Stabilizing Hydrogen Adsorption Through Theory-Guided Chalcogen Substitution In Chevrel-Phase Mo6x8 (X=S, Se, Te) Electrocatalysts

In this work, we implement a facile microwave-assisted synthesis method to yield three binary Chevrel-Phase chalcogenides (Mo6X8; X = S, Se, Te) and investigate the effect of increasing chalcogen electronegativity on hydrogen evolution catalytic activity. Density functional theory predictions indicate that increasing chalcogen electronegativity in these materials will yield a favorable electronic structure for proton reduction. This is confirmed experimentally via X-ray absorption spectroscopy as well as traditional electrochemical analysis. We have identified that increasing the electronegativity of X in Mo6X8 increases the hydrogen adsorption strength owing to a favorable shift in the p- band position as well as an increase in the Lewis basicity of the chalcogen, thereby improving hydrogen evolution reaction energetics. We find that Mo(6)S(8 )exhibits the highest hydrogen evolution activity of the Mo6X8 series of catalysts, requiring an overpotential of 321 mV to achieve a current density of 10 mA cm(-2) (ECSA), a Tafel slope of 74 mV per decade, and an exchange current density of 6.01 X 10(-4) mA cm(-2) (ECSA). Agreement between theory and experiment in this work indicates that the compositionally tunable Chevrel-Phase chalcogenide family is a promising framework for which electronic structure can be predictably modified to improve catalytic small-molecule reduction reactivity.