摘要
Natural mineral composite catalysts have attracted much attention due to their great potential in the fields of water treatment, air purification and energy conversion. In this study, porous TiO 2 materials were synthesized from ilmenite by a two-stage calcination and acid leaching process, and porous TiO 2 /CdS composites were prepared by a hydrothermal method. The results of photocatalytic experiments indicate that the porous TiO 2 /CdS composite (PTC-2) with a Ti/Cd molar ratio of 1:1 exhibits the highest photocatalytic activity, with the degradation rate of methylene blue achieving a maximum value of 96.6% at 80 min. Moreover, the composite maintains a degradation efficiency of 88.5% after five cycles. The findings demonstrate that the TiO 2 /CdS heterojunction significantly enhances the photocatalyst's absorption of visible light while facilitating the effective separation and transfer of photogenerated electron–hole (e − /h + ) pairs. The porous architecture of the composite facilitates superior electron transport pathways and effectively mitigates e − /h + recombination. Furthermore, a mechanism for the photocatalytic degradation of organic dyes using porous TiO 2 /CdS composites is proposed, wherein photogenerated superoxide radicals ( · O 2 − ) and hydroxyl radicals ( · OH) serve as the primary reactive species. This study explores the cost-effective synthesis of TiO 2 /CdS heterojunctions and makes a significant contribution to the advancement and utilization of natural minerals for pollution degradation.
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