A highly utilized and practical lithium-sulfur positive electrode enabled in all-solid-state batteries
Abstract
Abstract All-solid-state batteries using sulfur-based positive electrodes (cathodes) offer a cost-effective route to achieve high specific energy. However, low active material utilization and cycle life hinder performance. Here, we demonstrate a positive electrode design that employs sulfide solid-state electrolytes, where a high energy synthesis approach forms a metastable and ionically conductive interphase on the active material surface. This interphase facilitates high active material utilization and contributes capacity with cycling. We also show that tailoring active material particle sizes to the micron-scale improves rate performance and cycling stability. Structural analysis reveals that the substantial volume change of sulfur-based positive electrodes during operation can partially offset that of the negative electrodes, thereby mitigating internal mechanical stress. The combined design principles enable sulfur areal capacities up to 11 mAh cm -2 while maintaining stable cycling at 25 °C. We further demonstrate several specific-energy-focused cell architectures, particularly a Li 2 S anode-free pouch cell that operates under “low stack pressure” of 10 MPa. This work outlines practical design strategies for constructing high-specific-energy all-solid-state batteries for a broad range of emerging applications.
Article Details
Authors (19)
Ashley Cronk
Xiaowei Wang
Jin An Sam Oh
Department of Nano Engineering
So-Yeon Ham
Shuang Bai
Phillip Ridley
Department of Nano Engineering
Mehdi Chouchane
Chen-Jui Huang
Pritzker School of Molecular Engineering
Diyi Cheng
Grayson Deysher
Program of Materials Science and Engineering
Hedi Yang
Baharak Sayahpour
Marta Vicencio
Choonghyeon Lee
Dongchan Lee
Min-Sang Song
Jihyun Jang
Jeong Beom Lee
Ying Shirley Meng