在丰富的反矿石 (Li2Fe) SOSO中分离阴离子和阳离子氧化还原活性
Lennart Singer1, Bowen Dong1, Mohamed A A Mohamed2,3
1Kirchhoff Institute for Physics, Heidelberg University, 69120 Heidelberg, Germany.
ACS applied materials & interfaces
|July 30, 2024
概括
富含的抗矿石通过阴离子和阳离子的氧化还原活性提供高容量. 分离这些过程可以提高循环稳定性,从而提高储能应用的性能.
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
- 储能 储能 储能 储能 储能 储能
背景情况:
- 富含的反矿是有前途的高容量阴极材料.
- 它们的性能依赖于阴离子和阳离子的氧化还原活性.
- 了解这些过程的分离对于优化电池性能至关重要.
研究的目的:
- 为了研究 (Li2Fe) SO材料的电化学特性.
- 为了区分阴离子和阴离子氧化还原过程的影响.
- 确定用于改善丰富的抗矿中循环稳定的策略.
主要方法:
- 三种 (Li2Fe) SO材料的电化学表征.
- 专注于分离阴离子和阳离子的氧化还原贡献.
- 分析循环稳定性和容量保留.
主要成果:
- 阳离子过程最初产生高容量 (~400 mAh g-1),但导致循环稳定性差.
- 仅限于 (Li2Fe) SO-BM500中的阴离子过程,提高了性能,在~175 mAh g-1.的100个循环中保持稳定的循环运行.
- 合成条件,特别是二次相含量,对性能产生重大影响,而颗粒大小则不那么重要.
结论:
- 分离阴离子和阴离子的氧化还原活性是提高丰富的抗矿性能的关键.
- 优化合成以控制二级相对于稳定,高容量的阴极材料至关重要.
- 这种方法允许研究内在的反矿性质,不包括外在相贡献.
关键词:
阳离子氧化氧化还原剂反佩罗夫斯基派是指反佩罗夫斯基派.在天主教堂 (Cathode) 里.在LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB,LIB多电子存储器多电子存储器更多相关视频
07:55Elemental-sensitive Detection of the Chemistry in Batteries through Soft X-ray Absorption Spectroscopy and Resonant Inelastic X-ray Scattering
Published on: April 17, 2018
12.7K
10:03Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
Published on: November 11, 2013
25.4K
相关概念视频
Ionic Bonding and Electron Transfer
41.3K
Ions are atoms or molecules bearing an electrical charge. A cation (a positive ion) forms when a neutral atom loses one or more electrons from its valence shell, and an anion (a negative ion) forms when a neutral atom gains one or more electrons in its valence shell. Compounds composed of ions are called ionic compounds (or salts), and their constituent ions are held together by ionic bonds: electrostatic forces of attraction between oppositely charged cations and anions.
41.3K
Ladder Diagrams: Redox Equilibria
446
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+...
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+...
446
Precipitation and Co-precipitation
1.7K
Precipitation and coprecipitation methods can be used to separate a mixture of ions in a solution. In qualitative inorganic analysis, ions that form sparingly soluble precipitates with the same reagent are separated based on the differences in solubility products. For example, consider the separation of Cu(II) and Fe(II) ions by precipitation as insoluble sulfides. First, copper(II) sulfide is precipitated by the addition of acidic H2S, where the dissociation of H2S is suppressed. Adding H2S...
1.7K
Extraction: Advanced Methods
436
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...
436
Formation of Complex Ions
23.6K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
23.6K
Ion Exchange
570
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...
570
