Dendrite-free zinc metal anode for long-life zinc-ion batteries enabled by an artificial hydrophobic-zincophilic coating

被引:0
|
作者
Zhang, Hanning [1 ]
Shui, Tao [1 ]
Moloto, Nosipho [2 ]
Li, An [3 ]
Zhang, Ruogu [4 ]
Liu, Jiacheng [5 ]
Kure-Chu, Song-Zhu [5 ]
Hihara, Takehiko [5 ]
Zhang, Wei [1 ]
Sun, Zhengming [1 ]
机构
[1] Southeast Univ, Sch Mat Sci & Engn, Nanjing 211189, Peoples R China
[2] Univ Witwatersrand, Sch Chem, Mol Sci Inst, Private Bag 3, ZA-2050 Johannesburg, South Africa
[3] Southeast Univ, Anal & Testing Ctr, Nanjing 211189, Peoples R China
[4] Nanjing Jinling High Sch, Int Dept, 169 Zhongshan Rd, Nanjing 210009, Peoples R China
[5] Nagoya Inst Technol, Dept Mat Funct & Design, Gokiso Cho,Showa Ku, Nagoya, Aichi 4668555, Japan
基金
中国国家自然科学基金;
关键词
Hydrophobicity; Zincophilicity; Zinc borate; Dendrite-free anode; Aqueous zinc-ion batteries; DESIGN; LAYER;
D O I
10.1016/j.jcis.2024.09.092
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
Considering the desired energy density, safety and cost-effectiveness, rechargeable zinc-ion batteries (ZIBs) are regarded as one of the most promising energy storage units in next-generation energy systems. Nonetheless, the service life of the current ZIBs is significantly limited by rampant dendrite growth and severe parasitic reactions occurring on the anode side. To overcome these issues caused by poor interfacial ionic conduction and water erosion, we have developed a facile strategy to fabricate a uniform zinc borate layer at the zinc anode/electrolyte interface (ZnBO). Such protective layer integrates superhydrophobic-zincopholic properties, which can effectively eliminate the direct contact of water molecules on the anode, and homogenize the interfacial ionic transfer, thereby enhancing the cyclic stability of the zinc plating/stripping. As a result, the as-prepared ZnBO-coated anode exhibits extended lifespan of 1200 h at 1 mA cm(-2) and demonstrates remarkable durability of 570 h at 20 mA cm(-2) in Zn||Zn symmetric cells. Additionally, when coupled to an NH4V4O10 (NVO) cathode, it also delivers a superior cyclability (203.5 mAh/g after 2000 cycles at 5 A/g, 89.3 % capacity retention) in coin full cells and a feasible capacity of 2.5 mAh at 1 A/g after 200 cycles in pouch full cells. This work offers a unique perspective on integrating hydrophobicity and zincophilicity at the anode/electrolyte interface through an artificial layer, thereby enhancing the cycle lifespan of ZIBs.
引用
收藏
页码:1148 / 1157
页数:10
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