21:I[432972,["/_next/static/chunks/bb923814e1f4d2e9.js","/_next/static/chunks/dd3ee9f5b7716ca6.js","/_next/static/chunks/4204a0ae82542ca8.js","/_next/static/chunks/1270dead247da766.js","/_next/static/chunks/6e1aa89a642f40be.js","/_next/static/chunks/2d7aa753e81324a8.js","/_next/static/chunks/8ffd0b71567920d8.js","/_next/static/chunks/67ea6dfd21f16c5f.js","/_next/static/chunks/24eb4379f68013fd.js","/_next/static/chunks/b8cd775ffdf935bd.js","/_next/static/chunks/983103cd9eb7b428.js","/_next/static/chunks/263f2cdcb9aa2341.js","/_next/static/chunks/294b9525248c8e5f.js"],"default"] 22:T427,Zinc (Zn) metal anode suffers from uncontrollable Zn dendrites and parasitic side reactions at the interface, which restrict the practical application of aqueous rechargeable zinc batteries (ARZBs). Herein, an amphoteric cellulose-based double-network is introduced as hydrogel electrolyte to overcome these obstacles. On one hand, the amphoteric groups build anion/cation transport channels to regulate electro-deposition behavior on Zn (002) crystal plane enabled by homogenizing Zn²⁺ ions flux. On the other hand, the strong bonding between negatively charged carboxyl groups and Zn²⁺ ions promote the desolvation process of [Zn(H₂ O)₆ ]²⁺ to eliminate side reactions. Based on the above two functions, the hydrogel electrolyte enables an ultra-stable cycling with a cumulative capacity of 7 Ah cm^-2 at 20 mA cm^-2 /20 mAh cm^-2 for Zn||Zn cell. This work provides significant concepts for developing hydrogel electrolytes to realize stable anode for high-performance ARZBs.23:T467,Aqueous zinc batteries (AZBs) are considered one of the most promising candidates for grid-scale energy storage. However, achieving a stable electrode-electrolyte interface remains a challenge for developing high-performance AZBs. Herein, taking the Zn||phenazine (PNZ) system as a prototype, where the proton uptake/removal mechanism dominates in the cathode, a carboxylic acid-functionalized cellulose hydrogel electrolyte is designed to simultaneously solve the issues at both the anode and cathode interfaces. Specifically, the hydrogel electrolyte can not only regulate Zn²⁺ ions at the Zn anode side but also supply H⁺ ions at the PNZ cathode side to avoid the unfavored deposition of zinc sulfate hydroxides. Benefiting from the unique one-gel-for-two-electrodes strategy, the dendrite-free and side reaction-suppressed aqueous Zn||PNZ cells are developed with a high specific capacity (311 mAh g^-1, 99% utilization of the theoretical capacity) and a long cycle life (over 1500 cycles within 2 months). This study proposes a facile and low-cost electrolyte strategy for stabilizing AZBs.24:T5f7,

#	Concept	H-Index	Publications	Citations
1	Engineering	5	5	185
2	Chemistry	5	5	185
3	Batteries	4	4	171
4	Chemical Engineering	3	3	104
5	Materials Science	2	2	48

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