorbed PO43- The splitting into two or three voltammetric features and the irreversibility of the two features at more positive potential is ascribed to the deprotonation reaction leading to a surface species (i e phosphate) which needs to change its surface coordination At pH > 11 a reversible pre-wave and a sharp spike are observed ascribed to the co-adsorption of phosphate and hydroxide (C) 2010 Elsevier Ltd All rights reserved
引用
收藏
页码:7961 / 7968
页数:8
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