Tuning Surface Energy to Enhance MoS<sub>2</sub> Nanosheet Production <i>via</i> Liquid-Phase Exfoliation: Understanding the Electrochemical Adsorption of Cesium Chloride
Panwad Chavalekvirat, Patlapa Nakkiew, Tanatat Kunaneksin, Wisit Hirunpinyopas, Wutthikrai Busayaporn, Pawin Iamprasertkun
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 (MoS 2 ) with its extensive intercalation galleries of MoS 2 nanosheets for cesium removal via an electrochemical route. Liquid-phase exfoliation with water and N -methyl-2-pyrrolidone (NMP) was then used to produce MoS 2 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 MoO 3 . 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.