Abstract
CuS is an encouraging photoelectrode candidate that meets the essential requirements for efficient solar‐to‐hydrogen production, but it has not been thoroughly studied. A CuS light absorber layer is grown by the self‐assembly of copper and sulfur precursors on a carbon paper (CP) electrode. Simultaneously, rGO is introduced as a buffer layer to control the optical and electrical properties of the absorber. The well‐ordered microstructural arrangement suppresses the recombination loss of electrons and holes owing to enhanced charge‐carrier generation, separation, and transport. The potential reaching 10 mA cm−2 in 1.0 m KOH solution is significantly lowered to 0.87 V, and the photocurrent density at 1.23 V is 94.7 mA cm−2. The computational result reveals that the potential‐determining step is sensitive to O* stability; the lower stability of O* in the thin layer of CuS/rGO decreases the free‐energy gap between the initial and final states of the potential‐determining step, resulting in a lowering of the onset potential. The faradaic efficiency for the photoelectrochemical oxygen evolution reaction in the optimized 2CuS/1rGO/CP photoanode is 98.60%, and the applied bias photon‐to‐current and the solar‐to‐hydrogen efficiencies are 11.2% and 15.7%, respectively, and its ultra‐high performance is maintained for 250 h. These record‐breaking achievement indices may be a trigger for establishing a green hydrogen economy.
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