电解质
材料科学
阴极
极化(电化学)
水溶液
电化学
盐(化学)
金属
化学工程
腐蚀
电化学窗口
离子
高压
电压
无机化学
离子电导率
电极
化学
复合材料
冶金
电气工程
有机化学
物理化学
工程类
作者
Long Qian,Haojie Zhu,Tingting Qin,Rui Yao,Jianwei Zhao,Feiyu Kang,Cheng Yang
标识
DOI:10.1002/adfm.202301118
摘要
Abstract Aqueous Zn metal batteries are regarded as a promising pathway for large‐scale energy storage systems due to their green, low‐cost, and intrinsically safe characteristics. However, they have long been suffered from narrow voltage windows and severe parasitic reactions (e.g., hydrogen evolution, corrosion, etc.), which hinder their further development. The above challenges are essentially related to the existence of hydrated ions (i.e., Zn(H 2 O) x 2+ and SO 4 2− ·(H 2 O) x ), which are highly reactive species. Herein, a counterintuitive ultralow‐salt‐concentration electrolyte strategy to solve the aforementioned problems by decreasing Zn salt concentration to reduce active hydrated ions is presented, so as to minimize water‐induced side reactions and thus anomalously enlarge the electrolyte splitting voltage window. Additionally, the gap between the charge and discharge medium voltages of full cells is also narrowed due to the reduced polarization in the ultralow‐salt‐concentration electrolyte. By adopting this strategy, the Zn‐Fe 4 [Fe(CN) 6 ] 3 full cell stably works at a high‐voltage of 1.40–2.30 V with a high cathode loading of ≈7 mg cm −2 and the Zn‐polyaniline full cell can stably work at 0.50–1.50 V with a high cathode loading of ≈11 mg cm −2 .
科研通智能强力驱动
Strongly Powered by AbleSci AI