Department of Physics, College of Science, National University of Defense Technology, Changsha 410073, Hunan, People's Republic of China.
J Chem Phys. 2011 Jul 14;135(2):024505. doi: 10.1063/1.3608412.
The changes of structure and distribution of dipole moment of water with temperatures up to 2800 K and densities up to 2.2 g/cm(3) are investigated using ab initio molecular dynamics. Along the isochore of 1.0 g/cm(3), the structure of liquid water above 800 K is dramatically different from that at ambient conditions, where the hydrogen-bonds network collapses. Along the isotherm of 1800 K, the transition from the liquid state to an amorphous superionic phase occurs at 2.0 g/cm(3) (32.9 GPa), which is not observed along the isotherm of 2800 K. With increasing temperature, the average dipole moment of water molecules is decreased arising from the weakened polarization by the collapse of the hydrogen-bonds network, while it is contrarily increased with compression due to the strengthening effect upon the polarization of water molecules. Both higher temperature and pressure broaden the distribution of dipole moment of water molecules due to the enhanced intramolecular charge fluctuations.
利用从头算分子动力学研究了温度高达 2800 K 和密度高达 2.2 g/cm(3) 时偶极矩的结构和分布变化。在 1.0 g/cm(3) 的等压线上,高于 800 K 的液态水的结构与环境条件下的结构有很大的不同,在环境条件下,氢键网络崩溃。在 1800 K 的等温线上,从液态到无定形超离子相的转变发生在 2.0 g/cm(3)(32.9 GPa),而在 2800 K 的等温线上没有观察到这种转变。随着温度的升高,水分子的平均偶极矩减小,这是由于氢键网络的崩溃导致极化减弱所致,而随着压缩的增加,偶极矩增大,这是由于水分子的极化增强所致。由于分子内电荷波动的增强,较高的温度和压力都会使水分子偶极矩的分布变宽。