Metal-organic frameworks derived Bi2O2CO3/porous carbon nitride: A nanosized Z-scheme systems with enhanced photocatalytic activity

[Display omitted] •A MOFs derived strategy is developed to construct nanoscale Bi2O2CO3/g-C3N4 Z-scheme heterojunction.•The nanosized heterojunction enhances the visible-light absorption range and promotes spatial charge separation.•This structural feature serves to favor 1O2 generation.•BO/CN shows...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2020-06, Vol.267, p.118700, Article 118700
Hauptverfasser: Wang, Ziwei, Wang, Han, Zeng, Zhuotong, Zeng, Guangming, Xu, Piao, Xiao, Rong, Huang, Danlian, Chen, Xijian, He, Linwei, Zhou, Chengyun, Yang, Yang, Wang, Zixuan, Wang, Wenjun, Xiong, Weiping
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:[Display omitted] •A MOFs derived strategy is developed to construct nanoscale Bi2O2CO3/g-C3N4 Z-scheme heterojunction.•The nanosized heterojunction enhances the visible-light absorption range and promotes spatial charge separation.•This structural feature serves to favor 1O2 generation.•BO/CN shows improved visible-light photocatalytic activities for antibiotics degradation. A bismuth-based metal-organic frameworks (MOFs) derived strategy is developed to construct nanoscale Bi2O2CO3/porous g-C3N4 Z-scheme heterojunction. Bi2O2CO3 nanoparticles uniformly distribute in the surface, edge and interlayer of g-C3N4 nanosheets, thus significantly increasing intimate contact at the interface. Furthermore, the Z-scheme heterojunctions and doped N atoms escaping from g-C3N4 to Bi2O2CO3 provide a charge transport chain to promote the charge carriers separation and accelerate the oxidation of O2− by holes, as confirmed by photoluminescence, photoelectrochemical and electron spin resonance measurements. Benefitting from these, the optimized composites not only outperform the pristine g-C3N4 in the removal of sulfamethazine (SMT) within 90 min visible light illumination (λ > 420 nm) but also serve to selectively generate singlet oxygen (1O2) during the molecular oxygen activation. The present study provides some guidelines for the design of photocatalysts via a MOF-assisted route toward sustainable environmental remediation.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2020.118700