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Irina Skvortsova

Publications and source records attributed to Irina Skvortsova.

2 recordsLinked to original sources

A 4D-STEM Tomographic Framework Assisted by Object Tracking for Nanoparticle Structure Determination

Three-dimensional electron diffraction (3D ED) has emerged as a powerful method for solving the structures of sub-micron-sized particles down to nanoparticles. However, it faces technical challenges when applied to beam-sensitive samples or agglomerated nanoparticles. This study presents a novel approach that combines 4D-STEM tomography with object tracking and segmentation algorithms to overcome these limitations and achieve single-crystalline 3D ED datasets from nanopowder samples. The method and data quality are assessed on brookite TiO2 nanorods and beam-sensitive CsPbBr3 nanoparticles. To finely sample the reciprocal-space, the data acquisition was automated to acquire hundreds of 4D-STEM scans at fine tilt steps using a slightly convergent beam (0.6 to 1 mrad). Compared to conventional 3D ED methodologies, the proposed method provides enhanced signal-to-noise ratio, low illumination time for reducing beam damage, and the ability to analyze multiple particles from a single tomographic dataset. The procedure is optimized to be feasible using commercially available desktops and detectors. This extends the method applicability to systems and samples that were very challenging for conventional 3D ED methods, by eliminating several technical challenges for the data acquisition.

physics.ins-det

Halide Perovskite-Chalcohalide Nanocrystal Heterostructures as a Platform for the Synthesis and Investigation of the CsPbCl3-CsPbI3 Epitaxial Interface

Halide exchange in lead-based halide perovskites has been studied extensively. While mixed Cl-Br or Br-I alloy compositions can be formed with no miscibility gaps, this is precluded for mixed Cl-I compositions, due to the large difference in Cl and I ionic radii. Here, we exploit perovskite-chalcohalide CsPbCl3-Pb4S3Cl2 heterostructures to study the Cl-I exchange and isolate new types of intermediate structures. The epitaxial interface between the Pb4S3Cl2 chalcohalide and the CsPbCl3 perovskite domain significantly influences the intermediate stages of halide exchange in the perovskite domain, leading to coexisting CsPbCl3 and CsPbI3 domains, thereby delivering segmented CsPbI3-CsPbCl3-Pb4S3Cl2 energetically favorable heterostructures, with partial iodide alloying of the CsPbCl3 domain and at the perovskite-chalcohalide interface. The I:CsPbCl3 domain between CsPbI3 and Pb4S3Cl2 enables a gradual lattice expansion across the heterostructure. This design accommodates interfacial strain, with a 5.6% mismatch at the CsPbCl3-CsPbI3 interface and a 3.4% mismatch at the perovskite-chalcohalide interface. Full halide exchange leads to CsPbI3-Pb4S3Cl2 heterostructures. Both in intermediate and fully exchanged heterostructures, the CsPbI3 domain is emissive. In the intermediate structures, the band alignment between the two perovskite domains is type-I, with carriers photogenerated in the CsPbCl3 domain quickly transferring to the CsPbI3 domain, where they can recombine radiatively.

cond-mat.mtrl-sci