Dong, Hui, et al. "Directing Mg-storage chemistry in organic polymers toward high-energy Mg batteries." Joule 3.3 (2019): 782-793.
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Directing Mg-storage chemistry in organic polymers is crucial for achieving high-energy Mg batteries ^[Cang et al.]. Aqueous Mg-ion batteries (MIBs) have shown potential, but reliable anode materials are lacking ^[Cang et al.]. In this study, an avant-garde anode material, 3D-P(PDI-T), was designed and synthesized for MIBs ^[Cang et al.]. The increased aromatic structure of 3D-P(PDI-T) enhanced its structural stability and resulted in remarkable outcomes, including an extremely high rate capacity and significant reversible capacity in full cells ^[Cang et al.]. Covalent organic frameworks (COFs) were also explored as host materials for high-rate aqueous Mg2+ ion batteries ^[Zou et al.]. The Mg2+ ion diffusion kinetics in COFs were dominated by surface pseudocapacitive behavior, leading to favorable rate performance and durable cyclic stability ^[Zou et al.]. These findings provide insights into the development of organic materials and host materials for efficient charge-storage behavior in aqueous Mg-ion batteries ^[Cang et al.] ^[Zou et al.].
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| The provided paper is not the same as the one mentioned in the query. The provided paper is about a study on the reaction mechanism of a model organic cathode in magnesium-ion batteries. | |
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| The provided paper is not the same as the one mentioned in the query. The provided paper is about cathode materials and chemistries for magnesium batteries, while the query is about directing Mg-storage chemistry in organic polymers for high-energy Mg batteries. Therefore, the answer to the query cannot be found in the provided paper. |
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