Fig. 4.
(A) In situ Raman spectra of different oxidation systems. (B) EPR spectra using DMPO as trapping agents. (C) The inhibition efficiency of different quenchers on degradation of tetA by CoSA/Ti3C2Tx. (D) Concentration of free •OH generated in the process of PMS activation by CoSA/Ti3C2Tx. (E) Charge density of CoSA/Ti3C2Tx. (F) Optimized configurations of PMS adsorbed on CoSA/Ti3C2Tx. (G) Difference charge density for PMS adsorption on CoSA/Ti3C2Tx and the corresponding charge transfer. Yellow and green contours represent electron accumulation and deletion, respectively. (H) Reaction pathways of PMS activation to form surface-bound •OH (H, Left) and free •OH (H, Right) at Co sites.
