材料科学
电解质
纳米孔
阳极
化学工程
多孔性
离子
溶剂
纳米技术
电极
物理化学
复合材料
化学
有机化学
工程类
作者
Xue Li,Fangting Liu,Junjie Li,Anding Xu,Jie Shi,Baitao Li,Songping Wu,Liming Wang
标识
DOI:10.1021/acsami.4c20743
摘要
Sodium-ion batteries (SIBs) face challenges in practical applications due to substantial volume expansion of anode materials and unstable solid–electrolyte interphases (SEIs), limiting their cycling life, rate performance, and reaction kinetics. Here, we report the successful synthesis of unique N-doped carbon-coated WS2 hexahedral nanoporous core–shell structures (WS2@NC) combined with a Na+-solvation strategy for high capacity and long-life sodium storage. Nanoporous architecture facilitates sufficient electrolyte infiltration and buffers volume expansion. The uniform N-doped carbon shell improves the conductivity, the stable inorganic-rich SEI improves the cycle stability, and the Na+-solvent cointercalation partially avoids the desolvation process and realizes the rapid reaction kinetics. Unique structural design and excellent compatibility with electrolytes give the WS2@NC electrode unprecedented long cycling life and rate capability in SIBs (207.7 mAh g–1 after 10,000 cycles at 20 A g–1 and 343 mAh g–1 at 50 A g–1). This work provides critical insights into performance enhancement mechanisms, offering a crucial theoretical basis for SIB applications.
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