摘要
基于经典热力学约束平衡方法,采用新非平衡溶剂化理论研究了Np O+2-Np O2+2体系电子转移反应的溶剂重组能,采用限制密度泛函理论实现电荷定域,用积分方程可极化连续介质模型获得水溶液中极化电荷.计算结果表明,新双球模型和数值解都给出了一致的溶剂重组能理论计算值.
A novel nonequilibrium solvation theory established recently by the authors was introduced Differing from the traditional ones, the present theory was based on the constrained equilibrium principle of classical thermodynamics. The calculations of solvent reorganization energy were performed with the electron transfer system of NpO2-NpO2+2as an example. The constrained density functional theory was adopted for the charge localization of the system and IEF-PCM was used for the gain of polarization charges in water. Both two-sphere model and numerical solution give consistent and reasonable solvent reorganization energies.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2015年第11期2256-2261,共6页
Chemical Journal of Chinese Universities
基金
国家自然科学基金(批准号:91441132)资助~~
关键词
非平衡溶剂化
约束平衡态
电子转移
溶剂重组能
Nonequilibrium solvation
Constrained equilibrium state
Electron transfer
Solventreorganization energy