Copper hexacyanoferrate modified electrodes for hydrogen peroxide detection as studied by X-ray absorption spectroscopy

被引:17
作者
Giorgetti, Marco [1 ]
Tonelli, Domenica [1 ]
Berrettoni, Mario [2 ]
Aquilanti, Giuliana [3 ]
Minicucci, Marco [4 ]
机构
[1] Univ Bologna, INSTM, Dept Ind Chem Toso Montanari, UdR Bologna, I-40136 Bologna, Italy
[2] Univ Bologna, INSTM, UOs Unita Operat Sede, Dept Ind Chem Toso Montanari, I-40136 Bologna, Italy
[3] Sincrotrone Trieste SCpA, I-34149 Trieste, Italy
[4] Univ Camerino, Sch Sci & Technol, Div Phys, CNISM, I-62032 Camerino, MC, Italy
关键词
X-ray absorption spectroscopy; Hydrogen peroxide; Copper hexacyanoferrate; Graphite foil electrodes; Sensor; BODY DISTRIBUTION-FUNCTIONS; PRUSSIAN BLUE; CONDENSED MATTER; SOLID-STATE; IRON; ELECTROCHEMISTRY; IDENTITY;
D O I
10.1007/s10008-013-2343-5
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
X-ray absorption spectroscopy (XAS) has been used to monitor the local geometry of Fe and Cu sites of copper hexacyanoferrates (CuHCF)-modified electrodes which find application in the electrochemical detection of hydrogen peroxide. The XAS approach has permitted to check the nature of the Cu and Fe sites and to investigate their local structure around about 500 pm from the metal centres. The measurements have been done on electrodes prior and after the addition of known quantities of hydrogen peroxide at two different concentration ranges, following a protocol consisting of H2O2 addition, applied potential, and rest period. For the CuHCF-modified electrode, this protocol leads to the increasing conversion to an already present "inactive" component, which limits the usability of the sensor; whereas the electrode modified with the Cu2+-loaded CuHCF displays a better resistance to this unavoidable process. In particular, the formation of the "inactive" component takes place more slowly, confirming the capability, at molecular scale, of such Cu-enriched CuHCF used as electrode modifier to detect more efficiently hydrogen peroxide, as recently demonstrated in our previous paper.
引用
收藏
页码:965 / 973
页数:9
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