Controllable Fabrication of Zn2+ Self-Doped TiO2 Tubular Nanocomposite for Highly Efficient Water Treatment

Tailoring high-efficiency photocatalytic composites for various implementations is a major research topic. 1D TNTs-based nanomaterials show promise as a photocatalyst for the remediation of organic pigments in an aqueous solution. Despite this, TiO2 (TNTs) is only photoactive in the UV range due to its inherent restriction on absorption of light in the UV range. Herein, we provide a facile recipe to tailor the optical characteristics and photocatalytic activity of TNTs by incorporating Zn (II) ionic species via an ion-exchange approach in an aqueous solution. The inclusion of Zn (II) ions into the TNTs framework expands its absorption of light toward the visible light range, therefore TiO2 nanotubes shows the visible-light photo-performance. Activity performance on photocatalytic decontamination of RhB at ambient temperature demonstrates that Zn-TNTs offer considerable boosted catalytic performance compared with untreated tubular TiO2 during the illumination of visible light. RhB (10 mg L-1) degradation of around 95% was achieved at 120 min. Radical scavenger experiment demonstrated that when electron (e(-)) or holes (h(+)) scavengers are introduced to the photodegradation process, the assessment of decontamination efficacy decreased by 45% and 76%, respectively. This demonstrates a more efficient engagement of the photoexcited electrons over photogenerated holes in the photodegradation mechanism. Furthermore, there seems to be no significant decrease in the activity of the Zn-TNTs after five consecutive runs. As a result, the fabricated Zn-TNTs composite has a high economic potential in the energy and environmental domains.

Automated summary

Tailoring high-efficiency photocatalytic composites is crucial. Incorporating Zn (II) ions into TNTs can enhance their absorption of visible light and improve the photocatalytic performance. The Zn-TNTs composite shows significant degradation of RhB under visible light illumination, with a degradation rate of around 95% achieved in 120 minutes. The efficient engagement of photoexcited electrons over photogenerated holes in the photodegradation mechanism is observed.