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. 2023 Nov 27;13(23):3026.
doi: 10.3390/nano13233026.

Ti3C2-MXene/NiO Nanocomposites-Decorated CsPbI3 Perovskite Active Materials under UV-Light Irradiation for the Enhancement of Crystal-Violet Dye Photodegradation

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Ti3C2-MXene/NiO Nanocomposites-Decorated CsPbI3 Perovskite Active Materials under UV-Light Irradiation for the Enhancement of Crystal-Violet Dye Photodegradation

Asma A Alothman et al. Nanomaterials (Basel). .

Abstract

Ti3C2-MXene material, known for its strong electronic conductivity and optical properties, has emerged as a promising alternative to noble metals as a cocatalyst for the development of efficient photocatalysts used in environmental cleanup. In this study, we investigated the photodegradation of crystal-violet (CV) dye when exposed to UV light using a newly developed photocatalyst known as Ti3C2-MXene/NiO nanocomposite-decorated CsPbI3 perovskite, which was synthesized through a hydrothermal method. Our research investigation into the structural, morphological, and optical characteristics of the Ti3C2-MXene/NiO/CsPbI3 composite using techniques such as FTIR, XRD, TEM, SEM-EDS mapping, XPS, UV-Vis, and PL spectroscopy. The photocatalytic efficacy of the Ti3C2-MXene/NiO/CsPbI3 composite was assessed by evaluating its ability to degrade CV dye in an aqueous solution under UV-light irradiation. Remarkably, the Ti3C2-MXene/NiO/CsPbI3 composite displayed a significant improvement in both the degradation rate and stability of CV dye when compared to the Ti3C2-MXene/NiO nanocomposite and CsPbI3 perovskite materials. Furthermore, the UV-visible absorption spectrum of the Ti3C2-MXene/NiO/CsPbI3 composite demonstrated a reduced band gap of 2.41 eV, which is lower than that of Ti3C2-MXene/NiO (3.10 eV) and Ti3C2-MXene (1.60 eV). In practical terms, the Ti3C2-MXene/NiO/CsPbI3 composite achieved an impressive 92.8% degradation of CV dye within 90 min of UV light exposure. We also confirmed the significant role of photogenerated holes and radicals in the CV dye removal process through radical scavenger trapping experiments. Based on our findings, we proposed a plausible photocatalytic mechanism for the Ti3C2-MXene/NiO/CsPbI3 composite. This research may open up new avenues for the development of cost-effective and high-performance MXene-based perovskite photocatalysts, utilizing abundant and sustainable materials for environmental remediation.

Keywords: NiO; Ti3C2-MXene; UV-light irradiation; crystal violet; perovskite; photodegradation.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
(A) FTIR spectra and (B) XRD pattern of (a) Ti3C2-MXene nanosheets, (b) NiO, (c) Ti3C2-MXene/NiO, (d) CsPbI3, and (e) Ti3C2-MXene/NiO/CsPbI3 composites.
Figure 2
Figure 2
TEM images of (a,b) Ti3C2-MXene nanosheets and (c) the corresponding HRTEM image, TEM images of (d) Ti3C2-MXene/NiO and (eg) the corresponding HRTEM image, and TEM images of (h) Ti3C2-MXene/NiO/CsPbI3 composites and (ik) the corresponding HRTEM image.
Figure 3
Figure 3
FE-SEM images of (a,b) Ti3C2-MXene nanosheets, (c) NiO, (d,e) Ti3C2-MXene/NiO, (f) CsPbI3, and (gi) Ti3C2-MXene/NiO/CsPbI3 composites.
Figure 4
Figure 4
FE-SEM image and the corresponding EDS elemental mapping of Ti3C2-MXene/NiO/CsPbI3 composites.
Figure 5
Figure 5
(a) XPS survey scan spectrum of Ti3C2-MXene/NiO and high-resolution XPS spectra of elements (b) Ti2p, (c) C1s, (d) Ni2p, (e) O1s, (f) Cs3d, (g) Pb4f, and (h) I3d states for Ti3C2-MXene/NiO. (Black line; fitting and violet line; background).
Figure 6
Figure 6
(a) UV–Visible absorption spectra of Ti3C2-MXene nanosheets, Ti3C2-MXene/NiO, and Ti3C2-MXene/NiO/CsPbI3 composites and Tauc plot of (b) Ti3C2-MXene nanosheets, (c) Ti3C2-MXene/NiO, and (d) Ti3C2-MXene/NiO/CsPbI3 composites from UV–Visible absorption spectroscopy.
Figure 7
Figure 7
PL spectra of Ti3C2-MXene nanosheets, NiO, Ti3C2-MXene/NiO, and Ti3C2-MXene/NiO/CsPbI3 composites.
Figure 8
Figure 8
(a) Electrochemical impedance spectra and (b) photocurrent response of Ti3C2-MXene nanosheets, Ti3C2-MXene/NiO, and Ti3C2-MXene/NiO/CsPbI3 composites.
Figure 9
Figure 9
Absorption spectra of CV-dye photodegradation over, (a) Ti3C2-MXene nanosheets, (b) Ti3C2-MXene/NiO, and (c) Ti3C2-MXene/NiO/CsPbI3 composites.
Figure 10
Figure 10
Degradation curves profiles of CV dye over Ti3C2-MXene nanosheets, Ti3C2-MXene/NiO, and Ti3C2-MXene/NiO/CsPbI3 composites, (a) the degradation rate, (b) linear kinetic, (c) rate constant, and (d) percentage degradation of dye.
Figure 11
Figure 11
(a) Effect of different scavengers and (b) cyclic stability performance of Ti3C2-MXene/NiO/CsPbI3 composites in the photocatalytic removal of CV.
Figure 12
Figure 12
Schematic illustration of the proposed mechanism for photocatalytic degradation of CV dye using Ti3C2-MXene/NiO/CsPbI3 composites photocatalyst.

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