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相关概念视频

The Quantum-Mechanical Model of an Atom02:45

The Quantum-Mechanical Model of an Atom

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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.
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π Electron Effects on Chemical Shift: Overview01:27

π Electron Effects on Chemical Shift: Overview

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An applied magnetic field causes loosely bound π-electrons in organic molecules to circulate, producing a local or induced diamagnetic field over a large spatial volume. As the molecules tumble in solution, the field generated by π-electrons in spherical substituents results in a zero net field. However, the net field generated by π-electrons in non-spherical substituents is not zero. The effect of this induced field depends on the orientation of the molecule with respect to B0,...
1.1K
Electron Configurations02:46

Electron Configurations

16.6K
Electron configurations and orbital diagrams can be determined by applying the Aufbau principle (each added electron occupies the subshell of lowest energy available), Pauli exclusion principle (no two electrons can have the same set of four quantum numbers), and Hund’s rule of maximum multiplicity (whenever possible, electrons retain unpaired spins in degenerate orbitals).
The relative energies of the subshells determine the order in which atomic orbitals are filled (1s, 2s, 2p, 3s, 3p,...
16.6K
¹H NMR: Interpreting Distorted and Overlapping Signals01:02

¹H NMR: Interpreting Distorted and Overlapping Signals

1.0K
Spin systems where the difference in chemical shifts of the coupled nuclei is greater than ten times J are called first-order spin systems. These nuclei are weakly coupled, and their chemical shifts and coupling constant can generally be estimated from the well-separated signals in the spectrum.
As Δν decreases and the signals move closer, the doublets appear increasingly distorted. The intensities of the inner lines increase at the cost of those of the outer lines as the signals are...
1.0K
The Bohr Model02:18

The Bohr Model

53.6K
Following the work of Ernest Rutherford and his colleagues in the early twentieth century, the picture of atoms consisting of tiny dense nuclei surrounded by lighter and even tinier electrons continually moving about the nucleus was well established. This picture was called the planetary model since it pictured the atom as a miniature “solar system” with the electrons orbiting the nucleus like planets orbiting the sun. The simplest atom is hydrogen, consisting of a single proton as...
53.6K
Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals01:17

Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals

2.5K
Ideally, an unpaired electron shows a single peak in the EPR spectrum due to the transition between the two spin energy states. However, coupling interactions can occur between the spins of the unpaired electron and any neighboring spin-active nuclei. This hyperfine coupling results in hyperfine splitting, where the EPR signal is split into multiplets. The signals split into 2nI + 1 peaks, where n is the number of equivalent nuclei and I is the nuclear spin. These splitting patterns provide...
2.5K

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Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
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Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry

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一个电子的自我相互作用校正方法对于有小数电子的系统的性能有多好?

Rajendra R Zope1, Yoh Yamamoto1, Tunna Baruah1

  • 1Department of Physics, The University of Texas at El Paso, El Paso, Texas 79968, USA.

The Journal of chemical physics
|February 22, 2024
PubMed
概括

局部缩放的自我相互作用校正 (LSIC) 方法在解决电子结构计算中的移位错误方面,比Perdew-Zunger自我相互作用校正 (PZSIC) 方法更准确. 这两种方法都减少了错误,但LSIC在几个关键领域提供了卓越的性能.

科学领域:

  • 量子化学 是一个量子化学.
  • 计算材料科学科学 计算材料科学
  • 电子结构理论 电子结构理论

背景情况:

  • 自相互作用误差是密度函数理论 (DFT) 近似中的一个重要问题.
  • 佩尔杜-格尔自我相互作用校正 (PZSIC) 方法试图纠正这个错误,但表现出矛盾的行为.
  • 局部缩放的自我相互作用校正 (LSIC) 是一种较新的,单电子的SIC方法,旨在改进PZSIC.

研究的目的:

  • 评估LSIC方法在缓解移位错误方面的性能.
  • 为了比较LSIC与PZSIC在各种电子结构问题上的准确性.
  • 评估LSIC描述分子解离和分数电荷的能力.

主要方法:

  • 该研究采用LSIC方法,将动能密度 (zσ) 的比率作为同轨道指标.
  • 对分子解离 (H2+,He2+,LiF) 和垂直电离能进行了计算.
  • 对微分电荷的能量与电子数曲线的线性进行了分析.

主要成果:

  • 无论是LSIC还是PZSIC都准确地描述了H2+和He2+的解离,而LSIC的整体准确性更高.
  • 无论是LSIC还是PZSIC,都没有对孤立的原子的垂直电离能产生偏移错误.

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Excitonic Hamiltonians for Calculating Optical Absorption Spectra and Optoelectronic Properties of Molecular Aggregates and Solids
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Excitonic Hamiltonians for Calculating Optical Absorption Spectra and Optoelectronic Properties of Molecular Aggregates and Solids
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  • 这两种方法都显著减少了微分电荷的线性偏差,而PZSIC对于C,Ne和Ar更优越.
  • LSIC在LiF解离中证明了精确的电荷转移,与实验和初始数据保持一致.
  • 结论:

    • 在电子结构计算中,LSIC 方法大大减少了移位错误.
    • 与PZSIC相比,LSIC在特定情况下提供了更好的准确性和更好的费用转移描述.
    • 作为一个可靠的方法,LSIC显示了准确的电子结构预测的前景.