Due to the adjustable structure and the broad application prospects in energy and other fields, the exploration of porous organic materials [metal-organic polymers (MOPs), covalent organic frameworks (COFs), etc.] has attracted extensive attention. In this work, an imine-induced metal-organic and covalent organic coexisting framework (Co-MOP@COF) hybrid was designed based on the combination between the amino units from the organic ligands of Co-MOP and the aldehyde groups from COF. The obtained Co-MOP@COF hybrid with layer-decorated microsphere morphology exhibited good electrochemical cycling performance (a large reversible capacity of 1020 mAh g-1 after 150 cycles at 100 mA g-1 and a reversible capacity of 396 mAh g-1 at 500 mA g-1 ) as the anode for Li-ion batteries. The coexisting framework structure endowed the Co-MOP@COF hybrid with more surface area exposed in the exfoliated COF structure, which provided rapid Li-ion diffusion, better electrolyte infiltration, and effective activation of functional groups. Therefore, the Co-MOP@COF hybrid material achieved an enhanced Li storage mechanism involving multi-electron redox reactions, related to the CoII center and organic groups (C=C groups of benzene rings and C=N groups), and furthermore improved electrochemical performance.
Keywords: batteries; electrochemistry; hybrid materials; lithium storage; organic electrode.
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