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Direct investigation of the reorientational dynamics of A-site cations in 2D organic-inorganic hybrid perovskite by solid-state NMR

Limited methods are available for investigating the reorientational dynamics of A-site cations in two-dimensional organic–inorganic hybrid perovskites (2D OIHPs), which play a pivotal role in determining their physical properties. Here, we describe an approach to study the dynamics of A-site cations...

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Detalles Bibliográficos
Autores principales: Lin, Cheng-Chieh, Huang, Shing-Jong, Wu, Pei-Hao, Chen, Tzu-Pei, Huang, Chih-Ying, Wang, Ying-Chiao, Chen, Po-Tuan, Radeva, Denitsa, Petrov, Ognyan, Gelev, Vladimir M., Sankar, Raman, Chen, Chia-Chun, Chen, Chun-Wei, Yu, Tsyr-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938534/
https://www.ncbi.nlm.nih.gov/pubmed/35314691
http://dx.doi.org/10.1038/s41467-022-29207-6
Descripción
Sumario:Limited methods are available for investigating the reorientational dynamics of A-site cations in two-dimensional organic–inorganic hybrid perovskites (2D OIHPs), which play a pivotal role in determining their physical properties. Here, we describe an approach to study the dynamics of A-site cations using solid-state NMR and stable isotope labelling. (2)H NMR of 2D OIHPs incorporating methyl-d(3)-ammonium cations (d(3)-MA) reveals the existence of multiple modes of reorientational motions of MA. Rotational-echo double resonance (REDOR) NMR of 2D OIHPs incorporating (15)N- and ¹³C-labeled methylammonium cations ((13)C,(15)N-MA) reflects the averaged dipolar coupling between the C and N nuclei undergoing different modes of motions. Our study reveals the interplay between the A-site cation dynamics and the structural rigidity of the organic spacers, so providing a molecular-level insight into the design of 2D OIHPs.