単価イオンを持つ拡張濃縮超リン酸フレームワークは,リチウムの移動性と高い計算された電気化学的安定性を組み合わせます
Guopeng Han1, Andrij Vasylenko1, Alex R Neale1,2
1Department of Chemistry, University of Liverpool, Crown Street, Liverpool, L69 7ZD, United Kingdom.
Journal of the American Chemical Society
|October 22, 2021
まとめ
研究者らは,リチウム超リン酸材料であるLi3P5O14とLi4P6O17を開発し,先進リチウムイオン電池のイオン伝導性と電気化学的安定性を向上させました.
科学分野:
- 固体無機化学
- 材料科学
- 電気化学
背景:
- 拡張アニオンフレームワークは多様ですが,リチウム超リン酸は報告されていません.
- リン酸塩とシリケートは地球に豊富に存在するが,リチウムを含むその超リン酸塩の形態は未調査である.
- 新しい固体電解質の開発は 次世代のエネルギー貯蔵に不可欠です
研究 の 目的:
- 新しいリチウム超リン酸化合物を合成し特徴づけること.
- これらの新材料のイオン伝導性と電気化学的性質を調査する.
- リチウムイオン電池の 固体電解質としての可能性を探るため
主な方法:
- Li3P5O14とLi4P6O17の結晶構造の決定
- イオン伝導度測定のためのインペデンススペクトロスコーピーとDC極化.
- 電気化学的評価のためのNMRスペクトロスコーピーと 静電塗装/剥離
主要な成果:
- Li3P5O14の層状の超リン酸構造と,リ4P6O17のループ型の鎖を発見した.
- Li3P5O14は高いイオン伝導性 (8.5~5) ×10−7 S cm~1) と低い活性化エネルギー (0.43~7) を表している.
- 両化合物は酸化に対する高い熱力学的安定性を示し,Li3P5O14は4. 8Vに安定している.
結論:
- 新しいリチウム超リン酸は,固体電解質のための新しい構造基盤を提供します.
- Li3P5O14はリチウムイオン電池の用途に有望なイオン伝導性と電気化学的安定性を示しています.
- これらの材料は,電解質の性能を最適化するための新しい戦略を提供し,潜在的にカソッドコーティングです.
関連する概念動画
Ionic Bonding and Electron Transfer
44.2K
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.
44.2K
Complexation Equilibria: Factors Influencing Stability of Complexes
539
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...
539
Ion Exchange
722
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...
722
Metal-Ligand Bonds
22.2K
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...
22.2K
EDTA: Chemistry and Properties
2.4K
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...
2.4K
Extraction: Advanced Methods
573
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...
573


