Yamamoto Yuzuki, Kume Kazuki, Miyazaki Suzuka, Shinozaki Ayako, Song Peng, Hasan Sayed Sahriar, Hongo Kenta, Maezono Ryo, Ubukata Hiroki, Kageyama Hiroshi, Higuchi Mikio, Masubuchi Yuji
Graduate School of Chemical Sciences and Engineering, Hokkaido University, N13 W8, Kita-ku, Sapporo 060-8628, Japan.
Faculty of Science, Hokkaido University, N10 W8, Kita-ku, Sapporo 060-0810, Japan.
J Am Chem Soc. 2025 Apr 2;147(13):11390-11398. doi: 10.1021/jacs.5c00962. Epub 2025 Mar 24.
While high-pressure phase transitions have been widely studied in inorganic compounds such as oxides and chalcogenides, relatively little attention has been given to compounds containing molecular anions, such as carbodiimides and cyanamides. This study investigates the phase transition of marcasite-type orthorhombic BaMNCN carbodiimides, where a transformation to a CsCl-type tetragonal phase was observed at room temperature under hydrostatic pressure of 0.8 GPa (M = Ca) and 0.3 GPa (M = Sr). This transition, accompanied by an increase in the metal coordination under from 6 to 8, occurs at pressures significantly lower than those required for the high-pressure phase transitions of rock-salt-type metal halides and marcasite-type metal diantimonides. Remarkably, partial phase transitions were also induced by hand milling, a process that applies localized shear forces, distinct from the particle-crushing effects of high-energy ball milling. The transition mechanism, analyzed via variable-cell nudged elastic band (VCNEB) calculations, revealed that while the linear NCN anions remain stable, the shear-sliding of Ba cations and the rotation of NCN anions are critical to the structural transformation. These findings underscore the potential of hand milling to effectively induce phase transitions in compounds containing linear molecular anions, offering new strategies for predicting and controlling such transitions in similar materials.
虽然高压相变在氧化物和硫族化物等无机化合物中已得到广泛研究,但对于含有分子阴离子的化合物,如碳二亚胺和氰胺,关注相对较少。本研究调查了 marcasite 型正交晶系 BaMNCN 碳二亚胺的相变情况,发现在 0.8 GPa(M = Ca)和 0.3 GPa(M = Sr)的静水压力下,室温时会转变为 CsCl 型四方相。这种转变伴随着金属配位数从 6 增加到 8,发生时的压力明显低于岩盐型金属卤化物和 marcasite 型金属二锑化物高压相变所需的压力。值得注意的是,手动研磨(一种施加局部剪切力的过程,不同于高能球磨的颗粒破碎作用)也能诱导部分相变。通过可变晶胞推挤弹性带(VCNEB)计算分析得出的转变机制表明,虽然线性 NCN 阴离子保持稳定,但 Ba 阳离子的剪切滑动和 NCN 阴离子的旋转对结构转变至关重要。这些发现强调了手动研磨在有效诱导含线性分子阴离子化合物相变方面的潜力,为预测和控制类似材料中的此类转变提供了新策略。