TY - JOUR
T1 - Lithium-Ion Desolvation Induced by Nitrate Additives Reveals New Insights into High Performance Lithium Batteries
AU - Wahyudi, Wandi
AU - Ladelta, Viko
AU - Tsetseris, Leonidas
AU - Alsabban, Merfat
AU - Guo, Xianrong
AU - Yengel, Emre
AU - Faber, Hendrik
AU - Adilbekova, Begimai
AU - Seitkhan, Akmaral
AU - Emwas, Abdul-Hamid
AU - Hedhili, Mohamed N.
AU - Li, Lain-Jong
AU - Tung, Vincent
AU - Hadjichristidis, Nikos
AU - Anthopoulos, Thomas D.
AU - Ming, Jun
N1 - KAUST Repository Item: Exported on 2021-04-05
Acknowledgements: W.W. and V.L. contributed equally to this work. This work was supported by the King Abdullah University of Science and Technology (KAUST)and KAUST Solar Centre. L.T. acknowledges computational time at the GRNET HPC facility ARIS through project pr007037-STEM-2. J.M. also thanks the great support from the National Natural Science Foundation of China (21978281).
PY - 2021/4/2
Y1 - 2021/4/2
N2 - Electrolyte additives have been widely used to address critical issues in current metal (ion) battery technologies. While their functions as solid electrolyte interface forming agents are reasonably well-understood, their interactions in the liquid electrolyte environment remain rather elusive. This lack of knowledge represents a significant bottleneck that hinders the development of improved electrolyte systems. Here, the key role of additives in promoting cation (e.g., Li+) desolvation is unraveled. In particular, nitrate anions (NO3−) are found to incorporate into the solvation shells, change the local environment of cations (e.g., Li+) as well as their coordination in the electrolytes. The combination of these effects leads to effective Li+ desolvation and enhanced battery performance. Remarkably, the inexpensive NaNO3 can successfully substitute the widely used LiNO3 offering superior long-term stability of Li+ (de-)intercalation at the graphite anode and suppressed polysulfide shuttle effect at the sulfur cathode, while enhancing the performance of lithium–sulfur full batteries (initial capacity of 1153 mAh g−1 at 0.25C) with Coulombic efficiency of ≈100% over 300 cycles. This work provides important new insights into the unexplored effects of additives and paves the way to developing improved electrolytes for electrochemical energy storage applications.
AB - Electrolyte additives have been widely used to address critical issues in current metal (ion) battery technologies. While their functions as solid electrolyte interface forming agents are reasonably well-understood, their interactions in the liquid electrolyte environment remain rather elusive. This lack of knowledge represents a significant bottleneck that hinders the development of improved electrolyte systems. Here, the key role of additives in promoting cation (e.g., Li+) desolvation is unraveled. In particular, nitrate anions (NO3−) are found to incorporate into the solvation shells, change the local environment of cations (e.g., Li+) as well as their coordination in the electrolytes. The combination of these effects leads to effective Li+ desolvation and enhanced battery performance. Remarkably, the inexpensive NaNO3 can successfully substitute the widely used LiNO3 offering superior long-term stability of Li+ (de-)intercalation at the graphite anode and suppressed polysulfide shuttle effect at the sulfur cathode, while enhancing the performance of lithium–sulfur full batteries (initial capacity of 1153 mAh g−1 at 0.25C) with Coulombic efficiency of ≈100% over 300 cycles. This work provides important new insights into the unexplored effects of additives and paves the way to developing improved electrolytes for electrochemical energy storage applications.
UR - http://hdl.handle.net/10754/668497
UR - https://onlinelibrary.wiley.com/doi/10.1002/adfm.202101593
U2 - 10.1002/adfm.202101593
DO - 10.1002/adfm.202101593
M3 - Article
SN - 1616-301X
SP - 2101593
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -