基于线性响应pCCD的方法:LR-pCCD和LR-pCCD+S方法,用于高效可靠地建模激发国家财产
Somayeh Ahmadkhani1, Katharina Boguslawski1, Paweł Tecmer1
1Institute of Physics, Faculty of Physics, Astronomy, and Informatics, Nicolaus Copernicus University in Toruń, Toruń, Grudziadzka 5, Toruń 87-100, Poland.
Journal of chemical theory and computation
|November 20, 2024
概括
我们介绍了线性响应对合集群双与单 (LR-pCCD+S) 方法,用于准确的电子光谱计算. 这种具有成本效益的方法为激发能和过渡双极时刻提供了CCSD级准确性.
科学领域:
- 量子化学 是一个量子化学.
- 计算化学的计算化学
- 理论化学 理论化学
背景情况:
- 准确预测电子光谱对于理解分子性质至关重要.
- 对于复杂的系统,标准的电子结构方法在计算上可能很昂贵.
- 开发具有成本效益和准确的方法是计算化学的一个持续挑战.
研究的目的:
- 为了导出和验证线性响应对合集群双重与单一 (LR-pCCD+S) 方法.
- 评估LR-pCCD+S的性能,用于计算电子激发能量和过渡二极极矩.
- 评估轨道优化对LR-pCCD+S模型准确性的影响.
主要方法:
- 为LR-pCCD和LR-pCCD+S提供工作方程的导出.
- 对LR-pCCD+S与线性响应合集群单双 (LR-CCSD) 的比较.
- 分析轨道优化效应和统计错误分析.
主要成果:
- LR-pCCD+S准确地复制了小分子 (BH,H2O,H2CO, furan) 的过渡二极点时刻和激发能.
- 该方法证明了成本效益,接近CCSD准确性与平均场计算成本.
- 成功模拟了具有显著双激发贡献和聚光谱的电子转换.
结论:
- LR-pCCD+S是电子光谱建模的可靠和计算效率高的替代方案.
- 该方法对模拟复杂的电子转换和扩展联系统具有前景.
- 在pCCD中轨道优化对过渡二极极矩计算产生了积极的影响.
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