Abstract Due to the prevailing energy shortages, the quest for new alternative energy sources is growing increasingly urgent. Hydrogen production through water electrolysis has become a crucial method. However, the slow four-electron reaction in oxygen evolution reaction (OER) becomes the main rate-limiting step. In this study, we propose obtaining heterostructure La(OH)3@CuO-P after composite phosphatisation using nickel foam (NF) as the substrate material. The experimental results demonstrate that the heterostructure La(OH)3@CuO exhibits an overpotential of 365mV at a current density of 10mA/cm2 , and displays a Tafel slope value of 114.02mF/dec, a bilayer capacitance of 1.853mF/cm2 for OER in a 1 M KOH solution. After phosphating, the heterostructure La(OH)3@CuO-P exhibits exceptional catalytic performance with only 215 mV overpotential, a Tafel slope value of 79.36 mV/dec, and a bilayer capacitance of 34.73mF/cm2 at a current density of 10mA/cm2 . Moreover, it also exhibits relatively stable performance during cyclic voltammetry testing for up to1000 cycles. Analyses suggest that the formation of a heterojunction structure in La(OH)3@CuO-P effectively addresses the issues of insufficient conductivity of La(OH)3 and tendency for CuO monomer aggregation while maintaining excellent properties for each component. The substitutional P atom doping not only adjusts the electronic structure and optimizes the adsorption free energy of -OH but also reduces sample size and increases catalytic active sites, thereby further enhancing the OER performance of the material.
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Liang et al. (2024) studied this question.
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