Chloride-improved crystallization in sequentially vacuum-deposited perovskites for p–i–n perovskite solar cells

Journal Article (2025)
Author(s)

Jin Yan (TU Delft - Photovoltaic Materials and Devices)

Jasmeen Nespoli (TU Delft - ChemE/Opto-electronic Materials)

Reinder K. Boekhoff (TU Delft - Photovoltaic Materials and Devices)

Haoxu Wang (TU Delft - Photovoltaic Materials and Devices)

Timo Gort (Student TU Delft)

Martijn Tijssen (TU Delft - Photovoltaic Materials and Devices)

Bernardus Zijlstra (TU Delft - Photovoltaic Materials and Devices)

Arjan J. Houtepen (TU Delft - ChemE/Opto-electronic Materials)

Tom J. Savenije (TU Delft - ChemE/Opto-electronic Materials)

O Isabella (TU Delft - Photovoltaic Materials and Devices)

L. Mazzarella (TU Delft - Photovoltaic Materials and Devices)

Research Group
Photovoltaic Materials and Devices
DOI related publication
https://doi.org/10.1039/D4SE01744G
More Info
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Publication Year
2025
Language
English
Research Group
Photovoltaic Materials and Devices
Issue number
10
Volume number
9
Pages (from-to)
2729-2737
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Abstract

Sequential thermal evaporation is an emerging technique for obtaining perovskite (PVK) photoactive materials for solar cell applications. Advantages include solvent-free processing, accurate stoichiometry control, and scalable processing. Nevertheless, the power conversion efficiency (PCE) of PVK solar cells (PSCs) fabricated by evaporation still lags behind that of solution-processed PSCs. Here, based on multi-cycle sequential thermal evaporation, we systematically investigate the effects of the post-deposition annealing temperature on the PVK properties in terms of surface morphology, opto-electronic properties, and device performance. We find that the average grain size increases to almost 1 μm and charge carrier mobilities exceed 50 cm2 V−1 s−1 when the annealing temperature is increased to 170 °C. We introduce a trace of PbCl2 to the multi-cycle sequential deposition to improve the absorber crystallinity at a lower annealing temperature of 150 °C, as evidenced by the XRD and PL analyses. The resulting PSC in a p–i–n structure yields a PCE of 18.5% with a cell area of 0.09 cm2. With the same deposition parameters, the cell area is scaled up to 0.36 cm2, achieving champion PCEs of 17.06%. This indicates the great potential of this technology for the commercialization of PSCs in the future.