Revealing the stability of CuWO4/g-C3N4 nanocomposite for photocatalytic tetracycline degradation from the aqueous environment and DFT analysis
Graphitic carbon nitride (g-C3N4) is an emerging metal-free photocatalyst, however, engineering the photocatalytic efficiency for the effective degradation of hazardous molecules is still challenging. An unstable and low bandgap CuWO4 was composited with g-C3N4 to achieve synergistic benefits of tun...
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Veröffentlicht in: | Environmental research 2022-05, Vol.207, p.112112-112112, Article 112112 |
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Sprache: | eng |
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Zusammenfassung: | Graphitic carbon nitride (g-C3N4) is an emerging metal-free photocatalyst, however, engineering the photocatalytic efficiency for the effective degradation of hazardous molecules is still challenging. An unstable and low bandgap CuWO4 was composited with g-C3N4 to achieve synergistic benefits of tuning the visible light responsiveness and stability of CuWO4. CuWO4/g-C3N4 nanocomposite exhibited a relatively high visible light absorption region and the bandgap was modified from 2.77 to 2.53 eV evidenced via UV-DRS. Moreover, the fast electron transfer rate was observed with CuWO4/g-C3N4 nanocomposite as confirmed using PL and photocurrent studies. XRD, FT-IR, and HR-TEM analyses signified the formation of CuWO4/g-C3N4 nanocomposite. CuWO4/g-C3N4 nanocomposite showed enhanced photocatalytic degradation of Tetracycline (TC) about ∼7.4 fold greater than pristine g-C3N4 in 120 min. Notably, the OH• and •O2− radicals played a most significant role in photocatalytic TC degradation. Furthermore, the energy band structure, density of state, and Bader charge analyses of these molecules were performed.
•CuWO4/g-C3N4 exhibited enhanced photocatalytic degradation of Tetracycline.•The built-in electric field and the matched energy band triggered Z-scheme system.•The stability of nanocomposite improved up to 6 cycles compared with CuWO4.•The OH.• and •O2− played a significant role in the photocatalytic degradation•The energy band structure, density of state and Bader charge analyses were analysed. |
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ISSN: | 0013-9351 1096-0953 |
DOI: | 10.1016/j.envres.2021.112112 |