蒽醌
电解质
锂(药物)
溶解
阴极
电化学
材料科学
化学工程
无机化学
化学
工程类
电极
物理化学
医学
内分泌学
作者
An-Na Zhou,Junyang Zheng,Chengxi Lei,Jiaying Liang,Xiaotong Deng,Zetao Wu,Phaivanh Chuangchanh,Qing Chen,Ronghua Zeng
标识
DOI:10.1002/chem.202303683
摘要
Abstract Anthraquinone electrode materials are promising candidates for lithium‐ion batteries (LIBs) due to the abundance of anthraquinone and the high theoretical capacity, and good reversibility of the anthraquinone electrodes. However, the active anthraquinone materials are soluble in organic electrolytes, resulting in a sharp decay of capacity during the charge and discharge processes. Herein, we report on a two‐dimensional calcium anthraquinone 2,3‐dicarboxy metal‐organic framework (2D CaAQDC MOF) fabricated using a simple hydrothermal method. The 2D CaAQDC MOF not only effectively inhibits the dissolution of active electrode substances into the electrolyte, but also promotes the diffusion of lithium ion into the pores of the MOF. When used as a cathode for the LIBs, the resulting CaAQDC electrode delivers a high specific capacity of ~100 mAh g −1 at a current density of 50 mA g −1 after 200 cycles, demonstrating its good cycle stability. Even at a high current density of 200 mA g −1 , the CaAQDC electrode exhibits a specific capacity of ~60 mAh g −1 . The fabricated 2D coordination polymers effectively restrains the dissolution of anthraquinone into the organic electrolyte and enhances the structural stability, which greatly improves the electrochemical performance of anthraquinone. These research results offer a rational molecular design strategy to address the dissolution of this and other active organic electrode materials.
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