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NMR spectroscopy probes microstructure, dynamics and doping of metal halide perovskites.

Accepted version
Peer-reviewed

Type

Article

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Authors

Stranks, Samuel D 

Abstract

Solid-state magic-angle spinning NMR spectroscopy is a powerful technique to probe atomic-level microstructure and structural dynamics in metal halide perovskites. It can be used to measure dopant incorporation, phase segregation, halide mixing, decomposition pathways, passivation mechanisms, short-range and long-range dynamics, and other local properties. This Review describes practical aspects of recording solid-state NMR data on halide perovskites and how these afford unique insights into new compositions, dopants and passivation agents. We discuss the applicability, feasibility and limitations of 1H, 13C, 15N, 14N, 133Cs, 87Rb, 39K, 207Pb, 119Sn, 113Cd, 209Bi, 115In, 19F and 2H NMR in typical experimental scenarios. We highlight the pivotal complementary role of solid-state mechanosynthesis, which enables highly sensitive NMR studies by providing large quantities of high-purity materials of arbitrary complexity and of chemical shifts calculated using density functional theory. We examine the broader impact of solid-state NMR on materials research and how its evolution over seven decades has benefitted structural studies of contemporary materials such as halide perovskites. Finally, we summarize some of the open questions in perovskite optoelectronics that could be addressed using solid-state NMR. We, thereby, hope to stimulate wider use of this technique in materials and optoelectronics research.

Description

Keywords

3403 Macromolecular and Materials Chemistry, 34 Chemical Sciences, 3406 Physical Chemistry

Journal Title

Nat Rev Chem

Conference Name

Journal ISSN

2397-3358
2397-3358

Volume Title

5

Publisher

Springer Science and Business Media LLC

Rights

All rights reserved
Sponsorship
Royal Society (UF150033)
European Research Council (756962)
Engineering and Physical Sciences Research Council (EP/R023980/1)
European Commission Horizon 2020 (H2020) Marie Sk?odowska-Curie actions (841136)
This work has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No. 841136. This work was supported by Swiss National Science Foundation Grant No. 200020_178860. S.D.S. acknowledges the Royal Society and Tata Group (UF150033). CPG acknowledges the Royal Society.