聚烯 (烯) 基烯 (烯) 与醇吊用于性离子溶解聚合物电解质
Yifan Xia1, Sinu C Rajappan1, Si Chen2
1Department of Energy Conversion and Storage, Technical University of Denmark, Elektrovej, Building 375, Lyngby, 2800, Denmark.
ChemSusChem
|August 8, 2024
概括
新的四醇功能化膜作为性水电解的高效电极分离器. 这些先进的膜实现了高性能,为增强气生产提供了改进的气体屏障特性.
科学领域:
- 材料科学 材料科学 材料科学
- 电化学 电化学 电化学
- 聚合物化学 聚合物化学
背景情况:
- 性水电解需要强大而高效的电极分离器.
- 像Zirfon这样的现有分离器在厚度和气体屏障特性方面存在局限性.
- 新型离子溶解膜的开发对于推进电解技术至关重要.
研究的目的:
- 准备和表征新的四醇功能化聚烯基烯膜.
- 为了评估这些膜作为性水电解中的电极分离器.
- 评估它们的离子导电性,机械性能和在电解电池中的性能.
主要方法:
- 通过超酸催化聚酸基化合成一种基本的聚 ((烯基) 聚合物.
- 聚合物的功能化与四醇吊.
- 膜性质的表征,包括各种KOH度的离子导电性.
- 在使用未催化Ni-泡电极的性电解细胞试验中进行评估.
主要成果:
- 四醇功能化膜的峰值离子导电率为19 mS/cm在5重%的KOH中.
- 导电性在30重%KOH中略有下降至13mS/cm,表明稳定性良好.
- 在30重%KOH的电解试验中,在<2.6V时达到高达1000mA/cm2的电流密度.
- 与较厚的Zirfon分离器相比,膜显示出优越的气体屏障特性.
结论:
- 醇功能化的聚烯基烯膜是性水电解的有效电极分离器.
- 这些膜为传统分离器提供了有希望的替代品,可实现高电流密度和更高的安全性.
- 进一步优化可能会导致生产效率更高.
相关概念视频
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
2.9K
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...
2.9K
Ion Exchange
566
Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or...
566
Anionic Chain-Growth Polymerization: Overview
2.1K
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,...
2.1K
EDTA: Chemistry and Properties
1.8K
Polydentate ligands are most widely used in complexometric titrations because they form more stable complexes with the metal ions than mono- or bidentate ligands due to the chelate effect. Examples of polydentate ligands are ethylenediaminetetraacetic acid (EDTA), crown ethers, and cryptands. The most important feature of optimal polydentate ligands is the ability to form 1:1 complexes in a single-step process. Amino carboxylic acid derivatives are frequently used as complexing agents. EDTA is...
1.8K
Electrophilic Addition to Alkynes: Halogenation
8.2K
Introduction
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
8.2K
Aromatic Hydrocarbon Cations: Structural Overview
2.8K
Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
Removing one hydrogen from the intervening CH2 group...
Removing one hydrogen from the intervening CH2 group...
2.8K


