Enhanced Efficiency and Stability for the Inverted High‐Bandgap Perovskite Solar Cell via Bottom Passivation Strategy

The bottom perovskite with the hole transport layer (HTL) in inverted perovskite solar cells (PSCs) interface has received little attention due to challenges like interlayer dissolution during perovskite deposition. And voids at the perovskite/HTL interface can degrade cell performance. This work introduces a two‐dimensional (2D) perovskite layer between the perovskite and poly (N, N′‐bis‐4‐butylphenyl‐N, N′‐bisphenyl) benzidine (Poly‐TPD) HTL using a mixed solution of 4‐methylphenethylammonium chloride (4M‐PEA‐Cl), methylammonium iodide (MA‐I), and Poly(9,9‐bis(3′‐(N,N‐dimethyl)‐N‐ethylammoinium‐propyl‐2,7‐fluorene)‐alt‐2,7‐(9,9‐dioctylfluorene))dibromide (PFN‐Br). The amine functional groups in the organic salts improved HTL wettability, resulting in a void‐free interface. 4M‐PEA‐Cl, with its strong electron‐withdrawing benzene ring, outperformed other amine‐containing salts in passivating undercoordinated Pb 2+ ions. Incorporating this hybrid passivation layer in PSCs resulted in a 1.8% absolute increase in power conversion efficiency (PCE) to 19.1% with 1.68 eV perovskite bandgap. Additionally, the passivated PSCs demonstrated enhanced operational stability, retaining 91% of their initial efficiency after 800 hours of continuous 1‐sun illumination, compared to 84.7% for the control sample.

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Publication Details

Journal
Solar RRL
Published
2024-08-29
DOI
https://doi.org/10.1002/solr.202400391
Citations
7
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
1.46

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article

Enhanced Efficiency and Stability for the Inverted High‐Bandgap Perovskite Solar Cell via Bottom Passivation Strategy

Anh Dinh Bui, Grace Dansoa Tabi, Olivier Lee Cheong Lem, The Duong et al.
7 citations
Solar RRL
Perovskite Materials and Applications
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article

Enhanced Efficiency and Stability for the Inverted High‐Bandgap Perovskite Solar Cell via Bottom Passivation Strategy

Anh Dinh Bui, Grace Dansoa Tabi, Olivier Lee Cheong Lem, The Duong, Keqing Huang, Dang‐Thuan Nguyen, Xuan Minh Chau Ta, Frank Brink, Felipe Kremer, Viqar Uddin Ahmad, Klaus Weber, Leiping Duan, Anne Haggrén, Azul Osorio Mayon, Kylie Catchpole, Heping Shen, Hualin Zhan, Daniel Walter, Yihui Hou, Li‐Chun Chang, Wei Wang, Thomas P. White
article en
7 citations

Abstract

The bottom perovskite with the hole transport layer (HTL) in inverted perovskite solar cells (PSCs) interface has received little attention due to challenges like interlayer dissolution during perovskite deposition. And voids at the perovskite/HTL interface can degrade cell performance. This work introduces a two‐dimensional (2D) perovskite layer between the perovskite and poly (N, N′‐bis‐4‐butylphenyl‐N, N′‐bisphenyl) benzidine (Poly‐TPD) HTL using a mixed solution of 4‐methylphenethylammonium chloride (4M‐PEA‐Cl), methylammonium iodide (MA‐I), and Poly(9,9‐bis(3′‐(N,N‐dimethyl)‐N‐ethylammoinium‐propyl‐2,7‐fluorene)‐alt‐2,7‐(9,9‐dioctylfluorene))dibromide (PFN‐Br). The amine functional groups in the organic salts improved HTL wettability, resulting in a void‐free interface. 4M‐PEA‐Cl, with its strong electron‐withdrawing benzene ring, outperformed other amine‐containing salts in passivating undercoordinated Pb 2+ ions. Incorporating this hybrid passivation layer in PSCs resulted in a 1.8% absolute increase in power conversion efficiency (PCE) to 19.1% with 1.68 eV perovskite bandgap. Additionally, the passivated PSCs demonstrated enhanced operational stability, retaining 91% of their initial efficiency after 800 hours of continuous 1‐sun illumination, compared to 84.7% for the control sample.

Solar RRLVol. 8(19)
Australian National University (AU), The University of Sydney (AU)
Australian National Fabrication Facility, Australian Government
Affordable and clean energy
Openalex Percentile: Top 18%
Perovskite Materials and Applications
1.46
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