Architecting the High-Entropy Oxides on 2D MXene Nanosheets by Rapid Microwave-Heating Strategy with Robust Photoelectrochemical Oxygen Evolution Performance

High-entropy oxides (HEO) have recently concerned interest as the most promising electrocatalytic materials for oxygen evolution reactions (OER). In this work, a new strategy to the synthesis of HEO nanostructures on Ti3C2Tx MXene via rapid microwave heating and subsequent calcination at a low temperature is reported. Furthermore, the influence of HEO loading on Ti3C2Tx MXene is investigated toward OER performance with and without visible-light illumination in an alkaline medium. The obtained HEO/Ti3C2Tx-0.5 hybrid exhibited an outstanding photoelectrochemical OER ability with a low overpotential of 331 mV at 10 mA cm(-2) and a small Tafel slope of 71 mV dec(-1), which exceeded that of a commercial IrO2 catalyst (340 mV at 10 mA cm(-2)). In particular, the fabricated water electrolyzer with the HEO/Ti3C2Tx-0.5 hybrid as anode required a less potential of 1.62 V at 10 mA cm(-2) under visible-light illumination. Owing to the strong synergistic interaction between the HEO and Ti3C2Tx MXene, the HEO/Ti3C2Tx hybrid has a great electrochemical surface area, many metal active sites, high conductivity, and fast reaction kinetics, resulting in an excellent OER performance. This study offers an efficient strategy for synthesizing HEO-based materials with high OER performance to produce high-value hydrogen fuel.

Automated summary

In this study, HEO nanostructures were synthesized on Ti3C2Tx MXene via rapid microwave heating and subsequent calcination at a low temperature. The influence of HEO loading on Ti3C2Tx MXene and its performance in OER were investigated. The results showed that the HEO/Ti3C2Tx-0.5 hybrid exhibited outstanding OER ability and photoelectrochemical performance, surpassing that of a commercial IrO2 catalyst.