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• W4296457555 abstract "•Fast precipitation of Cs ions is found to induce the δ-CsPbI3 secondary phase •MACl is essential for forming pure-iodide wide-band-gap perovskites without δ phases •Pure-iodide perovskite films show excellent stability without halide-segregation •The best perovskite/Si tandem cell exhibits a high certified efficiency of 28.37% Halide perovskites, promising top-cell materials for efficient Si tandem solar cells, suffer from halide segregation, which results from the halide mixing necessary for achieving band-gap widening. We report pure-iodide wide-band-gap perovskite top cells that are fundamentally free of halide segregation. Cs and dimethylammonium cations were incorporated simultaneously into the A-site of perovskite structure to increase the band gap while maintaining the tolerance factor. However, the incorporation of dual cations resulted in the simultaneous formation of orthorhombic and hexagonal secondary phases rather than forming the pure perovskite phase, owing to the different precipitation kinetics between cations. We demonstrated that this strategy can only be implemented by the phase-controlled nucleation of the Cs-rich composition that governs the desired phase evolution. The pure-iodide perovskite top cell exhibited excellent photo-stability (1% degradation after 1,000 h of continuous operation; ISOS-L-1I, white LED), and its Si tandem exhibited a high conversion efficiency of 29.4% (28.37% certified). Halide perovskites, promising top-cell materials for efficient Si tandem solar cells, suffer from halide segregation, which results from the halide mixing necessary for achieving band-gap widening. We report pure-iodide wide-band-gap perovskite top cells that are fundamentally free of halide segregation. Cs and dimethylammonium cations were incorporated simultaneously into the A-site of perovskite structure to increase the band gap while maintaining the tolerance factor. However, the incorporation of dual cations resulted in the simultaneous formation of orthorhombic and hexagonal secondary phases rather than forming the pure perovskite phase, owing to the different precipitation kinetics between cations. We demonstrated that this strategy can only be implemented by the phase-controlled nucleation of the Cs-rich composition that governs the desired phase evolution. The pure-iodide perovskite top cell exhibited excellent photo-stability (1% degradation after 1,000 h of continuous operation; ISOS-L-1I, white LED), and its Si tandem exhibited a high conversion efficiency of 29.4% (28.37% certified)." @default.
• W4296457555 created "2022-09-20" @default.
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• W4296457555 date "2022-10-01" @default.
• W4296457555 modified "2023-10-10" @default.
• W4296457555 title "Stable pure-iodide wide-band-gap perovskites for efficient Si tandem cells via kinetically controlled phase evolution" @default.
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• W4296457555 doi "https://doi.org/10.1016/j.joule.2022.08.006" @default.
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