锂(药物)
碘
单体
碘化物
化学
成核
无机化学
氧化还原
碘化氢
氢
氢气储存
电解质
化学工程
碘化钠
碘化锂
材料科学
有机化学
电极
聚合物
物理化学
内分泌学
医学
工程类
作者
Chaofei Guo,Bo Han,Weiwei Sun,Yingnan Cao,Yifan Zhang,Yong Wang
标识
DOI:10.1002/anie.202213276
摘要
The rechargeable lithium/sodium-iodine battery (Li/Na-I2 ) is a promising candidate for meeting the growing energy demand. Herein, a flexible hydrogen-bonded organic framework (HOF) linked to the Ti3 C2 Tx MXene complex (HOF@Ti3 C2 Tx ) has been presented for iodine loading. HOF is self-assembled by organic monomers through hydrogen bonding interactions between each monomer. It leads to numerous cavities in HOF structure, which can encapsulate iodine through various adsorptive sites and intermolecular interactions. The unique structure of complex can accelerate the nucleation of iodine, achieve fast reaction kinetics, stabilize iodide and retard the shuttle effect, thus improving the cycling stability of I2 -based batteries. The I2 /HOF@Ti3 C2 Tx exhibits large reversible capacities of 260.2 and 207.6 mAh g-1 at 0.2 C after repeated cycling for Li-I2 and Na-I2 batteries, respectively. This work can gain insights into the HOF-related energy storage application with reversible iodine encapsulation and its related redox reaction mechanisms with Li and Na metal ions.
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