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. 2023 Jul 10;120(29):e2305705120. doi: 10.1073/pnas.2305705120

Fig. 4.

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.