4.6 Article

Probing Chemical-Composition-Induced Heterostructures and Interfaces in Lead Halide Perovskites

Journal

LANGMUIR
Volume 38, Issue 40, Pages 12103-12117

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.2c01586

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This article introduces different strategies employed in LHP thin films and nanocrystals to generate heterostructures for improved stability and photovoltaic efficiency, and discusses the application of variable energy photoelectron spectroscopy (VEPES) in probing the chemical composition variation in these materials and interfaces. The internal heterostructures of LHP nanocrystals generated by surface chemistry and post-synthesis anion exchange, as well as the heterostructures induced by the chemical composition of LHP thin films, are discussed in detail.
Lead halide perovskites (LHP) are of great interest for their optoelectronic properties and photovoltaic applications. Various heterostructures are created in these materials to achieve favorable optical properties and improved stability at the interfaces during the fabrication of devices. Such heterostructures are often assumed to be formed based on the reactivity of precursors and are not directly probed. In this Feature Article, we report how various strategies have been employed in LHP thin films and nanocrystals (NCs) that generate heterostructures to boost their stability and photovoltaic (PV) efficiencies and how variable energy photoelectron spectroscopy (VEPES) can probe the chemical composi-tion variation in heterostructured materials and interfaces. We specifically discussed the internal heterostructures of LHP NCs generated due to the surface chemistry and postsynthesis anion exchange followed by a detailed discussion of the heterostructures induced by the chemical composition (anion, cation, and degradation) of LHP thin films. The difficulties in determining heterostructures as well as the potential scope of the application of VEPES in unwrapping heterostructures in diverse materials are also discussed.

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