阴极
材料科学
聚丙烯腈
锂(药物)
聚合物
化学工程
X射线光电子能谱
电化学
锂硫电池
纳米技术
硫黄
复合材料
物理化学
电极
内分泌学
化学
冶金
工程类
医学
作者
Chen‐Jui Huang,Kuan‐Yu Lin,Yi‐Chen Hsieh,Wei‐Nien Su,Chia‐Hsin Wang,Gunther Brunklaus,Martin Winter,Jyh‐Chiang Jiang,Bing‐Joe Hwang
标识
DOI:10.1021/acsami.0c22811
摘要
Sulfurized polyacrylonitrile (S-cPAN) has been recognized as a particularly promising cathode material for lithium–sulfur (Li–S) batteries due to its ultra-stable cycling performance and high degree of sulfur utilization. Though the synthetic conditions and routes for modification of S-cPAN have been extensively studied, details of the molecular structure of S-cPAN remain yet unclear. Herein, a more reasonable molecular structure consisting of pyridinic/pyrrolic nitrogen (NPD/NPL) is proposed, based on the analysis of combined X-ray photoelectron spectroscopy, 13C/15N solid-state nuclear magnetic resonance, and density functional theory data. The coexistence of vicinal NPD/NPL entities plays a vital role in attracting S2 molecules and facilitating N–S bond formation apart from the generally accepted C–S bond in S-cPAN, which could explain the extraordinary electrochemical features of S-cPAN among various nitrogen-containing sulfurized polymers. This study provides new insights and a better understanding of structural details and relevant bond formation mechanisms in S-cPAN, providing a foundation for the design of new types of sulfurized cathode materials suitable for application in next-generation high-performance Li–S batteries.
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