4.7 Article

A Facile, One-Step Synthesis for Core-Shell Perovskite Materials via Molten Salt

Journal

CRYSTAL GROWTH & DESIGN
Volume 21, Issue 5, Pages 2581-2588

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.cgd.0c01249

Keywords

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Funding

  1. Department of Energy, National Energy Technology Laboratory [DE-FE0031205]

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This study successfully synthesized core-shell perovskite materials via molten salt synthesis, demonstrating for the first time the rapid preparation of two-phase perovskite composites in a molten salt. By adjusting various parameters, the characteristics of the core-shell composites can be controlled to achieve higher core-shell yield and uniform shell deposition.
Core-shell La0.6Sr0.4Co0.2Fe0.8O3 (LSCF)-La0.8Sr0.2MnO3 (LSM) heterostructure crystalline materials have been synthesized in a simple, one-step feeding method via a KNO3 molten salt solvent. Two-phase perovskite composites can be synthesized in times as short as 10 minutes and is demonstrated for the first time in a molten salt. A combination of X-ray diffraction and S/TEM energy dispersive X-ray spectroscopy has been utilized to confirm the formation of an LSM shell on LSCF cores in all samples when adjusting dwell time, core size, weight ratio between core and shell precursors, and weight ratio of powder to salt. Specifically, decreasing the LSCF core size increases core-shell yield. Smaller cores introduce a greater density of facets on the crystal surface and provide more favorable sites for LSM heterogeneous nucleation. Decreasing the weight ratio of shell precursor to core decreases shell thickness, reduces the number of homogeneously nucleated LSM nanoparticles, and increases core-shell yield. Increasing the amount of salt relative to powder decreases supersaturation in the melt and results in less uniform, isolated shell deposition on the cores. Overall, the molten salt synthesis of core-shell perovskite oxides is investigated and demonstrated as an expeditious method to synthesize core-shell composites for energy applications.

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