Highly efficient and robust noble-metal free bifunctional water electrolysis catalyst achieved via complementary charge transfer

The operating principle of conventional water electrolysis using heterogenous catalysts has been primarily focused on the unidirectional charge transfer within the heterostructure. Herein, multidirectional charge transfer concept has been adopted within heterostructured catalysts to develop an efficient and robust bifunctional water electrolysis catalyst, which comprises perovskite oxides (La0.5Sr0.5CoO3-delta, LSC) and potassium ion-bonded MoSe2 (K-MoSe2). The complementary charge transfer from LSC and K to MoSe2 endows MoSe2 with the electron-rich surface and increased electrical conductivity, which improves the hydrogen evolution reaction (HER) kinetics. Excellent oxygen evolution reaction (OER) kinetics of LSC/K-MoSe2 is also achieved, surpassing that of the noble metal (IrO2), attributed to the enhanced adsorption capability of surface-based oxygen intermediates of the heterostructure. Consequently, the water electrolysis efficiency of LSC/K-MoSe2 exceeds the performance of the state-of-the-art Pt/C||IrO2 couple. Furthermore, LSC/K-MoSe2 exhibits remarkable chronopotentiometric stability over 2,500h under a high current density of 100mAcm(-2). While water electrolysis offers a renewable means to obtain H-2, it is necessary to understand the roles adopted by catalytic components. Here, authors explore a heterostructured MoSe2/perovskite oxide catalyst that shows multidirectional charge transfer to boost electrocatalytic water splitting.

Automated summary

This study adopts the concept of multidirectional charge transfer to develop an efficient and robust water electrolysis catalyst using heterostructured catalysts. The catalyst shows excellent kinetics and stability, surpassing the performance of noble metals like IrO2.