ArticleNature chemistry2025
Synthesis of zero-dimensional octahedral metal halides through solvent incorporation and their photophysical properties.
Article in Nature chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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Who cites it
3 citing papers in PubMed.
- Low-Temperature Melting-Crystallization Transition in Perovskites With Self-Trapped Excitons for Photovoltaic Downconversion.Advanced materials (Deerfield Beach, Fla.) · 2026Article
- Highly Emissive and Stable Ge(II)- and Sn(II)-Based Vacancy-Ordered Iodide Double Perovskites.Angewandte Chemie (International ed. in English) · 2026Article
- A unified ligand-dimensional design to halt cation migration in perovskite photovoltaics.Science advances · 2026Article
Corrections and comments
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Authors and funding
16 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Zero-dimensional (0D) metal halides, which feature discrete metal halide octahedra interspersed with large organoammonium cations, are the building blocks of halide perovskites. The optical properties of these materials make them promising candidates in light-emitting devices. However, developing their general design principles remains challenging. Here we report an antisolvent incorporation approach that transforms a broad range of two-dimensional tin iodide perovskites into 0D structures. This approach accommodates diverse organic cations and antisolvent molecules and is extendable to germanium and lead analogues. We show that enhancing the structural rigidity in Sn-based octahedra-modulated by organic packing-increases the radiative recombination rate while decreasing the non-radiative recombination rate, achieving near-unity photoluminescence quantum yield. Ge- and Sn-based structures exhibit large Stokes shifts and microsecond-scale triplet lifetimes due to localized excited states, while their Pb-based counterpart shows faster recombination via triplet-singlet mixing, supported by theoretical calculations. This work offers a versatile synthetic platform for 0D metal halides and deepens our current understanding of excited-state dynamics in halide perovskites.
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40759738What OpenQuestion holds
Registered trials
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