Dual-defect enhanced piezocatalytic performance of C3N5 for multifunctional applications
An effective piezocatalytic semiconductor (C3N5−x-O) was prepared with a two-step thermal polymerization/etching method. Experimental characterizations and structural simulations revealed that the dual-defects of O doping and N vacancy in C3N5 not only increases the asymmetry and the exposure of tri...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2023-04, Vol.323, p.122196, Article 122196 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | An effective piezocatalytic semiconductor (C3N5−x-O) was prepared with a two-step thermal polymerization/etching method. Experimental characterizations and structural simulations revealed that the dual-defects of O doping and N vacancy in C3N5 not only increases the asymmetry and the exposure of triangular pores, but also optimizes the band structure and charge distribution of the thin-layered C3N5−x-O, endowing it with an enhanced piezoelectricity and increased active surfaces. Piezocatalysis-mediated pollutant degradation and H2O2 production were achieved with substantially improved efficiencies over the pristine carbon nitrides. Under ultrasound-assisted piezocatalysis, tetracycline was degraded with a kinetic rate of 0.0356 min−1 and this figure was further increased to 0.0561 min−1 in piezocatalytic-Fenton. A yield of 0.615 mM/g/h for piezocatalytic production of H2O2 was achieved in pure water. The synergistic effect of the defect sites revealed in present work could facilitate the more rational design of nitrogen-rich carbon nitrides for environmental remediation and the production of value-added chemicals.
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•Dual-defect C3N5 containing O doping and N vacancy was synthesized.•Defect engineering leads to an enhanced piezoelectricity and surface activities.•Dual-defect sites exhibit synergistic effect to improve piezocatalytic performance.•Effective piezocatalytic degradation, H2O2 evolution, and Fenton were demonstrated.•doping and N vacancy respectively act as O2 activation and TC adsorption sites. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2022.122196 |