All-Climate Energy-Dense Cascade Aqueous Zn-I2 Batteries Enabled by a Polycationic Hydrogel Electrolyte

IF 26.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Materials Pub Date : 2025-02-16 DOI:10.1002/adma.202415979
Yangyang Liu, Longhai Zhang, Ling Liu, Quanwei Ma, Rui Wang, Peng Xiong, Hongbao Li, Shilin Zhang, Junnan Hao, Chaofeng Zhang
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Abstract

The practical development of aqueous zinc-iodine (Zn-I2) batteries is greatly hindered by the low energy density resulting from conventional I0/I conversion and the limited temperature tolerance. Here, a temperature-insensitive polycationic hydrogel electrolyte borax-bacterial cellulose / p(AM-co-VBIMBr) (denoted as BAVBr) for achieving an energy-dense cascade aqueous Zn-I2 battery over a wide temperature range from −50 to 50 °C is designed. A comprehensive investigation, combining advanced spectroscopic investigation and DFT calculations, has revealed that the presence of Br species in the gel electrolyte facilitates the conversion reaction of Br0/Br. Simultaneously, it activates the high voltage I+/I0 redox reaction through interhalogen formation. Consequently, sequential and highly reversible redox reactions involving I0/I, I+/I0, and Br0/Br are achieved with the assistance of −NR3+ units in BAVBr, effectively suppressing interhalogen hydrolysis in aqueous electrolyte. The cascade reactions lead to a high area capacity of 0.76 mAh cm−2 at a low I2 loading of 1 mg cm−2 or 760 mAh g−1 based on the mass of iodine, demonstrating exceptional long-term cycling stability over a wide temperature range from −50 to 50 °C. This study offers valuable insights into the rational design of electrolytes for high-energy aqueous batteries, specifically tailored for wide-temperature operation.

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由多阳离子水凝胶电解质实现的全天候能量密集级联水锌- i2电池
传统的I0/I−转换导致的低能量密度和有限的耐温性极大地阻碍了水基锌碘(Zn-I2)电池的实际发展。在这里,设计了一种温度不敏感的多阳离子水凝胶电解质硼酸-细菌纤维素/ p(AM-co-VBIMBr)(表示为BAVBr),用于在- 50至50°C的宽温度范围内实现能量密集的级联水Zn-I2电池。一项综合研究,结合先进的光谱研究和DFT计算,揭示了Br在凝胶电解质中的存在促进了Br0/Br−的转化反应。同时,通过生成卤素间激活高压I+/I0氧化还原反应。因此,在BAVBr中的- NR3+单元的帮助下,实现了包括I0/I−,I+/I0和Br0/Br−在内的顺序和高度可逆的氧化还原反应,有效地抑制了水溶液中卤素间的水解。级联反应导致在1 mg cm - 2或760 mAh g- 1的低I2负载下的高面积容量为0.76 mAh cm - 2,基于碘的质量,在- 50至50°C的宽温度范围内表现出优异的长期循环稳定性。这项研究为高能水性电池电解质的合理设计提供了有价值的见解,特别是为宽温度操作量身定制的电解质。
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来源期刊
Advanced Materials
Advanced Materials 工程技术-材料科学:综合
CiteScore
43.00
自引率
4.10%
发文量
2182
审稿时长
2 months
期刊介绍: Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.
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