一石二鸟:基于二茂铁的锆(IV)-有机框架纳米片既具有高质子传导性,又可作为壳聚糖基复合膜的精细掺杂剂

IF 4.8 3区 材料科学 Q1 CHEMISTRY, APPLIED Microporous and Mesoporous Materials Pub Date : 2024-09-19 DOI:10.1016/j.micromeso.2024.113342
Yu-Ling Hong , Lu-Lu Kang , Bingbing Li , Zhi-Qiang Shi , Zifeng Li , Gang Li
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引用次数: 0

摘要

最近的研究表明,将具有突出质子传导性(σ)的金属有机框架(MOFs)作为填料与壳聚糖(CS)或纳菲翁(Nafion)等有机基质一起使用,是制备具有突出功能性的复合膜(CMs)的有效方法。受此启发,本研究成功制备了一种由 1,1′-二茂铁二羧酸 (H2FDA) 生成的具有纳米片状结构的极其稳定的 Zr(IV)-MOF (即 Zr-FDC),并随后将其用作填料,通过浇铸法合成了一系列基于 CS 的 CM。交流阻抗测定结果表明,Zr-FDC 和相关的 CS 基 CM(CS/MOF-x;x = 2、4、6、8,即 Zr-MOF 在 CM 中的质量百分比)均显示出超高的 σ 值,这表明了 Zr-MOF 的结构优势。进一步的研究证实,当 MOF 掺杂量为 4 % 时,CM(CS/MOF-4)的 σ 值最大,为 2.22 × 10-2 S/cm,在 100 °C 和 98 % 相对湿度(RH)条件下,比原始 MOF(3.2 × 10-3 S/cm)提高了近 10 倍。此外,CM 还具有优异的热稳定性和抗拉性。最后,考虑到 MOF 和 CS 的结构特征、活化能数据以及其他测定结果,我们对 MOF 框架和 CM 中的质子传导过程进行了深入的理论分析,为后续的质子交换膜设计提供了参考。
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Two birds with one stone: A ferrocene-based zirconium(IV)-organic framework nanosheet denoting intrinsic high proton conductivity and acting as a fine dopant to chitosan-based composite membranes
Recently, it was demonstrated that employing metal-organic frameworks (MOFs) with prominent proton conductivity (σ) as fillers with organic substrates such as chitosan (CS) or Nafion is an effective approach for preparing composite membranes (CMs) with outstanding functionalities. Inspired by this, one extremely stable Zr(IV)-MOF (namely Zr-FDC) with a nanosheet structure produced by 1,1′-ferrocene dicarboxylic acid (H2FDA) was successfully manufactured in this research and subsequently used as a filler to synthesize a series of CS-based CMs via casting method. The alternating current (AC) impedance determinations manifested that both Zr-FDC and the related CS-based CMs (CS/MOF-x; x = 2, 4, 6, 8 being the mass percentage of Zr-MOF in the CM) showed ultrahigh σ values, indicating the structural advantages of the Zr-MOF. Further research verified that when the MOF doping quantity is 4 %, the CM's (CS/MOF-4) σ is the greatest, being 2.22 × 10−2 S/cm, which is boosted by nearly tenfold at 100 °C and 98 % relative humidity (RH) compared to the original MOF (3.2 × 10−3 S/cm). Furthermore, the CM exhibits superior thermal stability and tensile resistance. Finally, considering the structural features of the MOF and CS, activation energy data, and other determinations, we thoroughly theorized the proton conduction process within the MOF framework and CMs, referencing the subsequent proton exchange membrane design.
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来源期刊
Microporous and Mesoporous Materials
Microporous and Mesoporous Materials 化学-材料科学:综合
CiteScore
10.70
自引率
5.80%
发文量
649
审稿时长
26 days
期刊介绍: Microporous and Mesoporous Materials covers novel and significant aspects of porous solids classified as either microporous (pore size up to 2 nm) or mesoporous (pore size 2 to 50 nm). The porosity should have a specific impact on the material properties or application. Typical examples are zeolites and zeolite-like materials, pillared materials, clathrasils and clathrates, carbon molecular sieves, ordered mesoporous materials, organic/inorganic porous hybrid materials, or porous metal oxides. Both natural and synthetic porous materials are within the scope of the journal. Topics which are particularly of interest include: All aspects of natural microporous and mesoporous solids The synthesis of crystalline or amorphous porous materials The physico-chemical characterization of microporous and mesoporous solids, especially spectroscopic and microscopic The modification of microporous and mesoporous solids, for example by ion exchange or solid-state reactions All topics related to diffusion of mobile species in the pores of microporous and mesoporous materials Adsorption (and other separation techniques) using microporous or mesoporous adsorbents Catalysis by microporous and mesoporous materials Host/guest interactions Theoretical chemistry and modelling of host/guest interactions All topics related to the application of microporous and mesoporous materials in industrial catalysis, separation technology, environmental protection, electrochemistry, membranes, sensors, optical devices, etc.
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