4.6 Article

Increasing the wettability and reducing excess PbI2 using diamine hydrobromides with different lengths at the buried interface of the 3D perovskite film

Journal

JOURNAL OF MATERIALS CHEMISTRY C
Volume 11, Issue 45, Pages 15959-15966

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3tc03434h

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In this study, the wettability of the perovskite solution in p-i-n type lead halide perovskite solar cells was improved by introducing diamine hydrobromides with different lengths. This resulted in a more uniform perovskite film and reduced trap density, as well as a decrease in excess PbI2. The best performance was achieved when hexanediamine hydrobromate (HDADBr) was used, leading to improved power conversion efficiency and enhanced device stability.
In p-i-n type lead halide perovskite solar cells (PSCs), the poor wettability of the perovskite solution on the typically used hole transport layer, poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA), is detrimental to obtaining high quality perovskite films. Moreover, the formation of excess lead iodide (PbI2) deteriorates the device stability. Herein, by introducing diamine hydrobromides with different lengths on the PTAA layer, its wettability is greatly increased, leading to a more uniform perovskite film and reduced trap density. Moreover, diamine hydrobromide can reduce excess PbI2. Density functional theory (DFT) calculations further prove the strong interaction between diamine hydrobromides and PbI2; diamine hydrobromides with different lengths present different binding energies with PbI2. Among them, hexanediamine hydrobromate (HDADBr) has the lowest binding energy with PbI2 and enables the least traps formed in the device. Moreover, HDADBr also has the weakest interaction with the I--rich perovskite surface, and the distribution of the I density of states is expanded, which is more conducive to the diffusion of charge carriers. The best-performing PSC is achieved when HDADBr is used, which exhibits an improved power conversion efficiency (PCE) of 20.22% from 18.41% of the control device. The device stability is also notably improved; the PCE of the unencapsulated PSC remains at 90% of the initial value after 400 h of degradation.

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