MXenes公司
材料科学
电解质
致潮剂
离子
无机化学
化学工程
纳米技术
有机化学
化学
物理化学
电极
工程类
作者
Liping Zhang,Leiqiang Qin,Yeying Li,Le Du,Manting Song,Y. Wang,Jingkun Xu,Baoyang Lu,Johanna Rosén,Jianxia Jiang
标识
DOI:10.1016/j.ensm.2025.104116
摘要
Optimizing electrolytes is essential for improving the electrochemical stability window (ESW) and energy storage capacity of aqueous energy storage devices. High-concentration electrolytes improve performance but face solubility, conductivity, and stability issues. Here, a strong chaotropic anion, ClO4-, is introduced into 1 M ZnSO4 to expand the ESW and boost performance in dilute electrolytes. Theoretical simulation and experimental results provide that perchlorate not only significantly enhances ionic conductivity, leading to faster ion diffusion, but also weakens hydrogen bonds formation, reduces free water at the electrode surface, and promote the desolvation of hydrated zinc ions. Collectively, these factors lead to an improvement in the ESW and enhance overall device performance. Therefore, in the mixed electrolyte of 0.005 M Zn(ClO4)2 and 1 M ZnSO4, the Zn// Mo2ScC2Tz aqueous zinc-ion hybrid supercapacitor (ZHSC) achieves a voltage window expansion from 1.0 to 1.3 V, delivering a high specific capacitance of 692.3 F g-1 at 0.2 A g- 1. Furthermore, an asymmetric supercapacitor with the same electrolyte operates at 1.8 V, delivering an energy density of 98.1 Wh kg-1 at 180 W kg-1 and maintaining 17 Wh kg-1 at 9000 W kg-1. Notably, this electrolyte design strategy is universally applicable for enhancing Zn-ion storage performance of MXene-based materials.
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