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硫化聚丙烯腈上的功能层增强了钠离子去溶剂化作用并促进其传输,以实现高倍率和长寿命钠硫电池。

Functional layer on sulfurized polyacrylonitrile enhancing Na de-solvation and transportation for high rate and long life sodium-sulfur batteries.

作者信息

Xiao Xueying, Jin Zhaoqing, Wang Baochun, Ye Yunzhen, Xu Ao, Xie Xintai, Pei Mengxian, Lu Jianhao, Wang Weikun, Huang Yaqin

机构信息

Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Key Laboratory of Biomedical Materials of Natural Macromolecules, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029, China; Chemical Defense Institute, Beijing 100191, China.

Chemical Defense Institute, Beijing 100191, China.

出版信息

J Colloid Interface Sci. 2025 Nov 15;698:137985. doi: 10.1016/j.jcis.2025.137985. Epub 2025 May 26.

Abstract

Rechargeable sulfurized polyacrylonitrile (SPAN)-based room temperature sodium-sulfur (RT Na/SPAN) batteries, which can operate stably at room temperature, are highly sought after due to the high coulombic efficiency, excellent reversibility and cycling stability. However, the practical battery performance of the Na/SPAN system is fundamentally limited by sluggish interfacial kinetics, particularly hindered Na transport and electron transfer at electrode-electrolyte interface. Herein, this study addresses these challenges through a low-temperature (180 ℃) polymeric carbon encapsulation strategy, which strategically constructs a polyfuran-rich amorphous carbon(AC) coating on SPAN microparticles (SPAN@AC). This synergistic mechanism operates through conjugated backbones that facilitate efficient electron transport, while the dual role of oxygen which providing strong Na coordination and weak bonding interactions, thereby simultaneously accelerating charge transfer and ion-desolvation kinetics at the interface. These strategies effectively mitigate interfacial kinetic limitations in sodium-ion batteries, resulting in improved cycling durability and rate capability during practical battery testing. Hence, the SPAN@AC electrode delivered a reversible capacity of 400 mAh g at 0.2 A g over 500 cycles and 248 mAh g at 1 A g over 750 cycles. This study develops a new approach to enhance SPAN's electrochemical properties, thereby establishing its viability as a high-performance cathode material for practical room temperature sodium-sulfur battery applications.

摘要

可充电的硫化聚丙烯腈(SPAN)基室温钠硫(RT Na/SPAN)电池能够在室温下稳定运行,因其具有高库仑效率、出色的可逆性和循环稳定性而备受青睐。然而,Na/SPAN体系的实际电池性能从根本上受到缓慢的界面动力学限制,特别是在电极-电解质界面处阻碍了钠的传输和电子转移。在此,本研究通过低温(180℃)聚合物碳封装策略应对这些挑战,该策略在SPAN微粒(SPAN@AC)上战略性地构建了富含聚呋喃的非晶碳(AC)涂层。这种协同机制通过促进有效电子传输的共轭主链起作用,而氧的双重作用提供了强钠配位和弱键相互作用,从而同时加速了界面处的电荷转移和离子去溶剂化动力学。这些策略有效减轻了钠离子电池中的界面动力学限制,在实际电池测试中提高了循环耐久性和倍率性能。因此,SPAN@AC电极在0.2 A g下500次循环中可逆容量为400 mAh g,在1 A g下750次循环中为248 mAh g。本研究开发了一种增强SPAN电化学性能的新方法,从而确立了其作为实用室温钠硫电池应用的高性能正极材料的可行性。

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