Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, CA 90095-1569, USA.
Science. 2010 Jul 2;329(5987):65-9. doi: 10.1126/science.1189588.
Since the discovery of the hydrated electron more than 40 years ago, a general consensus has emerged that the hydrated electron occupies a quasispherical cavity in liquid water. We simulated the electronic structure and dynamics of the hydrated electron using a rigorously derived pseudopotential to treat the electron-water interaction, which incorporates attractive oxygen and repulsive hydrogen features that have not been included in previous pseudopotentials. What emerged was a hydrated electron that did not reside in a cavity but instead occupied a approximately 1-nanometer-diameter region of enhanced water density. Both the calculated ground-state absorption spectrum and the excited-state spectral dynamics after simulated photoexcitation of this noncavity hydrated electron showed excellent agreement with experiment. The relaxation pathway involves a rapid internal conversion followed by slow ground-state cooling, the opposite of the mechanism implicated by simulations in which the hydrated electron occupies a cavity.
自 40 多年前发现水合电子以来,人们普遍认为水合电子占据液态水中的准球形腔。我们使用经过严格推导的赝势来模拟水合电子的电子结构和动力学,以处理电子-水相互作用,其中包含了以前的赝势中未包含的有吸引力的氧和排斥氢特征。结果表明,水合电子不是位于腔体内,而是占据了一个大约 1 纳米直径的增强水密度区域。计算得出的基态吸收光谱和模拟光激发后激发态光谱动力学都与实验非常吻合。弛豫途径涉及快速的内转换,然后是缓慢的基态冷却,与水合电子占据腔的模拟所涉及的机制相反。