多站点充电转移的快速方法. 处理过程II. 对cCASSCF(1,n) 和cCASSCF(2n-1,n) 波函数的分析核梯度和非adiabatic动态
1Department of Chemistry, Princeton University, Princeton, New Jersey 08540, USA.
The Journal of chemical physics
|December 19, 2025
概括
我们开发了用于模拟电子和孔转移的新计算方法,使电荷转移过程的高效模拟成为可能,例如化学系统中的质子合电子转移.
科学领域:
- 计算化学的计算化学
- 量子化学 是一个量子化学.
- 理论化学 理论化学
背景情况:
- 模拟电子和孔转移对于理解化学反应至关重要.
- 精确的模拟需要有效的方法来计算能量梯度和合.
研究的目的:
- 为受约束的完全活性空间自相一致场 (CASSCF) 推导和实施分析核梯度和导数合.
- 开发一个高效的算法,用于电荷转移过程的非adiabatic动态模拟.
主要方法:
- 利用拉格朗日形式主义来区分CASSCF能量和约束.
- 为受约束的CASSCF实施分析核梯度和衍生合.
- 将该方法应用于对质子合电子转移的表面跳跃模拟.
主要成果:
- 衍生和实施分析核梯度和衍生合.
- 开发了一种有效的算法,适用于非adiabatic动态模拟.
- 成功地运行了用于氧-系统的初始表面跳跃模拟.
结论:
- 开发的方法为建模电荷转移过程提供了一种高效的方法.
- 该算法适用于非adiabatic动态模拟.
- 证明了对研究质子合电子转移事件的实用性.
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