化金属有机框架用于提高离子电池中高阴极的性能
Heeju Ahn1, Yeonju Park1, Kwan Woo Nam1
1Department of Chemical Engineering and Materials Science, and Graduate Program in System Health and Engineering, Ewha Womans University, Seoul, 03760, Republic of Korea.
ChemSusChem
|August 22, 2024
概括
含有化剂的金属有机框架通过改善离子转移和减少金属交叉声来提高离子电池的性能. 这些添加剂提高了高阴极的能量密度和稳定性.
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
- 储能 储能 储能 储能 储能 储能
背景情况:
- 离子电池 (LIB) 对便携式电子产品,电动汽车和电网存储至关重要.
- 高 (Ni) 阴极,如LiNixCoyMnzO2 (NCM,x≥0.8),提供高能量密度,但面临挑战.
- 关键的限制包括缓慢的离子转移速率和过渡金属 (TM) 迁移到阳极,阻碍性能.
研究的目的:
- 调查金属有机框架 (MOF) 与合剂作为NCM阴极的添加剂的使用.
- 为了应对有限的离子动力学和TM交叉交谈在高Ni LIB中的挑战.
- 为了提高NCM阴极的电化学性能和稳定性.
主要方法:
- 在电极配方中将MOF与合剂作为添加材料的结合.
- MOF属性的表征:TM交叉谈话缓解,Li+部分溶解和离子固定.
- 修改NCM阴极的电化学测试,包括原始和循环后性能评估.
主要成果:
- 化MOF修改显著降低了NCM阴极中的电荷传输电阻.
- 在修改后的NCM阴极中,在100个循环后观察到改善的离子扩散系数.
- MOFs有效地减轻了TM向阳极的迁移,并促进了Li+离子转移.
结论:
- 含有合剂的MOF是提高LIB性能的有效添加材料.
- 这项研究展示了一种可行的策略,以克服高能量密度NCM阴极的动力限制.
- 这种方法对推动下一代离子电池的发展具有重大前景.
相关概念视频
Metal-Ligand Bonds
20.7K
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...
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...
20.7K
Extraction: Advanced Methods
433
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...
433
Complexation Equilibria: The Chelate Effect
485
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
485
Formation of Complex Ions
23.5K
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...
23.5K
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
Complexation Equilibria: Factors Influencing Stability of Complexes
348
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
348


