丁二腈
材料科学
电解质
极限抗拉强度
离子电导率
环氧乙烷
复合材料
电化学
增塑剂
化学工程
钠离子电池
氧化物
电极
聚合物
冶金
化学
共聚物
物理化学
法拉第效率
工程类
作者
Vasan Iyer,J. Petersen,Sebastian Geier,Peter Wierach
出处
期刊:Polymers
[MDPI AG]
日期:2024-10-03
卷期号:16 (19): 2806-2806
标识
DOI:10.3390/polym16192806
摘要
A new approach to developing structural sodium batteries capable of operating in ambient-temperature conditions has been successfully achieved. The developed multifunctional structural electrolyte (SE) using poly(ethylene oxide) (PEO) as a matrix integrated with succinonitrile (SN) plasticizers and glass-fiber (GF) reinforcements identified as GF_PEO-SN-NaClO4 showed a tensile strength of 32.1 MPa and an ionic conductivity of 1.01 × 10−4 S cm−1 at room temperature. It displayed a wide electrochemical stability window of 0 to 4.9 V and a high sodium-ion transference number of 0.51 at room temperature. The structural electrode (CF|SE) was fabricated by pressing the structural electrolyte with carbon fibers (CFs), and it showed a tensile strength of 72.3 MPa. The fabricated structural battery half-cell (CF||SE||Na) demonstrated good cycling stability and an energy density of 14.2 Wh kg−1, and it retained 80% capacity at the end of the 200th cycle. The cycled electrodes were observed using scanning electron microscopy, which revealed small dendrite formation and dense albeit uniform deposition of the sodium metal, helping to avoid a short-circuit of the cell and providing more cycling stability. The developed multifunctional matrix composites demonstrate promising potential for developing ambient-temperature sodium structural batteries.
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