Direct Electrochemical Seawater Splitting for Green Hydrogen and Artificial Reefs
Source abstract
Abstract
The electrochemical splitting of abundant seawater using renewable electricity to generate green hydrogen holds a great promise for energy transport and storage. However, direct seawater electrolysis suffers from side reactions and degradation of electrodes due to impurities. Here, we demonstrate a direct electrochemical seawater splitting device that uses only electricity and air. The seawater was desalinated first by oxygen reduction, which created an alkaline environment and concurrently captured CO 2 to remove Ca and Mg ions. Simultaneously, artificial reefs could be formed. The softened seawater was immediately utilized to produce hydrogen. This proof of concept shows that seawater splitting could be coupled with value-added processes, allowing for the direct utilization of seawater without pretreatment or purification and circumventing the challenges posed by impurities and cost. With the simultaneous production of H 2 and artificial reefs, CO 2 elimination, and powered solely by renewable electricity, this strategy provides an approach to seawater splitting for sustainable H 2 production.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Hybrid Renewable Energy Systems
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science, Fudan University, Shanghai 200433, PR China
Yiwu Research Institute of Fudan University, Yiwu City 322000, Zhejiang, PR China
Funding
National Key Research and Development Program of China · Science and Technology Commission of Shanghai Municipality · National Natural Science Foundation of China · Zhuhai Fudan Innovation Institute · Guangdong Provincial Key Laboratory of Advance Energy Storage Materials
References (27)
Show source-provided references
1. 10.1126/science.110319710.1126/science.1103197 ↗
2. 10.1021/ef060491u10.1021/ef060491u ↗
3. 10.1149/09601.0107ecst10.1149/09601.0107ecst ↗
4. 10.1080/15567249.2014.95039410.1080/15567249.2014.950394 ↗
5. 10.1016/j.joule.2020.09.02010.1016/j.joule.2020.09.020 ↗
6. 10.1002/aenm.20200318810.1002/aenm.202003188 ↗
7. 10.1021/acsenergylett.9b0022010.1021/acsenergylett.9b00220 ↗
8. 10.1016/j.rser.2020.11016610.1016/j.rser.2020.110166 ↗
9. 10.1038/s41560-020-0550-810.1038/s41560-020-0550-8 ↗
10. 10.1016/j.elecom.2011.03.03210.1016/j.elecom.2011.03.032 ↗
11. 10.1016/j.electacta.2008.09.05810.1016/j.electacta.2008.09.058 ↗
12. 10.1002/anie.20171212110.1002/anie.201712121 ↗
13. 10.1039/C6EE03768B10.1039/C6EE03768B ↗
14. 10.1002/aenm.20190133310.1002/aenm.201901333 ↗
15. 10.1021/acscatal.0c0434310.1021/acscatal.0c04343 ↗
16. 10.1039/D1EE00870F10.1039/D1EE00870F ↗
17. 10.1007/s10311-020-01002-z10.1007/s10311-020-01002-z ↗
18. 10.1016/j.rser.2011.02.01410.1016/j.rser.2011.02.014 ↗
19. Bjerge L. M. · 2014 · 63 · 6455
20. 10.3390/en1203055910.3390/en12030559 ↗
21. 10.1016/S0196-8904(99)00071-010.1016/S0196-8904(99)00071-0 ↗
22. 10.1021/es800366q10.1021/es800366q ↗
23. 10.1021/es102671x10.1021/es102671x ↗
24. 10.1038/s41558-018-0203-010.1038/s41558-018-0203-0 ↗
25. 10.1021/acssuschemeng.0c0856110.1021/acssuschemeng.0c08561 ↗
26. 10.1021/acsestengg.3c0000410.1021/acsestengg.3c00004 ↗
27. 10.1002/cssc.20210013410.1002/cssc.202100134 ↗