锂(药物)
材料科学
多硫化物
阴极
离子
储能
无机化学
插层(化学)
阳极
电化学
电解质
法拉第效率
硝酸锂
化学工程
纳米技术
电池(电)
电极
化学
离子键合
有机化学
功率(物理)
物理化学
内分泌学
工程类
物理
医学
量子力学
作者
Wandi Wahyudi,Viko Ladelta,Leonidas Tsetseris,Merfat M. Alsabban,Xianrong Guo,Emre Yengel,Hendrik Faber,Begimai Adilbekova,Akmaral Seitkhan,Abdul‐Hamid Emwas,Mohamed Nejib Hedhili,Lain‐Jong Li,Vincent Tung,Nikos Hadjichristidis,Thomas D. Anthopoulos,Jun Ming
标识
DOI:10.1002/adfm.202101593
摘要
Abstract 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 (NO 3 − ) 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 NaNO 3 can successfully substitute the widely used LiNO 3 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.
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