Unassisted Photoelectrochemical H<sub>2</sub>O<sub>2</sub> Production with <i>In Situ</i> Glycerol Valorization Using α-Fe<sub>2</sub>O<sub>3</sub>.
basic_science · Level V
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- Record sourced from PubMed, PMID 38526525.
- Also identified by DOI 10.1021/acs.nanolett.3c05136.
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Abstract
Photoelectrochemical (PEC) H<sub>2</sub>O<sub>2</sub> production via two-electron O<sub>2</sub> reduction is promising for H<sub>2</sub>O<sub>2</sub> production without emitting CO<sub>2</sub>. For PEC H<sub>2</sub>O<sub>2</sub> production, α-Fe<sub>2</sub>O<sub>3</sub> is an ideal semiconductor owing to its earth abundance, superior stability in water, and an appropriate band gap for efficient solar light utilization. Moreover, its conduction band is suitable for O<sub>2</sub> reduction to produce H<sub>2</sub>O<sub>2</sub>. However, a significant overpotential for water oxidation is required due to the poor surface properties of α-Fe<sub>2</sub>O<sub>3</sub>. Thus, unassisted solar H<sub>2</sub>O<sub>2</sub> production is not yet possible. Herein, we demonstrate unassisted PEC H<sub>2</sub>O<sub>2</sub> production using α-Fe<sub>2</sub>O<sub>3</sub> for the first time by applying glycerol oxidation, which requires less bias compared with water oxidation. We obtain maximum Faradaic efficiencies of 96.89 ± 0.6% and 100% for glycerol oxidation and H<sub>2</sub>O<sub>2</sub> production, respectively, with high stability for 25 h. Our results indicate that unassisted and stable PEC H<sub>2</sub>O<sub>2</sub> production is feasible with <i>in situ</i> glycerol valorization using the α-Fe<sub>2</sub>O<sub>3</sub> photoanode.