电解质
锂(药物)
X射线光电子能谱
材料科学
化学工程
聚合物
金属锂
准固态
扫描电子显微镜
纳米技术
化学
电极
复合材料
物理化学
内分泌学
工程类
医学
色素敏化染料
作者
Dechao Zhang,Zhengbo Liu,Yiwen Wu,Shaomin Ji,Zhanxiang Yuan,Jun Liu,Min Zhu
标识
DOI:10.1002/advs.202104277
摘要
Abstract Solid‐state lithium metal batteries (SLMBs) are attracting enormous attention due to their enhanced safety and high theoretical energy density. However, the alkali lithium with high reducibility can react with the solid‐state electrolytes resulting in the inferior cycle lifespan. Herein, inspired by the idea of interface design, the 1‐butyl‐1‐methylpyrrolidinium bis(trifluoromethanesulfonyl) imide as an initiator to generate an artificial protective layer in polymer electrolyte is selected. Time‐of‐flight secondary ion mass spectrometry and X‐ray photoelectron spectroscopy reveal the stable solid electrolyte interface (SEI) is in situ formed between the electrolyte/Li interface. Scanning electron microscopy (SEM) images demonstrate that the constructed SEI can promote homogeneous Li deposition. As a result, the Li/Li symmetrical cells enable stable cycle ultralong‐term for over 4500 h. Moreover, the as‐prepared LiFePO 4 /Li SLMBs exhibit an impressive ultra‐long cycle lifespan over 1300 cycles at 1 C, as well as 1600 cycles at 0.5 C with a capacity retention ratio over 80%. This work offers an effective strategy for the construction of the stable electrolyte/Li interface, paving the way for the rapid development of long lifespan SLMBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI