Press Release

Visualizing a photosensitizer complex in action

July 17, 2012

High Energy Accelerator Research Organization (KEK)
Tokyo Institute of Technology
Japan Science and Technology Agency

A research group comprised of Dr. Tokushi Sato, Professor Shunsuke Nozawa, and Professor Shin-ichi Adachi of the Institute of Materials Structure Science at KEK, Professor Hiroshi Fujii of the Institute of Molecular Science at the National Institutes of Natural Sciences, and Professor Shin-ya Koshihara of the Tokyo Institute of Technology successfully visualized electron transfer process in a photosensitizer molecule, which is the fundamental process in solar cells and photocatalysts, at a temporal resolution of 100 ps.

Improvements of the efficiency and the lifetime of solar cells and photocatalysts are necessary to solve energy and environmental problems. Understanding the electron motion due to light irradiation, which is common to all these devices, is very important in realizing such developments. The photoexcitation mechanism in Ruthenium(II)-tris-2,2′-bipyridine [RuII(bpy)3]2+, used in solar cells, was observed in this research. The absorption band wavelengths (400–500 nm) for charge transfer from metal to ligand (MLCT) in this material are close to the maximum intensity wavelengths of the Sun, and therefore, efficient charge separation induced by solar light occurs in this material. Therefore, it is frequently used in investigating photochemical reactions.

The research group used time-resolved X-ray absorption spectroscopy at the Photon Factory at KEK to observe the changes in the electronic state and the molecular structure. The observation of the electronic state before and after irradiation showed that there is electron transfer from ruthenium to bipyridine ligand within 100 ps, resulting in a change in the oxidation state of ruthenium from II to III. The bipyridine ligand moves toward the ruthenium atom by 0.04 Å with the charge transfer and a structurally distorted state exists in the photoexcited state .

This research elucidated the details of electron transfer, which is a fundamental process in solar cells and photocatalysts, and the change in molecular structure that accompanies electron transfer. This is important information in designing solar cells and photocatalysts, and it is expected to result in advances such as further improvements in device efficiency.

This work was supported by PRESTO, Japan Science and Technology Agency and by a Grant for Basic Science Research Projects from The Sumitomo Foundation.

Publication
“Coordination and Electronic Structure of Ruthenium(II)-tris-2,2’-Bipyridine in the Triplet Metal-to-Ligand Charge Transfer Excited State Observed by Picosecond Time-Resolved Ru K-edge XAFS” The Journal of Physical Chemistry C, Vol. 116, No. 25(June 28, 2012). doi:10.1021/jp3038285.
Authors:T. Sato, S. Nozawa, A. Tomita, M. Hoshino, S. Koshihara, H. Fujii, S. Adachi

image

Fig. 1: Schematic of the change in structure with electron transfer
An electron transfers from the ruthenium atom (green), at the center of the figure, to one of the coordinated bipyridine ligand, and thereafter, the electron hops between bipyridine molecules.

Media Contact

[ for research ]
Tokushi Sato
Institute of Materials Structure Science, High Energy Accelerator Research Organization (KEK)
TEL: +81-29-879-6185
FAX: +81-29-879-6187
E-mail: tokushi.sato@kek.jp

Prof. Shin-ichi Adachi
Institute of Materials Structure Science, High Energy Accelerator Research Organization (KEK)
TEL: +81-29-879-6022
FAX: +81-29-864-3202
E-mail: shinichi.adachi@kek.jp

Prof. Shin-ya Koshihara
Department of Materials Science, Graduate School of Science and Engineering, Tokyo Institute of Technology
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E-mail: skoshi@cms.titech.ac.jp

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