Study of Photoinduced Electron Transfer Process in Ruthenium Complex Modified Zinc Oxide Nanoparticles by Ultrafast Time-Resolved Transient Absorption Spectroscopy

We report the preparation of ruthenium complex functionalized zinc oxide nanoparticles and the studies of the photophysical properties by ultrafast time-resolved transient absorption spectroscopy. Diazonium group was used as the anchoring unit on ZnO surface and covalent linkage was formed between t...

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Veröffentlicht in:Journal of inorganic and organometallic polymers and materials 2017-11, Vol.27 (Suppl 1), p.39-47
Hauptverfasser: Xiong, Wenjuan, Yu, Lihong, Shi, Haiting, Phillips, David L., Chan, Wai Kin
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container_issue Suppl 1
container_start_page 39
container_title Journal of inorganic and organometallic polymers and materials
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creator Xiong, Wenjuan
Yu, Lihong
Shi, Haiting
Phillips, David L.
Chan, Wai Kin
description We report the preparation of ruthenium complex functionalized zinc oxide nanoparticles and the studies of the photophysical properties by ultrafast time-resolved transient absorption spectroscopy. Diazonium group was used as the anchoring unit on ZnO surface and covalent linkage was formed between the ruthenium complex and ZnO upon UV irradiation. The morphological and electron transfer properties of the ruthenium complex modified ZnO were studied. XPS and EDX results confirmed the presence of covalent linkage. The charge generation and the transport dynamics of this light harvesting system were probed by ultrafast transient absorption (TA) spectroscopy. No positive TA absorption band was observed, which suggested an ultrafast direct electron injection from the singlet 1 MLCT excited state of the ruthenium complex to the conduction band of ZnO without going via the triplet 3 MLCT excited state. The time constants for the ground states bleaching of the complex modified ZnO are 8.1 and 167 ps, both of which are shorter than those of the pure ruthenium complex (21.7 and 360 ps). This further suggests a strong electronic coupling between the ruthenium complex and ZnO.
doi_str_mv 10.1007/s10904-017-0522-z
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Diazonium group was used as the anchoring unit on ZnO surface and covalent linkage was formed between the ruthenium complex and ZnO upon UV irradiation. The morphological and electron transfer properties of the ruthenium complex modified ZnO were studied. XPS and EDX results confirmed the presence of covalent linkage. The charge generation and the transport dynamics of this light harvesting system were probed by ultrafast transient absorption (TA) spectroscopy. No positive TA absorption band was observed, which suggested an ultrafast direct electron injection from the singlet 1 MLCT excited state of the ruthenium complex to the conduction band of ZnO without going via the triplet 3 MLCT excited state. The time constants for the ground states bleaching of the complex modified ZnO are 8.1 and 167 ps, both of which are shorter than those of the pure ruthenium complex (21.7 and 360 ps). This further suggests a strong electronic coupling between the ruthenium complex and ZnO.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10904-017-0522-z</doi><tpages>9</tpages></addata></record>
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subjects Absorption spectra
Absorption spectroscopy
Anchoring
Bleaching
Charge transport
Chemistry
Chemistry and Materials Science
Conduction bands
Electron transfer
Electrons
Inorganic Chemistry
Nanoparticles
Organic Chemistry
Polymer Sciences
Ruthenium
Spectrum analysis
Zinc oxide
Zinc oxides
title Study of Photoinduced Electron Transfer Process in Ruthenium Complex Modified Zinc Oxide Nanoparticles by Ultrafast Time-Resolved Transient Absorption Spectroscopy
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