Achieving high performance organic solar cells with a closer π-π distance in branched alkyl-chain acceptors
Side-chain functional groups have been shown to not only ensure solubility but also influence molecular packing behavior, and side-chain modification is an important strategy in the optimization of photovoltaic performance. Instead of focusing on the size of the alkyl side chains, we have investigat...
Saved in:
Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 11; no. 17; pp. 9538 - 9545 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
02.05.2023
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Side-chain functional groups have been shown to not only ensure solubility but also influence molecular packing behavior, and side-chain modification is an important strategy in the optimization of photovoltaic performance. Instead of focusing on the size of the alkyl side chains, we have investigated the influence of side-chain configurations on the properties of acceptors and organic solar cells (OSCs). Two acceptor molecules,
BTIC-TCl-
b
and
BTIC-TCl-
l
were designed by changing the linear configuration of alkyl chain substituents on thiophene rings to a branched structure. The results show that the branched configuration of the side-chain can significantly improve the planarity and reduce the π π distances, leading to a more compact 3D-network structure. With the polymer donor PBDB-TF, an outstanding power conversion efficiency (PCE) of 16.17% was achieved by
BTIC-TCl-
b
, which is significantly higher than that found with
BTIC-TCl-
l
. Our study offers new insights for side-chain modification, regulation of the aggregation state, and optimization of photovoltaic performance.
This study describes a strategy for improving organic photovoltaic materials performance by adjusting the packing mode with a branched alkyl-chain,
BTIC-TCl-
b
. This modification significantly reduces the π-π distance and boosts the power conversion efficiency up to 16.71%. |
---|---|
Bibliography: | Electronic supplementary information (ESI) available. CCDC 2240316 For ESI and crystallographic data in CIF or other electronic format see DOI b BTIC-TCl- 2240315 and : l https://doi.org/10.1039/d3ta01049j |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d3ta01049j |