Abstract

A simple hydrothermal method was used to prepare the single-metal atom oxide (SMAO) catalyst. The prepared dual Cobalt and tungsten (CoW) single metal atom oxide anchored on the TiO2-Bi2MoO6-reduced graphene oxide (rGO), an interstitial atomic line of tungsten and cobalt. The prepared photocatalyst showed good photocatalytic hydrogen (H2) evolution and organic contaminant degradation. As co-catalysts, surface-dispersed CoW sites were created using a Co mono-substituted hetero-polyacid (HPA-Co). A larger quantity of single atoms were uniformly decorated on the TiO2-Bi2MoO6-Ethylenediamine (ED)-rGO catalyst. The presence of the CoW species was verified employing extended X-ray absorption near edge structure (XANES), high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), and extended X-ray absorption fine structure (EXAFS) analyses after a TiO2-Bi2MoO6-CoW-ED-rGO composite synthesized. The findings demonstrate that TiO2-Bi2MoO6-CoW-ED-rGO catalysts were more capable of producing hydrogen and degrading Ciprofloxacin (CIP) (21.46 mmol/g/h, 97.2%) than other bare and binary catalysts. Furthermore, it showed remarkable stability and reusability after five consecutive CIP photodegradation and H2 production cycles. Gas chromatography/mass spectroscopy (GC/MS) techniques were used to identify the intermediates in the photodegradation process. The prepared photocatalyst was significantly increased, and the separation of charge carriers was further boosted, thanks to the CoW material and the synergistic effect. A possible Z-scheme mechanism was proposed for the photocatalytic H2 production activity. More electrons can contribute to the reduction of H2 evolution because of the processability of the Z-scheme. This work created a recyclable, inexpensive, highly effective, and non-toxic catalytic material for H2 generation and CIP degradation.

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