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- W4385256192 abstract "Abstract Molybdenum disulfide (MoS 2 ), a promising two‐dimensional photothermal material, possesses the capability to convert solar irradiation into thermal energy. This conversion is beneficial for processes like wastewater treatment and seawater desalination. Nevertheless, the influence of the surface chemical properties of MoS 2 , particularly its wettability, on the evaporation rate of water confined to the surface remains unexplored. In our study, we demonstrate that the wettability degree of MoS 2 significantly influences its water evaporation rate performance. Interestingly, this parameter can be simply and accurately modulated by altering the synthesis time of MoS 2 . We synthesized MoS 2 via a simple hydrothermal method at three different durations: 16, 20, and 24 h, at 200°C. Subsequently, we impregnated the resultant MoS 2 onto air‐laid paper (ALP), forming a solar‐driven evaporator system. We found that the MoS 2 nanosheets synthesized within the shortest duration (MoS 2 ‐16 h) exhibited the highest evaporation rate of 1.77 kg m −2 h −1 , along with 92% energy efficiency. MoS2‐16 h resulted in MoS 2 rich in defects, featuring the largest surface area and the smallest contact angle. The hydrophilic areas of MoS 2 ‐16 h facilitated the continuous diffusion of water molecules through defect sites, treating them as contact lines. Additionally, the expansive surface area introduced a larger region for light absorption, enhancing water‐solid interactions. The presence of molybdenum oxide on the surface of the nanosheet system also contributed to superior wettability behavior. Notably, all the tested MoS 2 /ALP systems in this study displayed excellent performance in salt rejection and heavy metal ion concentration reduction." @default.
- W4385256192 created "2023-07-26" @default.
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- W4385256192 date "2023-07-25" @default.
- W4385256192 modified "2023-10-16" @default.
- W4385256192 title "Tuning surface wettability of <scp>MoS<sub>2</sub></scp> to enhance solar‐driven evaporation rates" @default.
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- W4385256192 doi "https://doi.org/10.1002/ep.14234" @default.
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