TY - JOUR
T1 - Revealing the crystalline packing structure of Y6 in the active layer of organic solar cells
T2 - the critical role of solvent additives
AU - Xia, Xinxin
AU - Mei, Le
AU - He, Chengliang
AU - Chen, Zeng
AU - Yao, Nannan
AU - Qin, Minchao
AU - Sun, Rui
AU - Zhang, Zhenzhen
AU - Pan, Yuyu
AU - Xiao, Yiqun
AU - Lin, Yuze
AU - Min, Jie
AU - Zhang, Fengling
AU - Zhu, Haiming
AU - Bredas, Jean Luc
AU - Chen, Hongzheng
AU - Chen, Xian Kai
AU - Lu, Xinhui
N1 - Publisher Copyright:
© 2023 The Royal Society of Chemistry.
PY - 2023/9/26
Y1 - 2023/9/26
N2 - The bulk heterojunction (BHJ) morphology of photovoltaic materials is crucial to the fundamental optoelectronic properties of organic solar cells (OSCs). However, in the photoactive layer, the intrinsic crystalline packing structure of Y6, currently the hallmark molecule among Y-series non-fullerene acceptors (NFAs), has not been unambiguously determined. Here, employing grazing-incidence wide-angle X-ray scattering (GIWAXS), we managed to uncover the intrinsic crystalline packing structure of Y6 in the BHJ active layer of OSCs, which is found to be different from its single-crystal structure reported previously. Moreover, we find that solvent additive 1-chloronaphthalene (CN) can induce highly ordered packing of Y6 in BHJ thin films. With the help of atomistic molecular dynamics simulations, it is revealed that π-π interactions generally exist between naphthalene derivatives and IC terminals of Y6 analogues, which would essentially improve their long-range ordering. Our work reveals the intrinsic crystalline packing structure of Y6 in the BHJ active layer as well as its crystallization mechanism in thin films, thus providing direct correlations between this crystalline packing and the device characteristics and photophysical properties.
AB - The bulk heterojunction (BHJ) morphology of photovoltaic materials is crucial to the fundamental optoelectronic properties of organic solar cells (OSCs). However, in the photoactive layer, the intrinsic crystalline packing structure of Y6, currently the hallmark molecule among Y-series non-fullerene acceptors (NFAs), has not been unambiguously determined. Here, employing grazing-incidence wide-angle X-ray scattering (GIWAXS), we managed to uncover the intrinsic crystalline packing structure of Y6 in the BHJ active layer of OSCs, which is found to be different from its single-crystal structure reported previously. Moreover, we find that solvent additive 1-chloronaphthalene (CN) can induce highly ordered packing of Y6 in BHJ thin films. With the help of atomistic molecular dynamics simulations, it is revealed that π-π interactions generally exist between naphthalene derivatives and IC terminals of Y6 analogues, which would essentially improve their long-range ordering. Our work reveals the intrinsic crystalline packing structure of Y6 in the BHJ active layer as well as its crystallization mechanism in thin films, thus providing direct correlations between this crystalline packing and the device characteristics and photophysical properties.
UR - https://www.scopus.com/pages/publications/85174494384
UR - https://www.scopus.com/pages/publications/85174494384#tab=citedBy
U2 - 10.1039/d3ta05177c
DO - 10.1039/d3ta05177c
M3 - Article
AN - SCOPUS:85174494384
SN - 2050-7488
VL - 11
SP - 21895
EP - 21907
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 40
ER -