Thermodynamic and Kinetic Influence of Oxygen Vacancies on the Solar Water Oxidation Reaction of α-Fe2O3 Photoanodes
Source abstract
Abstract
To reveal the role of oxygen vacancies in the solar water oxidation of α-Fe2O3 photoanodes, the kinetic and thermodynamic properties that are closely related to the water oxidation reaction of the α-Fe2O3 photoanode containing oxygen vacancies were investigated. Compared with the pristine α-Fe2O3 photoanode, the presence of surface oxygen vacancies can improve the water oxidation activity and stability of the α-Fe2O3 photoanode simultaneously, but the bulk oxygen vacancies have a negative effect on the water oxidation performance of the α-Fe2O3 photoanode. In thermodynamics, our investigations revealed that the presence of surface oxygen vacancies narrows the space charge region width of the α-Fe2O3 photoanode, which could boost the charge separation and transfer efficiency of the α-Fe2O3 photoanode during water oxidation. Because the surface property and hydrophilicity of α-Fe2O3 are modified owing to the presence of surface oxygen vacancies, the water oxidation kinetics of the α-Fe2O3 photoanode with surface oxygen vacancies is obviously boosted. Our findings in the present work provide comprehensive understanding of the thermodynamic and kinetic differences for α-Fe2O3 photoanodes with and without oxygen vacancies for solar water oxidation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Iron oxide chemistry and applications · Minerals Flotation and Separation Techniques · Copper-based nanomaterials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Environmental-Friendly Energy Materials, School of Materials Science and Engineering, Southwest University of Science and Technology, Mianyang 621010, China
Ecomaterials and Renewable Energy Research Center, School of Physics, Nanjing University, Nanjing 211102, China
College of Chemistry and Chemical Engineering, Shannxi University of Science & Technology, Xi’an 710021, China
Funding
National Natural Science Foundation of China · Southwest University of Science and Technology
References (44)
Show source-provided references
1. 10.1021/cr100232610.1021/cr1002326 ↗
2. 10.1002/anie.20171087310.1002/anie.201710873 ↗
3. 10.1039/c2ee00001f10.1039/c2ee00001f ↗
4. 10.1002/adma.20170750210.1002/adma.201707502 ↗
5. 10.1002/aenm.20147006710.1002/aenm.201470067 ↗
6. 10.1039/c2ee22681b10.1039/c2ee22681b ↗
7. 10.1021/jp200751j10.1021/jp200751j ↗
8. 10.1039/C5TA00257E10.1039/C5TA00257E ↗
9. 10.1021/cr300062610.1021/cr3000626 ↗
10. 10.1103/PhysRev.116.8410.1103/PhysRev.116.84 ↗
11. 10.1063/1.32935110.1063/1.329351 ↗
12. Zangwill A. · 198810.1017/CBO9780511622564 ↗
13. 10.1002/anie.20110746710.1002/anie.201107467 ↗
14. 10.1039/c2cp44352j10.1039/c2cp44352j ↗
15. 10.1021/acsami.5b0613110.1021/acsami.5b06131 ↗
16. 10.1039/C6CP06410H10.1039/C6CP06410H ↗
17. 10.1002/ange.20181058310.1002/ange.201810583 ↗
18. 10.1016/j.jcis.2017.10.03910.1016/j.jcis.2017.10.039 ↗
19. 10.1016/j.apcatb.2017.10.04910.1016/j.apcatb.2017.10.049 ↗
20. 10.1016/j.jcat.2017.04.02910.1016/j.jcat.2017.04.029 ↗
21. 10.1039/c3ta10689f10.1039/c3ta10689f ↗
22. 10.1021/acscatal.9b0240810.1021/acscatal.9b02408 ↗
23. 10.1039/C9NR04023D10.1039/C9NR04023D ↗
24. 10.1016/j.electacta.2017.09.18610.1016/j.electacta.2017.09.186 ↗
25. 10.1021/acscatal.8b0381910.1021/acscatal.8b03819 ↗
26. 10.1039/C5TA06978E10.1039/C5TA06978E ↗
27. 10.1016/j.electacta.2017.08.09010.1016/j.electacta.2017.08.090 ↗
28. 10.1002/(SICI)1097-4555(199711)28:11<873::AID-JRS177>3.0.CO;2-B10.1002/(SICI)1097-4555(199711)28:11<873::AID-JRS177>3.0.CO;2-B ↗
29. 10.1002/cssc.20130101310.1002/cssc.201301013 ↗
30. 10.1021/acs.jpclett.5b0071010.1021/acs.jpclett.5b00710 ↗
31. 10.1103/PhysRevB.94.23520910.1103/PhysRevB.94.235209 ↗
32. 10.1002/anie.20150222610.1002/anie.201502226 ↗
33. 10.1016/j.apcatb.2019.11825010.1016/j.apcatb.2019.118250 ↗
34. 10.1002/cssc.20140294510.1002/cssc.201402945 ↗
35. 10.1021/acscatal.8b0403410.1021/acscatal.8b04034 ↗
36. 10.1016/j.nanoen.2017.06.04910.1016/j.nanoen.2017.06.049 ↗
37. 10.1002/adma.20180048610.1002/adma.201800486 ↗
38. 10.1021/acs.inorgchem.8b0257010.1021/acs.inorgchem.8b02570 ↗
39. 10.1002/anie.20140680010.1002/anie.201406800 ↗
40. 10.1021/ja210755h10.1021/ja210755h ↗
41. 10.1021/acsaem.8b0044510.1021/acsaem.8b00445 ↗
42. 10.1039/c0cp02408b10.1039/c0cp02408b ↗
43. 10.1039/c2cp40991g10.1039/c2cp40991g ↗
44. 10.1039/C8RA08875F10.1039/C8RA08875F ↗