Zn-based aqueous batteries have attracted much attention because of their high theoretical-capacity, safety, and low-cost, yet the H2 -evolution, qualification or inhibition mechanism investigations that are closely related to the dendrite-growth are rare and challenging. Herein, a series of zincophilic metal-covalent organic frameworks (e.g., Zn-AAn-COF, Zn-DAAQ-COF, and Zn-DAA-COF) have been explored as model-platforms to manipulate the H2 -evolution and Zn2+ flux. Best of them, Zn-AAn-COF based cell only produces 0.002 mmol h-1 cm-2 H2 , which is >2 orders of magnitude lower than bare Zn. Noteworthy, it affords high stability for 3000 cycles (overpotential, <79.1 mV) at 20 mA cm-2 in symmetric-cell and enhanced cycling-stability up to 6000 cycles at 2000 mA g-1 in the assembled full-battery. Besides, mechanistic characterizations show that Zn-AAn-COF can enhance the energy-barrier of H2 -evolution and homogenize the ion-distribution or electric-filed to achieve high performance.
Keywords: Homogeneous Zinc Ion Flux; Inhibition Hydrogen Evolution; Metal-Covalent Organic Frameworks; Suppression the Zn Dendrite Growth.
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