Insights into the dual Z-scheme and piezoelectricity co-driven photocatalyst for ultra-speed degradation of nitenpyram
[Display omitted] •Improved activity by synergy of Z-scheme and piezoelectricity was firstly proposed.•The promotion mechanism of piezoelectricity on dual Z-scheme is explained.•The prepared material has strong anti-interference ability.•The degradation path of nitenpyram is explained in detail.•The...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2023-01, Vol.451, p.138399, Article 138399 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | [Display omitted]
•Improved activity by synergy of Z-scheme and piezoelectricity was firstly proposed.•The promotion mechanism of piezoelectricity on dual Z-scheme is explained.•The prepared material has strong anti-interference ability.•The degradation path of nitenpyram is explained in detail.•The toxicity of NTP’s intermediate products was also analyzed.
A highly active catalyst AgI/Ag3PO4/BaTiO3 with the synergistic effect of photocatalysis and piezoelectricity was prepared, which can remove 100 % of Nitenpyram (NTP) in a wide pH range within 10 min. This piezo-photocatalyst AgI/Ag3PO4/BaTiO3 with dual Z-scheme shows a higher NTP degradation rate than their mono-material and binary composites. The apparent rate constant of AgI/Ag3PO4/BaTiO3 in NTP removal is 2.12 times higher than the second-performing catalyst. In the quenching experiment, h+ and ·O2– were observed to be the main active substance in NTP degradation and the former contributes the most. The dual Z-scheme mechanism and the built-in electric field are both beneficial for the separation of electron-hole pairs, as well as the extension of the photo-generated carrier lifetime. At last, the effect factor experiments proved that the prepared AgI/Ag3PO4/BaTiO3 catalyst owns stable and efficient activity. This work provides novel guidance for the construction of highly efficient and stable piezo-photocatalytic heterojunction catalysts. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2022.138399 |