基质分子膜的自旋依赖性电离
John M Abendroth1,2, Kevin M Cheung1,2, Dominik M Stemer1,3
1California NanoSystems Institute , University of California, Los Angeles , Los Angeles , California 90095 , United States.
Journal of the American Chemical Society
|February 9, 2019
概括
旋转极化电子与性有机膜相互作用,影响光辐射. 这项研究揭示了分子结构和基质磁性如何影响电子自旋选择性和能量障碍.
科学领域:
- 表面科学
- 光谱学
- 有机电子
背景情况:
- 用奇拉性有机薄膜功能化的铁磁基板是旋电学中的关键.
- 了解光辐射中的旋转选择性对于开发新型电子设备至关重要.
研究的目的:
- 分析有机膜覆盖的铁磁基板的光辐射中的自旋选择性.
- 研究分子结构和基质磁化对光电子属性的影响.
主要方法:
- 在室温下进行紫外光电子光谱 (UPS).
- 分析来自铁磁基板和性有机薄膜的光电子.
- 对自组装的α螺旋和蛋白质膜 (牛血清白蛋白) 的研究.
主要成果:
- 光电子的光谱宽度取决于基质磁化方向和极化.
- 螺旋依赖的分子电离截面导致旋转极化孔.
- 基板磁化会影响电离能和工作功能,从而可以测量自旋依赖的能量障碍.
结论:
- 体有机薄膜与光电子具有自旋依赖的相互作用.
- 这项研究量化了通过奇拉膜传输电子的自旋依赖性能量障碍.
- 这些发现提供了关于旋转极化孔生成和旋转电子学潜在应用的见解.
相关概念视频
Ionization Energy
43.3K
The amount of energy required to remove the most loosely bound electron from a gaseous atom in its ground state is called its first ionization energy (IE1). The first ionization energy for an element, X, is the energy required to form a cation with 1+ charge:
43.3K
Chirality
29.4K
Chirality is a term that describes the lack of mirror symmetry in an object. In other words, chiral objects cannot be superposed on their mirror images. For example, our feet are chiral, as the mirror image of the left foot, the right foot, cannot be superposed on the left foot.
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
29.4K
Chirality in Nature
17.2K
Chirality is the most intriguing yet essential facet of nature, governing life’s biochemical processes and precision. It can be observed from a snail shell pattern in a macroscopic world to an amino acid, the minutest building block of life. Most of the snails around the world have right-coiled shells because of the intrinsic chirality in their genes. All the amino acids present in the human body exist in an enantiomerically pure state, except for glycine - the sole achiral amino acid.
17.2K
NMR Spectroscopy: Spin–Spin Coupling
3.2K
The spin state of an NMR-active nucleus can have a slight effect on its immediate electronic environment. This effect propagates through the intervening bonds and affects the electronic environments of NMR-active nuclei up to three bonds away; occasionally, even farther. This phenomenon is called spin–spin coupling or J-coupling. Coupling interactions are mutual and result in small changes in the absorption frequencies of both nuclei involved. While nuclei of the same element are involved...
3.2K
Spin–Spin Coupling: One-Bond Coupling
1.5K
Coupling interactions are strongest between NMR-active nuclei bonded to each other, where spin information can be transmitted directly through the pair of bonding electrons. While nuclei polarize their electrons to the opposite spins, the bonding electron pair has opposite spins. Configurations with antiparallel nuclear spins are expected to be lower in energy. When coupling makes antiparallel states more favorable, J is considered to have a positive value. The one-bond coupling constant, 1J,...
1.5K
Spin–Spin Coupling Constant: Overview
1.5K
In bromoethane, the three methyl protons are coupled to the two methylene protons that are three bonds away. In accordance with the n+1 rule, the signal from the methyl protons is split into three peaks with 1:2:1 relative intensities. The methylene protons appear as a quartet, with the relative intensities of 1:3:3:1.
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
1.5K


