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Near-Complete Suppression of Oxygen Evolution for Photoelectrochemical H<sub>2</sub>O Oxidative H<sub>2</sub>O<sub>2</sub> Synthesis
279
Citations
45
References
2020
Year
Solar energy-assisted water oxidative hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) production on an anode combined with H<sub>2</sub> production on a cathode increases the value of solar water splitting, but the challenge of the dominant oxidative product, O<sub>2</sub>, needs to be overcome. Here, we report a SnO<sub>2-<i>x</i></sub> overlayer coated BiVO<sub>4</sub> photoanode, which demonstrates the great ability to near-completely suppress O<sub>2</sub> evolution for photoelectrochemical (PEC) H<sub>2</sub>O oxidative H<sub>2</sub>O<sub>2</sub> evolution. Based on the surface hole accumulation measured by surface photovoltage, downward quasi-hole Fermi energy at the photoanode/electrolyte interface and thermodynamic Gibbs free energy between 2-electron and 4-electron competitive reactions, we are able to consider the photoinduced holes of BiVO<sub>4</sub> that migrate to the SnO<sub>2-<i>x</i></sub> overlayer kinetically favor H<sub>2</sub>O<sub>2</sub> evolution with great selectivity by reduced band bending. The formation of H<sub>2</sub>O<sub>2</sub> may be mediated by the formation of hydroxyl radicals (OH·), from 1-electron water oxidation reactions, as evidenced by spin-trapping electron paramagnetic resonance (EPR) studies conducted herein. In addition to the H<sub>2</sub>O oxidative H<sub>2</sub>O<sub>2</sub> evolution from PEC water splitting, the SnO<sub>2-<i>x</i></sub>/BiVO<sub>4</sub> photoanode can also inhibit H<sub>2</sub>O<sub>2</sub> decomposition into O<sub>2</sub> under either electrocatalysis or photocatalysis conditions for continuous H<sub>2</sub>O<sub>2</sub> accumulation. Overall, the SnO<sub>2-<i>x</i></sub>/BiVO<sub>4</sub> photoanode achieves a Faraday efficiency (FE) of over 86% for H<sub>2</sub>O<sub>2</sub> generation in a wide potential region (0.6-2.1 V vs reversible hydrogen electrode (RHE)) and an H<sub>2</sub>O<sub>2</sub> evolution rate averaging 0.825 μmol/min/cm<sup>2</sup> at 1.23 V vs RHE under AM 1.5 illumination, corresponding to a solar to H<sub>2</sub>O<sub>2</sub> efficiency of ∼5.6%; this performance surpasses almost all previous solar energy-assisted H<sub>2</sub>O<sub>2</sub> evolution performances. Because of the simultaneous production of H<sub>2</sub>O<sub>2</sub> and H<sub>2</sub> by solar water splitting in the PEC cells, our results highlight a potentially greener and more cost-effective approach for "solar-to-fuel" conversion.
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