柔性电弹性体通过可混性驱动的尼特分子旋转来实现
Moonseok Jang1, Bitgaram Kim1,2, Ji-Hun Seo1
1Department of Materials Science and Engineering, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul, 02841, Republic of Korea.
Advanced science (Weinheim, Baden-Wurttemberg, Germany)
|November 7, 2025
概括
这项研究探讨了聚合物网络中的苏奇尼尼特 (SN) 塑料晶体中的柔电性. 交叉连接的基于SN的复合材料展示了高效的机械到电能转换,突出了软材料的设计原则.
科学领域:
- 材料科学 材料科学 材料科学
- 固态物理 固态物理
- 聚合物科学 聚合物科学
背景情况:
- 塑料晶体具有独特的顺序/混乱特性,在应变梯度下允许柔电,尽管缺乏压电.
- 一种极性塑料晶体苏奇尼尼特 (SN),由于其分子动力学,显示出电机应用的潜力.
- 之前的研究集中在纯或合的SN上,不探讨聚合物网络的影响.
研究的目的:
- 研究共振交联聚合物网络如何影响SN的旋转动力学和柔电性质.
- 确定聚合物-SN混合性,微观结构,分子移动性和机电合之间的关系.
- 建立用于机械到电能转换的新型软材料的设计原则.
主要方法:
- 在复合网中聚合物-SN混合性的系统变化.
- 在机械应力下测量机电性能 (电压,电流) (手指敲击).
- 通过三点曲试验,通过介电分析和DFT计算来确定柔电系数.
主要成果:
- SN_MMA复合材料表现出最高的电机性能,产生2.79 V和0.082 μA cm−2.2.
- 在SN_MMA复合材料中记录了22.8 nC m-1的最高柔电系数.
- 最佳性能归因于界面应力局部化,并保留了聚合物网络内的 SN 定向自由.
结论:
- 联交联的聚合物网络可以显著增强succinonitrile的柔电特性.
- 微观结构和SN分子流动性是实现这些软材料高效电机械合的关键因素.
- 该SN_MMA复合材料作为设计高性能,非零电能收获材料的模型.
相关概念视频
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
3.1K
Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
3.1K
Olefin Metathesis Polymerization: Overview
2.5K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
2.5K
Cationic Chain-Growth Polymerization: Mechanism
2.8K
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
2.8K
Thermal and Photochemical Electrocyclic Reactions: Overview
2.9K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
2.9K
Thermal Electrocyclic Reactions: Stereochemistry
2.5K
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
2.5K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
2.2K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
2.2K


