基于状态平均长距离CASSCF短距离DFT的激发状态方法.
Benjamin Helmich-Paris1, Erik Rosendahl Kjellgren2, Hans Jørgen Aa Jensen2
1Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, D-45470 Mülheim an der Ruhr, Germany. helmichparis@kofo.mpg.de.
Physical chemistry chemical physics : PCCP
|July 10, 2025
概括
两个新的方法,SA-CAS-srDFT和CI-srDFT,使用密度函数理论计算激发状态. CI-srDFT显示有机分子的精度提高,为电子刺激能量计算提供了更可靠的方法.
科学领域:
- 计算化学计算化学
- 量子化学 是一个量子化学.
- 理论化学 理论化学
背景情况:
- 精确计算激发状态对于理解分子性质和反应至关重要.
- 像CASSCF-DFT这样的现有方法在准确性和适用性方面存在局限性,特别是在复杂的系统中.
研究的目的:
- 开发和评估基于状态平均 (SA) 的新方法来计算激发状态.
- 将这些新方法的性能与各种分子系统的现有方法进行比较.
主要方法:
- 提出了两个不同的基于状态平均 (SA) 的方法:SA-CAS-srDFT和CI-srDFT.
- 使用了长距离完全活跃空间自我一致场 (CASSCF) 短距离密度函数理论 (DFT) 方法 (CAS-srDFT).
- 采用总一体和顶部对密度 (OTPD) 来进行最终能量评估,并与多重配置对密度函数理论 (MC-PDFT) 进行基准测试.
主要成果:
- 与SA-CAS-srDFT不同,CI-srDFT为乙烯提供了物理正确的潜在曲线.
- CI-srDFT显示激发能量的依赖性减少了对平均状态数量的依赖性.
- 使用sr-ctPBE功能,CI-srDFT在有机染色体的单点激发能达到0.17 eV的平均绝对误差.
- 开发的方法对有机分子显示了令人印象深刻的准确性,但不能转移到过渡金属复合体.
结论:
- 与SA-CAS-srDFT相比,CI-srDFT是计算有机分子激发状态的更准确,更可靠的方法.
- 当前的CASSCF-DFT和MC-PDFT方法对CASSCF激发能没有持续的改进,特别是对于过渡金属复合体.
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