V “Bridged” CoO to Eliminate Charge Transfer Barriers and Drive Lattice Oxygen Oxidation during Water‐Splitting
Source abstract
Abstract
Abstract Oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) play significant role on the practical applications of water splitting for producing clean fuel. Although some low‐cost metal oxides are active on catalyzing OER and HER, the instinct drawback of sluggish charges carriers transfer mobility decrease the reactions kinetic and hinder their application. To overcome the issue, CoV oxide is successfully built‐up with a CoOV structure to eliminate energy barrier during carriers transfer by the spin‐flip hopping process, which can be coated on various substrate to stimulate OER and HER. Moreover, the V “bridge” between CoO bonds stimulates the OER through more effective lattice oxygen oxidation mechanism, which can directly format OO bond in more effective pathway. The protocol could be spread on rational design of such OER electrocatalysts on various electrode to lower‐cost water splitting.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Heavy Oil Processing College of Chemical Engineering University of Petroleum (East China) Qingdao 266580 China
School of Physics Nankai University Tianjin 300071 China
Funding
National Natural Science Foundation of China · Fundamental Research Funds for the Central Universities
References (43)
Show source-provided references
1. 10.1021/acscatal.7b0180010.1021/acscatal.7b01800 ↗
2. 10.1021/acs.accounts.6b0063510.1021/acs.accounts.6b00635 ↗
3. 10.1039/C8NR01032C10.1039/C8NR01032C ↗
4. 10.1002/anie.20171254910.1002/anie.201712549 ↗
5. 10.1016/j.jechem.2018.09.01610.1016/j.jechem.2018.09.016 ↗
6. 10.1016/j.nanoen.2017.11.04510.1016/j.nanoen.2017.11.045 ↗
7. 10.1002/anie.20171137610.1002/anie.201711376 ↗
8. 10.1021/acscatal.7b0350910.1021/acscatal.7b03509 ↗
9. 10.1002/adma.20190117410.1002/adma.201901174 ↗
10. 10.1021/cs500713d10.1021/cs500713d ↗
11. 10.1021/ja508255310.1021/ja5082553 ↗
12. 10.1039/C7EE01917C10.1039/C7EE01917C ↗
13. 10.1038/s41467-017-01872-y10.1038/s41467-017-01872-y ↗
14. 10.1038/ncomms1287610.1038/ncomms12876 ↗
15. 10.1002/adma.20150269610.1002/adma.201502696 ↗
16. 10.1016/j.jpcs.2004.11.00210.1016/j.jpcs.2004.11.002 ↗
17. 10.1002/anie.20170243010.1002/anie.201702430 ↗
18. 10.1038/nchem.269510.1038/nchem.2695 ↗
19. 10.1038/s41560-019-0355-910.1038/s41560-019-0355-9 ↗
20. 10.1016/j.ceramint.2018.07.17110.1016/j.ceramint.2018.07.171 ↗
21. 10.1038/s41467-018-05341-y10.1038/s41467-018-05341-y ↗
22. 10.1038/ncomms1198110.1038/ncomms11981 ↗
23. 10.1016/j.apsusc.2010.07.08610.1016/j.apsusc.2010.07.086 ↗
24. 10.1021/acscatal.7b0379510.1021/acscatal.7b03795 ↗
25. 10.1038/s41467-019-11765-x10.1038/s41467-019-11765-x ↗
26. 10.1002/adfm.20170345510.1002/adfm.201703455 ↗
27. 10.1149/1.156874110.1149/1.1568741 ↗
28. 10.1021/jp204492r10.1021/jp204492r ↗
29. 10.1002/adfm.20170444710.1002/adfm.201704447 ↗
30. 10.1103/PhysRevB.66.02040210.1103/PhysRevB.66.020402 ↗
31. 10.1103/PhysRevB.47.1612410.1103/PhysRevB.47.16124 ↗
32. 10.1021/jacs.7b0888110.1021/jacs.7b08881 ↗
33. 10.1021/ja201269b10.1021/ja201269b ↗
34. 10.1016/j.nanoen.2014.08.01310.1016/j.nanoen.2014.08.013 ↗
35. 10.1002/adfm.20150550910.1002/adfm.201505509 ↗
36. 10.1021/acscatal.6b0071310.1021/acscatal.6b00713 ↗
37. 10.1021/ja200559j10.1021/ja200559j ↗
38. 10.1021/jacs.5b0777910.1021/jacs.5b07779 ↗
39. 10.1016/j.jelechem.2006.11.00810.1016/j.jelechem.2006.11.008 ↗
40. 10.1021/acscatal.6b0071310.1021/acscatal.6b00713 ↗
41. 10.1021/ja200559j10.1021/ja200559j ↗
42. 10.1038/376238a010.1038/376238a0 ↗
43. 10.1016/0039-6028(96)00588-210.1016/0039-6028(96)00588-2 ↗