AI Article Synopsis

  • Researchers are focusing on creating efficient composite photocatalysts that enhance charge transfer and light absorption.
  • The innovative CdS/FeO@N-doped graphene aerogel microtube/N-doped TiO photocatalyst is designed with a unique layered structure to optimize electron and hole transfer in photocatalysis.
  • This composite demonstrates remarkable effectiveness in degrading pollutants like methyl orange, bisphenol A, and tetracycline hydrochloride, while also showing strong stability and the involvement of free radicals in its catalytic processes.

Article Abstract

The development of composite photocatalysts with high charge transfer efficiency, great visible light absorption, and quick recovery has aroused the interest of many researchers. Herein, based on the hydrothermal assisted vacuum freeze drying method, CdS, FeO, and N-TiO were, respectively, fixed in the inner, middle, and outer layers of nitrogen-doped graphene aerogel for preparation of the site-specific magnetic porous Z-scheme CdS/FeO@N-doped graphene aerogel microtube/N-doped TiO (CdS/FeO@NGAM/N-TiO) photocatalyst. For the composite, FeO@NGAM carrier with porous and tubular structure not only helps the recycle and reactants/productions mass transport in the photocatalytic process but also ensures the well-steered transfer of electrons and holes from CdS and N-TiO in the Z-type heterojunction system, greatly improving the separation of photogenerated carriers. Besides, FeO can also work as a Fenton catalyst to activate hydrogen peroxide which is generated in situ by CdS. Thus, the CdS/FeO@NGAM/N-TiO composite presents excellent degradation efficiencies towards methyl orange ((MO) 98% removal rate within 50 min), bisphenol A ((BPA) 96% removal rate within 50 min), tetracycline hydrochloride ((TCH) 96% removal rate within 120 min) and strong stabilities after 6 cycles. The free radical removal experiments show that ·O and ·OH are the main active substances of catalysis, which further confirms the synergistic effect of photocatalysis and Fenton catalysis.

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http://dx.doi.org/10.1007/s11356-024-32190-8DOI Listing

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