Photoreduction of chromium hexavalent ions (Cr6+) from the aquatic environment is urgently needed due to its impairing effect on human health. Adsorption, photoreduction, and desorption of reduced trivalent chromium (Cr3+) at the photocatalyst surface are all significant factors for determining photocatalytic reduction efficiency. Herein, we report a facile, template-free hydrothermal approach to fabricate green and homogeneous mixed-phase (1 T/2H) molybdenum disulfide (MoS2) nanosheets for highly efficient removal of Cr6+ ions and pharmaceuticals from wastewater. The nanostructure and morphology of the obtained (1 T/2H) MoS2 are investigated; the calculated crystallite size of the (2H/1 T) MoS2 nanosheets is found to be 1.7 nm. The presence of surface functional groups adsorption, and photoreduction processes is confirmed by spectroscopic studies using Fourier transform infrared (FTIR) spectra. Additionally, Raman spectra confirmed the formation of 1 T/2H mixed-phase MoS2 which illustrates its crystal phases, structure, and chemical composition. Moreover, the point-of-zero charge analysis revealed the positively charged surface in the acid system. The obtained results revealed the non-toxicity of MoS2 nanosheets at doses lower than 1000 ppm. The results reveal that the (1 T/2H) MoS2 exhibited impressive reduction performance for Cr6+; the reduction efficiency of chromium Cr6+ is 100% under simulated sunlight, 90 min at pH (3). Further spectroscopic study results confirm the importance of the adsorption step in Cr6+ ions photoreduction. Different pharmaceuticals are also completely degraded over (1 T/2H) MoS2 nanosheets. Interestingly, complete removals of E. coli O157:H7, Listeria monocytogenes, and Candida albicans were observed at a dose of MoS2 nanosheets of 250 ppm after a contact time of 30, 30, and 45 min, respectively. The results of the current work could lead to a rational design of high-performance nanosheets for the efficient decontamination of heavy metals, pharmaceuticals, and pathogens from aquatic environments. [ABSTRACT FROM AUTHOR]