雅恩-泰勒效应
材料科学
锰
原位
羧酸盐
图层(电子)
失真(音乐)
无机化学
氧化锰
纳米技术
化学工程
光电子学
离子
冶金
有机化学
化学
放大器
工程类
CMOS芯片
作者
Mingfeng Li,Junjie Shi,Mengdi Guo,Tao Huang,Wenqiao Liu,Yanping Shen,Zhiwei Gao,Chuankun Zhang,Xiao Luo,Xu Li,Yang Yue,Meng Qin,Yanan Ma
标识
DOI:10.1002/adfm.202512344
摘要
Abstract Manganese oxides, known for their high theoretical capacity and operating voltage, have garnered significant attention in aqueous zinc‐ion batteries. However, irreversible phase transitions and manganese dissolution in Mn‐free electrolytes result in poor electrochemical performance. To solve those problems, an in‐situ cathode electrolyte interphase (CEI) layer formed by the adsorption of lactate ions (SC − ) on the cathode that allows Zn 2+ and H + de‐intercalation while preventing Mn 2+ from entering the electrolyte during charging is proposed. The inhibited Mn 2+ is reversibly oxidized under an external power source, making the Jahn–Teller distortion reversible. Additionally, SC − can stabilize pH and modulate solvation structure of the electrolyte, which can suppress the side reactions. Consequently, the Zn//manganese oxide batteries deliver a remarkable reversible capacity (294.9 mAh g −1 at 0.1 A g −1 ), outstanding rate capability (119.0 mAh g −1 at 2.0 A g −1 ), and robust cyclic stability (81.7% after 1000 cycles at 0.3 A g −1 ). More importantly, the carboxyl‐Zn 2+ interaction achieves uniform Zn deposition on the (002) plane, enabling high‐performance pouch cells. This study provides new insights into the CEI layers, which will promote the commercialization of Zn//manganese oxide batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI