Temperature-controlled anti-solvent engineering enables the fabrication of reproducible and stable tin-based perovskite solar cells by decoupling the kinetic fragility

Abstract

Tin-based perovskites are among the most promising lead-free, solution-processed photovoltaic absorbers. However, their practical deployment is limited by uncontrolled crystallization kinetics, a narrow process window and severe energetic disorder resulting from rapid nucleation. Here, we demonstrate that modulation of anti-solvent temperature (cool to hot anti-solvent treatment) leads to a significant impact on crystallinity, grain packing and electronic features of the films. This transformation allows for governing the crystallization process with temperature and makes it fabrication-tolerant. We also examine the pre-annealing passivation of precursor films (passivation before post-thermal annealing). This dual control suppresses energetic disorder and non-radiative recombination without altering the optical bandgap or absorbance. This improvement increases the power conversion efficiency from 3.50% to 9.12%. In situ optical spectroscopy reveals a dramatic change in perovskite formation during the post-annealing process. Our synergistic control of thermal processes enhances efficiency, operational stability and reproducibility, paving the way to overcome defects in tin-halide perovskite photovoltaics.

Graphical abstract: Temperature-controlled anti-solvent engineering enables the fabrication of reproducible and stable tin-based perovskite solar cells by decoupling the kinetic fragility

Supplementary files

Article information

Article type
Paper
Submitted
20 Apr 2026
Accepted
27 May 2026
First published
09 Jun 2026
This article is Open Access
Creative Commons BY license

J. Mater. Chem. A, 2026, Advance Article

Temperature-controlled anti-solvent engineering enables the fabrication of reproducible and stable tin-based perovskite solar cells by decoupling the kinetic fragility

T. Liu, R. Nishikubo, C. Chen, A. Wakamiya and A. Saeki, J. Mater. Chem. A, 2026, Advance Article , DOI: 10.1039/D6TA03298B

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