% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Wu:1046019,
author = {Wu, Jianchang and Zhang, Jiyun and Wang, Luyao and
Jakšić, Jovana and Barabash, Anastasia and Veljković,
Dušan and Bornschlegl, Andreas J. and Jovanov, Vladislav
and Lahn, Leopold and Kasian, Olga and Pérez-Ojeda, M.
Eugenia and Götz, Klaus and Unruh, Tobias and Li, Chaohui
and Peng, Zijian and Wang, Yunuo and Hauch, Jens and Deng,
Lin-Long and Maslak, Veselin and Mitrović, Aleksandra and
Li, Gang and Brabec, Christoph},
title = {{D}iastereomeric {F}ullerene {C}omposite {E}ngineering for
{E}nhanced {P}erovskite {S}olar {C}ells},
journal = {Journal of the American Chemical Society},
volume = {147},
number = {35},
issn = {0002-7863},
address = {Washington, DC},
publisher = {ACS Publications},
reportid = {FZJ-2025-03659},
pages = {32045 - 32053},
year = {2025},
abstract = {Achieving high performance and long-term stability in
perovskite solar cells (PSCs) typically requires the use of
surface passivation layers to suppress the interfacial
defects. However, these additional passivation agents often
introduce chemical and structural instabilities, limiting
the device lifetime. Here, we present a molecular
engineering strategy utilizing a chiral series of
C60-Furan-Sugar (CFS) fullerene derivatives blended with
[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) to modify
the electron transport layer (ETL). The incorporation of
CFSs significantly enhances the electron mobility and
dielectric constant of the ETL, while their intrinsic
passivation functionality effectively passivates perovskite
surface defects. As a result, PSCs employing PCBM:CFS-RS
blends achieve a power conversion efficiency (PCE) of
$25.81\%$ without the use of additional passivation layers
and retain $95\%$ of their initial performance after 1000 h
of aging. Notably, CFS-RS is a chiral molecule bearing a
side chain with R/S configurational isomers, which
facilitates interfacial compatibility and contributes to the
enhanced device performance. This work demonstrates that
tuning the orientation of polar substituents in fullerene
side chains can effectively influence the optoelectronic
properties of the blended films, thereby simultaneously
enhancing both efficiency and stability in PSCs.},
cin = {IET-2},
ddc = {540},
cid = {I:(DE-Juel1)IET-2-20140314},
pnm = {1213 - Cell Design and Development (POF4-121)},
pid = {G:(DE-HGF)POF4-1213},
typ = {PUB:(DE-HGF)16},
pubmed = {40839343},
UT = {WOS:001555400300001},
doi = {10.1021/jacs.5c10340},
url = {https://juser.fz-juelich.de/record/1046019},
}