Issue 29, 2017

A new n-type semiconducting molecule with an asymmetric indenothiophene core for a high-performing non-fullerene type organic solar cell

Abstract

Herein, a new asymmetric n-type semiconducting molecule (PhITBD) with an indenothiophene core was designed, synthesized using tethering 2-(benzo[c][1,2,5]-thiadiazol-4-ylmethylene)-malononitrile (BM) as terminal groups, and applied to polymer solar cells (PSCs). The PSCs with asymmetric PhITBD displayed improved power conversion efficiencies (PCE) of 6.57% as compared to those with the symmetric molecule IDT-2BM. The higher PCE value of the PhITBD-based PSC was mainly attributed to the enhanced photovoltaic properties, the Voc, Jsc, FF induced by complementary light absorption (550–600 nm range), morphological improvement, and balanced charge carrier transport in the active layer. Due to the effective morphological control and absorption enhancement, asymmetric structured n-type-conjugated molecules are potential candidates for improving the performance of bulk heterojunction non-fullerene type PSCs.

Graphical abstract: A new n-type semiconducting molecule with an asymmetric indenothiophene core for a high-performing non-fullerene type organic solar cell

Supplementary files

Article information

Article type
Paper
Submitted
15 Feb 2017
Accepted
29 May 2017
First published
30 May 2017

J. Mater. Chem. C, 2017,5, 7182-7190

A new n-type semiconducting molecule with an asymmetric indenothiophene core for a high-performing non-fullerene type organic solar cell

Y. Un Kim, G. Eun Park, S. Choi, D. Hee Lee, M. Ju Cho and D. H. Choi, J. Mater. Chem. C, 2017, 5, 7182 DOI: 10.1039/C7TC00706J

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