Guo Chaofei, Han Bo, Sun Weiwei, Cao Yingnan, Zhang Yifan, Wang Yong
School of Environmental and Chemical Engineering, Shanghai University, 99 Shangda Road, Shanghai, 200444, P. R. China.
School of Metallurgy and Environment, Central South University, 932 Lushan South Road, Changsha, 410083, P. R. China.
Angew Chem Int Ed Engl. 2022 Nov 25;61(48):e202213276. doi: 10.1002/anie.202213276. Epub 2022 Oct 26.
The rechargeable lithium/sodium-iodine battery (Li/Na-I ) is a promising candidate for meeting the growing energy demand. Herein, a flexible hydrogen-bonded organic framework (HOF) linked to the Ti C T MXene complex (HOF@Ti C T ) 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 I -based batteries. The I /HOF@Ti C T exhibits large reversible capacities of 260.2 and 207.6 mAh g at 0.2 C after repeated cycling for Li-I and Na-I 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.
可充电锂/钠-碘电池(Li/Na-I)是满足不断增长的能源需求的一个有前景的候选者。在此,已提出一种与Ti C T MXene复合物相连的柔性氢键有机框架(HOF)(HOF@Ti C T)用于碘负载。HOF由有机单体通过每个单体之间的氢键相互作用自组装而成。这导致HOF结构中存在大量空腔,这些空腔可通过各种吸附位点和分子间相互作用封装碘。复合物的独特结构可加速碘的成核,实现快速反应动力学,稳定碘化物并抑制穿梭效应,从而提高基于碘的电池的循环稳定性。对于Li-I和Na-I电池,经过反复循环后,I /HOF@Ti C T在0.2 C下分别表现出260.2和207.6 mAh g的大可逆容量。这项工作可以深入了解与HOF相关的具有可逆碘封装的储能应用及其与锂和钠金属离子的相关氧化还原反应机制。