The breakthrough offers a low‑cost, scalable route to produce H₂O₂ using sunlight, addressing demand for sustainable oxidants in chemical and environmental applications.
Polymeric carbon nitride has long been prized for its metal‑free photocatalytic properties, yet integrating alkali‑metal dopants at scale remained elusive. By leveraging a vapor‑phase condensation over KCl‑coated substrates, researchers achieve uniform potassium incorporation without compromising film integrity. This approach not only simplifies the synthesis workflow but also introduces cyano‑group defects that effectively narrow the band gap, allowing the material to harvest a broader spectrum of solar photons.
The doped panels translate these electronic advantages into tangible performance gains. In pure ethanol, the potassium‑doped CN delivers hydrogen peroxide at 3.0 × 10² mM m⁻² h⁻¹, an 18‑fold increase over pristine CN, and generates charge carriers below the undoped band edge, accelerating the oxygen reduction reaction. Such metrics position the material as a competitive alternative to conventional H₂O₂ production routes that rely on energy‑intensive processes.
Beyond laboratory metrics, the study demonstrates real‑world viability through a 46 cm² continuous‑flow reactor operating for four days. The system maintains steady H₂O₂ output, underscoring the method’s scalability and potential for integration into decentralized chemical manufacturing or water‑treatment facilities. As industries seek greener oxidant sources, potassium‑doped polymeric carbon nitride panels could become a cornerstone of solar‑driven, on‑site hydrogen peroxide generation.
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