异质结
材料科学
阳极
插层(化学)
碳纤维
热液循环
纳米技术
化学工程
降级(电信)
相(物质)
吸附
离子
催化作用
电子转移
动力学
工作(物理)
光电子学
电极
氟
作者
Xin Zhang,Yanchen Fan,Hui Li,Guanyi Wang,Zhaoying Li,Jiantao Li,Chunrong Ma
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-12-12
卷期号:11 (1): 925-935
被引量:7
标识
DOI:10.1021/acsenergylett.5c03845
摘要
The practical application of sodium-ion batteries is hindered by slow ion transport and structural degradation of anodes during cycling. To address this, we report an iodine-doped MoS2 heterostructure with carbon intercalation (I-MoS2@C), constructed via an in situ hydrothermal strategy that integrates phase engineering with interfacial modulation. Glucose-derived carbon layers confine reversible 2H-1T phase transformations, enhancing structural adaptability and ion transport. Concurrently, electron transfer from iodine stabilizes the 1T phase, improving Na+ adsorption and electronic conductivity. At the interface, I–C catalytic sites promote fluorine release and the formation of a NaF-rich SEI, strengthening interfacial ion kinetics and stability. As a result of these synergistic effects, the I-MoS2@C anode exhibits high-rate capability (220 mAh g–1 at 20 A g–1) and exceptional cycling durability. This work demonstrates a strategy for designing dynamically reconstructable, interface-optimized heterostructures for high-performance sodium-ion storage.
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