Local studies of photoelectrochemical reactions at nanostructured oxides

Abstract The conversion of photon energy to chemical energy and vice versa requires the close arrangement of absorber/emitters and (electro)chemical reactions sites. This review considers local measurement techniques aiding in the design of efficient oxide systems for the utilization of light as energy source and as efficient detection principle. Artificial photoelectrochemical systems are often build on oxides as they are abundant and have semiconducting properties. However, no single oxide fulfills all requirements for an efficient conversion of sunlight to chemical energy and thus complex oxides are explored. These oxides might be obtained by doping oxides with other metal cations or by combining different oxides for absorbance and catalyzing the desired reaction, mainly water splitting. Due to the enormous amount of possible combinations combinatorial search for new material systems has been pursued and accelerated around the world making use of local photoelectrochemical characterization techniques in the screening step. Local detection schemes based on scanning electrochemical microscopy and scanning electrochemical cell microscopy also provide details about the kinetics for heterogeneous charge transfer and the release of soluble reaction products. During the recent years the scanning probe methods have been complemented by local detection of fluorescent reaction products that are formed by heterogeneous electron transfer reactions from and non-fluorescent precursor molecules. Such detection is possible with single molecule sensitivity and spatial resolution exceeding the diffraction limit (superresolution). Such approaches enabled the discovery of population within ensembles of metal oxide nanoparticles that are distinguished by the location and reactivity of their reaction sites. Optical techniques for measuring Faradaic currents hold great promise for the measurement of very low currents beyond the study of photoelectrochemistry of metal oxides.