TY - JOUR
T1 - Electrolyte engineering for thermally stable Li-S batteries operating from -20 °C to 100 °C
AU - Guo, Dong
AU - Thomas, Simil
AU - El-Demellawi, Jehad K.
AU - Shi, Zixiong
AU - Zhao, Zhiming
AU - Canlas, Christian G.
AU - Lei, Yongjiu
AU - Yin, Jian
AU - Zhang, Yaping
AU - Hedhili, Mohamed Nejib
AU - Arsalan, Muhammad
AU - Zhu, Yunpei
AU - Bakr, Osman M.
AU - Mohammed, Omar F.
AU - Alshareef, Husam N.
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2024/9/19
Y1 - 2024/9/19
N2 - Lithium-sulfur (Li-S) batteries are deemed one of the most promising high-energy density battery technologies. However, their operation under thermal extremes, e.g., subzero and above 60 °C, remains largely underexplored. Especially, high temperatures (HT) accelerate sulfur dissolution and undesired side reactions, presenting significant challenges for electrolyte design. In this work, contrary to traditional understanding, we discovered that even (localized) high-concentration electrolytes (HCEs), which have shown promise within moderate temperature ranges (0-60 °C), fail at temperatures above 80 °C. Detailed investigations revealed that Li-anion aggregates in HCE trigger uncontrolled reductive decomposition at the Li anode side once the temperature exceeds a threshold of 80 °C. The resultant parasitic byproducts caused serious crosstalk and cathode oxidation in HT Li-S batteries. To counter this issue, we developed a localized medium-concentration electrolyte that features a well-mediated solvation structure and energy level, demonstrating excellent thermodynamic stability at high temperatures with superb kinetics at low temperatures. Consequently, high-performance and safely operating Li-S pouch cells are achieved over an unprecedented range of −20 to 100 °C. These findings link electrolyte microstructure, temperature, SEI structure, and degradation mechanism, offering a design protocol for the reliable function of batteries in extreme environments.
AB - Lithium-sulfur (Li-S) batteries are deemed one of the most promising high-energy density battery technologies. However, their operation under thermal extremes, e.g., subzero and above 60 °C, remains largely underexplored. Especially, high temperatures (HT) accelerate sulfur dissolution and undesired side reactions, presenting significant challenges for electrolyte design. In this work, contrary to traditional understanding, we discovered that even (localized) high-concentration electrolytes (HCEs), which have shown promise within moderate temperature ranges (0-60 °C), fail at temperatures above 80 °C. Detailed investigations revealed that Li-anion aggregates in HCE trigger uncontrolled reductive decomposition at the Li anode side once the temperature exceeds a threshold of 80 °C. The resultant parasitic byproducts caused serious crosstalk and cathode oxidation in HT Li-S batteries. To counter this issue, we developed a localized medium-concentration electrolyte that features a well-mediated solvation structure and energy level, demonstrating excellent thermodynamic stability at high temperatures with superb kinetics at low temperatures. Consequently, high-performance and safely operating Li-S pouch cells are achieved over an unprecedented range of −20 to 100 °C. These findings link electrolyte microstructure, temperature, SEI structure, and degradation mechanism, offering a design protocol for the reliable function of batteries in extreme environments.
UR - http://www.scopus.com/inward/record.url?scp=85205599552&partnerID=8YFLogxK
U2 - 10.1039/d4ee03191a
DO - 10.1039/d4ee03191a
M3 - Article
AN - SCOPUS:85205599552
SN - 1754-5692
VL - 17
SP - 8151
EP - 8161
JO - Energy and Environmental Science
JF - Energy and Environmental Science
IS - 21
ER -