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Synergistic effect of oxygen vacancies and plasmonic Au nanoparticles in anatase-brookite TiO2 for efficient solar-driven 2-methylbenzimidazole and hydrogen Co-production. / Банеманн, Детлеф Вернер; El-Hosainy, Hamza M.; Esmat, Mohamed ; El-Sheikh, Said M.; Hakki, Amer; Doustkhah, Esmail ; Tahawy, Rafat ; Ismail, Adel A.; El-Bery, Haitham M. ; Jevasuwan, Wipakorn ; Fukata, Naoki ; Ide, Yusuke ; El-Kemary, Maged .

In: Solar Energy Materials and Solar Cells, Vol. 295, 113973, 15.01.2026.

Research output: Contribution to journalArticlepeer-review

Harvard

Банеманн, ДВ, El-Hosainy, HM, Esmat, M, El-Sheikh, SM, Hakki, A, Doustkhah, E, Tahawy, R, Ismail, AA, El-Bery, HM, Jevasuwan, W, Fukata, N, Ide, Y & El-Kemary, M 2026, 'Synergistic effect of oxygen vacancies and plasmonic Au nanoparticles in anatase-brookite TiO2 for efficient solar-driven 2-methylbenzimidazole and hydrogen Co-production', Solar Energy Materials and Solar Cells, vol. 295, 113973. https://doi.org/10.1016/j.solmat.2025.113973

APA

Банеманн, Д. В., El-Hosainy, H. M., Esmat, M., El-Sheikh, S. M., Hakki, A., Doustkhah, E., Tahawy, R., Ismail, A. A., El-Bery, H. M., Jevasuwan, W., Fukata, N., Ide, Y., & El-Kemary, M. (2026). Synergistic effect of oxygen vacancies and plasmonic Au nanoparticles in anatase-brookite TiO2 for efficient solar-driven 2-methylbenzimidazole and hydrogen Co-production. Solar Energy Materials and Solar Cells, 295, [113973]. https://doi.org/10.1016/j.solmat.2025.113973

Vancouver

Банеманн ДВ, El-Hosainy HM, Esmat M, El-Sheikh SM, Hakki A, Doustkhah E et al. Synergistic effect of oxygen vacancies and plasmonic Au nanoparticles in anatase-brookite TiO2 for efficient solar-driven 2-methylbenzimidazole and hydrogen Co-production. Solar Energy Materials and Solar Cells. 2026 Jan 15;295. 113973. https://doi.org/10.1016/j.solmat.2025.113973

Author

Банеманн, Детлеф Вернер ; El-Hosainy, Hamza M. ; Esmat, Mohamed ; El-Sheikh, Said M. ; Hakki, Amer ; Doustkhah, Esmail ; Tahawy, Rafat ; Ismail, Adel A. ; El-Bery, Haitham M. ; Jevasuwan, Wipakorn ; Fukata, Naoki ; Ide, Yusuke ; El-Kemary, Maged . / Synergistic effect of oxygen vacancies and plasmonic Au nanoparticles in anatase-brookite TiO2 for efficient solar-driven 2-methylbenzimidazole and hydrogen Co-production. In: Solar Energy Materials and Solar Cells. 2026 ; Vol. 295.

BibTeX

@article{3d5df2ec89a941118f7c855ab00d4086,
title = "Synergistic effect of oxygen vacancies and plasmonic Au nanoparticles in anatase-brookite TiO2 for efficient solar-driven 2-methylbenzimidazole and hydrogen Co-production",
abstract = "In this study, TiO2 heterostructures with anatase and brookite phases, as well as oxygen vacancies, were synthesized using a modified sol-gel method and a heat treatment process. Subsequently, Au nanoparticles (Au NPs) were deposited onto TiO2 through photo-deposition. Detailed structural and chemical analyses verified the successful creation of anatase-brookite phases, efficient incorporation of Au NPs, and strong interactions between the Au NPs and the oxygen vacancies on the TiO2 surface. Spectroscopic analysis revealed the presence of localized surface plasmon resonance (LSPR) from the Au NPs, indicating enhanced light absorption properties. The photocatalytic efficiency of the Au-TiO2 composites was evaluated under solar light irradiation for the conversion of o-phenylenediamine to 2-methylbenzimidazole and hydrogen (H2) production. Notably, the 2 %Au-TiO2 catalyst achieved a remarkable 99.7 % conversion rate of o phenylenediamine, with 90 % selectivity toward 2-methylbenzimidazole and the highest H2 production rate within 9 h, significantly outperforming 2 % Au/UV100 (commercial TiO2), 2 % Pd/TiO2, and pure TiO2. This enhanced photocatalytic performance is attributed to increased surface acidity (from both Lewis and Br{\o}nsted acid sites), efficient charge separation, increased photocurrent, reduced charge transfer resistance and the synergistic interactions between Au NPs and surface oxygen vacancies in TiO2. These findings highlight the potential of Au-TiO2 heterostructures for advancing solar-driven catalytic applications, promoting both clean energy generation and efficient organictransformations.",
keywords = "Oxygen vacancies, Au NPs, Anatase-brookite, Solar-driven, Hydrogen, 2-methylbenzimidazole, 2-methylbenzimidazole, Anatase-brookite, Au NPs, Hydrogen, Oxygen vacancies, Solar-driven",
author = "Банеманн, {Детлеф Вернер} and El-Hosainy, {Hamza M.} and Mohamed Esmat and El-Sheikh, {Said M.} and Amer Hakki and Esmail Doustkhah and Rafat Tahawy and Ismail, {Adel A.} and El-Bery, {Haitham M.} and Wipakorn Jevasuwan and Naoki Fukata and Yusuke Ide and Maged El-Kemary",
year = "2026",
month = jan,
day = "15",
doi = "10.1016/j.solmat.2025.113973",
language = "English",
volume = "295",
journal = "Solar Energy Materials and Solar Cells",
issn = "0927-0248",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Synergistic effect of oxygen vacancies and plasmonic Au nanoparticles in anatase-brookite TiO2 for efficient solar-driven 2-methylbenzimidazole and hydrogen Co-production

AU - Банеманн, Детлеф Вернер

AU - El-Hosainy, Hamza M.

AU - Esmat, Mohamed

AU - El-Sheikh, Said M.

AU - Hakki, Amer

AU - Doustkhah, Esmail

AU - Tahawy, Rafat

AU - Ismail, Adel A.

AU - El-Bery, Haitham M.

AU - Jevasuwan, Wipakorn

AU - Fukata, Naoki

AU - Ide, Yusuke

AU - El-Kemary, Maged

PY - 2026/1/15

Y1 - 2026/1/15

N2 - In this study, TiO2 heterostructures with anatase and brookite phases, as well as oxygen vacancies, were synthesized using a modified sol-gel method and a heat treatment process. Subsequently, Au nanoparticles (Au NPs) were deposited onto TiO2 through photo-deposition. Detailed structural and chemical analyses verified the successful creation of anatase-brookite phases, efficient incorporation of Au NPs, and strong interactions between the Au NPs and the oxygen vacancies on the TiO2 surface. Spectroscopic analysis revealed the presence of localized surface plasmon resonance (LSPR) from the Au NPs, indicating enhanced light absorption properties. The photocatalytic efficiency of the Au-TiO2 composites was evaluated under solar light irradiation for the conversion of o-phenylenediamine to 2-methylbenzimidazole and hydrogen (H2) production. Notably, the 2 %Au-TiO2 catalyst achieved a remarkable 99.7 % conversion rate of o phenylenediamine, with 90 % selectivity toward 2-methylbenzimidazole and the highest H2 production rate within 9 h, significantly outperforming 2 % Au/UV100 (commercial TiO2), 2 % Pd/TiO2, and pure TiO2. This enhanced photocatalytic performance is attributed to increased surface acidity (from both Lewis and Brønsted acid sites), efficient charge separation, increased photocurrent, reduced charge transfer resistance and the synergistic interactions between Au NPs and surface oxygen vacancies in TiO2. These findings highlight the potential of Au-TiO2 heterostructures for advancing solar-driven catalytic applications, promoting both clean energy generation and efficient organictransformations.

AB - In this study, TiO2 heterostructures with anatase and brookite phases, as well as oxygen vacancies, were synthesized using a modified sol-gel method and a heat treatment process. Subsequently, Au nanoparticles (Au NPs) were deposited onto TiO2 through photo-deposition. Detailed structural and chemical analyses verified the successful creation of anatase-brookite phases, efficient incorporation of Au NPs, and strong interactions between the Au NPs and the oxygen vacancies on the TiO2 surface. Spectroscopic analysis revealed the presence of localized surface plasmon resonance (LSPR) from the Au NPs, indicating enhanced light absorption properties. The photocatalytic efficiency of the Au-TiO2 composites was evaluated under solar light irradiation for the conversion of o-phenylenediamine to 2-methylbenzimidazole and hydrogen (H2) production. Notably, the 2 %Au-TiO2 catalyst achieved a remarkable 99.7 % conversion rate of o phenylenediamine, with 90 % selectivity toward 2-methylbenzimidazole and the highest H2 production rate within 9 h, significantly outperforming 2 % Au/UV100 (commercial TiO2), 2 % Pd/TiO2, and pure TiO2. This enhanced photocatalytic performance is attributed to increased surface acidity (from both Lewis and Brønsted acid sites), efficient charge separation, increased photocurrent, reduced charge transfer resistance and the synergistic interactions between Au NPs and surface oxygen vacancies in TiO2. These findings highlight the potential of Au-TiO2 heterostructures for advancing solar-driven catalytic applications, promoting both clean energy generation and efficient organictransformations.

KW - Oxygen vacancies

KW - Au NPs

KW - Anatase-brookite

KW - Solar-driven

KW - Hydrogen

KW - 2-methylbenzimidazole

KW - 2-methylbenzimidazole

KW - Anatase-brookite

KW - Au NPs

KW - Hydrogen

KW - Oxygen vacancies

KW - Solar-driven

UR - https://www.mendeley.com/catalogue/2a6bfa8f-929f-3e28-b2a3-40152c7f64b7/

U2 - 10.1016/j.solmat.2025.113973

DO - 10.1016/j.solmat.2025.113973

M3 - Article

VL - 295

JO - Solar Energy Materials and Solar Cells

JF - Solar Energy Materials and Solar Cells

SN - 0927-0248

M1 - 113973

ER -

ID: 143366098