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Electrochemistry is the science involved in the interconversion of electrical and chemical reactions. Such reactions are called reduction-oxidation, or redox reactions. These important reactions are defined by changes in oxidation states for one or more reactant elements and include a subset of reactions involving the transfer of electrons between reactant species. Electrochemistry as a field has evolved to yield sufficient insights on the fundamental principles of redox chemistry and multiple...
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In a galvanic cell, the electrical work is done by a redox system on its surroundings as electrons produced by the spontaneous redox reactions are transferred through an external circuit. Alternatively, an external circuit does work on a redox system by imposing a voltage sufficient to drive an otherwise nonspontaneous reaction in a process known as electrolysis. For instance, recharging a battery involves the use of an external power source to drive the spontaneous (discharge) cell reaction in...
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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...
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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.
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可充电多价离子电池中的可逆电化学离子还氧化

Ankur L Jadhav1, Taylor R Juran2, Matthew A Kim3

  • 1Department of Chemical Engineering, The City College of New York, CUNY, New York, New York 10031, United States.

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概括

可充电的多价离子电池是有前途的,但多价离子介质的阴极材料稀缺. 这项研究揭示了环相中独特的阳离子氧化还原机制,使稳定的多价值离子间隔成为可能.

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科学领域:

  • 材料科学
  • 电化学
  • 固态化学

背景情况:

  • 可充电的多价离子电池具有高容量,但缺乏适合有效的离子间隔材料.
  • 晶体切弗勒相是罕见的阴极材料,可以反向插入多价.
  • 缺乏设计规则阻碍了稳定的多价离子间隔电极的开发.

研究的目的:

  • 为了阐明在多价子介质过程中切弗勒相电极中的电荷储存机制.
  • 确定新型介质电极的设计原则,以促进多价值离子的插入.

主要方法:

  • 固态核磁共振 (NMR) 光谱
  • 同步射线近边结构 (XANES) 的测量
  • 操作同步射线衍射
  • 密度函数理论 (DFT) 的计算

主要成果:

  • 电子在离子介质时被选择性地转移到离子基框架中.
  • 过渡金属 (Mo) 八面体在过程中保持无氧化活性.
  • 在不破坏化学键的情况下发生可逆电化学离子氧化还原机制.

结论:

  • 切弗勒相中的电荷储存涉及可逆的阳离子氧化还原,与典型的过渡金属电极不同.
  • 这种机制的理解为先进的多价离子电池阴极提供了设计原则.
  • 这项工作为开发高效的多价离子存储的新介质电极铺平了道路.