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Here, we report a dual soft\u2010gel electrode aqueous battery enabled by a water competition effect between sulfate anions and water\u2010soluble polymers. By confining redox\u2010active 1,8\u2010bis(2\u2010(2\u2010(2\u2010hydroxyethoxy)\u2010ethoxy)ethoxy)anthracene\u20109,10\u2010dione and iodide within the anode and cathode soft\u2010gel phases, respectively, together with an electronically conductive network, a dual\u2010soft\u2010gel electrode battery configuration is realized. This architecture delivers stable electrochemical operation while maintaining effective ionic and electronic transport. Importantly, the concept is further validated in a cylindrical cell with substantially increased electrode dimensions, which exhibits consistent cycling behavior, highlighting the potential of dual soft\u2010gel electrodes as a deployable platform for practical aqueous batteries.<\/jats:p>","DOI":"10.1002\/smtd.70732","type":"journal-article","created":{"date-parts":[[2026,5,23]],"date-time":"2026-05-23T05:50:16Z","timestamp":1779515416000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Dual Soft\u2010Gel Electrodes Enabling Near\u2010Practical and Deployable Aqueous Batteries"],"prefix":"10.1002","volume":"10","author":[{"given":"Kaiqiang","family":"Zhang","sequence":"first","affiliation":[{"name":"School of Energy Sciences and Engineering Nanjing Tech University  Nanjing Jiangsu 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