Marin Timothy W, Takahashi Kenji, Bartels David M
Chemistry Department, Benedictine University, Lisle, IL 60532, USA.
J Chem Phys. 2006 Sep 14;125(10):104314. doi: 10.1063/1.2338521.
Characteristics of the ultraviolet absorption band edge of high-pressure light and heavy water are reported over the temperature range of 25-400 degrees C, extending into the supercritical regime. A gradual redshift in the absorption band edge of approximately 0.6 eV is observed with increasing temperature. This shift cannot be explained by vibrational hot band growth or changes in the degree of Rayleigh scattering with increasing temperature, and is ascribed to a shift of the electronic transition energy. The density dependence for the absorption edge in 400 degrees C supercritical water was also examined, and showed a surprising approximately 0.1 eV blueshift over a factor of 3.5 decrease in density. This shift may be due to a narrowing of the absorption spectrum with decreasing density. It is proposed that the previously reported "red tail" of the water absorption extending into the near ultraviolet and visible could be attributed to preresonant Rayleigh scattering, and that the true onset of liquid water absorption is approximately 5.8 eV at 25 degrees C.
报道了高压轻水和重水在25至400摄氏度温度范围内的紫外吸收带边缘特征,该范围延伸至超临界区域。随着温度升高,观察到吸收带边缘逐渐红移约0.6电子伏特。这种位移不能用振动热谱带增长或随着温度升高瑞利散射程度的变化来解释,而是归因于电子跃迁能量的位移。还研究了400摄氏度超临界水中吸收边缘的密度依赖性,结果表明,在密度降低3.5倍的情况下,出现了约0.1电子伏特的惊人蓝移。这种位移可能是由于吸收光谱随着密度降低而变窄。有人提出,先前报道的延伸至近紫外和可见光区域的水吸收“红尾”可能归因于预共振瑞利散射,并且液态水吸收的真正起始点在25摄氏度时约为5.8电子伏特。