Synergistic photothermal conversion and visible-light photodegradation of antibiotic in S-type TiO2 derived Ti3C2-MXene loaded on NaYF4: Tm3+, Er3+, Yb3+ @BiOI
Here, the collaboration of photocatalysis and photothermal conversion has been defined as an efficient strategy for converting unusable near-infrared (NIR) light to operational ultraviolet–visible (UV–vis) photons. For this, a new heterostructured photocatalyst NaYF4: Tm3+, Er3+, Yb3+ @ BiOI was suc...
Saved in:
| Main Authors: | , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2025-06-01
|
| Series: | Journal of Science: Advanced Materials and Devices |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2468217925000048 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | Here, the collaboration of photocatalysis and photothermal conversion has been defined as an efficient strategy for converting unusable near-infrared (NIR) light to operational ultraviolet–visible (UV–vis) photons. For this, a new heterostructured photocatalyst NaYF4: Tm3+, Er3+, Yb3+ @ BiOI was successfully synthesized using a simple hydrothermal approach paired with electrostatic self-assembly. The results show that BiOI can indirectly use the NIR portion to produce electron-hole pairs due to the presence of upconversion nanoparticles (UCNPs). On the other hand, loading TiO2 derived Ti3C2 MXenes on NaYF4: Tm3+, Er3+, Yb3+ @ BiOI increased tetracycline (TC) degradation to 36% and 90%, compared to narrow band gap BiOI, within 120 min under NIR light irradiation and sunlight irradiation, respectively. Moreover, the reaction rate of UCNP@BiOI@TiO2–Ti3C2 was found to be 2.85 times higher under sunlight compared to NIR. It can be attributed to the synergistic photocatalytic and photothermal effects triggered by NIR light. In addition, the broad photoresponse range of TiO2 and the Schottky junction formed by Ti3C2 MXenes between TiO2 and BiOI facilitate charge separation while reducing photo-generated electron-hole pair recombination. The reduced recombination rate in the synthesized heterojunction was further substantiated by the larger photocurrent response and smaller EIS arc. Excellent catalytic activity is explained by the S-scheme mechanism, which produces holes at the valence band and superoxide radicals at the conductive band in the BiOI and Ti3C2, respectively. Significantly, the cycling results demonstrated that the photocatalysts had the requisite reusability and recyclability for real-world applications. The cooperative MXene and UCNPs utilized in this study provide a helpful basis for the logical design of full-spectrum photocatalysts. |
|---|---|
| ISSN: | 2468-2179 |