Noguchi Naoki, Okuchi Takuo
Institute for Planetary Materials, Okayama University, Misasa, Tottori 682-0193, Japan.
J Chem Phys. 2016 Jun 21;144(23):234503. doi: 10.1063/1.4953688.
The self-diffusion of ice VII in the pressure range of 5.5-17 GPa and temperature range of 400-425 K was studied using micro Raman spectroscopy and a diamond anvil cell. The diffusion was monitored by observing the distribution of isotope tracers: D2O and H2 (18)O. The diffusion coefficient of hydrogen reached a maximum value around 10 GPa. It was two orders of magnitude greater at 10 GPa than at 6 GPa. Hydrogen diffusion was much faster than oxygen diffusion, which indicates that protonic diffusion is the dominant mechanism for the diffusion of hydrogen in ice VII. This mechanism is in remarkable contrast to the self-diffusion in ice Ih that is dominated by an interstitial mechanism for the whole water molecule. An anomaly around 10 GPa in ice VII indicates that the rate-determining process for the proton diffusion changes from the diffusion of ionic defects to the diffusion of rotational defects, which was suggested by proton conductivity measurements and molecular dynamics simulations.
利用显微拉曼光谱和金刚石对顶砧池,研究了冰VII在5.5 - 17吉帕压力范围和400 - 425开尔文温度范围内的自扩散。通过观察同位素示踪剂D₂O和H₂¹⁸O的分布来监测扩散情况。氢的扩散系数在10吉帕左右达到最大值。在10吉帕时,其值比在6吉帕时大两个数量级。氢的扩散比氧的扩散快得多,这表明质子扩散是冰VII中氢扩散的主要机制。这种机制与冰Ih中的自扩散形成显著对比,冰Ih中的自扩散由整个水分子的间隙机制主导。冰VII中10吉帕左右的异常现象表明,质子扩散的速率决定过程从离子缺陷的扩散转变为旋转缺陷的扩散,这是由质子电导率测量和分子动力学模拟所表明的。