极化连续模型和格林函数形式主义:关于溶剂电子的动态
Ivan Duchemin1, David Amblard2, Xavier Blase2
1CEA, IRIG-MEM-L_Sim, Université Grenoble Alpes, 38054 Grenoble, France.
Journal of chemical theory and computation
|September 3, 2024
概括
在多体GW计算中简化溶剂介电反应,即使具有静态光学介电常数,也会产生精确的溶液能量转移. 一个新的单极模型只使用静电介电常数就能进行动态计算.
科学领域:
- 计算化学计算化学
- 量子力学就是量子力学.
- 材料科学 材料科学 材料科学
背景情况:
- 多体GW形式主义对于计算电离电位和电子亲和度至关重要.
- 准确的GW计算取决于溶剂的依赖频率的介电函数.
- 极化连续模型 (PCM) 常用于估计溶剂效应.
研究的目的:
- 调查在GW计算中简化水的依赖频率的介电函数的影响.
- 为了评估使用静态光电介电常数 (ε∞) 而不是完全依赖频率的准确性.
- 开发一个简化的模型,用于在凝结阶段的动态GW计算.
主要方法:
- 在水的极化连续模型中采用多体GW形式主义.
- 使用完全依赖频率的介电函数的计算与使用静态 ε∞ 的计算进行了比较.
- 引入并验证了一个单极模型来模拟频率依赖.
主要成果:
- 将溶剂介电反应限制在静态 ε∞ 上,在能量水平转移中只会引入几百分之一的误差.
- 拟议的单极模型准确地复制了可见-紫外线范围内的完全频率依赖的影响.
- 这种简化使得完全动态的嵌入式GW计算只使用静电介电常数.
结论:
- 静态光电介电常数是GW能量水平计算中溶剂效应的可行和准确近似.
- 开发的单极模型提供了一种高效的方式,可以使用简化溶剂模型执行动态GW计算.
- 这项工作为研究凝结相溶液的电子性质提供了计算效率高的途径.
相关概念视频
Chemical Shift: Internal References and Solvent Effects
620
In an NMR sample, precise measurement of the absolute absorption frequencies of nuclei is difficult. A standard internal reference compound is added, and the frequency difference between the reference signal and sample signals is measured.
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
620
Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model
278
Various dissolution theories provide insight into the factors that influence the dissolution rate. Danckwerts' Model suggests that turbulence, rather than a stagnant layer, characterizes the dissolution medium at the solid-liquid interface. In this model, the agitated solvent contains macroscopic packets that move to the interface via eddy currents, facilitating the absorption and delivery of the drug to the bulk solution. The regular replenishment of solvent packets maintains the...
278
Chemical and Solubility Equilibria
4.1K
The free energy change associated with dissolving a solute in a liter of solvent is called the free energy of a solution, ΔGsolution. The overall ΔGsolution is expressed as the balance of ΔGinteraction against the always-favorable free-energy of mixing, ΔGmixing. Solution formation is favorable if ΔGsolution is less than zero, whereas it is unfavorable if ΔGsolution is greater than zero. In short, for a solution to form and complete dissolution to take place,...
4.1K
Intermolecular Forces in Solutions
33.2K
The formation of a solution is an example of a spontaneous process, a process that occurs under specified conditions without energy from some external source.
When the strengths of the intermolecular forces of attraction between solute and solvent species in a solution are no different than those present in the separated components, the solution is formed with no accompanying energy change. Such a solution is called an ideal solution. A mixture of ideal gases (or gases such as helium and argon,...
When the strengths of the intermolecular forces of attraction between solute and solvent species in a solution are no different than those present in the separated components, the solution is formed with no accompanying energy change. Such a solution is called an ideal solution. A mixture of ideal gases (or gases such as helium and argon,...
33.2K
Intermolecular Forces
58.0K
Atoms and molecules interact through bonds (or forces): intramolecular and intermolecular. The forces are electrostatic as they arise from interactions (attractive or repulsive) between charged species (permanent, partial, or temporary charges) and exist with varying strengths between ions, polar, nonpolar, and neutral molecules. The different types of intermolecular forces are ion–dipole, dipole–dipole, hydrogen bonds, and dispersion; among these, dipole–dipole, hydrogen...
58.0K
Molecular Geometry and Dipole Moments
12.7K
The VSEPR theory can be used to determine the electron pair geometries and molecular structures as follows:
12.7K


