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Title: Pseudo-halide anion engineering for efficient quasi-2D Ruddlesden-Popper tin perovskite solar cells

Abstract

Quasi-two-dimensional (2D) organic-inorganic hybrid tin perovskites have emerged as promising alternatives to lead-based perovskites in thin-film photovoltaics because of their reduced toxicity and improved stability. However, the undesired small n-value 2D phases and disordered crystal orientation enormously restrict the efficiency of quasi-2D tin perovskite solar cells (PSCs) due to uncontrollable nucleation and crystal growth processes. Here, we propose a mixed pseudo-halide anion engineering approach by using acetate (Ac-) and tetrafluoroborate (BF4-) anions to make quasi-2D Ruddlesden-Popper perovskites with a target formula of PEA2FA4Sn5I16. We find that the mixed Ac- and BF4- anions can not only promote homogeneously distributed PEA+ cations in the precursor by effectively breaking the PEA+···PEA+ stacking but also retard the crystallization process by coordinating with unbonded SnI2, thereby, significantly reducing small n-value 2D phases, improving the crystal orientation, and suppressing the Sn2+ oxidation. The resulting PSC exhibits up to 9% power conversion efficiency and 400 h stability.

Authors:
 [1];  [1];  [1]; ORCiD logo [2];  [2];  [1]; ORCiD logo [1]
  1. Cornell University, Ithaca, NY (United States)
  2. Brookhaven National Laboratory (BNL), Upton, NY (United States). Center for Functional Nanomaterials (CFN)
Publication Date:
Research Org.:
Brookhaven National Lab. (BNL), Upton, NY (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES); National Science Foundation (NSF)
OSTI Identifier:
1922715
Report Number(s):
BNL-223927-2023-JAAM
Journal ID: ISSN 2666-3864
Grant/Contract Number:  
SC0012704; ECCS-2054942; EPM-2114350; DMR-1719875
Resource Type:
Accepted Manuscript
Journal Name:
Cell Reports Physical Science
Additional Journal Information:
Journal Volume: 3; Journal Issue: 10; Journal ID: ISSN 2666-3864
Publisher:
Elsevier
Country of Publication:
United States
Language:
English
Subject:
36 MATERIALS SCIENCE; Ruddlesden-Popper phase perovskite; tin perovskite solar cell; pseudo-halide anion; crystal growth; charge transport

Citation Formats

Li, Hao, Xu, Yuanze, Ramakrishnan, Shripathi, Zhang, Yugang, Cotlet, Mircea, Xu, Tony Lou, and Yu, Qiuming. Pseudo-halide anion engineering for efficient quasi-2D Ruddlesden-Popper tin perovskite solar cells. United States: N. p., 2022. Web. doi:10.1016/j.xcrp.2022.101060.
Li, Hao, Xu, Yuanze, Ramakrishnan, Shripathi, Zhang, Yugang, Cotlet, Mircea, Xu, Tony Lou, & Yu, Qiuming. Pseudo-halide anion engineering for efficient quasi-2D Ruddlesden-Popper tin perovskite solar cells. United States. https://doi.org/10.1016/j.xcrp.2022.101060
Li, Hao, Xu, Yuanze, Ramakrishnan, Shripathi, Zhang, Yugang, Cotlet, Mircea, Xu, Tony Lou, and Yu, Qiuming. Tue . "Pseudo-halide anion engineering for efficient quasi-2D Ruddlesden-Popper tin perovskite solar cells". United States. https://doi.org/10.1016/j.xcrp.2022.101060. https://www.osti.gov/servlets/purl/1922715.
@article{osti_1922715,
title = {Pseudo-halide anion engineering for efficient quasi-2D Ruddlesden-Popper tin perovskite solar cells},
author = {Li, Hao and Xu, Yuanze and Ramakrishnan, Shripathi and Zhang, Yugang and Cotlet, Mircea and Xu, Tony Lou and Yu, Qiuming},
abstractNote = {Quasi-two-dimensional (2D) organic-inorganic hybrid tin perovskites have emerged as promising alternatives to lead-based perovskites in thin-film photovoltaics because of their reduced toxicity and improved stability. However, the undesired small n-value 2D phases and disordered crystal orientation enormously restrict the efficiency of quasi-2D tin perovskite solar cells (PSCs) due to uncontrollable nucleation and crystal growth processes. Here, we propose a mixed pseudo-halide anion engineering approach by using acetate (Ac-) and tetrafluoroborate (BF4-) anions to make quasi-2D Ruddlesden-Popper perovskites with a target formula of PEA2FA4Sn5I16. We find that the mixed Ac- and BF4- anions can not only promote homogeneously distributed PEA+ cations in the precursor by effectively breaking the PEA+···PEA+ stacking but also retard the crystallization process by coordinating with unbonded SnI2, thereby, significantly reducing small n-value 2D phases, improving the crystal orientation, and suppressing the Sn2+ oxidation. The resulting PSC exhibits up to 9% power conversion efficiency and 400 h stability.},
doi = {10.1016/j.xcrp.2022.101060},
journal = {Cell Reports Physical Science},
number = 10,
volume = 3,
place = {United States},
year = {Tue Sep 20 00:00:00 EDT 2022},
month = {Tue Sep 20 00:00:00 EDT 2022}
}

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