School of Physics and Astronomy, Tel Aviv University, 69978, Tel Aviv, Israel.
Phys Rev Lett. 2013 Oct 25;111(17):175501. doi: 10.1103/PhysRevLett.111.175501. Epub 2013 Oct 24.
Under high pressures the hydrogen bonds were predicted to transform from a highly asymmetric soft O-H···O to a symmetric rigid configuration in which the proton lies midway between the two oxygen atoms. Despite four decades of research on hydroxyl containing compounds, pressure induced hydrogen bond symmetrization remains elusive. Following single crystal x-ray diffraction, Mössbauer and Raman spectroscopy measurements supported by ab initio calculations, we report the H-bonds symmetrization in iron oxyhydroxide, FeOOH, resulting from the Fe(3+) high-to-low spin crossover at above 45 GPa.
在高压下,预测氢键会从高度不对称的软 O-H···O 转变为对称的刚性构型,其中质子位于两个氧原子的中间。尽管对含羟基化合物进行了四十年的研究,但压力诱导的氢键对称化仍然难以捉摸。通过单晶 X 射线衍射、穆斯堡尔和拉曼光谱测量,并辅以从头算计算,我们报告了在 45 GPa 以上压力下,由于 Fe(3+) 的高到低自旋交叉,导致羟基氧化铁,FeOOH 中的氢键对称化。