Journal Home > Volume 13 , Issue 1

As a renewable and environment-friendly technology for seawater desalination and wastewater purification, solar energy triggered steam generation is attractive to address the long-standing global water scarcity issues. However, practical utilization of solar energy for steam generation is severely restricted by the complex synthesis, low energy conversion efficiency, insufficient solar spectrum absorption and water extraction capability of state-of-the-art technologies. Here, for the first time, we report a facile strategy to realize hydrogen bond induced self-assembly of a polydopamine (PDA)@MXene microsphere photothermal layer for synergistically achieving wide-spectrum and highly efficient solar absorption capability (~ 96% in a wide solar spectrum range of 250-1,500 nm wavelength). Moreover, such a system renders fast water transport and vapor escaping due to the intrinsically hydrophilic nature of both MXene and PDA, as well as the interspacing between core-shell microspheres. The solar-to-vapor conversion efficiencies under the solar illumination of 1 sun and 4 sun are as high as 85.2% and 93.6%, respectively. Besides, the PDA@MXene photothermal layer renders the system durable mechanical properties, allowing producing clean water from seawater with the salt rejection rate beyond 99%. Furthermore, stable light absorption performance can be achieved and well maintained due to the formation of ternary TiO2/C/MXene complex caused by oxidative degradation of MXene. Therefore, this work proposes an attractive MXene-assisted strategy for fabricating high performance photothermal composites for advanced solar-driven seawater desalination applications.

File
12274_2019_2608_MOESM1_ESM.pdf (6 MB)
Publication history
Copyright
Acknowledgements

Publication history

Received: 18 September 2019
Revised: 15 November 2019
Accepted: 14 December 2019
Published: 27 December 2019
Issue date: January 2020

Copyright

© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2019

Acknowledgements

This work was supported by the National Natural Science Foundation of China (Nos. 51873126, 51422305, and 51721091). We greatly appreciate the help of Dr. Guiping Yuan from the Analytical and Testing Center of Sichuan University for providing the TEM measurement facility.

Return