Separation-free artificial photosynthesis of concentrated hydrogen peroxide and value-added fuels over Ta atomic sites.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41038862.
- Also identified by DOI 10.1038/s41467-025-63838-9 and PMC identifier 12491456.
- Licence recorded as CC BY-NC-ND.
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Abstract
Solar-driven artificial photosynthesis of hydrogen peroxide and high-value chemicals from oxygen and biomass is promising but is hindered by poor light absorption, sluggish kinetics of biomass dehydrogenation, and low oxygen reduction selectivity. Herein, we develop a resorcinol-formaldehyde resin/carbon-supported Ta-N<sub>2</sub>O<sub>2</sub> single-atom catalyst (RF/C-TaSA) that enables broad-spectrum light harvesting (> 932 nm) and selective biomass conversion in a solid-organic-aqueous three-phase system. RF/C-TaSA achieves a high 3.0% quantum yield at 635 nm, with Ta-N<sub>2</sub>O<sub>2</sub> sites stabilizing intermediates and reducing the energy barrier for biomass conversion. We further demonstrate that RF/C-TaSA enables efficient artificial photosynthesis of H<sub>2</sub>O<sub>2</sub> and value-added chemicals from more available thatch, pine needles and wastepaper. Combining catalyst innovation and system engineering, we build a solar-powered RF/C-TaSA-based photocatalytic device for directly producing commercially viable H<sub>2</sub>O<sub>2</sub> at a high concentration of 3 wt% and high-value-added chemical without requiring energy-intensive separation processes for 70-day operation. Furthermore, the produced crude concentrated H<sub>2</sub>O<sub>2</sub> can also be readily converted to solid H<sub>2</sub>O<sub>2</sub> powder (Na<sub>2</sub>CO<sub>3</sub> ∙ 1.5 H<sub>2</sub>O<sub>2</sub>) for ease of storage and transport with high sterilization activities even after 6 months.