Nature Communications · 2019 · 383 citations · 67 references
Natural SciencesMaterials EngineeringMaterials ScienceElectrochemistryInorganic ChemistrySurface ScienceElectrochemical Energy ConversionElectrode MaterialsOxygen EvolutionPhotochemistryPhotoelectrochemistryRedox-active MaterialsCo-catalystsOxygen Evolution CatalystsPhosphorenePhotoanodesPhotocatalytic MaterialsPhotocatalytic Water SplittingPhotocurrent GenerationWater Splitting
Abstract As the development of oxygen evolution co-catalysts (OECs) is being actively undertaken, the tailored integration of those OECs with photoanodes is expected to be a plausible avenue for achieving highly efficient solar-assisted water splitting. Here, we demonstrate that a black phosphorene (BP) layer, inserted between the OEC and BiVO 4 can improve the photoelectrochemical performance of pre-optimized OEC/BiVO 4 (OEC: NiOOH, MnO x, and CoOOH) systems by 1.2∼1.6-fold, while the OEC overlayer, in turn, can suppress BP self-oxidation to achieve a high durability. A photocurrent density of 4.48 mA·cm −2 at 1.23 V vs reversible hydrogen electrode (RHE) is achieved by the NiOOH/BP/BiVO 4 photoanode. It is found that the intrinsic p -type BP can boost hole extraction from BiVO 4 and prolong holes trapping lifetime on BiVO 4 surface. This work sheds light on the design of BP-based devices for application in solar to fuel conversion, and also suggests a promising nexus between semiconductor and electrocatalyst.
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