Anchoring Side Chains to Carbonate Groups for Reviving Stable Polycarbonate-Based Solid-State Lithium Metal Batteries

Polycarbonate-based electrolytes are ideal electrolytes for solid-state lithium metal batteries (LMBs) due to their wider electrochemical windows and considerable ionic conductivities compared with conventional solid polymer electrolytes. However, polycarbonates encounter severe interfacial side reactions with lithium metal, leading to the interfacial degradation of polymers. Herein, a spontaneously formed restricted conformation is designed via the in situ anchoring of side chains to suppress the interfacial degradation of polycarbonate-based electrolytes. The restricted conformation enables the side chains to shield and protect the degradable ester bonds of cyclic carbonates, suppressing contact and interfacial degradation between polycarbonates and lithium metal anodes. As a proof of concept, the protected polycarbonate-based electrolyte demonstrates a stable cycling capability of the Li/Li cell beyond 1000 h at a current density of 0.5 mA cm<sup>-2</sup>, and the assembled LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub>/Li pouch cell also achieves similar improvement in cycling performance. This work indicates that the strategy of constructing restricted conformations via anchoring side chains is a feasible avenue for fabricating highly stable polycarbonate-based solid-state LMBs.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-05-01
DOI
https://doi.org/10.1021/jacs.5c00760
Citations
18
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
13.15

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article

Anchoring Side Chains to Carbonate Groups for Reviving Stable Polycarbonate-Based Solid-State Lithium Metal Batteries

Jingyuan Yu, Wei Deng, Juncai Long, Hantao Xu et al.
18 citations
Journal of the American Chemical Society
Advanced Battery Materials and Technologies
13.15
article

Anchoring Side Chains to Carbonate Groups for Reviving Stable Polycarbonate-Based Solid-State Lithium Metal Batteries

Jingyuan Yu, Wei Deng, Juncai Long, Hantao Xu, Lin Xu, Lei Shi, Chaobin He, Wenwei Zhang
article en
18 citations

Abstract

Polycarbonate-based electrolytes are ideal electrolytes for solid-state lithium metal batteries (LMBs) due to their wider electrochemical windows and considerable ionic conductivities compared with conventional solid polymer electrolytes. However, polycarbonates encounter severe interfacial side reactions with lithium metal, leading to the interfacial degradation of polymers. Herein, a spontaneously formed restricted conformation is designed via the in situ anchoring of side chains to suppress the interfacial degradation of polycarbonate-based electrolytes. The restricted conformation enables the side chains to shield and protect the degradable ester bonds of cyclic carbonates, suppressing contact and interfacial degradation between polycarbonates and lithium metal anodes. As a proof of concept, the protected polycarbonate-based electrolyte demonstrates a stable cycling capability of the Li/Li cell beyond 1000 h at a current density of 0.5 mA cm<sup>-2</sup>, and the assembled LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub>/Li pouch cell also achieves similar improvement in cycling performance. This work indicates that the strategy of constructing restricted conformations via anchoring side chains is a feasible avenue for fabricating highly stable polycarbonate-based solid-state LMBs.

Journal of the American Chemical SocietyVol. 147(19)
Agency for Science, Technology and Research (SG), National University of Singapore (SG), Wuhan University of Technology (CN), Institute of Materials Research and Engineering (SG), Division of Materials Science and Engineering (AU), Materials Processing (United States) (US)
National Research Foundation Singapore, National Natural Science Foundation of China, China Scholarship Council, National Key Research and Development Program of China
Openalex Percentile: Top 1%
Advanced Battery Materials and Technologies
13.15
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