纳米复合材料
兴奋剂
材料科学
固态
聚合物
离子
聚合物纳米复合材料
钠
纳米技术
化学工程
化学
光电子学
复合材料
有机化学
冶金
工程类
物理化学
作者
Yang Pan,Zhenhua Wu,Mingli Li,Cheng Zhang,Yiqing Wang,Yutong Zhu,Meng Li,Yun Wang,Dong‐Sheng Li,Hao Chen,Shanqing Zhang
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-10-18
卷期号:64 (6): e202417778-e202417778
被引量:15
标识
DOI:10.1002/anie.202417778
摘要
Due to the seamless interfaces between solid polymer electrolytes (SPEs) and electrode materials, SPEs-based all-solid-state sodium-ion batteries (ASSSIBs) are considered promising energy storage systems. However, the sluggish Na+ transport and uncontrollable Na dendrite propagation still hinder the practical application of SPEs-based ASSSIBs. Herein, Ca-doped CeO2 (Ca-CeO2) nanotube framework is synthesized and integrated with poly (ethylene oxide) methyl ether acrylate-perfluoropolyether copolymer (PEOA-PFPE), resulting in multifunctional solid nanocomposite electrolytes (namely SNEs, i.e., PEOA-PFPE/Ca-CeO2). Our investigations demonstrate that the fluorous effect incurred by the fluorine-containing PEOA-PFPE and the oxygen vacancy effect induced by the Ca-CeO2 framework could synergistically promote the dissociation of sodium salt, ultimately enhancing the Na+ mobility in SNEs. Besides, the resultant SNEs construct rapid Na+ transport channels and homogenize the Na deposition in SNEs/Na interface, which effectively prevents the Na dendrite growth. Furthermore, the assembled carbon-coated sodium vanadium phosphate (NVP@C)||PEOA-PFPE/Ca-CeO2||Na coin cell delivers impressive rate capability of 97.9 mAh g-1 at 2 C and outstanding cycling stability with capacity retention of 84.3 % after 300 cycles at 1 C. This work illustrates that constructing multifunctional SNEs via incorporating functional inorganic frameworks into fluorine-containing SPEs could be a promising strategy for the commercialization of robust and high-performance ASSSIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI