一种可生物降解的基性聚合物使高性能,物理短暂的有机记忆成为可能
Jaehyoung Ko1, Soeun Kim2, Daeun Kim1,3
1Functional Composite Materials Research Center, Korea Institute of Science and Technology, Jeonbuk, 55324, Republic of Korea.
Angewandte Chemie (International ed. in English)
|April 28, 2025
概括
研究人员使用激进聚合物开发了可持续的,短暂的电子. 这些材料能够实现先进的神经形态计算和生物分离,减少未来生物电子设备的电子废物.
科学领域:
- 材料科学 材料科学 材料科学
- 电子工程 电子工程
- 生物技术是生物技术.
背景情况:
- 电子设备面临的可靠性要求,但有助于电子垃圾.
- 物理过渡性电子产品提供了一个可持续的替代品,特别是生物电子产品.
- 记忆材料是节能神经形态计算的关键.
研究的目的:
- 在软材料中,将记忆性特性与短暂行为结合起来.
- 创建先进的计算材料,也可以可持续地分离.
- 加强整合使用可调节,生物相容和经济高效的软材料.
主要方法:
- 一个基聚物的分子工程.
- 制造双终端记忆设备.
- 开发灵活的,短暂的横杆阵列.
主要成果:
- 特殊的内存性能: >10^6开/关比, >10^4秒的保留时间, 250+周期的稳定性.
- 过渡性设备通过>3,000个曲周期保持性能.
- 在室温水中完全解离.
结论:
- 展示了一种用于短暂记忆材料的新型分子工程策略.
- 开发了高性能,灵活和可生物降解的电子元件.
- 推进了用于神经形态生物电子学的多功能,生物现实平台的开发.
相关概念视频
Radical Chain-Growth Polymerization: Overview
2.3K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
2.3K
Free-Radical Chain Reaction and Polymerization of Alkenes
7.6K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
7.6K
Radical Chain-Growth Polymerization: Mechanism
2.4K
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this...
2.4K
Radical Chain-Growth Polymerization: Chain Branching
1.9K
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
1.9K
Radical Reactivity: Steric Effects
1.9K
The presence of electron-donating, electron-withdrawing, or conjugating groups adjacent to a radical center, imparts electronic stabilization to the radicals. Examples of such electronically-stabilized radicals are triphenylmethyl, tetramethylpiperidine‐N‐oxide, and 2,2‐diphenyl‐1‐picrylhydrazyl. These radicals are remarkably stable and are known as persistent radicals. Some of the persistent radicals can even be isolated and purified.
Along with electronic...
Along with electronic...
1.9K
Anionic Chain-Growth Polymerization: Overview
2.0K
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
2.0K


