Enhanced Electrochemical Water Splitting with Chiral Molecule-Coated Fe3O4 Nanoparticles
Source abstract
Abstract
Photoelectrochemical (PEC) water splitting is a promising approach for generating hydrogen from water. In order to enhance PEC water splitting efficiency, it is essential to inhibit the production of the hydrogen peroxide byproduct and to reduce the overpotential required by an inexpensive catalyst and with high current density. In the past, it was shown that coating TiO2 electrodes by chiral molecules or chiral films enhances the hydrogen production and reduces the production of H2O2 byproduct. This was explained to be a result of the chiral-induced spin selectivity (CISS) effect that induces spin correlation between the electrons transferred to the anode. However, typically the current observed in those studies was in the range of 1–100 μA/cm2. Here we report currents in the range of 10 mA/cm2 obtained by adsorbing chiral molecules on a well-established Fe3O4 nanoparticle (NP) catalyst deposited on the anode. The results indicate a new strategy for designing low-cost earth-abundant catalysts where the advantages of the CISS effect are combined with the large effective area provided by the NPs to promote PEC water splitting with high current density.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Iron oxide chemistry and applications · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Biological Physics, Weizmann Institute of Science, Rehovot 76100, Israel
Funding
Israel Science Foundation · Government of Jiangsu Province · U.S. Department of Energy · National Natural Science Foundation of China · H2020 Excellent Science
References (28)
Show source-provided references
1. 10.1038/3510460710.1038/35104607 ↗
2. 10.1038/s41570-017-010510.1038/s41570-017-0105 ↗
3. 10.1039/C3CS60378D10.1039/C3CS60378D ↗
4. 10.1038/nmat300810.1038/nmat3008 ↗
5. 10.1021/acscatal.6b0247910.1021/acscatal.6b02479 ↗
6. 10.1021/acsenergylett.7b0132610.1021/acsenergylett.7b01326 ↗
7. 10.1039/C5EE00457H10.1039/C5EE00457H ↗
8. 10.1126/science.aaa314510.1126/science.aaa3145 ↗
9. 10.1039/c2cc33644h10.1039/c2cc33644h ↗
10. 10.1021/cm101946910.1021/cm1019469 ↗
11. 10.1021/acs.jpclett.5b0241910.1021/acs.jpclett.5b02419 ↗
12. 10.1021/jacs.6b1297110.1021/jacs.6b12971 ↗
13. 10.1002/smtd.20170031310.1002/smtd.201700313 ↗
14. 10.1021/acs.jpcc.7b0419410.1021/acs.jpcc.7b04194 ↗
15. 10.1021/jz300793y10.1021/jz300793y ↗
16. 10.1146/annurev-physchem-040214-12155410.1146/annurev-physchem-040214-121554 ↗
17. 10.1039/C6CS00369A10.1039/C6CS00369A ↗
18. 10.1073/pnas.141490111210.1073/pnas.1414901112 ↗
19. 10.1002/anie.20170642610.1002/anie.201706426 ↗
20. 10.1016/j.pmatsci.2018.02.00210.1016/j.pmatsci.2018.02.002 ↗
21. 10.1039/b704636g10.1039/b704636g ↗
22. 10.1021/ja906894r10.1021/ja906894r ↗
23. 10.1021/acs.chemrev.6b0075510.1021/acs.chemrev.6b00755 ↗
24. 10.1039/C5PY01549A10.1039/C5PY01549A ↗
25. 10.1002/aoc.333310.1002/aoc.3333 ↗
26. 10.1021/acs.nanolett.6b0188010.1021/acs.nanolett.6b01880 ↗
27. 10.1021/acs.jpcc.5b0946910.1021/acs.jpcc.5b09469 ↗
28. 10.1016/B978-1-4832-8375-3.50018-710.1016/B978-1-4832-8375-3.50018-7 ↗