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Efficient Standalone Flexible Small Molecule Organic Solar Cell Devices: Structure-Performance Relation Among Tetracyanoquinodimethane Derivatives

[Image: see text] Currently, very few dicyano and tetracyanoquinodimethane (TCNQ) based molecules are utilized as active layers, sandwiched between the electron and hole transport layer in organic solar cell (OSC) devices. Nevertheless, simple mono- and disubstituted TCNQ derivatives as exclusively...

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Autores principales: Mohitkar, Anuradha, H, Renuka, Goel, Sanket, Jayanty, Subbalakshmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620877/
https://www.ncbi.nlm.nih.gov/pubmed/37929146
http://dx.doi.org/10.1021/acsomega.3c05939
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author Mohitkar, Anuradha
H, Renuka
Goel, Sanket
Jayanty, Subbalakshmi
author_facet Mohitkar, Anuradha
H, Renuka
Goel, Sanket
Jayanty, Subbalakshmi
author_sort Mohitkar, Anuradha
collection PubMed
description [Image: see text] Currently, very few dicyano and tetracyanoquinodimethane (TCNQ) based molecules are utilized as active layers, sandwiched between the electron and hole transport layer in organic solar cell (OSC) devices. Nevertheless, simple mono- and disubstituted TCNQ derivatives as exclusively active layers are yet unexplored and provide scope for further investigation. In this study, TCNQ derivatives with varying amine substituents, namely, AEPYDQ (1), BMEDDQ (2), MATBTCNQ (3), and MITATCNQ (4), were explored as efficient standalone, flexible, all small molecule OSC devices. Particularly, 1 resulted in the highest device efficiency of 11.75% with an aromatic amine, while 2 possessing an aliphatic amine showed the lowest power conversion efficiency (PCE; 2.12%). Notably, the short circuit current density (J(SC)) of device 1 increased from 2 mA/cm(2) in the dark to 9.12 mA/cm(2) under light, indicating a significant boost in the current generation. Further, 1 manifested more crystallinity than others. Interestingly, 4 exhibited a higher PCE (5.90%) than 3 (PCE is 2.58%), though 3 is disubstituted with an aromatic amine, probably attributed to the electron-withdrawing effects of the −CF(3) and −CN groups in 3 reducing the available π-electron density for stacking. Therefore, this study emphasizes crystallinity, significantly on the PCE, offering insights into the design of many such efficient OSCs.
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spelling pubmed-106208772023-11-03 Efficient Standalone Flexible Small Molecule Organic Solar Cell Devices: Structure-Performance Relation Among Tetracyanoquinodimethane Derivatives Mohitkar, Anuradha H, Renuka Goel, Sanket Jayanty, Subbalakshmi ACS Omega [Image: see text] Currently, very few dicyano and tetracyanoquinodimethane (TCNQ) based molecules are utilized as active layers, sandwiched between the electron and hole transport layer in organic solar cell (OSC) devices. Nevertheless, simple mono- and disubstituted TCNQ derivatives as exclusively active layers are yet unexplored and provide scope for further investigation. In this study, TCNQ derivatives with varying amine substituents, namely, AEPYDQ (1), BMEDDQ (2), MATBTCNQ (3), and MITATCNQ (4), were explored as efficient standalone, flexible, all small molecule OSC devices. Particularly, 1 resulted in the highest device efficiency of 11.75% with an aromatic amine, while 2 possessing an aliphatic amine showed the lowest power conversion efficiency (PCE; 2.12%). Notably, the short circuit current density (J(SC)) of device 1 increased from 2 mA/cm(2) in the dark to 9.12 mA/cm(2) under light, indicating a significant boost in the current generation. Further, 1 manifested more crystallinity than others. Interestingly, 4 exhibited a higher PCE (5.90%) than 3 (PCE is 2.58%), though 3 is disubstituted with an aromatic amine, probably attributed to the electron-withdrawing effects of the −CF(3) and −CN groups in 3 reducing the available π-electron density for stacking. Therefore, this study emphasizes crystallinity, significantly on the PCE, offering insights into the design of many such efficient OSCs. American Chemical Society 2023-10-22 /pmc/articles/PMC10620877/ /pubmed/37929146 http://dx.doi.org/10.1021/acsomega.3c05939 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Mohitkar, Anuradha
H, Renuka
Goel, Sanket
Jayanty, Subbalakshmi
Efficient Standalone Flexible Small Molecule Organic Solar Cell Devices: Structure-Performance Relation Among Tetracyanoquinodimethane Derivatives
title Efficient Standalone Flexible Small Molecule Organic Solar Cell Devices: Structure-Performance Relation Among Tetracyanoquinodimethane Derivatives
title_full Efficient Standalone Flexible Small Molecule Organic Solar Cell Devices: Structure-Performance Relation Among Tetracyanoquinodimethane Derivatives
title_fullStr Efficient Standalone Flexible Small Molecule Organic Solar Cell Devices: Structure-Performance Relation Among Tetracyanoquinodimethane Derivatives
title_full_unstemmed Efficient Standalone Flexible Small Molecule Organic Solar Cell Devices: Structure-Performance Relation Among Tetracyanoquinodimethane Derivatives
title_short Efficient Standalone Flexible Small Molecule Organic Solar Cell Devices: Structure-Performance Relation Among Tetracyanoquinodimethane Derivatives
title_sort efficient standalone flexible small molecule organic solar cell devices: structure-performance relation among tetracyanoquinodimethane derivatives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620877/
https://www.ncbi.nlm.nih.gov/pubmed/37929146
http://dx.doi.org/10.1021/acsomega.3c05939
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