化学
剥离(纤维)
镁
化学工程
阳极
纳米尺度
沉积(地质)
金属
降级(电信)
纳米技术
电极
材料科学
复合材料
物理化学
古生物学
工程类
有机化学
生物
电信
计算机科学
沉积物
作者
Xin‐Cheng Hu,Shuang‐Yan Lang,Yang Shi,Rui Wen,Li‐Jun Wan
标识
DOI:10.1016/j.jelechem.2021.115301
摘要
Magnesium (Mg) metal batteries have attracted increased attention due to their high theoretical energy densities, low cost and high safety. However, severe capacity degradation induced by irreversible Mg deposition/stripping processes limits the long-term durability of Mg metal batteries. Direct visualization of the dynamic processes of Mg deposition/stripping is of great significance to intensively understand the degradation mechanism. Herein, we systematically investigated the morphological changes during Mg deposition and stripping at the nanoscale by in situ atomic force microscopy (AFM) in diglyme (DEG)/ ionic liquid (IL) system. The formation processes of sphere-shaped and crystallized Mg, as well as their stripping processes are directly observed. In the combination with in situ optical imaging, we found that the irreversible stripping process of deposited Mg results in the loss of active materials, potentially leading to severe capacity fading and poor cycling stability. Our results provide direct insights into the interfacial evolution at the nanoscale and the structure–reactivity correlation, which offer useful information for the design of high performance Mg metal batteries.
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