锂(药物)
阳极
电化学
多硫化物
电解质
氧化还原
化学
无机化学
锂硫电池
X射线光电子能谱
电极
化学工程
磷酸钒锂电池
材料科学
物理化学
内分泌学
工程类
医学
作者
Misganaw Adigo Weret,Shi‐Kai Jiang,Kassie Nigus Shitaw,Chia‐Yu Chang,Teshager Mekonnen Tekaligne,Jeng-Chian Chiou,Sheng‐Chiang Yang,Nigusu Tiruneh Temesgen,Yosef Nikodimos,She‐Huang Wu,Chun‐Chieh Wang,Wei‐Nien Su,Bing‐Joe Hwang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-05-31
卷期号:8 (6): 2817-2823
被引量:11
标识
DOI:10.1021/acsenergylett.3c00622
摘要
Anode-free lithium–sulfur batteries (AFLSBs) show a surprisingly prolonged cycle life 2-fold higher than anode-free lithium metal batteries. The principal difference is the presence of an intrinsic polysulfide (PS) shuttle between electrodes in AFLSBs. However, the underlying mechanism for the impact of PS redox species on the electrochemical performance of AFLSBs is not clearly understood. Herein, we investigate the role of PS redox species in retrieving inactive lithium for compensating lithium inventory loss using titration gas chromatography, thereby quantifying inactive lithium accumulated after several cycles. Moreover, XPS analysis reveals reduced lithium sulfide (Li2S/Li2S2) species formed through PS redox shuttle refresh inactive solid electrolyte interface (SEI) composition and stabilize the consecutive cycle lithium deposition. Interestingly, synchrotron-based operando transmission X-ray microscopy (TXM) reveals dense and granular electrodeposited lithium morphologies in AFLSBs. Therefore, the interplay between reviving inactive lithium for compensating lithium inventory loss and stabilizing lithium electrodeposition endows high electrochemical performance in AFLSBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI