Highly Entangled Hydrogel Enables Stable Zinc Metal Batteries via Interfacial Confinement Effect

被引:49
作者
He, Qiong [1 ]
Chang, Zhi [1 ]
Zhong, Yue [1 ]
Chai, Simin [1 ]
Fu, Chunyan [1 ]
Liang, Shuquan [1 ]
Fang, Guozhao [1 ]
Pan, Anqiang [1 ,2 ]
机构
[1] Cent South Univ, Sch Mat Sci & Engn, Key Lab Elect Packaging & Adv Funct Mat Hunan Prov, Changsha 410083, Hunan, Peoples R China
[2] Xinjiang Univ, Sch Phys & Technol, Urumqi 830046, Xinjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
FRACTURE;
D O I
10.1021/acsenergylett.3c02139
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydrogel electrolytes are expected to be useful for stable zinc metal batteries; however, it is extremely challenging to develop a hydrogel electrolyte that balances mechanical properties, ionic conductivity, and interface stability. Herein, we report a highly entangled hydrogel electrolyte that achieves pronounced mechanical properties (446 kPa tensile strength) and high ionic conductivity (3.93 mS cm(-1)) by optimizing the dense reversible conformation of hydrophilic chains. Moreover, due to the interfacial confinement effect, the highly entangled hydrogel electrolyte enables a dynamically stabilized anode with a non-dendritic planar morphology. Thus, the zinc anode with this electrolyte system exhibits a long-term cycle stability of 6000 h at 0.5 mA cm(-2) and over 220 h at an impressive depth-of-discharge of 68.4%. This work provides an important concept for realizing practical high-performance wearable zinc-manganese batteries.
引用
收藏
页码:5253 / 5263
页数:11
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