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PAM基復合水凝膠電解質的制備及其在Zn–MnO2電池中的應用

Preparation and application of PAM-based composite hydrogel electrolyte in Zn?MnO2 battery

  • 摘要: 水系鋅離子電池具有低成本、安全、環保等優點,在規模化儲能和智能可穿戴方面極具應用前景. 提高其循環穩定性以及循環壽命是實現水系鋅離子電池進一步應用的關鍵問題之一. 本工作采用二維層狀蒙脫土(MMT)和丙烯酰胺單體,通過兩步法合成了具有三維網狀結構的蒙脫土–聚丙烯酰胺水凝膠電解質(Montmorillonite–polyacrylamide hydrogel,MMT–PAM). 蒙脫土的加入為丙烯酰胺單體的原位聚合提供了吸附位點,并通過MMT和PAM高分子鏈之間的氫鍵作用顯著提高了水凝膠的機械性能,抑制了鋅枝晶生長(在0.5 mA?cm?1電流密度下穩定循環250 h). 此外,蒙脫土表面豐富的負電荷為Zn2+的快速傳輸提供更多離子傳輸通道,提高其離子電導率(室溫下為34 mS?cm?1),賦予MMT–PAM水凝膠電解質更好的倍率性能和循環穩定性. 基于上述優點,組裝的水系Zn–MnO2電池在0.2 A?g?1的電流密度下提供了289 mA·h?g?1的比容量,且可穩定循環2000次. 此外,使用MMT–PAM水凝膠作為電解質制備的柔性電池在經過不同外界條件沖擊下依然可正常工作,表現出了其在柔性電子領域的應用可行性.

     

    Abstract: With the advantages of being cheap, safe, and environmentally friendly, aqueous Zn-ion batteries (AZIBs) show promise in large-scale energy storage and smart wearables. Moreover, with the expansion of the field of flexible electronics, the huge demand potential of wearable smart electronic devices is increasingly being underscored, which proposes higher requirements for the structural and electrochemical stability of energy storage devices and device safety in physical deformation processes. Aqueous electrolyte-based AZIBs are prone to interface separation during bending, which affects battery stability and makes it difficult to realize further practical applications in flexible electronics. Unlike aqueous electrolytes, hydrogel electrolytes are flexible and foldable, assuring the structural and performance stability of flexible energy storage devices under the action of external impacts. Particularly, polyacrylamide (PAM)-based hydrogels are the preferred materials for preparing hydrogel electrolytes due to their better ionic conductivity, strain, and stability. Herein, montmorillonite–PAM hydrogel (MMT–PAM) electrolytes with a three-dimensional network structure were produced by a two-step process using two-dimensional layered montmorillonite and acrylamide monomer. The addition of montmorillonite provides adsorption sites for the in situ polymerization of acrylamide monomer to enhance the mechanical properties of the hydrogel and facilitates the rapid transport of Zn2+ through the abundant negative charge on the MMT surface, increasing its ionic conductivity (34 mS?cm?1 at room temperature is much higher than that of the PAM hydrogel electrolyte (17 mS?cm?1)) to obtain MMT–PAM hydrogel electrolytes with better electrochemical properties. The MMT–PAM hydrogel electrolyte-based Zn–MnO2 batteries –demonstrated a specific capacity of 289 mA·h?g?1 at a current density of 0.2 A?g?1 and could be stably cycled for 2000 cycles, whereas the PAM hydrogel electrolyte-based Zn–MnO2 batteries only cycled for hundreds of cycles at the same current density before short-circuiting, thus demonstrating the long battery cycle life of the MMT–PAM hydrogel electrolyte-based Zn–MnO2 batteries. The MMT–PAM-based batteries maintained a high specific capacity even at a high current density of 4 A?g?1. Furthermore, flexible batteries based on MMT–PAM hydrogel electrolytes could still work properly under different external impacts, such as cutting and piercing. The prepared flexible batteries were folded and immersed in aqueous solution to provide stable voltage and remarkable water resistance, demonstrating their possible application in flexible electronics. Therefore, this work sheds light on the possibility of further application of hydrogel electrolytes in aqueous Zn–MnO2 batteries and the further development of flexible energy storage devices based on hydrogel electrolytes.

     

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