Nanostructured MoS2 grafted by anthraquinone for energy storage

被引:1
|
作者
Tobis, Maciej [1 ]
Frackowiak, Elzbieta [1 ]
机构
[1] Poznan Univ Tech, Inst Chem & Tech Electrochem, PL-60965 Poznan, Poland
关键词
TRANSITION-METAL DICHALCOGENIDES; EXFOLIATED MOLYBDENUM-DISULFIDE; INTERCALATION PSEUDOCAPACITANCE; ELECTROCHEMICAL REDUCTION; HYDROGEN EVOLUTION; CARBON; ELECTRODES; NANOSHEETS; FUNCTIONALIZATION; SUPERCAPACITORS;
D O I
10.1016/j.jpowsour.2024.234862
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two-dimensional materials such as molybdenum disulfide (MoS 2 ) can be employed as an electrode material in energy systems due its good electrical conductivity and high reachable capacity/capacitance. We demonstrate the concept of a covalent modification of nanostructured MoS 2 with anthraquinone (AQ) molecules through diazonium salt chemistry for electrochemical capacitors and lithium -ion storage. AQ molecules are chemically bonded to MoS 2 which was proved experimentally by spectroscopic techniques. Here, AQ is grafted (ca. 20 wt%) to the outer surface of nanostructured MoS 2 , but also confined within the MoS 2 interlayer spacing. Modified AQ-MoS 2 exhibited faradaic response which improved the overall charge stored from 191 F g -1 (461 F cm -3 ) to 263 F g -1 (631 F cm -3 ) at 0.2 A g -1 in 1 M H 2 SO 4 . The process of intercalation of ions within interlayer spacing of AQ-MoS 2 was not hindered by the presence of confined AQ molecules. Impedance spectroscopy and voltammetry analysis revealed comparable non -diffusion limited response of MoS 2 before and after modification. The MoS 2 modification was likely conducted on the defect sites limiting the catalytic activity of MoS 2 towards hydrogen evolution improving stability of electrodes. In organic medium, the pseudocapacitive response of MoS 2 , enhanced by additional redox reactions of grafted AQ was observed during lithium -ion storage.
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页数:13
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