Tianke Zhu, Gang Wang, Junyu Hou, Wu Sun, Changsheng Song, Qunyao Yuan, Ce Zhang, Xingyu Lei, Yang Su, Min Chen, Yun Song, Jie Zhao
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The polyvinylidene fluoride (PVDF) layer toward the cathode improves high voltage compatibility to 4.8 V, while the boron nitride (BN) layer toward the anode provides sufficient mechanical strength, regulates Li-ions transport and promotes the formation of an inorganic-rich solid electrolyte interphase (SEI). The effect of the hetero-layered structure is then verified in an easy-to-process in situ polymerized poly(1,3-dioxane) (PDOL) electrolyte, that seamlessly integrates multiple interfaces, bridging cathode, PVDF, BN, and Li metal. This solid electrolyte is characterized by high room temperature (RT) ionic conductivity (2.1 × 10<sup>−3</sup> S<sup> </sup>cm<sup>−1</sup>), and high Li-ions transference number (0.801). Most importantly, the Li|LiNi<sub>0.6</sub>Co<sub>0.2</sub>Mn<sub>0.2</sub>O<sub>2</sub>(NCM622) full batteries show remarkable cycling performance with capacity retention of 90.3% over 200 cycles at 0.5 C. 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引用次数: 0
摘要
具有高安全性和高能量密度的固态锂金属电池是储能系统的终极目标。瓶颈在于固体电解质,无论是锂阳极还是高压阴极,都必须保持完美的固-固接触和电化学稳定。在这里,我们开发了一种原位聚合异质层电解质,同时拓宽了电化学窗口并解决了多个组分之间的界面问题。阴极方向的聚偏氟乙烯(PVDF)层将高压兼容性提高到4.8 V,而阳极方向的氮化硼(BN)层提供了足够的机械强度,调节了锂离子的传输,促进了富无机固体电解质界面(SEI)的形成。然后在易于加工的原位聚合聚(1,3-二氧六环)(PDOL)电解质中验证了异质层结构的效果,该电解质无缝集成了多个界面,桥接阴极,PVDF, BN和Li金属。该固体电解质具有高室温离子电导率(2.1 × 10−3 S cm−1)和高锂离子转移数(0.801)的特点。最重要的是,Li|LiNi0.6Co0.2Mn0.2O2(NCM622)全电池在0.5℃下循环200次,容量保持率达到90.3%,具有无缝原位聚合界面的异质层状结构为高能固态lmb提供了新的途径。
Heterogeneous Engineered Solid Electrolyte for Seamless and Stable Integration of Anode and Cathode
Solid-state lithium metal batteries (LMBs) with high safety and energy density are the ultimate goal for energy storage systems. The bottleneck lies in the solid electrolytes, which must maintain perfect solid–solid contact and be electrochemically stable for both Li anode and high-voltage cathode. Here, we develop an in situ polymerized hetero-layered electrolyte that simultaneously broadens the electrochemical window and addresses interfacial issues between multiple components. The polyvinylidene fluoride (PVDF) layer toward the cathode improves high voltage compatibility to 4.8 V, while the boron nitride (BN) layer toward the anode provides sufficient mechanical strength, regulates Li-ions transport and promotes the formation of an inorganic-rich solid electrolyte interphase (SEI). The effect of the hetero-layered structure is then verified in an easy-to-process in situ polymerized poly(1,3-dioxane) (PDOL) electrolyte, that seamlessly integrates multiple interfaces, bridging cathode, PVDF, BN, and Li metal. This solid electrolyte is characterized by high room temperature (RT) ionic conductivity (2.1 × 10−3 Scm−1), and high Li-ions transference number (0.801). Most importantly, the Li|LiNi0.6Co0.2Mn0.2O2(NCM622) full batteries show remarkable cycling performance with capacity retention of 90.3% over 200 cycles at 0.5 C. The hetero-layered structure with a seamless in situ polymerized interface provides a new avenue for high-energy, solid-state LMBs.
期刊介绍:
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