电解质
材料科学
阳极
锂(药物)
化学工程
离子电导率
金属锂
准固态
聚丙烯腈
聚合物
电极
复合材料
化学
色素敏化染料
内分泌学
工程类
物理化学
医学
作者
Jaehyeong Bae,Keonwoo Choi,Hyunsub Song,Do Heung Kim,Doo Young Youn,Su‐Ho Cho,Dogyeong Jeon,Jiyoung Lee,Junyoung Lee,Wontae Jang,Changhyeon Lee,Youson Kim,Chanhoon Kim,Ji‐Won Jung,Sung Gap Im,Il‐Doo Kim
标识
DOI:10.1002/aenm.202203818
摘要
Abstract The lithium metal anode is notoriously unstable and reactive to electrolytes, forming brittle solid‐electrolyte interphase (SEI) layers with uneven distribution, exacerbating Li dendrites that ultimately limit the battery life. Here, this work passivates Li metal with electrolyte‐swellable polymer nanolayers deposited monolithically by the initiated chemical vapor deposition (iCVD) to reinforce the native SEI layers and stabilize their interface. The 100 nm iCVD poly(dimethylaminomethyl styrene) (pDMAMS) layer is swelled by 264% under a carbonate electrolyte, establishing the electrolyte‐filled soft scaffold for Li‐ion transport. Notably, the solvogel accommodates homogeneous Li 2 O‐free and Li 2 CO 3 ‐rich native SEI layers, providing a record‐high Li‐ion transference number of 0.95 and ionic conductivity of 6.54 mS cm −1 . The developed pDMAMS‐Li anodes extend the cycle life by 550% in Li–Li symmetric cells and 600% in LiNi 0.6 Mn 0.2 Co 0.2 O 2 full cells compared to pristine Li metal. The mechanistic details of the swollen‐soft‐scaffold strategy are elucidated by depth profile analysis of the pDMAMS homopolymer compared to pDMAMS/electrolyte‐phobic copolymers, providing new insights to manage the interface of liquid‐state electrolyte and solid‐state Li metal by using a novel class of bifunctional solvogel.
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