Issue 40, 2023

Impact of substituent's position on the DSSC performances of new 1,1′-bis-(diphenylphosphino)ferrocene appended nickel(ii) methoxy cyanodithiolates

Abstract

Three new isomeric 1,1′-bis-(diphenylphosphino)ferrocene (dppf) appended nickel(II) dithiolates o-NiL, m-NiL and p-NiL (disodium 2-cyano-2-(2-methoxyphenyl)ethene-1,1-dithiolate (o-L), disodium 2-cyano-2-(3-methoxyphenyl)ethene-1,1-dithiolate (m-L) and disodium 2-cyano-2-(4-methoxyphenyl)ethene-1,1-dithiolate (p-L)) have been synthesized and characterized. The single X-ray analyses revealed that in all three complexes, nickel(II) adopts a distorted square planar geometry arising from the bidentate chelating coordination of two sulfur centers of the dithiolate ligand and two phosphorus centers of the dppf co-ligand. The distortion in geometry is because of the strained four membered NiS2C chelate ring formed from the dithiolate ligand as well as small variation in Ni–S and Ni–P bond lengths. The weak interactions existing in these newly synthesized sensitizers have been addressed with the help of Hirshfeld surface analysis. The electronic absorption spectra of all three compounds display absorption bands between ∼400–500 nm and ∼500–600 nm arising from the d–d transition of ferrocene and Ni(II), respectively. These compounds have been used as photo-sensitizers in dye sensitized solar cells (DSSCs). The experiments revealed that amongst all three sensitizer based DSSC set-ups, the assembly fabricated using p-NiL exhibited the best photovoltaic performance due to stronger electronic coupling between the sensitizer and the semiconductor resulting in enhanced electron injection with 3.40% efficiency (η) with a short circuit current (Jsc) of 7.10 mA cm−2, open circuit voltage (Voc) of −0.748 V and incident photon to current conversion efficiency of 63%. Also, the ageing experiment for the DSSC cell set-up fabricated using p-NiL revealed that after 700 h the set-up retained 93% of its efficiency which indicates that such a type of molecular system can be used as an apt sensitizer for DSSC fabrication.

Graphical abstract: Impact of substituent's position on the DSSC performances of new 1,1′-bis-(diphenylphosphino)ferrocene appended nickel(ii) methoxy cyanodithiolates

Supplementary files

Article information

Article type
Paper
Submitted
20 Jun 2023
Accepted
02 Sep 2023
First published
07 Sep 2023

CrystEngComm, 2023,25, 5660-5672

Impact of substituent's position on the DSSC performances of new 1,1′-bis-(diphenylphosphino)ferrocene appended nickel(II) methoxy cyanodithiolates

D. Srivastava, A. Kushwaha, G. Kociok-Köhn, S. W. Gosavi, R. Chauhan, M. Ashokkumar, A. Kumar and Mohd. Muddassir, CrystEngComm, 2023, 25, 5660 DOI: 10.1039/D3CE00621B

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