Chemical and Structural Stability of CsPbX3 Nanorods during Postsynthetic Anion-Exchange: Implications for Optoelectronic Functionality
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide We examine halide anion-exchange reactions on CsPbX 3 nanorods (NRs), and we identify reaction conditions that provide complete anion exchange while retaining both the highly quantum-confined 1-D morphology and metastable crystal lattice configurations that span a range between tetragonal structures and thermodynamically preferred orthorhombic structures. We find that the chemical stability of CsPbBr 3 NRs is degraded by the presence of alkyl amines that etch CsPbBr 3 and result in the formation of Cs 4 PbBr 6 and 2-D bromoplumbates. Our study outlines strategies for maintaining metastable states of the soft lattices of perovskite nanocrystals undergoing exchange reactions, despite the thermodynamic driving force toward more stable lattice configurations during this disruptive chemical transformation. These strategies can be used to fine-tune the band gap of LHP-based nanostructures while preserving structure–property relationships that are contingent on metastable shapes and crystal configurations, aiding optoelectronic applications of these materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Solid-state spectroscopy and crystallography · 2D Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Texas A&M University, College Station, Texas 77843-3255, United States
Department of Materials Science and Engineering, Texas A&M University, College Station, Texas 77843-3255, United States
Funding
Welch Foundation · National Science Foundation
References (39)
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