TY  - JOUR
AU  - Dukić, Miljana
AU  - Sredojević, Dušan
AU  - Férová, Marta
AU  - Slovak, Vaclav
AU  - Lončarević, Davor
AU  - Dostanić, Jasmina
AU  - Šalipur, Hristina
AU  - Lazić, Vesna
AU  - Nedeljković, Jovan
PY  - 2024
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/12989
AB  - The interfacial charge transfer (ICT) complex formation is a simple procedure to bring optical absorption of widebandgap oxide materials in the visible spectral range, crucial for enhancing their use in photo-driven reactions. The optical absorption of the prepared ICT complexes between ZnO and five different colorless benzene derivatives is red-shifted compared to pristine ZnO nanopowder. The density functional theory (DFT) calculations provided realistic energy level alignment in hybrid systems. Also, the DFT-calculated infrared spectra support the binding structures derived based on experimental measurements of free and adsorbed ligands onto ZnO surfaces. The photocatalytic performance of prepared hybrids was evaluated using photocatalytic hydrogen generation in the water-splitting reaction. The ZnO nanopowders modified with catechol and caffeic acid have over 50% higher hydrogen production rate than pristine ZnO, displaying steady hydrogen production under long-run working conditions.
T2  - International Journal of Hydrogen Energy
T1  - Interfacial charge transfer complexes between ZnO and benzene derivatives: Characterization and photocatalytic hydrogen production
VL  - 62
SP  - 628
EP  - 636
DO  - 10.1016/j.ijhydene.2024.03.075
ER  - 

@article{
author = "Dukić, Miljana and Sredojević, Dušan and Férová, Marta and Slovak, Vaclav and Lončarević, Davor and Dostanić, Jasmina and Šalipur, Hristina and Lazić, Vesna and Nedeljković, Jovan",
year = "2024",
abstract = "The interfacial charge transfer (ICT) complex formation is a simple procedure to bring optical absorption of widebandgap oxide materials in the visible spectral range, crucial for enhancing their use in photo-driven reactions. The optical absorption of the prepared ICT complexes between ZnO and five different colorless benzene derivatives is red-shifted compared to pristine ZnO nanopowder. The density functional theory (DFT) calculations provided realistic energy level alignment in hybrid systems. Also, the DFT-calculated infrared spectra support the binding structures derived based on experimental measurements of free and adsorbed ligands onto ZnO surfaces. The photocatalytic performance of prepared hybrids was evaluated using photocatalytic hydrogen generation in the water-splitting reaction. The ZnO nanopowders modified with catechol and caffeic acid have over 50% higher hydrogen production rate than pristine ZnO, displaying steady hydrogen production under long-run working conditions.",
journal = "International Journal of Hydrogen Energy",
title = "Interfacial charge transfer complexes between ZnO and benzene derivatives: Characterization and photocatalytic hydrogen production",
volume = "62",
pages = "628-636",
doi = "10.1016/j.ijhydene.2024.03.075"
}

Dukić, M., Sredojević, D., Férová, M., Slovak, V., Lončarević, D., Dostanić, J., Šalipur, H., Lazić, V.,& Nedeljković, J.. (2024). Interfacial charge transfer complexes between ZnO and benzene derivatives: Characterization and photocatalytic hydrogen production. in International Journal of Hydrogen Energy, 62, 628-636.
https://doi.org/10.1016/j.ijhydene.2024.03.075

Dukić M, Sredojević D, Férová M, Slovak V, Lončarević D, Dostanić J, Šalipur H, Lazić V, Nedeljković J. Interfacial charge transfer complexes between ZnO and benzene derivatives: Characterization and photocatalytic hydrogen production. in International Journal of Hydrogen Energy. 2024;62:628-636.
doi:10.1016/j.ijhydene.2024.03.075 .

Dukić, Miljana, Sredojević, Dušan, Férová, Marta, Slovak, Vaclav, Lončarević, Davor, Dostanić, Jasmina, Šalipur, Hristina, Lazić, Vesna, Nedeljković, Jovan, "Interfacial charge transfer complexes between ZnO and benzene derivatives: Characterization and photocatalytic hydrogen production" in International Journal of Hydrogen Energy, 62 (2024):628-636,
https://doi.org/10.1016/j.ijhydene.2024.03.075 . .