High-Performance Osmotic Power Generators Based on the 1D/2D Hybrid Nanochannel System
Source abstract
Abstract
Extracting clean energy by converting the salinity gradient between river and sea into energy is an effective way to reduce the global pollution and carbon emissions. Reverse electrodialysis (RED) is of great importance to realize the energy conversion assisting the ion-selective membrane. However, its higher ion resistance and lower conversion efficiency results in the undesirable power conversion performance. Here, we demonstrate a 1D/2D hybrid nanochannel system to achieve high osmotic energy conversion and output power. This heterogeneous structure is composed of two structures, in which the subnanometer nanochannels in graphene oxide membrane (GOM) can serve as a selective layer and reduce the ion diffusion energy barrier, while the nanochannel in the polymer can introduce asymmetry to enhance ionic rectification and conversion efficiency. This heterogeneous membrane exhibits excellent cation selectivity and enhanced ionic current rectification (ICR) performance. The application of the GOM/PET hybrid nanochannel system in osmotic energy harvesting is evaluated, and the output power can reach up to 118.2 pW with the energy conversion efficiency of 40.3%. Theoretical calculation indicates that the 1D/2D hybrid system can effectively take the advantage of excellent cation selectivity of 2D lamellar nanochannels to improve its RED performance significantly.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanopore and Nanochannel Transport Studies · Membrane-based Ion Separation Techniques · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou730000, PR China
Key Laboratory for Magnetism and Magnetic Materials of Ministry of Education, Lanzhou University, Lanzhou730000, PR China
University of Chinese Academy of Sciences, Beijing100049, PR China
Advanced Energy Science and Technology Guangdong Laboratory, Huizhou516000, PR China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (63)
Show source-provided references
1. 10.1016/j.fuel.2014.10.03010.1016/j.fuel.2014.10.030 ↗
2. 10.1016/j.pnucene.2017.07.00210.1016/j.pnucene.2017.07.002 ↗
3. 10.1016/j.rser.2013.11.04910.1016/j.rser.2013.11.049 ↗
4. 10.15302/j-eng-201504610.15302/j-eng-2015046 ↗
5. 10.1016/j.joule.2020.09.00910.1016/j.joule.2020.09.009 ↗
6. 10.1038/s41578-021-00300-410.1038/s41578-021-00300-4 ↗
7. 10.1002/smll.20200601310.1002/smll.202006013 ↗
8. 10.1038/nnano.2009.33210.1038/nnano.2009.332 ↗
9. 10.1038/s41578-019-0126-z10.1038/s41578-019-0126-z ↗
10. 10.1002/adfm.20090231210.1002/adfm.200902312 ↗
11. 10.1038/nature1187610.1038/nature11876 ↗
12. 10.1021/ja503692z10.1021/ja503692z ↗
13. 10.1039/c8ta10848j10.1039/c8ta10848j ↗
14. 10.1038/s41467-019-11792-810.1038/s41467-019-11792-8 ↗
15. 10.1021/jacs.8b1349710.1021/jacs.8b13497 ↗
16. 10.1038/nature1859310.1038/nature18593 ↗
17. 10.1016/j.nanoen.2018.12.07510.1016/j.nanoen.2018.12.075 ↗
18. 10.1002/adfm.20160362310.1002/adfm.201603623 ↗
19. 10.1002/ange.20191599310.1002/ange.201915993 ↗
20. 10.1021/acsnano.9b0257910.1021/acsnano.9b02579 ↗
21. 10.1021/acsnano.0c0984510.1021/acsnano.0c09845 ↗
22. 10.1016/j.joule.2019.09.00510.1016/j.joule.2019.09.005 ↗
23. 10.1016/s0168-583x(01)00722-410.1016/s0168-583x(01)00722-4 ↗
24. 10.1039/c9cs00751b10.1039/c9cs00751b ↗
25. 10.1126/science.123609810.1126/science.1236098 ↗
26. 10.1038/s41467-017-02479-z10.1038/s41467-017-02479-z ↗
27. 10.1038/ncomms671610.1038/ncomms6716 ↗
28. 10.1103/physrevb.61.1409510.1103/physrevb.61.14095 ↗
29. 10.1038/s41467-020-20296-910.1038/s41467-020-20296-9 ↗
30. 10.1002/anie.20191301010.1002/anie.201913010 ↗
31. 10.1002/adfm.20190880410.1002/adfm.201908804 ↗
32. 10.1039/d0nr01054e10.1039/d0nr01054e ↗
33. 10.1021/acsnano.0c0445310.1021/acsnano.0c04453 ↗
34. 10.1002/adfm.20180107910.1002/adfm.201801079 ↗
35. 10.1021/acs.analchem.0c0530310.1021/acs.analchem.0c05303 ↗
36. 10.1016/j.nanoen.2018.09.01510.1016/j.nanoen.2018.09.015 ↗
37. 10.1007/s10404-010-0641-010.1007/s10404-010-0641-0 ↗
38. 10.1021/acsnano.0c0862810.1021/acsnano.0c08628 ↗
39. 10.1038/s41467-019-10885-810.1038/s41467-019-10885-8 ↗
40. 10.1021/acsnano.9b0816810.1021/acsnano.9b08168 ↗
41. 10.1038/ncomms1140810.1038/ncomms11408 ↗
42. 10.1021/acsnano.1c0271910.1021/acsnano.1c02719 ↗
43. 10.1126/science.124571110.1126/science.1245711 ↗
44. 10.1038/s41467-019-09178-x10.1038/s41467-019-09178-x ↗
45. 10.1016/j.nanoen.2020.10495410.1016/j.nanoen.2020.104954 ↗
46. 10.1016/j.memsci.2005.05.00210.1016/j.memsci.2005.05.002 ↗
47. 10.1021/acs.jpcc.9b0227910.1021/acs.jpcc.9b02279 ↗
48. 10.1039/c9tc03251g10.1039/c9tc03251g ↗
49. 10.1039/d0mh00979b10.1039/d0mh00979b ↗
50. 10.1016/j.joule.2019.11.01010.1016/j.joule.2019.11.010 ↗
51. 10.1039/c7nr04387b10.1039/c7nr04387b ↗
52. 10.1063/1.170198610.1063/1.1701986 ↗
53. 10.1038/s41565-020-0713-610.1038/s41565-020-0713-6 ↗
54. 10.1002/admt.20180074210.1002/admt.201800742 ↗
55. 10.1039/c1ee01088c10.1039/c1ee01088c ↗
56. 10.1016/j.memsci.2017.09.00810.1016/j.memsci.2017.09.008 ↗
57. 10.1021/acsami.9b0176810.1021/acsami.9b01768 ↗
58. 10.1016/j.joule.2019.04.01110.1016/j.joule.2019.04.011 ↗
59. 10.1016/j.nanoen.2020.10461210.1016/j.nanoen.2020.104612 ↗
60. 10.1021/acsami.0c0510210.1021/acsami.0c05102 ↗
61. 10.1002/adfm.20200958610.1002/adfm.202009586 ↗
62. 10.1021/acsnano.0c0130910.1021/acsnano.0c01309 ↗
63. 10.1021/acs.accounts.1c0043110.1021/acs.accounts.1c00431 ↗