Abstract
In this study, we present a novel method for controlling the growth of perovskite crystals in the vacuum thermal evaporation process by utilizing a vacuum-processable additive, propylene urea (PU). By coevaporation of perovskite precursors with PU to form the perovskite layer, PU, acting as a Lewis base additive, retards the direct reaction between the perovskite precursors. This facilitates a larger domain size and reduced defect density. Following the removal of the residual additive, the perovskite layer, exhibiting improved crystallinity, demonstrates reduced charge recombination, as confirmed by a time-resolved microwave conductivity analysis. Consequently, there is a notable enhancement in open-circuit voltage and power conversion efficiency, increasing from 1.05 to 1.15 V and from 17.17 to 18.31%, respectively.
Original language | English |
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Pages (from-to) | 21915-21923 |
Number of pages | 9 |
Journal | ACS Applied Materials and Interfaces |
Volume | 16 |
Issue number | 17 |
DOIs | |
State | Published - 1 May 2024 |
Bibliographical note
Publisher Copyright:© 2024 American Chemical Society.
Keywords
- coevaporation
- crystallinity
- Lewis base additive
- morphology
- perovskite growth
- perovskite solar cells
- thermal evaporation
- vacuum deposition