AI Article Synopsis

  • Recent computational studies have identified new ternary nitrides, pointing to potential new materials, but synthesizing them is challenging due to high cohesive energies that slow down diffusion.
  • The authors successfully synthesized two new phases, calcium zirconium nitride (CaZrN) and calcium hafnium nitride (CaHfN), through solid state metathesis reactions involving calcium nitride (CaN) and metal chlorides (Zr, Hf).
  • It was found that a slight excess of CaN (about 20 mol %) is necessary to achieve the correct stoichiometry of CaN for producing the desired phases, as revealed by advanced synchrotron X-ray diffraction studies, which also helped explain the synthesis process compared to

Article Abstract

Recent computational studies have predicted many new ternary nitrides, revealing synthetic opportunities in this underexplored phase space. However, synthesizing new ternary nitrides is difficult, in part because intermediate and product phases often have high cohesive energies that inhibit diffusion. Here, we report the synthesis of two new phases, calcium zirconium nitride (CaZrN) and calcium hafnium nitride (CaHfN), by solid state metathesis reactions between CaN and Cl ( = Zr, Hf). Although the reaction nominally proceeds to the target phases in a 1:1 ratio of the precursors via CaN + Cl → CaN + 2 CaCl, reactions prepared this way result in Ca-poor materials (CaN, < 1). A small excess of CaN (ca. 20 mol %) is needed to yield stoichiometric CaN, as confirmed by high-resolution synchrotron powder X-ray diffraction. synchrotron X-ray diffraction studies reveal that nominally stoichiometric reactions produce Zr intermediates early in the reaction pathway, and the excess CaN is needed to reoxidize Zr intermediates back to the Zr oxidation state of CaZrN. Analysis of computationally derived chemical potential diagrams rationalizes this synthetic approach and its contrast from the synthesis of MgZrN. These findings additionally highlight the utility of diffraction studies and computational thermochemistry to provide mechanistic guidance for synthesis.

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http://dx.doi.org/10.1021/jacs.3c12114DOI Listing

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