Abstract
AbstractThe development of high‐energy‐density lithium metal batteries has been significantly hampered mainly due to the poor electrolyte–electrode compatibility, narrow operating temperature range, and stringent safety concerns of conventional electrolytes. Here, an in situ cross‐linked plastic crystal‐based electrolyte (CPCE) with an optimized composition design is proposed. Based on the interaction of succinonitrile (SN) and ethoxylated trimethylolpropane triacrylate (ETPTA) with polar carbonyl groups, CPCE delivers well‐tuned energy levels and a concentrated coordination structure, leading to an improved electrochemical window and stable electrode–electrolyte interface. In addition, the crystallization of SN molecules is also inhibited, ensuring suitable ion migration in bulky CPCE over a wide temperature range. Moreover, both the nonleakage of cross‐linked ETPTA and the nonflammability of the plastic crystal electrolyte (PCE) further reinforce the safety of CPCE. As a result, the well‐designed CPCE achieves high ion conductivity with a wide electrochemical window (≈5.4 V vs Li+/Li) and a broad operating temperature range (−20 to 100 °C). It also delivers dendrite‐free lithium plating with high Coulombic efficiency of up to ≈99.1%. The Cu|CPCE|LiNi0.8Co0.1Mn0.1O2 anode‐free pouch cell exhibits high energy density (≈1520 Wh L‐1) and high safety during abuse tests. This study paves a new pathway to realize the practical application of high‐energy‐density lithium metal battery energy storage systems.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.