Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/36018
Title: Ligand-bridged charge extraction and enhanced quantum efficiency enable efficient n-i-p perovskite/silicon tandem solar cells
Authors: Aydin, E
Liu, J
Ugur, E
Azmi, R
Harrison, GT
Hou, Y
Chen , B
Zhumagali, S
De Bastiani, M
Wang, MC
Raja, W
Allen, TG
Rehman, AU
Subbiah, AS
Babics, M
BABAYIGIT, Aslihan 
Isikgor, FH
Wang, K
Van Kerschaver, E
Tsetseris, L
Sargent, EH
Laquai, F
De Wolf , S
Issue Date: 2021
Publisher: ROYAL SOC CHEMISTRY
Source: Energy & environmental science (Print), 14 (8) , p. 4377 -4390
Abstract: Translating the high power conversion efficiencies of single-junction perovskite solar cells in their classic, non-inverted (n-i-p) architecture to efficient monolithic n-i-p perovskite/silicon tandem solar cells with high current densities has been a persistent challenge due to the lack of low-temperature processable, chemically-insoluble contact materials with appropriate polarity and sufficient optical transparency. To address this, we developed sputtered amorphous niobium oxide (a-NbOx) with ligand-bridged C-60 as an efficient electron-selective contact, deposited on the textured-silicon bottom cell. For the sunward, hole-selective contact we implemented a stack of molecularly doped broadband transparent evaporated 2,2 ',7,7 '-tetra(N,N-di-p-tolyl)amino-9,9-spirobifluorene (spiro-TTB) and atomic layer deposited vanadium oxide, which further enhances the device quantum efficiency. Combining these contact materials with two-dimensional perovskite passivation on the micrometer-thick solution-processed perovskite top cell yields 27% efficient monolithic n-i-p perovskite/silicon tandem solar cells, which represents one of the highest power conversion efficiencies reported on pyramidal textured crystalline silicon bottom cells, and the highest with this polarity.
Document URI: http://hdl.handle.net/1942/36018
ISSN: 1754-5692
e-ISSN: 1754-5706
DOI: 10.1039/d1ee01206a
ISI #: 000670654700001
Rights: The Royal Society of Chemistry 2021. Open Access Article. Published on 30 June 2021. Downloaded on 7/5/2024 2:01:36 PM. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Category: A1
Type: Journal Contribution
Validations: ecoom 2022
Appears in Collections:Research publications

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