Uranyl Peroxide Nanocage Assemblies for Solid-State Electrolytes

被引:8
作者
Hu, Jie [1 ,2 ]
Cai, Linkun [1 ,2 ]
Wang, Huihui [1 ,2 ]
Chen, Kun [1 ,2 ]
Yin, Panchao [1 ,2 ]
机构
[1] South China Univ Technol, Sch Mol Sci & Engn, South China Adv Inst Soft Matter Sci & Technol, Guangdong Prov Key Lab Funct & Intelligent Hybrid, Guangzhou 510640, Peoples R China
[2] South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
uranyl peroxide nanocage; nanocomposites; microphase separation; solid-state electrolyte; molecular cluster; charge interaction; POLYMER ELECTROLYTES; CONDUCTIVITY RELAXATION; IONIC TRANSPORT; METAL; COMPOSITES; COMPLEXES; BATTERIES; DYNAMICS; CLUSTERS; MODEL;
D O I
10.1021/acsanm.1c00130
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Hybrid nanocomposites of uranyl peroxide nanocages are assembled from the ionic interaction between anionic uranyl peroxide nanocage clusters (Li44K16[UO2(O-2)(OH)](60), U-60) and cationic surfactants. As a porous nanocapsule, one U-60 cluster can uptake as much as similar to 44 Li+ ions, serving as the Li+ storage and transportation center. The nanocomposites show enriched microphase-separated structures ranging from lamellar to hexagonal columnar structures depending on the geometries of introduced surfactants. The U-60 enriched phases serve as nanochannels for Li+ ion transportation. The Li+ conductivity of the nanocomposites exhibits a crossover at 295 K from the Vogel-Fulcher-Tammann temperature dependence law to Arrhenius law, suggesting different Li+ conducting mechanisms across the critical temperature (T-c) phase-transition temperature of the hybrid materials. The Li+ ions diffuse through dynamic segmental motion of the nanocomposites above Tc and through a typical hopping mechanism below Tc. The design of the nanocomposites offers approaches to decouple the ionic transportation and dynamics of surfactant chains and therefore paves a way to fabricate solid-state electrolytes with both high ion conductivities and promising mechanical strengths.
引用
收藏
页码:3597 / 3603
页数:7
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