Issue 2, 2024

Designed fabrication of MoS2 hollow structures with different geometries and the comparative investigation toward capacitive properties

Abstract

Hollow MoS2 cubes and spheres were synthesized by a one-step hydrothermal method with the hard template method. The structure and morphology were characterized, and their electrochemical properties were studied. It is concluded that the specific capacitance of the hollow MoS2 cubes (335.7 F g−1) is higher than that of the hollow MoS2 spheres (256.1 F g−1). The symmetrical supercapacitors were assembled, and the results indicate that the specific capacitance of the device composed of hollow MoS2 spheres (32.9 F g−1) is slightly lower than that of the hollow MoS2 cube (37.4 F g−1) device. Furthermore, the symmetrical supercapacitor (MoS2-cube//MoS2-cube) provides a maximum energy density of 4.93 W h kg−1, which is greater than that of the symmetrical capacitor (MoS2-sphere//MoS2-sphere, 3.65 W h kg−1). This may indicate that hollow molybdenum disulfide cubes with substructures have more efficient charge transfer capabilities and better capacitance characteristics than hollow spheres. After 8000 cycles, the coulombic efficiency of the two symmetrical capacitors is close to 100%. The capacity retention of the MoS2 sphere device (95.2%) is slightly higher than that of the MoS2 cube device (90.1%). These results show that the pore structure, specific surface, and active site of MoS2 with different hollow structures have a greater impact on its electrochemical properties.

Graphical abstract: Designed fabrication of MoS2 hollow structures with different geometries and the comparative investigation toward capacitive properties

Supplementary files

Article information

Article type
Paper
Submitted
26 Oct 2023
Accepted
24 Nov 2023
First published
25 Nov 2023

Phys. Chem. Chem. Phys., 2024,26, 1156-1165

Designed fabrication of MoS2 hollow structures with different geometries and the comparative investigation toward capacitive properties

Y. Xu, H. Feng, C. Dong, Y. Yang, M. Zhou, Y. Wei, H. Guo, Y. Wei, J. Su, Y. Ben and X. Zhang, Phys. Chem. Chem. Phys., 2024, 26, 1156 DOI: 10.1039/D3CP05196J

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