The toxic dyeing wastewater containing both carcinogenic Cr(VI) and refractory dyes poses serious threats to ecological safety and human health. Herein, a novel composite photocatalytic material e-LDH/t-BiOCl/Bi2S3 with an ultrathin sandwich structure constructed achieves removal rate constants of 0.044 and 0.019 min-1 for Cr(VI) and reactive red 2 by adsorption-photocatalysis synergistic mechanism in full-spectrum illumination. This structure employs the interface conditions and built-in electric field to form multilevel short-range charge migration channel, achieving the targeted reduction and oxidation of Cr(VI) and azoxy dyes by electrons (e-) and holes (h+). Besides facilitating the reduction of Cr(VI), e- can also enhance the effective utilization of h+ and mediate the formation of other reactive oxygen species that target RR2 degradation. The degradation mechanism, pathway, and biological toxicity of RR2 single and Cr(VI)/RR2 coexistence reaction system were discussed by DFT calculation, LC-MS characterization, and T.E.S.T. evaluation. Moreover, we further investigated the photocatalytic activity and cost-effectiveness of the e-LDH/t-BiOCl/Bi2S3 system under continuous flow and real water settings, and determined the primary water quality parameters that influence photocatalytic performance. This work establishes a new concept for the rational design of robust ternary heterostructure photocatalysts with desirable morphology and competitive performance for photocatalytic applications.
Keywords: Continuous flow; Full-spectrum; Multistage interface; Synergistic effect; Toxicity.
Copyright © 2024. Published by Elsevier Inc.