journal article·2022-08-01

Tailoring Sulfonated Poly(phenyl-alkane)s of Intrinsic Microporosity Membrane for Advanced Osmotic Energy Conversion

Shengyang Zhou, Xiangbin Lin, Yuhao Hu, Lin Fu, Qixing Luo, Linsen Yang, Shuhua Hou, Xiang-Yu Kong, Lei Jiang, Liping Wen

ACS Materials Letters· Volume 4· Issue 8
Publisher page

Abstract

The capture of sustainable osmotic energy from salinity gradients has huge potential to solve the global issues of energy shortage and environmental pollution. However, developing membranes with high-performance ion transport and ion selectivity to achieve a high energy conversion efficiency is challenging. Herein, based on novel sulfonated microporous polymers (SPIMs), we report a series of membranes with densely distributed and subnanometer charged nanochannels. The inefficient packing of SPIM chains not only provide an interconnected microporous structure as three-dimensional nanofluidic channels to facilitate a fast ion transport but also ensure high cation permselectivity via the negatively charged sulfonated groups. The maximum power density of SPIM membrane reaches up to 9.58 W m–2 under a 50-fold salinity gradient, which is superior to that of Nafion 117. This work can inspire the design of membrane materials for advanced osmotic energy conversion systems.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanopore and Nanochannel Transport Studies · Membrane Separation Technologies · Fuel Cells and Related Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Laboratory of Bio-Inspired Materials and Interfacial Science, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China

School of Future Technology, University of Chinese Academy of Sciences, Beijing 100049, P. R. China

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China

References (36)

Show source-provided references
1. 10.1038/nature1147710.1038/nature11477 ↗
2. 10.1016/j.joule.2019.11.01010.1016/j.joule.2019.11.010 ↗
3. 10.1038/nature1859310.1038/nature18593 ↗
4. 10.1038/nature1187610.1038/nature11876 ↗
5. 10.1039/D1SC03581A10.1039/D1SC03581A ↗
6. 10.1073/pnas.200389811710.1073/pnas.2003898117 ↗
7. 10.1002/advs.20200028610.1002/advs.202000286 ↗
8. 10.1021/jacs.1c0209010.1021/jacs.1c02090 ↗
9. 10.1039/D1TA02400K10.1039/D1TA02400K ↗
10. 10.1016/j.joule.2017.10.01510.1016/j.joule.2017.10.015 ↗
11. 10.1038/s41565-020-0641-510.1038/s41565-020-0641-5 ↗
12. 10.1002/ange.20210020510.1002/ange.202100205 ↗
13. 10.1039/b600349d10.1039/b600349d ↗
14. 10.1021/acs.chemrev.7b0062910.1021/acs.chemrev.7b00629 ↗
15. 10.1038/s41563-019-0536-810.1038/s41563-019-0536-8 ↗
16. 10.1016/j.joule.2019.08.02510.1016/j.joule.2019.08.025 ↗
17. 10.1002/anie.20200001210.1002/anie.202000012 ↗
18. 10.1007/s11426-017-9058-x10.1007/s11426-017-9058-x ↗
19. 10.1021/acs.macromol.5b0119610.1021/acs.macromol.5b01196 ↗
20. 10.1002/cssc.20160035410.1002/cssc.201600354 ↗
21. 10.1021/ma200918h10.1021/ma200918h ↗
22. 10.1021/acs.macromol.1c0046810.1021/acs.macromol.1c00468 ↗
23. 10.1021/acsmacrolett.7b0038510.1021/acsmacrolett.7b00385 ↗
24. 10.1021/ma901430q10.1021/ma901430q ↗
25. 10.1021/acs.macromol.7b0133210.1021/acs.macromol.7b01332 ↗
26. 10.1016/j.memsci.2017.04.03910.1016/j.memsci.2017.04.039 ↗
27. 10.1038/s41467-019-11792-810.1038/s41467-019-11792-8 ↗
28. 10.1021/acsenergylett.9b0229610.1021/acsenergylett.9b02296 ↗
29. 10.1038/s41467-019-10885-810.1038/s41467-019-10885-8 ↗
30. 10.1002/anie.20200632010.1002/anie.202006320 ↗
31. 10.1038/s41467-020-14674-610.1038/s41467-020-14674-6 ↗
32. 10.1002/anie.20191599310.1002/anie.201915993 ↗
33. 10.1002/cnma.20190032610.1002/cnma.201900326 ↗
34. 10.1021/jacs.5b0991810.1021/jacs.5b09918 ↗
35. 10.1093/nsr/nwaa05710.1093/nsr/nwaa057 ↗
36. 10.1002/adma.20210841010.1002/adma.202108410 ↗