Journal
ELECTROCHIMICA ACTA
Volume 376, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2021.137987
Keywords
Supercapacitor; Pseudo-capacitor; Alkali metals; Tin disulfide; Flower-like structure; Binder-free
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In this study, flower-like pure SnS2 and alkali metals doped-SnS2 nanostructures were successfully synthesized by a simple single-step solvothermal method. The presence of dopants in SnS2 led to increased interlayer distance and dislocation intensity, resulting in better electrochemical performance. Among the alkali metals, Na doping showed the highest current density and capacitance performance, attributed to its higher conductivity and expanded interlayer spacing.
Tin disulfide can be a good electrode material in supercapacitors due to the presence of significant interlayer space in crystalline structures and large surface area. However, there are only a few reports of its supercapacitor applications. In this study, we report flower-like pure SnS2 and alkali metals (Li, Na, K and Cs) doped-SnS2 nanostructures synthetized by simple single-step solvothermal method without use of any surfactants. Results show that due to the presence of dopants, with increasing radius of the dopant element, the interlayer distance and dislocation intensity increase. This leads to an increase in the expanded space between interlayer and electro-active sites, and therefore, it is possible to intercalate more ions from the electrolyte. But due to the higher conductivity of Na than the other alkali metals, Na doped-SnS2 shows higher current density at constant voltage and thus better capacitance performance than the others. Na doped-SnS2 exhibits higher supercapacitor performance with a high capacitance of 269 Fg(-1) at a current density of 1 Ag-1. The significant electrochemical performance of Na doped-SnS2 can be attributed to its particularly good surface area due to the expansion of interlayer space, increasing of electro-active sites and greater conductivity due to the presence of Na. (C) 2021 Elsevier Ltd. All rights reserved.
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