法拉第效率
阳极
水溶液
锌
阴极
材料科学
钝化
电池(电)
化学工程
电极
金属
纳米技术
纳米颗粒
电化学
耐久性
电偶阳极
寄主(生物学)
碳纤维
图层(电子)
金属有机骨架
过渡金属
作者
Jingjie Sun,Tianyu Shen,Mingyue Zhang,Yizhi Xing,Jie Wei,Qianchuan Yu,Zuoxiu Tie,Zhong Jin
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-08-05
卷期号:12 (32): eaeh4699-eaeh4699
标识
DOI:10.1126/sciadv.aeh4699
摘要
Developing dendrite-free zinc metal anodes with high durability poses a great challenge for aqueous zinc-ion batteries. Herein, we propose an in situ constructed 3D restrained host frameworks with multi-component gradients that induces a controllable and rapid stack-type zinc plating/stripping behavior, enabling a unique “first-in/last-out” mode. Typically, hydrophobic amino-functionalized polysilane passivation layer and zincophilic Ag nanoparticles are successively self-assembled on carbon paper scaffold to form opposite concentration gradients, namely g’ -Ag/ g -PSiO x -NH 2 /CP. The g -PSiO x -NH 2 inhibits side-reactions and promotes Zn 2+ desolvation, meanwhile the g’ -Ag guides preferential Zn 2+ deposition. Consequently, the zinc-deposited g’ -Ag/ g -PSiO x -NH 2 /CP electrodes exhibit high Coulombic efficiency and long cyclability, surpassing 5000 hours at 10 mA cm −2 /10 mAh cm −2 in symmetric cells. The as-assembled Zn||MnO 2 full batteries deliver a specific capacity of 200.1 mAh g −1 with 82.2% retention after 800 cycles. Large-size pouch-type battery with zinc-deposited g’ -Ag/ g -PSiO x -NH 2 /CP anode and high-loading MnO 2 cathode (∼15 mg cm −2 ) also exhibit good rate capability and cyclability. This scalable strategy offers a feasible solution to develop high-durability rechargeable metal-based batteries.
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