Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Molecular Orbital Theory II03:51

Molecular Orbital Theory II

19.1K
Molecular Orbital Energy Diagrams
19.1K
The Quantum-Mechanical Model of an Atom02:45

The Quantum-Mechanical Model of an Atom

42.2K
Shortly after de Broglie published his ideas that the electron in a hydrogen atom could be better thought of as being a circular standing wave instead of a particle moving in quantized circular orbits, Erwin Schrödinger extended de Broglie’s work by deriving what is now known as the Schrödinger equation. When Schrödinger applied his equation to hydrogen-like atoms, he was able to reproduce Bohr’s expression for the energy and, thus, the Rydberg formula governing hydrogen spectra.
42.2K
Stability of Conjugated Dienes01:28

Stability of Conjugated Dienes

3.3K
Introduction
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
3.3K
Maxwell-Boltzmann Distribution: Problem Solving01:20

Maxwell-Boltzmann Distribution: Problem Solving

1.4K
Individual molecules in a gas move in random directions, but a gas containing numerous molecules has a predictable distribution of molecular speeds, which is known as the Maxwell-Boltzmann distribution, f(v).
This distribution function f(v) is defined by saying that the expected number N (v1,v2) of particles with speeds between v1 and v2 is given by
1.4K
MO Theory and Covalent Bonding02:40

MO Theory and Covalent Bonding

10.4K
The molecular orbital theory describes the distribution of electrons in molecules in a manner similar to the distribution of electrons in atomic orbitals. The region of space in which a valence electron in a molecule is likely to be found is called a molecular orbital. Mathematically, the linear combination of atomic orbitals (LCAO) generates molecular orbitals. Combinations of in-phase atomic orbital wave functions result in regions with a high probability of electron density, while...
10.4K
Hybridization of Atomic Orbitals I03:24

Hybridization of Atomic Orbitals I

46.9K
The mathematical expression known as the wave function, ψ, contains information about each orbital and the wavelike properties of electrons in an isolated atom. When atoms are bound together in a molecule, the wave functions combine to produce new mathematical descriptions that have different shapes. This process of combining the wave functions for atomic orbitals is called hybridization and is mathematically accomplished by the linear combination of atomic orbitals. The new orbitals that...
46.9K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Toward the "Gold Standard" in Bootstrap Embedding.

Journal of chemical theory and computation·2025
Same author

Efficient acceleration of the convergence of the minimum free energy path via a path-planning generated initial guess.

Journal of computational chemistry·2024
Same author

Toward a Full Configurational Accuracy Calculation of an Arbitrary Molecule via Fragment Embedding and a Stochastic Solver.

The journal of physical chemistry letters·2024
查看所有相关文章

相关实验视频

Updated: Jun 20, 2025

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
12:11

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry

Published on: April 8, 2020

8.2K

加速密度矩阵嵌入与随机密度拟合理论:对结集群的应用.

Yi Sun1

  • 1Department of Chemistry, Chicago Center for Theoretical Chemistry, James Franck Institute, and Institute for Biophysical Dynamics, The University of Chicago, Chicago, Illinois 60637, United States.

Journal of chemical theory and computation
|July 19, 2024
PubMed
概括

半定态密度拟合 (ss-DF) 通过减少辅助轨道来加速量子嵌入计算. 这种方法在复杂的分子模拟中大大节省了时间,有效捕捉弱相互作用.

科学领域:

  • 计算化学计算化学
  • 量子嵌入理论 量子嵌入理论
  • 材料科学 材料科学 材料科学

背景情况:

  • 自相一致的密度矩阵嵌入理论 (DMET) 是一种强大的量子化学方法,用于研究大型系统.
  • 传统的DMET计算可能由于处理积分而具有昂贵的计算成本.
  • 密度匹配 (DF) 技术可以加快这些计算,但确定性DF (d-DF) 仍然存在挑战.

研究的目的:

  • 为了证明使用半静态密度拟合 (ss-DF) 的DMET计算的加速.
  • 研究ss-DF对计算效率和准确性的影响.
  • 展示基于ss-DF的DMET在分子集群中恢复弱相互作用的能力.

主要方法:

  • 在DMET框架内实施半静态密度适配 (ss-DF).
  • 减少三指数 DF 积分中的辅助轨道,以节省计算时间.
  • 应用于与结合的集群 (水和化) 和分析Hartree-Fock矩阵结构和积分转换.

主要成果:

  • 在构建Hartree-Fock矩阵和使用ss-DF转换积分方面实现了显著的时间节约.
  • 对 (H2O) 10集群的分析表明,决定性空间大小对计算质量的影响.
  • 与d-DF相比,ss-DF在水集群 (6-30个分子) 中表现出更高的计算效率,具有三次-ζ基础集.

更多相关视频

Spatial Separation of Molecular Conformers and Clusters
10:37

Spatial Separation of Molecular Conformers and Clusters

Published on: January 9, 2014

8.9K
Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics
10:52

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics

Published on: April 12, 2019

12.8K

相关实验视频

Last Updated: Jun 20, 2025

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
12:11

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry

Published on: April 8, 2020

8.2K
Spatial Separation of Molecular Conformers and Clusters
10:37

Spatial Separation of Molecular Conformers and Clusters

Published on: January 9, 2014

8.9K
Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics
10:52

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics

Published on: April 12, 2019

12.8K
  • 数字结构优化证实了DMET通过反转换能量公式恢复弱相互作用的能力.
  • 结论:

    • 半定态密度拟合 (ss-DF) 提供了一种有前途的方法来加速像DMET这样的量子嵌入理论.
    • 该方法提供了显著的计算加速,而不会影响相关化学系统的准确性.
    • 基于ss-DF的DMET有效捕捉弱相互作用,这对于理解分子结构和特性至关重要.