材料科学
阴极
电解质
聚合物
化学工程
碳酸丙烯酯
锂(药物)
吸附
粘弹性
能量密度
乙醚
钠
阳极
电极
储能
金属锂
悬挂(拓扑)
作者
Xiaoniu Guo,Shuai Guo,Shaohua Ge,Longfei Wen,Zhichao Gong,Yi Yang,Junyu Li,Ruixue Wang,Zhengkun Xie,Jiyu Zhang,Jun Luo,Jianqiang Kang,Lingfei Zhao,J J Lu,Junhua Shao,W G Chen
摘要
Abstract Gel polymer electrolytes (GPEs) paired with abundant sodium (Na) and high-voltage polyanion cathode, offer improved energy density and superior safety, positioning them as scalable candidates for resource-limited lithium batteries. However, such technologies are plagued by critical interfacial engineering challenges: existing GPEs fail to sustain (electro)-chemical stability and mechanical close contact at high-loading cathode and high-reactive anode. Here, we report a rationally-engineered GPE featuring biphasic polymer, creating step channels and polymer-solvent dipole adsorption to address the key issues. The volume-constrained bidirectional transport of infilling linear ether and cyclic carbonate solvents and differential polymer mechanical viscoelasticity bearing high-loading cathode and ductile Na anode. Therefore, a high-energy-density full cell of Na||Na3V2(PO4)3 (34.1 mg cmcathode−2, 194.4 Wh kg−1, based on total cell mass) and a stable pouch cell of 4.5 V-class Na||Na2.466Fe1.724Mg0.043(SO4)3 (18.7 mg cmcathode−2, ~100% after 100 cycles) were demonstrated, with safety validation included. The design principles were established for this new chemical engineering pathway towards practical solid-state batteries.
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