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@ARTICLE{Ji:1052856,
author = {Ji, Sang-Geun and Noh, Eunseo and Kim, Jongbeom and Duan,
Weiyuan and Kang, Bong Joo and Lee, Yonghui and Ding,
Kaining and Seok, Sang Il},
title = {{C}ooperative {D}ipole {E}ngineering {U}nlocks $92.8\%$
{S}hockley–{Q}ueisser {V}oltage {L}imit in
{W}ide-{B}andgap {P}erovskites for {T}andem {P}hotovoltaics},
journal = {ACS energy letters},
volume = {11},
number = {1},
issn = {2380-8195},
address = {Washington, DC},
publisher = {American Chemical Society},
reportid = {FZJ-2026-01212},
pages = {442 - 450},
year = {2026},
abstract = {Wide-bandgap (WBG) perovskite solar cells (PSCs, Eg ≃
1.67 eV) still suffer from pronounced open-circuit-voltage
(VOC) deficits. Here, we report a synergistic
surface-passivation strategy that coassembles a dipolar
quaternary-ammonium salt, acetylcholine chloride (ACCl),
with an electron-rich long-chain alkylammonium halide,
n-octylammonium iodide (OAI). A mixed ACCl:OAI treatment
reconstructs the perovskite surface, lowers surface-trap
density, and aligns the valence band with the hole-transport
layer. Consequently, the champion WBG PSC delivers VOC =
1.29 V, JSC = 20.0 mA cm–2, FF = $82.8\%,$ and PCE =
$21.27\%,$ corresponding to $92.8\%$ of the
Shockley–Queisser voltage limit. When integrated as the
top absorber in a monolithic n-i-p perovskite/p-type Si
tandem, the passivated WBG cell contributed to a PCE of
$26.8\%$ with a VOC of 1.91 V. These results reveal that
cooperative defect passivation and energy-level engineering
are both essential to unlock the full voltage potential of
WBG perovskites.},
cin = {IMD-3},
ddc = {333.7},
cid = {I:(DE-Juel1)IMD-3-20101013},
pnm = {1213 - Cell Design and Development (POF4-121)},
pid = {G:(DE-HGF)POF4-1213},
typ = {PUB:(DE-HGF)16},
UT = {WOS:001644774500001},
doi = {10.1021/acsenergylett.5c02738},
url = {https://juser.fz-juelich.de/record/1052856},
}