We've updated our Privacy Policy to make it clearer how we use your personal data. We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Advertisement

New Electrolyte Paves the Way for Safe and Long-Cyclable Lithium Metal Batteries

A battery with small sections inside, illustrating charge.
Credit: iStock
Listen with
Speechify
0:00
Register for free to listen to this article
Thank you. Listen to this article using the player above.

Want to listen to this article for FREE?

Complete the form below to unlock access to ALL audio articles.

Read time: 1 minute

In recent years, batteries have become ubiquitous in consumers’ daily lives. However, existing commercial battery technologies, which use liquid electrolytes and carbonaceous anodes, have certain drawbacks such as safety concerns, limited lifespan, and inadequate power density particularly at high temperatures.


Yet, there is an increasing need for batteries that can operate in extreme conditions, such as the high temperatures required in various industrial sectors, including medical device sterilisation, subsurface exploration, and thermal reactors.


This has prompted researchers to search for solid electrolytes that are safe and compatible with lithium metal anodes, which are known for their high theoretical specific power capacity.


A research team led by Professor Dong-Myeong Shin of Department of Mechanical Engineering at the University of Hong Kong (HKU) has developed a new generation of lithium metal batteries, representing a significant advancement in the field. Their innovation centres on microcrack-free polymer electrolytes, integral to these batteries, which promise extended lifespan and enhanced safety at elevated temperatures.


The findings have been published in the journal Advanced Science with the title “Accelerated Selective Li+ Transports Assisted by Microcrack-Free Anionic Network Polymer Membranes for Long Cyclable Lithium Metal Batteries”.

Want more breaking news?

Subscribe to Technology Networks’ daily newsletter, delivering breaking science news straight to your inbox every day.

Subscribe for FREE
The microcrack-free polymer electrolytes developed by Professor Shin's team are synthesised via a straightforward one-step click reaction, exhibiting notable attributes including resistance to dendrite growth and non-flammability, demonstrating a high electrochemical stability window up to 5 V, and an ionic conductivity of 3.1 × 10−5 S cm−1 at high tempuratures.


These enhancements are attributed to tethered borate anions within the microcrack-free membranes, which facilitate accelerated selective transport of Li+ ions and suppress dendrite formation. Ultimately, these anionic network polymer membranes enable lithium metal batteries to function as safe, long-cycling energy storage devices at high temperatures, maintaining 92.7% capacity retention and averaging 99.867% coulombic efficiency over 450 cycles at 100°C. Normally, the cycling performance of conventional liquid electrolytes Li metal batteries is fewer than 10 cycles at high temperatures.


The breakthrough by the research team potentially paves the way for future advancements in anionic polymer electrolyte design for next-generation lithium batteries.


“We believe this innovation opens doors for new battery chemistries that can revolutionise rechargeable batteries for high-temperature applications, emphasising safety and longevity,” said Dr Jingyi Gao, the first author of the paper.


"Apart from applications in high-temperature scenarios, the microcrack-free electrolyte membranes also have the potential to enable fast charging due to low overpotential. This capability could allow electric vehicles to recharge in the time it takes to drink a cup of coffee, marking a significant advancement towards a clean energy future," Professor Shin added.


Reference: Gao J, Zhou J, Chen X, et al. Accelerated selective Li+ transports assisted by microcrack-free anionic network polymer membranes for long cyclable lithium metal batteries. Adv Sci. 2024;11(17):2308530. doi: 10.1002/advs.202308530

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source. Our press release publishing policy can be accessed here.