ABSTRACT
Environmental pollution caused by radionuclides like Cs-137 and Cs-134 has increased global attention toward public health. Electrochemical adsorption has emerged as a feasible, rapid, and scalable method to treat contaminated water sources. However, graphene and its derivatives have limitations in ion adsorption via physisorption, forming a double layer that restricts the electrode's adsorption capacity. To address this, we propose the use of molybdenum disulfide (MoS2) with its extensive intercalation galleries of MoS2 nanosheets for cesium removal via an electrochemical route. Liquid-phase exfoliation with water and N-methyl-2-pyrrolidone (NMP) was then used to produce MoS2 nanosheets in a scalable quantity (high-yield production). The formation of a mixed solvent possessing relatively equivalent surface energy for exfoliation enabled us to achieve a remarkable exfoliation yield of up to ca. 1.26 mg mL-1, which is one of the highest yields reported to date (without a surfactant being added) and to the best of our knowledge. The 35% v/v of water in NMP displayed a maximum yield while maintaining the structure of the as-exfoliated one. Water exceeding over 66.7% v/v led to the formation of MoO3. Moreover, an insight into the cesium ion removal mechanism through the electrochemical route was demonstrated. It is found that the Cs+ removal follows electrochemical intercalation rather than adsorption. This work aids the understanding of cesium intercalation coupled with a mass-scale production method, which should lead to more efficient and cost-effective removal of radionuclides from contaminated water sources, opening new research avenues in materials and environmental science.
