对氨酸固化剂桥接组对铜/环氧接口中电荷注射的影响进行研究
Liuhuo Wang1, Sukai Hu1, Zhiwu Xiong2
1Guangdong Power Grid, Guangzhou 510080, China.
Materials (Basel, Switzerland)
|November 13, 2025
概括
了解金属/环氧接口的电荷注入对于高压直流 (HVDC) 气体绝缘开关装置 (GIS) 至关重要. 这项研究揭示了不同的固化剂如何影响电荷注入屏障,指导开发更可靠的电气设备.
科学领域:
- 材料科学 材料科学 材料科学
- 电气工程 电气工程
- 计算化学计算化学
背景情况:
- 准确了解金属/环氧接口的电荷注入对于高压电气设备至关重要.
- 在高压直流 (HVDC) 气体绝缘开关装置 (GIS) 内绝缘体中的表面电荷积累需要详细的调查.
研究的目的:
- 在HVDC GIS中调查金属/环氧接口的电荷注入行为.
- 评估不同氨基固化剂对界面电荷动态的影响.
主要方法:
- 使用第一原理计算来建模Cu(111) 和具有特定固化剂 (DDM和6FDAM) 的环氧树脂之间的接口.
- 评估的关键参数:注入障碍,电荷转移和真空能量水平的变化.
- 通过宏观电荷注入实验验验证了计算结果.
主要成果:
- 具有-C2F6键的分子结构显示出比具有-CH2.2.的更高的电子和孔注入障碍.
- 由于低电子负性,DDM降低了界面电荷注入障碍,并改善了电荷传输.
- 6FDAM由于其强烈的电负性质,增加了屏障高度.
结论:
- 固化剂的选择显著影响金属/环氧接口上的电荷注入和传输.
- 这些发现为设计和应用先进的高压直流GIS设备提供了宝贵的见解.
- 在HVDC应用中,DDM是一种有前途的固化剂,可减少电荷注入障碍.
相关概念视频
Basicity of Heterocyclic Aromatic Amines
6.9K
Heterocyclic amines, where the N atom is a part of an alicyclic system, are similar in basicity to alkylamines. Interestingly, the heterocyclic amine having a nitrogen atom as part of an aromatic ring has much less basicity than its corresponding alicyclic counterpart. For this reason, as presented in Figure 1, piperidine (pKb = 2.8) is significantly more basic than pyridine (pKb = 8.8).
6.9K
Basicity of Aromatic Amines
8.0K
The basicity of aromatic amines is much weaker than that of aliphatic amines due to the involvement of the lone pair of electrons over the N atom in resonance with the aryl rings. Generally, the electron-donating ability of any substituents on the aryl ring of aromatic amines increases the basicity of the amine by increasing electron density, and hence the availability of lone pair on the nitrogen. On the other hand, electron-withdrawing functional groups on the aryl ring of amines decrease the...
8.0K
Diazonium Group Substitution: –OH and –H
3.3K
Nitrous acid, a weak acid, is prepared in situ via the reaction of sodium nitrite with a strong acid under cold conditions. This nitrous acid prepared in situ reacts with primary arylamines to form arenediazonium salts. Such reactions are known as diazotization reactions. As shown in Figure 1, the formation of arenediazonium salts begins with the decomposition of nitrous acid in an acidic solution to give nitrosonium ions.
3.3K
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
3.6K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para...
3.6K
π Electron Effects on Chemical Shift: Overview
1.6K
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,...
1.6K
Complexation Equilibria: The Chelate Effect
1.2K
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
1.2K


