Multinuclear solid state nuclear magnetic resonance for studying CsPbBr3 nanocubes

Author:

Scarperi Andrea1,Landi Noemi1ORCID,Gabbani Alessio12ORCID,Jarmouni Nabila13ORCID,Borsacchi Silvia45ORCID,Calucci Lucia45ORCID,Pucci Andrea1ORCID,Carignani Elisa45ORCID,Pineider Francesco12ORCID,Geppi Marco1ORCID

Affiliation:

1. Department of Chemistry and Industrial Chemistry , University of Pisa , via G. Moruzzi 13 , Pisa , Italy

2. Department of Physics and Astronomy , University of Florence , Sesto Fiorentino (FI) , Italy

3. Department of Chemistry , Laboratory of Physical Chemistry of Materials , Faculty of sciences Ben M’sik , University Hassan II of Casablanca , Av Driss El Harti, Sidi Othmane Casablanca, , Casablanca , Morocco

4. Institute for the Chemistry of Organometallic Compound , National Council of Research (ICCOM-CNR) , via G. Moruzzi 1 , Pisa , Italy

5. Center for Instrument Sharing of the University of Pisa (CISUP) , Pisa , Italy

Abstract

Abstract Cesium lead bromide perovskite (CsPbBr3) nanocrystals have raised impressive interest as efficient and stable optoelectronic materials. Size and morphology play important roles in the final performances of these materials and advanced characterization studies are needed to elucidate structural and surface properties. In this work, CsPbBr3 cubic nanocrystals were obtained by colloidal synthesis and characterized by multinuclear Solid State NMR (SSNMR), complemented by X-Ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and optical spectroscopy. The multinuclear NMR approach allowed the different components of the nanocubes to be separately observed. In particular, the surface ligands and their interactions with the nanocubes surface were investigated by 1H and 13C NMR experiments, while the structural investigation of the perovskite nanocubes was addressed by exploiting 207Pb and 133Cs spectral properties in comparison with bulk CsPbBr3. Static 207Pb NMR spectra indicated a possible contribution of chemical shift anisotropy from the 207Pb nuclei of the outer layer. The 133Cs NMR spectra showed signals with different chemical shifts for cesium atoms in at least three regions of the nanocubes, from the inner core to the surface, which were interpreted in terms of cubic layers with different distances from the surface using a simple geometrical model. This interpretation was also supported by 133Cs longitudinal relaxation time measurements.

Funder

Ministero dell’Università e della Ricerca

Regione Toscana

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

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