journal article·2023-03-15

Strongly Solvating Ether Electrolytes for High-Voltage Lithium Metal Batteries

Shunqiang Chen, Weiduo Zhu, Lijiang Tan, Digen Ruan, JiaJia Fan, Yunhua Chen, Xianhui Meng, Qingshun Nian, Xin Zhao, Jinyu Jiang, Zihong Wang, Shuhong Jiao, Xiaojun Wu, Xiaodi Ren

ACS Applied Materials & Interfaces· Volume 15· Issue 10
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Abstract

Ethers are promising electrolytes for lithium (Li) metal batteries (LMBs) because of their unique stability with Li metal. Although intensive research on designing anion-enriched electrolyte solvation structures has greatly improved their electrochemical stabilities, ether electrolytes are approaching an anodic bottleneck. Herein, we reveal the strong correlation between electrolyte solvation structure and oxidation stability. In contrast to previous designs of weakly solvating solvents for enhanced anion reactivities, the triglyme (G3)-based electrolyte with the largest Li + solvation energy among different linear ethers demonstrates greatly improved stability on Ni-rich cathodes under an ultrahigh voltage of 4.7 V (93% capacity retention after 100 cycles). Ether electrolytes with a stronger Li + solvating ability could greatly suppress deleterious oxidation side reactions by decreasing the lifetime of free labile ether molecules. This study provides critical insights into the dynamics of the solvation structure and its significant influence on the interfacial stability for future development of high-efficiency electrolytes for high-energy-density LMBs.
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Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Polyoxometalates: Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China

Department of Physics, Hefei University of Technology, Hefei, Anhui 230009, China

NIO Inc., Shanghai 201804, China

Funding

Central University Basic Research Fund of China · National Natural Science Foundation of China · NIO Research Programme

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