Issue 7, 2018

Photoinduced electron transfer in a molecular dyad by nanosecond pump–pump–probe spectroscopy

Abstract

The design of robust and inexpensive molecular photocatalysts for the conversion of abundant stable molecules like H2O and CO2 into an energetic carrier is one of the major fundamental questions for scientists nowadays. The outstanding challenge is to couple single photoinduced charge separation events with the sequential accumulation of redox equivalents at the catalytic unit for performing multielectronic catalytic reactions. Herein, double excitation by nanosecond pump–pump–probe experiments was used to interrogate the photoinduced charge transfer and charge accumulation on a molecular dyad composed of a porphyrin chromophore and a ruthenium-based catalyst in the presence of a reversible electron acceptor. An accumulative charge transfer state is unattainable because of rapid reverse electron transfer to the photosensitizer upon the second excitation and the low driving force of the forward photodriven electron transfer reaction. Such a method allows the fundamental understanding of the relaxation mechanism after two sequential photon absorptions, deciphering the undesired electron transfer reactions that limit the charge accumulation efficiency. This study is a step toward the improvement of synthetic strategies of molecular photocatalysts for light-induced charge accumulation and more generally, for solar energy conversion.

Graphical abstract: Photoinduced electron transfer in a molecular dyad by nanosecond pump–pump–probe spectroscopy

Supplementary files

Article information

Article type
Paper
Submitted
30 Қаң. 2018
Accepted
12 Мам. 2018
First published
14 Мам. 2018

Photochem. Photobiol. Sci., 2018,17, 903-909

Photoinduced electron transfer in a molecular dyad by nanosecond pump–pump–probe spectroscopy

M.-H. Ha-Thi, V.-T. Pham, T. Pino, V. Maslova, A. Quaranta, C. Lefumeux, W. Leibl and A. Aukauloo, Photochem. Photobiol. Sci., 2018, 17, 903 DOI: 10.1039/C8PP00048D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements