| Literature DB >> 33314518 |
Hua Wang1, Lin Guo2, Jiangchun Chen2, Qiaonan Zhu2, Li Jiang3, Rongyang Liu3, Yan Yang2, Mengyao Tang4, Jiawei Wang2.
Abstract
Aqueous aluminum-ion batteries (AABs) are regarded as a promising next-generation energy storage device, and the current reported cathodes for AABs mainly focused on inorganic materials which usually implement a typical Al 3+ ions (de)insertion mechanism. However, the strong electrostatic forces between Al 3+ and the host materials usually lead to sluggish kinetics, poor reversibility and inferior cycling stability. Herein, we employ an organic compound with redox-active moieties, phenazine (PZ), as the cathode material in AABs. Different from conventional inorganic materials confined by limited lattice spacing and rigid structure, the flexible organic molecules allow a large-size Al-complex co-intercalation via reversible redox active centers (-C=N-) of PZ. This co-intercalation behavior can effectively reduce desolvation penalty, and substantially lower the Coulombic repulsion during the ion (de)insertion process. Consequently, this organic cathode exhibits a high capacity and excellent cyclability, which exceeds those of most reported electrode materials for AABs. This work highlights the anion co-intercalation chemistry of redox-active organic materials, which is expected to boost the development of high-performance multivalent-ion battery systems.Entities:
Keywords: Electrolyte; aqueous aluminum-ion batteries; co-intercalaion mechanism; multielectron redox; organic cathode
Year: 2020 PMID: 33314518 DOI: 10.1002/anie.202011144
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336