Embedding Amorphous Molybdenum Sulfide within a Porous Poly(3,4-ethylenedioxythiophene) Matrix to Enhance its H -evolving Catalytic Activity and Robustness.

Amorphous molybdenum sulfide (MoS ) is a promising alternative to Pt catalyst for the H evolution in water. However, it is suffered of an electrochemical corrosion. In this report, we present a strategy to tack this issue by embedding the MoS catalyst within a porous poly(3,4-ethylenedioxythiophene) (PEDOT) matrix. The PEDOT host is firstly grown onto a fluorine-doped tin oxide (FTO) electrode by electrochemical polymerization of EDOT monomer in an acetonitrile solution to perform a porous structure. The MoS catalyst is subsequently deposited onto the PEDOT by an electrochemical oxidation of [MoS ] monomer. In a 0.5 M H SO electrolyte solution, the MoS /PEDOT shows higher H -evolving catalytic activities (current density of 34.2 mA/cm at -0.4 V vs RHE) in comparison to a pristine MoS grown on a planar FTO electrode having similar catalyst loading (24.2 mA/cm ). The PEDOT matrix contributes to enhance the stability of MoS catalyst by a significant manner. As such, the MoS /PEDOT retains 81 % of its best catalytic activity after 1000 potential scans from 0 to -0.4 V vs. RHE, whereas a planar MoS catalyst is completely degraded after about 240 potential scans, due to its complete corrosion.