journal article·2023-06-12Open access

Half-Electrolysis of Water with the Aid of a Supercapacitor Electrode

Yao Chen, George Zheng Chen

ACS Applied Energy Materials· Volume 6· Issue 11

Abstract

High Resolution Image Download MS PowerPoint Slide Half-electrolysis runs one desirable half-cell reaction with the aid of a counter supercapacitor electrode which replaces the other unwanted half-cell reaction occurred inevitably in conventional electrolysis. Herein, it is developed to complete the whole cell reaction of water electrolysis, in alternative steps, with a capacitive activated carbon (AC) electrode and an electrolysis Pt electrode. When positively charging the AC electrode, a hydrogen evolution reaction occurs at the Pt electrode. By reversing the current, the charge stored in the AC electrode is discharged to assist the oxygen evolution reaction on the same Pt electrode. Consecutive completion of the two processes realizes the overall reaction of water electrolysis. This strategy leads to stepwise production of H 2 and O 2 without the need of a diaphragm in the cell and hence results in a lower energy consumption compared with the practical conventional electrolysis.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Supercapacitor Materials and Fabrication

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

Affiliations

The State Key Laboratory of Refractories and Metallurgy, College of Materials and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081, P. R. China

Department of Chemical and Environmental Engineering, Faculty of Engineering, University of Nottingham, Nottingham NG2 7RD, U.K.

Funding

Research Councils UK · Innovate UK · National Natural Science Foundation of China

References (38)

Show source-provided references
1. 10.1038/s41560-021-00775-z10.1038/s41560-021-00775-z ↗
2. 10.1038/s41560-021-00824-710.1038/s41560-021-00824-7 ↗
3. 10.1002/aenm.20200395110.1002/aenm.202003951 ↗
4. 10.1186/s13054-021-03469-w10.1186/s13054-021-03469-w ↗
5. 10.1021/acsenergylett.9b0022010.1021/acsenergylett.9b00220 ↗
6. 10.1016/j.joule.2021.07.01410.1016/j.joule.2021.07.014 ↗
7. 10.1039/d0ee00921k10.1039/d0ee00921k ↗
8. 10.1016/s1872-2067(17)62949-810.1016/s1872-2067(17)62949-8 ↗
9. 10.1016/j.cej.2021.13238310.1016/j.cej.2021.132383 ↗
10. 10.1016/j.jpowsour.2017.09.00610.1016/j.jpowsour.2017.09.006 ↗
11. 10.1016/j.memsci.2019.11767410.1016/j.memsci.2019.117674 ↗
12. 10.1016/j.ijhydene.2021.02.04010.1016/j.ijhydene.2021.02.040 ↗
13. 10.1038/nchem.162110.1038/nchem.1621 ↗
14. 10.1038/ncomms1174110.1038/ncomms11741 ↗
15. 10.1038/nmat487610.1038/nmat4876 ↗
16. 10.1002/ange.20180043610.1002/ange.201800436 ↗
17. 10.1038/s41467-018-02877-x10.1038/s41467-018-02877-x ↗
18. 10.1038/s41560-019-0462-710.1038/s41560-019-0462-7 ↗
19. 10.1016/j.joule.2019.12.00610.1016/j.joule.2019.12.006 ↗
20. 10.1021/acsomega.1c0230510.1021/acsomega.1c02305 ↗
21. 10.1021/jacs.0c0951010.1021/jacs.0c09510 ↗
22. 10.1039/c3ee43817a10.1039/c3ee43817a ↗
23. 10.1039/d0ta08979f10.1039/d0ta08979f ↗
24. 10.1002/smll.20190645810.1002/smll.201906458 ↗
25. 10.1021/acsenergylett.1c0137310.1021/acsenergylett.1c01373 ↗
26. 10.1002/smll.20220427510.1002/smll.202204275 ↗
27. 10.1039/c9ta03285a10.1039/c9ta03285a ↗
28. 10.1016/j.ijhydene.2021.11.00210.1016/j.ijhydene.2021.11.002 ↗
29. 10.1038/s41560-020-00710-810.1038/s41560-020-00710-8 ↗
30. 10.1002/anie.20211244710.1002/anie.202112447 ↗
31. 10.1007/s12274-017-1593-410.1007/s12274-017-1593-4 ↗
32. 10.1016/j.carbon.2018.02.10010.1016/j.carbon.2018.02.100 ↗
33. 10.1002/eem2.1210110.1002/eem2.12101 ↗
34. 10.3866/pku.whxb20190402510.3866/pku.whxb201904025 ↗
35. 10.1002/aenm.20180033810.1002/aenm.201800338 ↗
36. 10.1002/adma.20200243510.1002/adma.202002435 ↗
37. 10.1021/acscatal.8b0041310.1021/acscatal.8b00413 ↗
38. 10.1002/adfm.20200648410.1002/adfm.202006484 ↗