Shenghang Zhang, Fu Sun, Xiangchun Zhuang, Lixuan Yang, Rongxian Wu, Bin Xie, Jiedong Li, S F Wang, Lixin Qiao, Jinzhi Wang, André Hilger, Ingo Manke, Shanmu Dong, Zili Cui, Gaojie Xu, Guanglei Cui
Lithium sulfonimide salts have significantly advanced the development of lithium metal batteries (LMBs). Nevertheless, sulfonimide salt-based electrolytes exhibit severe corrosion behavior toward the aluminum (Al) current collector when exceeding 4.0 V (vs Li/Li + ). Herein, the corrosion chemistry of lithium bis(trifluoromethylsulfonyl)imide (LiTFSI)-based electrolytes in LMBs has been elucidated. It is revealed that, in addition to Al 3+ dissolution, corrosion reactions also involve the Li anode, accompanied by decompositions of solvents. The corrosion byproducts, including Al 3+ and a series of carbonate anions ( e.g ., CH 3 CH 2 OCO 2 – ), will engage in crosstalk between electrodes to intensify the corrosion process. Herein, a series of cyano-group (−CN)-containing auxiliary salts are adopted to inhibit crosstalk effects by enabling strong anticorrosion coordination and interphase passivation. Encouragingly, the as-designed electrolyte enables the 468 Wh kg –1 LiNi 0.8 Co 0.1 Mn 0.1 O 2 ||Li pouch cell to exhibit 80% capacity retention after 280 cycles. The as-designed electrolyte also mitigates exothermic reactions under thermal abuse, effectively delaying the thermal runaway.