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. TheXAS 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 Cuenriched CuHCF used as electrode modifier to detect more efficiently hydrogen peroxide, as recently demonstrated in our previous paper
Marco Giorgetti, Domenica Tonelli, Mario Berrettoni, Giuliana Aquilanti, Marco Minicucci (2014). Copper hexacyanoferrate modified electrodes for hydrogen peroxide detection as studied by X-ray absorption spectroscopy. JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 18, 965-973 [10.1007/s10008-013-2343-5].
Copper hexacyanoferrate modified electrodes for hydrogen peroxide detection as studied by X-ray absorption spectroscopy
GIORGETTI, MARCO;TONELLI, DOMENICA;BERRETTONI, MARIO;
2014
Abstract
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. TheXAS 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 Cuenriched CuHCF used as electrode modifier to detect more efficiently hydrogen peroxide, as recently demonstrated in our previous paperI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.