Issue 15, 2015

Stokes shift/emission efficiency trade-off in donor–acceptor perylenemonoimides for luminescent solar concentrators

Abstract

Perylenediimides (PDIs) are among the best performing organic luminescent materials, both in terms of emission efficiency and chemical and photochemical stability because of their rigid, symmetric and planar structure; however, they exhibit very small Stokes shifts. The sizeable reabsorption of the emitted light limits the performances of perylenediimides in imaging applications and luminescent solar concentrators. Perylenemonoimides (PMIs) having an electron donating substituent in one of the free peri positions feature larger Stokes shift values while retaining high chemical stability. The selection of the most appropriate donor, both in terms of electron donating capability and steric demand, boosts emission efficiency and limits reabsorption losses. The synthesis, optical spectroscopy, molecular orbital computations, UPS, electrochemical, spectroelectrochemical, and multinuclear NMR investigation of a series of PMI derivatives functionalized with donors having different electronic characteristics and steric demands are discussed. Results are relevant for the fabrication of single layer plastic luminescent solar concentrators (LSC).

Graphical abstract: Stokes shift/emission efficiency trade-off in donor–acceptor perylenemonoimides for luminescent solar concentrators

Supplementary files

Article information

Article type
Paper
Submitted
11 Feb 2015
Accepted
20 Feb 2015
First published
20 Feb 2015

J. Mater. Chem. A, 2015,3, 8045-8054

Author version available

Stokes shift/emission efficiency trade-off in donor–acceptor perylenemonoimides for luminescent solar concentrators

R. Turrisi, A. Sanguineti, M. Sassi, B. Savoie, A. Takai, G. E. Patriarca, M. M. Salamone, R. Ruffo, G. Vaccaro, F. Meinardi, T. J. Marks, A. Facchetti and L. Beverina, J. Mater. Chem. A, 2015, 3, 8045 DOI: 10.1039/C5TA01134E

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.

Social activity

Spotlight

Advertisements