Efficient optimization of electron transfer pathway by constructing phosphide/ceria interface boosts seawater hydrogen production

Abstract

Developing efficient and durable hydrogen evolution reaction (HER) electrocatalysts is one of the most important issues for the commercialization of seawater electrolysis, but it remains challenging. Here, we report a CeO2-CoP nanoneedle array catalyst loaded on Ti mesh (CeO2-CoP/TM) with work-function-induced directional charge transport properties. The CeO2-CoP/TM catalyst showed superior HER catalytic activity and stability, with overpotentials of 41 and 60 mV to attain 10 mA cm−2, in 1 M KOH and 1 M KOH + seawater electrolyte, respectively. Experimental results and theoretical calculations reveal that the work function drives the charge transfer from CeO2 to CoP, which effectively balances the electronic density of CoP and CeO2, optimizes the d-band center, and accelerates the water activation kinetics, thus enhancing the HER activity. The solar-driven water electrolysis device displays a high and stable solar-to-hydrogen conversion efficiency of 19.6%. This study offers a work function-induced directional charge transport strategy to design efficient and durable catalysts for hydrogen production.