Oxide Relay: An Efficient Mechanism for Catalytic Water Oxidation at Hydrophobic Electrode Surfaces
Source abstract
Abstract
In order to combine the advantages of molecular catalysts with the stability of solid-state catalysts, hybrid systems with catalysts immobilized on carbon nanotubes are prominent candidates. Here we explore our recent mechanistic proposal for Ru(tda)(py) 2, the oxide relay mechanism, in a hybrid system from an experimental study. It reacts with the same efficiency but with increased stability compared to the homogeneous molecular catalyst. We used the empirical valence bond method and molecular dynamics with enhanced sampling approaches to investigate the two key steps in the mechanism: the intramolecular O–O bond formation and the OH – nucleophilic attack. The results on these calculations show that the oxide relay mechanism remains unaltered in the new environment. We believe that the principles should apply to other oxide containing dangling groups and to other metal centers, opening new possibilities of future developments on hybrid molecular catalyst-based water splitting devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Electrochemical Analysis and Applications · Analytical Chemistry and Sensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Departament of Theoretical Chemistry and Biology, School of Engineering Sciences in Chemistry Biotechnology and Health, KTH Royal Institute of Technology, 10691 Stockholm, Sweden
Funding
Vetenskapsr?det · Knut och Alice Wallenbergs Stiftelse · China Scholarship Council
References (28)
Show source-provided references
1. Ingenhousz, Jan. Experiments upon vegetables: discovering their great power of purifying the common air in the sunshine, and of injuring it in the shade and at night. To which is joined, a new method of examining the accurate degree of salubrity of the atmosphere. Printed for P. Elmsly and H. Payne, 1779.10.5962/bhl.title.60931 ↗
2. 10.1126/science.36.926.38510.1126/science.36.926.385 ↗
3. 10.1021/ar200301310.1021/ar2003013 ↗
4. 10.1126/science.118772110.1126/science.1187721 ↗
5. 10.1021/ar900209b10.1021/ar900209b ↗
6. 10.1073/pnas.121225410910.1073/pnas.1212254109 ↗
7. 10.1038/238037a010.1038/238037a0 ↗
8. 10.1021/ja00378a05310.1021/ja00378a053 ↗
9. 10.1111/j.1751-1097.2011.00966.x10.1111/j.1751-1097.2011.00966.x ↗
10. 10.1038/s41467-019-12994-w10.1038/s41467-019-12994-w ↗
11. 10.1021/jacs.8b1286210.1021/jacs.8b12862 ↗
12. 10.1021/acs.chemrev.8b0053710.1021/acs.chemrev.8b00537 ↗
13. 10.1039/C8CS00897C10.1039/C8CS00897C ↗
14. 10.1073/pnas.150611111210.1073/pnas.1506111112 ↗
15. 10.1021/cr100018g10.1021/cr100018g ↗
16. 10.1002/anie.20160916710.1002/anie.201609167 ↗
17. 10.1002/anie.20090643910.1002/anie.200906439 ↗
18. 10.1021/jacs.8b0043310.1021/jacs.8b00433 ↗
19. 10.1021/ar400169p10.1021/ar400169p ↗
20. 10.1021/jacs.5b0654110.1021/jacs.5b06541 ↗
21. 10.1021/jacs.9b0258510.1021/jacs.9b02585 ↗
22. 10.1016/j.softx.2015.06.00110.1016/j.softx.2015.06.001 ↗
23. 10.1021/ja962176010.1021/ja9621760 ↗
24. 10.1021/acs.organomet.8b0054410.1021/acs.organomet.8b00544 ↗
25. 10.1002/qua.2448110.1002/qua.24481 ↗
26. 10.1002/wcms.1010.1002/wcms.10 ↗
27. Warshel, A. Computer Modelling of Chemical Reactions in Enzymes and Solutions; Wiley-Interscience: New York, 1997.
28. 10.1021/ja077205t10.1021/ja077205t ↗