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相关概念视频

Redox Reactions01:24

Redox Reactions

58.1K
Oxidation-reduction or redox reactions involve the transfer of electrons from one molecule or atom to another. When an atom gains an electron, another atom must lose an electron, meaning oxidation and reduction must occur together. Since the redox occurs in pairs, the atom that gets oxidized is also called the reducing agent or reductant, and the atom that is reduced is also called the oxidizing agent or oxidant. A straightforward way to remember the definitions of oxidation and reduction is...
58.1K
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

23.6K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
23.6K
Ladder Diagrams: Redox Equilibria01:30

Ladder Diagrams: Redox Equilibria

716
Ladder diagrams are useful tools for understanding redox equilibrium reactions, especially the effects of concentration changes on the electrochemical potential of the reaction. The vertical axis in the redox ladder diagrams represents the electrochemical potential, E. The area of predominance is demarcated using the Nernst equation.
Consider the Fe3+/Fe2+ half-reaction, which has a standard-state potential of +0.771 V. At potentials more positive than +0.771 V, Fe3+ predominates, whereas Fe2+...
716
Redox Titration: Other Oxidizing and Reducing Agents01:26

Redox Titration: Other Oxidizing and Reducing Agents

1.3K
Besides iodine, other oxidizing or reducing agents can serve as titrants in redox titrations. Common oxidizing titrants include KMnO4, cerium(IV), and K2Cr2O7. The choice of oxidizing titrants depends on factors like stability, cost, analyte strength, and reaction rate between the analyte and titrant. KMnO4 is a strong oxidizing titrant that reduces from Mn(VII) to Mn(II) in a highly acidic solution, simultaneously oxidizing the analyte to a higher oxidation state. In this case, KMnO4 acts as a...
1.3K
Extraction: Advanced Methods00:56

Extraction: Advanced Methods

1.0K
Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
1.0K
Redox Equilibria: Overview01:23

Redox Equilibria: Overview

1.5K
A reduction-oxidation reaction is commonly called a redox reaction. In a redox reaction, electrons are transferred from one species to another rather than being shared between or among atoms. The reducing agent or reductant is the species that loses electrons and gets oxidized in the process. The species that gains electrons and gets reduced in the process is the oxidizing agent or oxidant. Redox reactions are represented as two separate equations called half-reactions, where one equation...
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Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
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对于具有可调节的反氧导电性有机金属框架的固体溶液方法

Gavin S Mohammad-Pour, Kendrich O Hatfield, David C Fairchild

    Journal of the American Chemical Society
    |December 3, 2019
    PubMed
    概括

    研究人员开发了可调节导电性的金属有机框架 (MOF) 薄膜电极. 这种进步可以精确控制电荷传输,从而改善能量和传感应用.

    科学领域:

    • 材料科学
    • 电化学
    • 纳米技术

    背景情况:

    • 金属有机框架 (MOF) 提供可调节的孔隙性和合成控制,但其电化学应用受到导电性的限制.
    • 系统调整MOF导电性对于将其特性整合到储能和传感技术中至关重要.
    • 反氧活性吊可以促进MOF中的电荷转移,但受控的集成仍然是一个挑战.

    研究的目的:

    • 引入一种新的策略,用于准备具有精确控制的氧化还原悬挂含量的氧化还原活性MOF薄膜电极.
    • 调查氧化还原悬挂度和由此产生的MOF电极电导率之间的关系.
    • 评估这些工程MOF材料中的电化学稳定性和电荷传递机制.

    主要方法:

    • 使用固体溶液方法制造MOF薄膜电极,具有不同比例的氧化还原活性 (酸铁素) 和非活性链接剂.
    • 在MOF合成过程中,系统调节氧化还原悬挂含量以控制导电性.
    • 电化学特性,包括导电性测量和数千次氧化还原循环的稳定性测试.
    • 电分析研究以阐明电荷转移机制 (例如,扩散,跳跃,透).

    主要成果:

    • 成功准备的MOF薄膜电极具有可调节的氧化还原导电性.
    • 实现了1.10mS m-1的最大电子导电性.

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  • 在成千上万的氧化还原循环中表现出极好的晶体和电化学稳定性.
  • 观察到与非线性扩散系数类似的扩散控制导电性行为.
  • 结论:

    • 开发的策略可以通过控制的氧化还原悬挂来微调MOF中的氧化还原导电性.
    • MOF电极表现出强大的稳定性,并表现出与跳跃和透模型相一致的电荷转移.
    • 这项工作为电池和传感器等电化学设备设计先进的氧化还原活性MOF开辟了新的途径.