Electrochemically Switchable Double-Gate Nanofluidic Logic Device as Biomimetic Ion Pumps
Source abstract
Abstract
Biological ion pumps with two separate gates can actively transport ions against the concentration gradient. Developing an artificial nanofluidic device with multiple responsive sites is of great importance to improve its controllability over ion transport to further explore its logic function and mimic the biological process. Here, we propose an electrochemical polymerization method to fabricate electrochemically switchable double-gate nanofluidic devices. The ion transport of the double-gate nanofluidic device can be in situ and reversibly switched among four different states. The logic function of this nanofluidic device is systematically investigated by assuming the gate state as the input and the transmembrane ionic conductance as the output. A biomimetic electrochemical ion pump is then established by alternately applying two different specific logic combinations, realizing an active ion transport under a concentration gradient. This work would inspire further studies to construct complex logical networks and explore bioinspired ion pump systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Fuel Cells and Related Materials · Nanopore and Nanochannel Transport Studies · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China
Funding
Ministry of Science and Technology of the People's Republic of China · Nanjing University · National Natural Science Foundation of China
References (31)
Show source-provided references
1. 10.1126/science.111366610.1126/science.1113666 ↗
2. 10.1038/nnano.2008.27410.1038/nnano.2008.274 ↗
3. 10.1002/adfm.20130031510.1002/adfm.201300315 ↗
4. 10.1021/acs.analchem.5b0101610.1021/acs.analchem.5b01016 ↗
5. 10.1021/jacs.5b0163810.1021/jacs.5b01638 ↗
6. 10.1002/smll.20080131810.1002/smll.200801318 ↗
7. 10.1002/adfm.20180850110.1002/adfm.201808501 ↗
8. 10.1021/jacs.9b0356910.1021/jacs.9b03569 ↗
9. 10.1002/adfm.20140416010.1002/adfm.201404160 ↗
10. 10.1021/jacs.8b1052710.1021/jacs.8b10527 ↗
11. 10.1021/jacs.9b0175910.1021/jacs.9b01759 ↗
12. 10.1038/nrm266810.1038/nrm2668 ↗
13. 10.1002/anie.20190781610.1002/anie.201907816 ↗
14. 10.1021/acsnano.0c0130910.1021/acsnano.0c01309 ↗
15. 10.1002/adma.20180486210.1002/adma.201804862 ↗
16. 10.1021/ja403766910.1021/ja4037669 ↗
17. 10.1002/anie.20170413710.1002/anie.201704137 ↗
18. 10.1021/jacs.7b1147210.1021/jacs.7b11472 ↗
19. 10.1021/jacs.5b1069210.1021/jacs.5b10692 ↗
20. 10.1002/adma.20170097210.1002/adma.201700972 ↗
21. 10.1021/acs.analchem.0c0150410.1021/acs.analchem.0c01504 ↗
22. 10.1021/acs.nanolett.8b0273810.1021/acs.nanolett.8b02738 ↗
23. 10.1002/adma.20170292610.1002/adma.201702926 ↗
24. 10.1021/acsami.9b0596110.1021/acsami.9b05961 ↗
25. 10.1002/adma.20170332310.1002/adma.201703323 ↗
26. 10.1039/c4ta00484a10.1039/c4ta00484a ↗
27. 10.1039/c9cc04021h10.1039/c9cc04021h ↗
28. 10.1038/s41565-018-0181-410.1038/s41565-018-0181-4 ↗
29. 10.1021/acsnano.9b0575810.1021/acsnano.9b05758 ↗
30. 10.1007/s00339005114310.1007/s003390051143 ↗
31. 10.1021/acs.langmuir.8b0398610.1021/acs.langmuir.8b03986 ↗