Issue 25, 2020

New cyclic and acyclic imidazole-based sensitizers for achieving highly efficient photoanodes for dye-sensitized solar cells by a potential-assisted method

Abstract

A series of systematically tailored aryl acyclic (biphenyl, dye 1 and 2), cyclic (phenanthrene, dye 3 and 4) and methyl-substituted (dye 5) imidazole derivatives were synthesized and characterized for application in dye-sensitized solar cells (DSSCs). The anisole ancillary donor was attached to the –NH position in the imidazole center to obtain dyes 2 and 4. Cyclic voltammetry and UV-visible studies of all the dyes indicate their suitability for DSSC applications. Among the as-synthesized dyes, dye 4 with a phenanthrene donor and anisole ancillary donor showed the highest power conversion efficiency (PCE) of 7.16% (JSC = 13.07 mA cm−2, VOC = 0.831 V, FF = 0.659). Dye 2 displayed the highest electron lifetime in the conduction band of the photoanode; hence, the open circuit voltage of the DSSC based on dye 2 was the highest among the studied dyes (0.865 V). By using a novel potential-assisted dye staining process, the dye loading on the photoanode was enhanced by 18% in 1 h, which in turn enhanced the PCE to 8.10%.

Graphical abstract: New cyclic and acyclic imidazole-based sensitizers for achieving highly efficient photoanodes for dye-sensitized solar cells by a potential-assisted method

Supplementary files

Article information

Article type
Paper
Submitted
11 Jan 2020
Accepted
30 Mar 2020
First published
31 Mar 2020

New J. Chem., 2020,44, 10207-10219

New cyclic and acyclic imidazole-based sensitizers for achieving highly efficient photoanodes for dye-sensitized solar cells by a potential-assisted method

J. Sivanadanam, I. S. Aidhen and K. Ramanujam, New J. Chem., 2020, 44, 10207 DOI: 10.1039/D0NJ00137F

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