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Microscopic pathways of structural phase transitions are difficult to probe because they occur over multiple, disparate time and length scales. Using $in$ $situ$ nanoscale cathodoluminescence microscopy, we visualize the thermally-driven transition to the perovskite phase in hundreds of non-perovskite phase nanowires, resolving the initial nanoscale nucleation and subsequent mesoscale growth and quantifying the activation energy for phase propagation. In combination with molecular dynamics computer simulations, we reveal that the transformation does not follow a simple martensitic mechanism, and proceeds via ion diffusion through a liquid-like interface between the two structures. While cations are disordered in this liquid-like region, the halide ions retain substantial spatial correlations. We find that the anisotropic crystal structure translates to faster nucleation of the perovskite phase at nanowire ends and faster growth along the long nanowire axis. These results represent a significant step towards manipulating structural phases at the nanoscale for designer materials properties.
Nanostructured semiconductors emit light from electronic states known as excitons[1]. According to Hunds rules[2], the lowest energy exciton in organic materials should be a poorly emitting triplet state. Analogously, the lowest exciton level in all
We report a strongly temperature dependent luminescence Stokes shift in the electronic spectra of both hybrid and inorganic lead-bromide perovskite single crystals. This behavior stands in stark contrast to that exhibited by more conventional crystal
Inorganic halide perovskites have emerged as a promising platform in a wide range of applications from solar energy harvesting to computing, and light emission. The recent advent of epitaxial thin film growth of halide perovskites has made it possibl
We study the thermodynamics of binary mixtures wherein the volume fraction of the minority component is less than the amount required to form a flat interface. Based on an explicit microscopic mean field theory, we show that the surface tension domin
2D Ruddlesden Popper perovskites have been extensively studied for their exceptional optical and electronic characteristics while only a few studies have shed light on their mechanical properties. The existing literature mainly discusses the mechanic