Two-dimensional (2D) materials such as transition metal dichalcogenides (TMDC) are well-recognized as excellent electrode materials for energy storage applications due to the ion intercalation characteristic. However, gas evolution is central to the problems that limit the potential window of these materials in the energy storage context. This is because the TMDC can behave as an electrocatalyst, especially in an acid environment. Herein, a novel design of electrode materials for avoiding gas evolution in supercapacitor devices was formed using the sandwich configuration between graphene (GP) and TMDC. A family of transition metal dichalcogenide (TMDC) materials e.g., molybdenum disulfide (MoS2), molybdenum diselenide (MoSe2), tungsten disulfide (WS2), and tungsten diselenide (WSe2) including GP was constructed as a layer-by-layer electrode materials, like a “sandwich”. In this work, we provide a straightforward method for creating GP/TMDCs/GP free-standing electrodes that have the necessary properties, such as large surface area and high conductivity for electrolyte diffusion. The GP sandwich on both sides of the electrode can diminish the gas evolution of TMDCs in acidic conditions. This makes the sandwiched electrodes perform a wider electrochemical window up to 1.0 V, in 1.0 M H2SO4. Note that the gas evolution e.g. hydrogen typically occurs at about −0.35 V (onset). Compared with conventional GP/activated carbon, the specific capacitances of “sandwich” GP/MoS2/GP, GP/MoSe2/GP, GP/WS2/GP, and GP/WSe2/GP devices are improved by 7.4, 6.2, 14.8, and 17.3 %, respectively. The findings also indicate that the developed sandwich electrode may be a suitable choice for the creation of future large energy storage systems with a high intercalation capacitance in layered materials.
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