Multiple Pathways in the Triplet States Population for a Naphthalenediimide‐C60 Dyad

Author:

Ye Kaiyue1ORCID,Carbonera Donatella2ORCID,Liao Sheng3ORCID,Zhang Xue1ORCID,Chen Xi1ORCID,Xiao Xiao1ORCID,Zhao Jianzhang1ORCID,Shanmugam Muralidharan4ORCID,Li Mingde3ORCID,Barbon Antonio2ORCID

Affiliation:

1. State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials School of Chemical Engineering Dalian University of Technology 2 Ling Gong Road Dalian 116024 P. R. China

2. Department of Chemical Sciences University of Padova Via Marzolo 1 35134 Padova Italy

3. Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structure Materials of Guangdong Province Shantou University Shantou 515063 P. R. China

4. Manchester Institute of Biotechnology and Photon Science Institute University of Manchester 131 Princess St Manchester M1 7DN UK

Abstract

AbstractThe link of an antenna dye with an electron spin converter, in this case naphthalenediimide and C60, produces a system with a rich photophysics including the detection of more than one triplet state on the long timescale (tens of μs). Beside the use of optical spectroscopies in the ns and in the fs time scale, we used time‐resolved Electron Paramagnetic Resonance (TREPR) to study the system evolution following photoexcitation. TREPR keeps track of the formation path of the triplet states through specific spin polarization patterns observed in the spectra. The flexibility of the linker and solvent polarity play a role in favouring either electron transfer or energy transfer processes.

Funder

European Commission

National Natural Science Foundation of China

National Key Research and Development Program of China

Dalian University of Technology

Fundamental Research Funds for the Central Universities

Ministero degli Affari Esteri e della Cooperazione Internazionale

Publisher

Wiley

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