摘要
Cellulose-based hydrogels hold great promise as electrolytes for aqueous Zinc-ion batteries (ZIBs), yet their performance is hindered by chain aggregation, overly strong Zn 2+ -cellulose coordination that slows ion transport, and parasitic reactions triggered by free water and sulfate species. Here, we design a multifunctional cellulose nanofiber (CNF) hydrogel electrolyte incorporating copper hybrid cluster Cu 4 I 4 (L) 4 (L = 3-Fluoropyridine (3-FPy)) to address these intrinsic limitations. Strong interactions between the clusters and cellulose chains prevent molecular aggregation and introduce additional crosslinking, reorganizing the network into a more continuous and uniform 3D architecture. Unexpectedly, the hydrogel develops a sandwiched structure consisting of dense outer layers that homogenize Zn 2+ flux and shield the anode from free water, and a porous intermediate layer that serves as an electrolyte reservoir to facilitate long-range ion migration. The clusters exhibit weaker affinity toward Zn 2+ than cellulose, mitigating excessive Zn 2+ -polymer coordination and enabling faster ion movement. Their spatially polarized charge distribution also provides sequential Zn 2+ hopping sites, further promoting directional ion transport. Meanwhile, strong binding with H 2 O and SO 4 2− converts free water into bound water and immobilizes anions, thereby suppressing H 2 O- and SO 4 2− -driven parasitic reactions. Benefiting from this cooperative regulation of microstructure, ion coordination, and water chemistry, the CNF@Cu 4 I 4 (L) 4 hydrogel exhibits high ionic conductivity, stable Zn plating/stripping, and effectively suppressed side reactions. As a result, Zn anodes achieve a long-term cycling stability up to 1200 h, and capacity retention of 99.5% over 2000 cycles for Zn||Polyaniline full cells. This work establishes a robust strategy for engineering cluster-modified hydrogels toward safe, durable, and high-performance aqueous ZIBs.
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