材料科学
降级(电信)
反应性(心理学)
机制(生物学)
氧化还原
锂(药物)
二聚体
化学工程
化学稳定性
反应机理
四氢呋喃
动力学
化学分解
组合化学
化学反应
还原剂
化学动力学
分子
光化学
表征(材料科学)
半反应
纳米技术
侧链
电池(电)
计算化学
可逆反应
化学
作者
Shiwei Xu,Yue Liu,Yejing Li,Mengyan Cao,QingLi Wu,Bingyun Ma,Jiayi Zhang,Qiu Fang,Liquan Chen,Zhaoxiang Wang,Tao Cheng,Xuefeng Wang
标识
DOI:10.1002/aenm.202402941
摘要
Abstract Organolithium solutions, especially Li‐arene solutions (LASs) with high reactivity and controllable redox potentials, have gained significant attention because of their wide applications in chemical lithiation, liquid anodes, and battery recycling. However, the sudden loss of reactivity when stored or applied at room temperature is still puzzling and inhibits the application of LASs. In this work, the degradation mechanism of LASs is fully investigated and revealed by combining various experimental characterization and computational simulations. A hierarchical reaction mechanism for lithium biphenyl/2‐methyl tetrahydrofuran (Li‐Bp‐2MT), a lithiation solution used for most anodes, explains degradation and side product formation. Specifically, the dimerization of the active component Li 1 Bp[2MT] 1 forms an inactive dimer that is irreversibly reduced in the presence of locally accumulated highly reductive Li 0 . This reaction mechanism reveals the atomic origins of lithiation solution deactivation and accounts for all solid and gaseous byproducts. LiH is identified as the dominating solid byproduct, indicating irreversible destruction of the active components and facilitating side reactions producing H 2 and CH 4. Based on reaction mechanism insights, modifying molecular interactions and reaction kinetics are experimentally shown to inhibit Li 0 aggregation kinetics, enhancing long‐term prelithiation performance. This research provides comprehensive guidelines for practical applications of LASs.
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