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Spontaneous bidirectional ordering of CH(3)NH(3)(+) in lead iodide perovskites at room temperature: The origins of the tetragonal phase
CH(3)NH(3)PbI(3) is a hybrid organic-inorganic material with a perovskite structure and a temperature-dependent polymorphism whose origins are still unclear. Here we perform ab initio molecular dynamics simulations in order to investigate the structural properties and atom dynamics of CH(3)NH(3)PbI(...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832208/ https://www.ncbi.nlm.nih.gov/pubmed/27079383 http://dx.doi.org/10.1038/srep24443 |
Sumario: | CH(3)NH(3)PbI(3) is a hybrid organic-inorganic material with a perovskite structure and a temperature-dependent polymorphism whose origins are still unclear. Here we perform ab initio molecular dynamics simulations in order to investigate the structural properties and atom dynamics of CH(3)NH(3)PbI(3) at room temperature. Starting from different initial configurations, we find that a single-crystalline system undergoes a spontaneous ordering process which brings the [Image: see text] ions to alternately point towards the center of two out of the six faces of the cubic [Image: see text] framework, i.e. towards the 〈100〉 and 〈010〉 directions. This bidirectional ordering gives rise to a preferential distortion of the inorganic lattice on the a-b plane, shaping the observed tetragonal symmetry of the system. The process requires tens of picoseconds for CH(3)NH(3)PbI(3) supercells with just eight [Image: see text] ions. |
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