TY - JOUR
T1 - Mitigation of Defect Formation at the NiOx/Perovskite Interface in p-i-n Perovskite Solar Cells
AU - Hajhemati, Javid
AU - Mallik, Nitin
AU - Dufoulon, Vincent
AU - Frégnaux, Mathieu
AU - Regaldo, Davide
AU - Coutancier, Damien
AU - Schneider, Nathanaelle
AU - Tondelier, Denis
AU - Desta, Derese
AU - Boyen, Hans Gerd
AU - Bonnassieux, Yvan
AU - Cacovich, Stefania
AU - Aureau, Damien
AU - Schulz, Philip
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society
PY - 2025/12/10
Y1 - 2025/12/10
N2 - Nickel oxide (NiOx) is widely utilized as an inorganic hole transport layer (HTL) in inverted metal halide perovskite (MHP) solar cells due to its high bandgap, transparency, stability, and scalability. However, its high surface reactivity and the presence of interfacial defects at the NiOx/MHP interface negatively impact the device performance. To address these issues, the community has explored ultraviolet ozone (UVO) post-treatment of NiOxand the use of organic molecules for surface passivation. Nevertheless, the individual effects of these processes and their influence on the bulk and surface characteristics of NiOx, as well as the NiOx/MHP interface, have not been thoroughly investigated and understood. This study based on photoemission analyses reveals that the UVO process increases the NiOxreactivity and introduces defects. We identify the nature of defect states at the interface of pristine and UVO-treated NiOxwith MHP and demonstrate that the implementation of MeO-2PACz (M2P) as an organic interlayer mitigates this issue. Additionally, we find that neither UVO treatment nor M2P molecule anchoring significantly impacts the bulk properties of NiOx.
AB - Nickel oxide (NiOx) is widely utilized as an inorganic hole transport layer (HTL) in inverted metal halide perovskite (MHP) solar cells due to its high bandgap, transparency, stability, and scalability. However, its high surface reactivity and the presence of interfacial defects at the NiOx/MHP interface negatively impact the device performance. To address these issues, the community has explored ultraviolet ozone (UVO) post-treatment of NiOxand the use of organic molecules for surface passivation. Nevertheless, the individual effects of these processes and their influence on the bulk and surface characteristics of NiOx, as well as the NiOx/MHP interface, have not been thoroughly investigated and understood. This study based on photoemission analyses reveals that the UVO process increases the NiOxreactivity and introduces defects. We identify the nature of defect states at the interface of pristine and UVO-treated NiOxwith MHP and demonstrate that the implementation of MeO-2PACz (M2P) as an organic interlayer mitigates this issue. Additionally, we find that neither UVO treatment nor M2P molecule anchoring significantly impacts the bulk properties of NiOx.
KW - ALD-NiO
KW - MeO-2PACz
KW - atomic layer deposition
KW - interface
KW - metal halide perovskite
KW - photoelectron spectroscopy
KW - ultraviolet ozone treatment
UR - https://www.scopus.com/pages/publications/105024381721
U2 - 10.1021/acsami.5c18456
DO - 10.1021/acsami.5c18456
M3 - Article
C2 - 41299879
AN - SCOPUS:105024381721
SN - 1944-8244
VL - 17
SP - 66683
EP - 66695
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 49
ER -