Magnetron sputtering strategy for Zr-Fe2O3 nanorod photoanode fabricated from ZrOx/β-FeOOH nanorods for photoelectrochemical water splitting

Synchronized surface modification and doping of hematite nanorod via sputtering is one of the impressive methods to develop photoanodes for practical application. In this paper, we report the role of Zr sputtering and 800 degrees C quenching on the structural and electrochemical properties of FeOOH NRs. The amount of ZrOx loading onto beta-FeOOH NRs was controlled by varying the sputtering time. FESEM and TEM images revealed that high-temperature quenching of Zr-sputtered beta-FeOOH NR's confirms the Zr doping and non-uniform ZrO2 nano-particles on vertically aligned Zr-doped hematite (Zr-Fe2O3 NRs). XPS analysis represented a tradeoff between extrinsic Zr doping and intrinsic Sn diffusion with increasing the thickness of deposited Zr layer in Zr-Fe2O3 NRs. A maximum achieved photocurrent density (1.23 mA/cm(2) at 1.23 V vs RHE) for the 7 nm Zr-Fe2O3 sample is 48% higher than that of pristine photoanode (Fe2O3 NRs). The electrochemical impedance spectroscopy and Mott-Schottky analyses revealed that the charge transfer properties and donor densities were effectively improved for Zr-Fe2O3 NRs photoanode. The photoelectrochemical reactor consisted of an optimum 7 nm Zr-Fe2O3 based photoanode exhibits the 115 and 165 mu mol, respectively O-2 and H-2 evolution over 10 h of 1 sun illumination. These results demonstrate the Zr sputtering approach followed by high-temperature quenching allows controlled Zr doping in vertically aligned Fe2O3 NRs for PEC water splitting applications.

Automated summary

This paper explores a method of surface modification and doping of hematite nanorods using sputtering, which has led to improved performance of photoanodes. By controlling the sputtering time, the loading of Zr onto FeOOH NRs was effectively managed. The study demonstrates that combining Zr sputtering with high-temperature quenching allows for controlled Zr doping in Fe2O3 NRs.