Issue 66, 2016

Synthesis and characterization of 2,2′-bithiophene end-capped dihexyloxy phenylene pentamer and its application in a solution-processed organic ultraviolet photodetector

Abstract

In this work a new solution processable small organic material, namely 2,2′-bithiophene end-capped dihexyloxy phenylene pentamer (BHBT2) was synthesized, characterized and applied in the fabrication of an organic ultraviolet photodetector. The material was synthesized via Williamson etherification, bromination and Suzuki coupling. FTIR and NMR spectroscopies were recorded for BHBT2 along with its optical, thermal and electrochemical properties. Finally, BHBT2 was used as donor material to produce a solution-processed UV photodetector based on a BHBT2 : PC61BM organic active layer. Results showed that in forward biasing, the photodetector exhibited a photovoltaic effect with Jsc = 1.80 mA, Voc = 0.66 V, FF = 0.30 and PCE = 0.98%, while in reverse biasing, the photodetector exhibited a fast, reversible and stable response with the highest detectivity of 1.47 × 109 jones. The realization of efficient UV detection was attributed to the strong absorption of BHBT2 and PC61BM in the UV region. Hence, the BHBT2 pentamer coupled with PC61BM can be considered as a potential material to be applied in a solution-processed organic UV photodetector.

Graphical abstract: Synthesis and characterization of 2,2′-bithiophene end-capped dihexyloxy phenylene pentamer and its application in a solution-processed organic ultraviolet photodetector

Article information

Article type
Paper
Submitted
15 Jun 2016
Accepted
17 Jun 2016
First published
21 Jun 2016

RSC Adv., 2016,6, 61848-61859

Author version available

Synthesis and characterization of 2,2′-bithiophene end-capped dihexyloxy phenylene pentamer and its application in a solution-processed organic ultraviolet photodetector

L. W. Lim, C. H. Teh, R. Daik, N. M. Sarih, M. A. Mat Teridi, F. F. Muhammad and K. Sulaiman, RSC Adv., 2016, 6, 61848 DOI: 10.1039/C6RA15534K

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