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Separation-free artificial photosynthesis of concentrated hydrogen peroxide and value-added fuels over Ta atomic sites

  • Hao Tan
  • , Peng Zhou
  • , Yu Gu
  • , Youxing Liu
  • , Wenxing Chen
  • , Hongyu Guo
  • , Fangxu Lin
  • , Heng Luo
  • , Xiaoqing Cao
  • , Lingyou Zeng
  • , Mingchuan Luo
  • , Shaojun Guo*
  • *Corresponding author for this work
  • School of Materials Science and Engineering
  • Peking University
  • CAS - Institute of Metal Research
  • School of Environment and Energy
  • Beijing Institute of Technology

Research output: Contribution to journal › Article › peer-review

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-N2O2 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-N2O2 sites stabilizing intermediates and reducing the energy barrier for biomass conversion. We further demonstrate that RF/C-TaSA enables efficient artificial photosynthesis of H2O2 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 H2O2 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 H2O2 can also be readily converted to solid H2O2 powder (Na2CO3 ∙ 1.5 H2O2) for ease of storage and transport with high sterilization activities even after 6 months.

Original languageEnglish
Article number8784
JournalNature Communications
Volume16
Issue number1
DOIs
Publication statusPublished - Dec 2025
Externally publishedYes

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