Close-space sublimation as a versatile deposition process for efficient perovskite silicon tandem solar cells
Abstract The envisaged breakthrough of perovskite photovoltaic technologies demands rapid advances in scalable and robust high-throughput fabrication methods. Here we present close-space sublimation (CSS) as a vacuum-based, industrially relevant deposition method for the conversion of sublimed PbI 2 inorganic scaffolds into high-quality wide-bandgap perovskite absorbers (MAPb(I 0.79 Br 0.21 ) 3 , 1.64 eV), employing a reusable mixed-halide organic source for stable bandgap control. We provide mechanistic insights into the substitution-reaction-limited CSS process and achieve power conversion efficiencies (PCEs) of up to 18.5% for fully vacuum-processed p–i–n single-junction devices. Monolithic integration in tandem solar cells onto planar, nano- and micro-textured silicon bottom cells reveals consistent optoelectronic and morphological properties across all configurations without requiring adjustments of deposition parameters, as corroborated by comprehensive characterization techniques. The resulting perovskite/silicon tandem solar cells reach PCEs up to 24.3%, with minimal variation across the different bottom cells. Our findings highlight the broad process window and versatility of CSS, positioning it as an industry-suitable deposition method for solvent-free high-throughput fabrication.
Institutions
- Karlsruhe Institute of Technology (DE)
- Consejo Nacional de Investigaciones Científicas y Técnicas (AR)
- Universitat de València (ES)
- Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR)
- Parc Científic de la Universitat de València (ES)
- Laboratoire d’Innovation pour les Technologies des Énergies Nouvelles et les nanomatériaux (FR)
- Instituto de Física del Litoral (AR)
- Université Grenoble Alpes (FR)
Publication Details
- Journal
- Nature Energy
- Published
- 2026-05-19
- DOI
- https://doi.org/10.1038/s41560-026-02068-9
- Primary Topic
- Perovskite Materials and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00