丙烯腈
材料科学
多硫化物
阴极
电化学
法拉第效率
傅里叶变换红外光谱
共价键
X射线光电子能谱
魔角纺纱
化学工程
聚合物
有机化学
核磁共振波谱
复合材料
电极
共聚物
电解质
物理化学
化学
工程类
作者
Misganaw Adigo Weret,Chung‐Feng Jeffrey Kuo,Tamene Simachew Zeleke,Tamene Tadesse Beyene,Meng‐Che Tsai,Chen−Jui Huang,Gebregziabher Brhane Berhe,Wei‐Nien Su,Bing−Joe Hwang
标识
DOI:10.1016/j.ensm.2019.11.022
摘要
Sulfurized−poly(acrylonitrile) compound (SPAN) cathode decipher polysulfide dissolution and shuttling effect and deliver promising electrochemical performance. However, the synthesis reaction mechanism, chemical structure, and lithium storage mechanism of the compound are yet not clearly understood. Herein we report a plausible synthesis reaction mechanism, chemical structure, and lithium storage mechanism of SPAN using high−resolution cross−polarization/magic angle spinning (CP−MAS) solid states nuclear magnetic resonance (ssNMR), Fourier transform infrared spectroscopy (FTIR), X−ray photoelectron spectroscopy (XPS), elemental analysis (EA) techniques, and electrochemical analysis. The analysis reveals that the SPAN structure contains N–S and NC–S bonds in addition to C–S and S–S bonds. Electrochemical cleavage of the covalent bonds results in high initial discharge capacity with high voltage polarization in the first cycle. Once the covalent bonds are cleaved in the first cycle, the electron-donating effect of the Li–C and Li–N bonds increases the electron density of the conjugated heterocyclic structure and benefits the decrease of the charge/discharge voltage hysteresis after the second cycle. As a result, it provides high reversible specific capacity, high coulombic efficiency, and extended cycle life with low voltage hysteresis after the second cycle. The results show that the covalent molecular interactions of SPAN cathode completely overcome the polysulfide dissolution, thereby prevent the loss of active materials. Furthermore, the structural elucidation is further applicable for designing an organic cathode achieving high active materials loading concomitantly with improving the electrochemical performances.
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