Phosphorus-Rich Colloidal Cobalt Diphosphide (CoP₂ ) Nanocrystals for Electrochemical and Photoelectrochemical Hydrogen Evolution.

Abstract

Developing earth-abundant and efficient electrocatalysts for photoelectrochemical water splitting is critical to realizing a high-performance solar-to-hydrogen energy conversion process. Herein, phosphorus-rich colloidal cobalt diphosphide nanocrystals (CoP₂ NCs) are synthesized via hot injection. The CoP₂ NCs show a Pt-like hydrogen evolution reaction (HER) electrocatalytic activity in acidic solution with a small overpotential of 39 mV to achieve -10 mA cm^-2 and a very low Tafel slope of 32 mV dec^-1 . Density functional theory (DFT) calculations reveal that the high P content both physically separates Co atoms to prevent H from over binding to multiple Co atoms, while simultaneously stabilizing H adsorbed to single Co atoms. The catalytic performance of the CoP₂ NCs is further demonstrated in a metal-insulator-semiconductor photoelectrochemical device consisting of bottom p-Si light absorber, atomic layer deposition Al-ZnO passivation layers, and the CoP₂ cocatalyst. The p-Si/AZO/TiO₂ /CoP₂ photocathode shows a photocurrent density of -16.7 mA cm^-2 at 0 V versus reversible hydrogen electrode (RHE) and an output photovoltage of 0.54 V. The high performance and stability are attributed to the junction between p-Si and AZO, the corrosion-resistance of the pinhole-free TiO₂ protective layer, and the fast HER kinetics of the CoP₂ NCs.