Photocatalytic Reactions over TiO2-Based Interfacial Charge Transfer Complexes
2024
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The present review is related to the novel approach for improvement of the optical properties of wide bandgap metal oxides, in particular TiO2, based on the formation of the inorganic–organic hybrids that display absorption in the visible spectral range due to the formation of interfacial charge transfer (ICT) complexes. We outlined the property requirements of TiO2-based ICT complexes for efficient photo-induced catalytic reactions, emphasizing the simplicity of the synthetic procedure, the possibility of the fine-tuning of the optical properties supported by the density functional theory (DFT) calculations, and the formation of a covalent linkage between the inorganic and organic components of hybrids, i.e., the nature of the interface. In addition, this study provides a comprehensive insight into the potential applications of TiO2-based ICT complexes in photo-driven catalytic reactions (water splitting and degradation of organic molecules), including the identification of the reacti...ve species that participate in photocatalytic reactions by the spin-trapping electron paramagnetic resonance (EPR) technique. Considering the practically limitless number of combinations between the inorganic and organic components capable of forming oxide-based ICT complexes and with the knowledge that this research area is unexplored, we are confident it is worth studying, and we emphasized some further perspectives. © 2024 by the authors.
Ključne reči:
EPR spin trapping / interface properties / interfacial charge transfer complexes / optical properties / photocatalytic oxidation reactions / solar energy conversion / titanium dioxide / water-splitting reactionIzvor:
Catalysts, 2024, 14, 11, 810-Finansiranje / projekti:
- Ministarstvo nauke, tehnološkog razvoja i inovacija Republike Srbije, institucionalno finansiranje - 200017 (Univerzitet u Beogradu, Institut za nuklearne nauke Vinča, Beograd-Vinča) (RS-MESTD-inst-2020-200017)
- 2023-07-17 HYDIS - Multifunctional visible-light-responsive inorganic- organic hybrids for efficient hydrogenproduction and disinfection (RS-ScienceFundRS-Prizma2023_TT-5354)
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VinčaTY - JOUR AU - Lazić, Vesna M. AU - Nedeljković, Jovan PY - 2024 UR - https://vinar.vin.bg.ac.rs/handle/123456789/14110 AB - The present review is related to the novel approach for improvement of the optical properties of wide bandgap metal oxides, in particular TiO2, based on the formation of the inorganic–organic hybrids that display absorption in the visible spectral range due to the formation of interfacial charge transfer (ICT) complexes. We outlined the property requirements of TiO2-based ICT complexes for efficient photo-induced catalytic reactions, emphasizing the simplicity of the synthetic procedure, the possibility of the fine-tuning of the optical properties supported by the density functional theory (DFT) calculations, and the formation of a covalent linkage between the inorganic and organic components of hybrids, i.e., the nature of the interface. In addition, this study provides a comprehensive insight into the potential applications of TiO2-based ICT complexes in photo-driven catalytic reactions (water splitting and degradation of organic molecules), including the identification of the reactive species that participate in photocatalytic reactions by the spin-trapping electron paramagnetic resonance (EPR) technique. Considering the practically limitless number of combinations between the inorganic and organic components capable of forming oxide-based ICT complexes and with the knowledge that this research area is unexplored, we are confident it is worth studying, and we emphasized some further perspectives. © 2024 by the authors. T2 - Catalysts T1 - Photocatalytic Reactions over TiO2-Based Interfacial Charge Transfer Complexes VL - 14 IS - 11 SP - 810 DO - 10.3390/catal14110810 ER -
@article{
author = "Lazić, Vesna M. and Nedeljković, Jovan",
year = "2024",
abstract = "The present review is related to the novel approach for improvement of the optical properties of wide bandgap metal oxides, in particular TiO2, based on the formation of the inorganic–organic hybrids that display absorption in the visible spectral range due to the formation of interfacial charge transfer (ICT) complexes. We outlined the property requirements of TiO2-based ICT complexes for efficient photo-induced catalytic reactions, emphasizing the simplicity of the synthetic procedure, the possibility of the fine-tuning of the optical properties supported by the density functional theory (DFT) calculations, and the formation of a covalent linkage between the inorganic and organic components of hybrids, i.e., the nature of the interface. In addition, this study provides a comprehensive insight into the potential applications of TiO2-based ICT complexes in photo-driven catalytic reactions (water splitting and degradation of organic molecules), including the identification of the reactive species that participate in photocatalytic reactions by the spin-trapping electron paramagnetic resonance (EPR) technique. Considering the practically limitless number of combinations between the inorganic and organic components capable of forming oxide-based ICT complexes and with the knowledge that this research area is unexplored, we are confident it is worth studying, and we emphasized some further perspectives. © 2024 by the authors.",
journal = "Catalysts",
title = "Photocatalytic Reactions over TiO2-Based Interfacial Charge Transfer Complexes",
volume = "14",
number = "11",
pages = "810",
doi = "10.3390/catal14110810"
}
Lazić, V. M.,& Nedeljković, J.. (2024). Photocatalytic Reactions over TiO2-Based Interfacial Charge Transfer Complexes. in Catalysts, 14(11), 810. https://doi.org/10.3390/catal14110810
Lazić VM, Nedeljković J. Photocatalytic Reactions over TiO2-Based Interfacial Charge Transfer Complexes. in Catalysts. 2024;14(11):810. doi:10.3390/catal14110810 .
Lazić, Vesna M., Nedeljković, Jovan, "Photocatalytic Reactions over TiO2-Based Interfacial Charge Transfer Complexes" in Catalysts, 14, no. 11 (2024):810, https://doi.org/10.3390/catal14110810 . .



