Abstract

An in situ study with dispersive EXAFS (Extended X-Ray Absorption Spectroscopy) at the Ir-LIIIedge is performed to characterize Electrodeposited Iridium Oxide Films (EIROF) under chronoamperometric conditions. The technique monitors the local chemical environment and electronic structure of iridium during the oxidation of Ir(III) to Ir(IV) with a time resolution of milliseconds. The study is performed in both acidic and basic media. The Fourier transforms of the time-resolved EXAFS signals clearly show that the short-range structure of Ir is similar to that of rutile-type IrO2and is maintained during the reaction, thus accounting for the flexibility of the structure of the electrode material in accommodating different oxidation states. From a more general point of view, the work demonstrates the capabilities of in situ experiments based on state-of-the-art dispersive EXAFS in clarifying the mechanistic aspects of electrochemical processes.

Highlights

  • When dealing with the mechanism and the kinetics of heterogeneous catalytic reactions, one of the main challenges is to investigate the processes with sufficient time resolution

  • In this paper we present a short-range investigation of electrodeposited IrOx material by means of in situ dispersive EXAFS spectroscopy at the Ir-LIII edge aimed at monitoring the local geometrical structure within the second coordination shell of iridium in chronoamperometric conditions

  • The peaks between 3.4 and 3.8 > are mainly due to Ir and O atoms that are the nearest neighbors (NNN) around Ir of IrO2. This is by itself a quite remarkable result, if attention is paid to the fact that at the beginning of the reaction Ir is present as Ir(III), and nicely demonstrates the flexibility of the Electrodeposited Iridium Oxide Films (EIROF) matrix in accommodating different oxidation states

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Summary

Introduction

When dealing with the mechanism and the kinetics of heterogeneous catalytic reactions, one of the main challenges is to investigate the processes with sufficient time resolution. In the setup of a time-resolved-XAS experiment, the standard monochromator is replaced by a polychromator so that the sample is crossed by a polychromatic beam which is Journal of Spectroscopy subsequently dispersed onto a detector This strategy allows recording spectra with a time resolution of milliseconds but only in the transmission mode. In recent works [15, 16], we employed XAS spectroscopy to study the turnover mechanism of Ir catalyst in the water splitting process: Ir was proposed to cycle between the Ir(III) and Ir(V) states In this context the knowledge of the possible variations in the local chemical structure of Ir with time during the application of different potential steps would be of primary interest; so, in situ time-resolved measurements are processed in order to obtain EXAFS signals for a short-range investigation

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