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T-Shaped-N-Doped Polycyclic Aromatic Hydrocarbons: A New Concept of Dopant-Free Organic Hole-Transporting Materials for Perovskite Solar Cells.

Authors :
Wagner J
Chavan RD
Kruszyńska J
Ans M
Mahapatra A
Mrkyvkova N
Siffalovic P
Yadav P
Ebic M
Akin S
Kubas A
Lindner M
Prochowicz D
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2024 Nov 18. Date of Electronic Publication: 2024 Nov 18.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Although metal halide perovskites are positioned as the most powerful light-harvesting materials for sustainable energy conversion, there is a need for a thorough understanding of molecular design principles that would guide better engineering of organic hole-transporting materials, which are vital for boosting the performance and stability of perovskite solar cells. To address this formidable challenge, here, we developed a new design strategy based on the curved N-doped polycyclic aromatic hydrocarbon merged with T-shaped phenazines being decorated with (phenyl)-di- p -methoxyphenylamine (OMeTAD)─N-PAH23/24 and -3,6-ditertbutyl carbazole (TBCz)─N-PAH25/26. As N-PAH23/24 exhibited satisfying thermal stability, the comparative studies performed with various experimental and simulation methods revealed a pronounced correlation between the depth of the central cyclazine core and the form of the T-shape units. This proved to be a crucial factor in controlling their π-π intermolecular interaction as well as self-assembly behavior with the perovskite layer, leading to enhanced humidity resistance, operational stability, and a maximum power conversion efficiency of 20.39% denoted for N-PAH23, which is superior to the benchmarked device with doped spiro-OMeTAD (19.23%). These studies not only resulted in optimized stability and device performance but also opened a conceptually new chemical space in the photovoltaic technology.

Details

Language :
English
ISSN :
1944-8252
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
39557578
Full Text :
https://doi.org/10.1021/acsami.4c18636