局部化中等度电解质具有快速动力学,用于金属电池
Pengcheng Li1, Zhiqing Zhang1, Ziwei Zhao1
1Department of Mechanical Engineering, University of Alberta, 9211-116 Street NW, Edmonton, Alberta, T6G 1H9, Canada.
Angewandte Chemie (International ed. in English)
|January 5, 2024
概括
一种新的局部化中度电解质 (LMCE) 为金属阳极提供了具有成本效益和环保的替代品. 这种新型电解质表现出卓越的性能和兼容性,克服了以前的局限性.
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:
- 局部化高度电解质是先进的,但由于高含量而昂贵.
- 高含量增加了生产成本和环境影响.
研究的目的:
- 为金属阳极开发一种新,经济高效,环保的电解质.
- 为了解决当前高度电解质的局限性.
主要方法:
- 通过稀释中度的电解质来设计和生产局部化中度电解质 (LMCE).
- 研究了LMCE与金属阳极的兼容性和电化学性能.
主要成果:
- LMCE 呈现出超低度 (0.1 M),具有显著的金属阳极兼容性.
- 在各种电池配置 (Li/Cu,Li/Li,LiFePO4/Li,NCM811/Li) 中实现了出色的动力学.
- 在高压 (>4V) 条件下抑制了电流收集器腐蚀.
结论:
- LMCE提供了一种突破性的方法,可以从以前不兼容的配方中制造兼容的电解质.
- 这一创新为各种电解质设计开辟了新的可能性,包括全液体电池系统.
更多相关视频
11:04Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature
Published on: December 20, 2016
13.0K
10:03Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
Published on: November 11, 2013
25.5K
相关概念视频
Formation of Complex Ions
23.7K
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...
23.7K
Extraction: Advanced Methods
447
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...
447
Batteries and Fuel Cells
27.4K
A battery is a galvanic cell that is used as a source of electrical power for specific applications. Modern batteries exist in a multitude of forms to accommodate various applications, from tiny button batteries such as those that power wristwatches to the very large batteries used to supply backup energy to municipal power grids. Some batteries are designed for single-use applications and cannot be recharged (primary cells), while others are based on conveniently reversible cell reactions that...
27.4K
Electrolysis
26.4K
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...
26.4K
Electrolyte and Nonelectrolyte Solutions
63.1K
Substances that undergo either a physical or a chemical change in solution to yield ions that can conduct electricity are called electrolytes. If a substance yields ions in solution, that is, if the compound undergoes 100% dissociation, then the substance is a strong electrolyte. Complete dissociation is indicated by a single forward arrow. For example, water-soluble ionic compounds like sodium chloride dissociate into sodium cations and chloride anions in aqueous solution.
63.1K
Ionic Strength: Effects on Chemical Equilibria
1.5K
The addition of an inert ionic compound increases the solubility of a sparingly soluble salt. For example, adding potassium nitrate to a saturated solution of calcium sulfate significantly enhances the solubility of calcium sulfate. Le Châtelier's principle cannot predict this shift in the equilibrium. Instead, this could be explained in terms of changes in the effective concentration of the ions in solution in the presence of added inert salt.
In this solution, the primary...
In this solution, the primary...
1.5K
