Acta Phys. -Chim. Sin. ›› 2024, Vol. 40 ›› Issue (3): 2304036.doi: 10.3866/PKU.WHXB202304036

• ARTICLE • Previous Articles     Next Articles

A Fumed SiO2-based Composite Hydrogel Polymer Electrolyte for Near-Neutral Zinc-Air Batteries

Ke Qiu, Fengmei Wang, Mochou Liao, Kerun Zhu, Jiawei Chen, Wei Zhang, Yongyao Xia*(), Xiaoli Dong*(), Fei Wang*()   

  1. Department of Chemistry, Department of Materials Science, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, China
  • Received:2023-04-20 Revised:2023-05-16 Accepted:2023-05-17 Published:2023-05-25
  • Contact: Email: feiw@fudan.edu.cn (Fei Wang)xldong@fudan.edu.cn (Xiaoli Dong)yyxia@fudan.edu.cn (Yongyao Xia)
  • Supported by:
    the National Key R&D Program of China(2021YFA1201900); the Science and Technology Commission of Shanghai Municipality(21511103300)

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Abstract:

Near-neutral zinc-air batteries show great promise for long-cycle applications in ambient air owing to their impressive deposition/stripping compatibility with zinc anodes and greater chemical stability towards CO2 in ambient air compared to batteries with traditional alkaline electrolytes. However, the inherent water volatilization of liquid electrolytes and the flexibility of electrolytes required for wearable devices severely limit the practical application of this system. In this study, a fumed SiO2-based composite hydrogel polymer electrolyte (SiO2-HPE) was prepared for application in near-neutral zinc-air batteries. The design of the SiO2-HPE was carried out considering the following three aspects. Firstly, it is widely acknowledged that the polyacrylamide polymer skeleton is beneficial to excellent ionic conductivity and the mechanical strength of the SiO2-HPE. Secondly, fumed SiO2 bearing multiple silicon hydroxyl groups is a suitable option as a water-retaining additive. Thirdly, the near-neutral liquid electrolyte (1 mol·kg−1 Zn(OTf)2) absorbed in the SiO2-HPE is stable towards CO2 in ambient air. In conclusion, these three aspects of the electrolyte design contribute to the practical application of the SiO2-HPE. Raman spectroscopy and scanning electron microscopy revealed that the synthesized SiO2-HPE exhibited a high degree of polymerization, plentiful surface pores, and a uniform distribution of elements. According to the infrared and Raman spectra, the abundant hydroxyl groups located on the surface of the SiO2 particles enhanced water molecule binding by altering the hydrogen bond network within the SiO2-HPE. This conclusion was further confirmed by thermogravimetry and differential scanning calorimetry. After exposure to ambient air (30% relative humidity) for 96 h, the SiO2-HPE exhibited a water retention capacity of 49.52%, which is 6.23% and 1.73% higher than those for 1 mol·kg−1 Zn(OTf)2 and the HPE (hydrogel polymer electrolyte without SiO2). Moreover, owing to the dynamic recombination of the hydrogen bonds between the silicon hydroxyl groups and the gel skeleton, SiO2-HPE exhibited a higher mechanical strength and modulus than HPE under tensile and compressive conditions, respectively. This further rendered it an ideal electrolyte for flexible zinc-air batteries. The near-neutral zinc-air battery assembled with the SiO2-HPE exhibited a cycle life of up to 200 h under 30% relative humidity, far exceeding those of 1 mol·kg−1 Zn(OTf)2 and the HPE. Based on such remarkable performance, the flexible near-neutral zinc-air battery device assembled by the SiO2-HPE has shown a satisfactory performance under special conditions, such as bending and cutting, and can be used as a power supply for different electronic devices, making it a promising next-generation electrochemical energy storage device. Overall, this work provides new insight into the development of flexible zinc-air battery devices with long-term stability in ambient air.

Key words: Zinc-air battery, Hydrogel polymer electrolyte, Near-neutral, Fumed SiO2, Water retention