Dual‐Enhanced Doping in ReSe(2) for Efficiently Photoenhanced Hydrogen Evolution Reaction

Rhenium dichalcogenides (ReX(2), X = S or Se) are catalysts that have great promise for the photoenhanced hydrogen evolution reaction (PE‐HER) because of their unique physiochemical properties. However, the catalytic performance is still restricted by their low concentration of electrocatalytic activity sites and poor injection of hot electrons. Herein, dual‐enhancement in ReSe(2) nanosheets (NSs) with high concentration of active sites and efficient use of hot electrons is simultaneously achieved with moderate Mo doping. Contributions from exposed catalytically active sites, improved electrical conductivity, and enhanced solar spectral response are systematically investigated. Superior PE‐HER catalytical performance is obtained in Re(0.94)Mo(0.06)Se(2), which has more catalytically active sites and optimized band structure than other Re(1−) (x)Mo(x)Se(2) samples. Here, it is demonstrated that only doping can reduce the overpotential (η(10)) from 239 to 174 mV at −10 mA cm(−2) (Δ1η(10) = 65 mV). Then, η(10) is further improved to 137 mV under simulated AM 1.5 sun illumination (Δ2η(10) = 37 mV). The total improvement (Δη(10)) toward PE‐HER is 102 mV (Δ1η(10) + Δ2η(10) = 102 mV) in optimal Re(0.94)Mo(0.06)Se(2). This work presents a new perspective for researching high‐efficiency photoenhanced HER ReSe(2)‐based electrocatalysts and other layered transition metal dichalcogenides.