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Traditional thermoelectric generators (TEGs) face scalability challenges due to high-temperature, long-duration curing processes and rare-earth/toxic chalcogenides such as bismuth telluride. 

MXenes are a newer class of 2D materials, possess with desirable properties such as large specific surface area, conductivity, and hydrophilicity, making them attractive for various environmental applications, including remediation and as membranes for water treatment. Until recently, the practical implementation of MXenes was hindered by their instability in water, although improved synthesis procedures have largely addressed this issue. Consequently, it is now important to assess the stability of MXenes in engineered environments relevant to drinking water and membrane operation (e.g. backwashing). In this study, Ti3C2Tx MXenes were found to remain stable upon exposure to an aqueous environment saturated with oxygen and to UVC and UVA light at circumneutral pH, but were transformed upon exposure to Fe(III) chloride and free chlorine. The chlorination reaction kinetics are 1st order with respect to Ti3C2Tx and free chlorine concentration, with a rate constant that increased at pH ≤ 7.5, implicating HOCl as the reactive species. We propose that MXene reactions with HOCl occur by an electrophilic attack of Cl+, forming TiO2 and degrading the MXene. AFM data shows that transformations are initiated at the edges of the MXene sheets and localized areas on the MXene, suggesting that the initial sites for Cl+ attack are defect sites and/or uncoordinated Ti atoms. During the initial stages of the oxidative degradation, the sheet-like structure of colloidal MXenes is preserved, although prolonged chlorine exposure leads to three-dimensional crystalline (anatase) TiO2 formation. The degradation of MXenes during chlorinationThis contrasts with the inertness of nanoscale TiC, highlighting the need to devise surface modification processes that will allow MXenes to resist the oxidative conditions associated with membrane regeneration/backwashing. 

Semiconductor InSe 2D nanomaterials have emerged as potential photoresponsive materials for broadly distributed photodetectors and wearable electronics technologies due to their high photoresponsivity and thermal stability. This paper addresses an environmental concern about the fate of InSe 2D nanosheets when disposed and released into the environment after use. Semiconducting materials are potentially reactive and often form environmentally damaging species, for example reactive oxygen and nitrogen species, when degraded. InSe nanosheets are prepared using a semi bottom-up approach which involves a reaction between indium and selenium precursors at elevated temperature in an oxygen-free environment to prevent oxidation. InSe nanosheets are formed as a stable intermediate with micrometer-sized lateral dimensions and a few monolayer thickness. The InSe 2D nanosheets are obtained when the reaction is stopped after 30 minutes by cooling. Keeping the reaction at elevated temperature for a longer period, for example 60 minutes leads to the formation of InSe 3D nanoparticles of about 5 nm in diameter, a thermodynamically more stable form of InSe. The paper focuses on the colloidal stabilization of InSe nanosheets in an aqueous solution that contains epigallocatechin gallate (EGCG), a natural organic matter (NOM) simulant. We show that EGCG coats the surface of the hydrophobic, water-insoluble InSe nanosheets via physisorption. The formed EGCG-coated InSe nanosheets are colloidally stable in aqueous solution. While unmodified semiconducting InSe nanosheets could produce reactive oxygen species (ROS) when illuminated, our study shows low levels of ROS generation by EGCG-coated InSe nanosheets under ambient light, which might be attributed to ROS quenching by EGCG. Growth-based viability (GBV) assays show that the colloidally stable EGCG-coated InSe nanosheets adversely impact the bacterial growth of Shewanella oneidensis MR-1, an environmentally relevant Gram-negative bacterium in aqueous media. The impact on bacterial growth is driven by the EGCG coating of the nanosheets. In addition, live/dead assays show insignificant membrane damage of the Shewanella oneidensis MR-1 cells by InSe nanosheets, suggesting a weak association of EGCG-coated nanosheets with the cells. It is likely that the adverse impact of EGCG-coated nanosheets on bacterial growth is the result of increasing local concentration of EGCG either when adsorbed on the nanosheets when the nanosheets interact with the cells, or when desorbed from the EGCG-coated nanosheets to interact with the bacterial cells.