Enhanced Oxygen Evolution Activity of CoO–La0.7Sr0.3MnO3−δ Heterostructured Thin Film
Source abstract
Abstract
The design and fabrication of highly efficient oxygen evolution reaction (OER) electrocatalysts is crucial for further development of electrochemical conversion devices. In this paper, the pulsed laser deposition technique was first used to fabricate high quality and well-defined CoO–La0.7Sr0.3MnO3−δ (LSMO) heterostructured electrocatalysts. The current density was about 70 and 20 times larger with respect to single-phase CoO and LSMO thin film electrocatalysts, respectively. The enhancement of electrocatalytic activity was investigated in detail by using electrochemical and X-ray photoemission/absorption spectroscopies. The introduction of the LSMO intermediate layer not only promoted charge transfer kinetics but also resulted in a larger Co3+/Co2+ ratio due to the partial oxidation of the CoO layer during film growth. The design of coatings with a tunable oxygen electrocatalytic activity implementing the heterostructure engineering approach was demonstrated.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, P. R. China
Center for Excellence in Superconducting Electronics, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050, China
School of Materials and Energy, University of Electronic Science and Technology of China, 2006 Xiyuan Road, Chengdu 611731, Sichuan, P. R. China
Funding
ShanghaiTech University · National Natural Science Foundation of China
References (65)
Show source-provided references
1. 10.1126/science.125744310.1126/science.1257443 ↗
2. 10.1021/acscatal.6b0247910.1021/acscatal.6b02479 ↗
3. 10.1021/cr200035s10.1021/cr200035s ↗
4. 10.1002/fuce.20040004510.1002/fuce.200400045 ↗
5. 10.1039/C4CY00669K10.1039/C4CY00669K ↗
6. 10.1038/ncomms519110.1038/ncomms5191 ↗
7. 10.1039/C5EE03316K10.1039/C5EE03316K ↗
8. 10.1021/cs300309810.1021/cs3003098 ↗
9. 10.1021/jz201650710.1021/jz2016507 ↗
10. 10.1002/anie.20140645510.1002/anie.201406455 ↗
11. 10.1002/adma.20160227010.1002/adma.201602270 ↗
12. 10.1021/jz502692a10.1021/jz502692a ↗
13. 10.1021/jacs.5b1171310.1021/jacs.5b11713 ↗
14. 10.1126/sciadv.160320610.1126/sciadv.1603206 ↗
15. 10.1039/C9TA04949E10.1039/C9TA04949E ↗
16. 10.1021/acsami.0c0398310.1021/acsami.0c03983 ↗
17. 10.1021/acsami.9b1383410.1021/acsami.9b13834 ↗
18. 10.1016/j.electacta.2017.05.08310.1016/j.electacta.2017.05.083 ↗
19. 10.1039/C8TA12477A10.1039/C8TA12477A ↗
20. 10.1039/C5TA03885E10.1039/C5TA03885E ↗
21. 10.1038/s41598-018-20974-110.1038/s41598-018-20974-1 ↗
22. 10.1038/srep2708110.1038/srep27081 ↗
23. 10.1016/j.jpowsour.2017.08.00710.1016/j.jpowsour.2017.08.007 ↗
24. 10.1016/j.electacta.2017.11.02810.1016/j.electacta.2017.11.028 ↗
25. 10.1038/ncomms1287610.1038/ncomms12876 ↗
26. 10.1039/C7EE00628D10.1039/C7EE00628D ↗
27. 10.1021/jacs.6b0352010.1021/jacs.6b03520 ↗
28. 10.1002/aenm.20180384610.1002/aenm.201803846 ↗
29. 10.1016/j.chempr.2017.09.00310.1016/j.chempr.2017.09.003 ↗
30. 10.1039/C9CP02278C10.1039/C9CP02278C ↗
31. 10.1021/ja500995410.1021/ja5009954 ↗
32. 10.1140/epjb/e2004-00233-710.1140/epjb/e2004-00233-7 ↗
33. 10.1103/PhysRevB.51.1410310.1103/PhysRevB.51.14103 ↗
34. 10.1016/j.nanoen.2018.12.08510.1016/j.nanoen.2018.12.085 ↗
35. 10.1016/j.jelechem.2010.05.01610.1016/j.jelechem.2010.05.016 ↗
36. http://www.consultrsr.net/resources/ref/refpotls.htm#ssce.
37. 10.1016/j.jpowsour.2012.08.07210.1016/j.jpowsour.2012.08.072 ↗
38. 10.1002/adfm.20080176810.1002/adfm.200801768 ↗
39. 10.1007/s40243-012-0006-610.1007/s40243-012-0006-6 ↗
40. 10.1021/acsnano.7b0622810.1021/acsnano.7b06228 ↗
41. 10.1039/C3EE42696C10.1039/C3EE42696C ↗
42. 10.1039/C8CS00848E10.1039/C8CS00848E ↗
43. 10.1002/adma.20150353210.1002/adma.201503532 ↗
44. 10.1002/anie.20140899810.1002/anie.201408998 ↗
45. 10.1021/acs.jpclett.5b0043910.1021/acs.jpclett.5b00439 ↗
46. 10.1039/C6TA03644A10.1039/C6TA03644A ↗
47. 10.1021/jacs.7b0321110.1021/jacs.7b03211 ↗
48. 10.1038/ncomms962510.1038/ncomms9625 ↗
49. 10.1039/C6CS00230G10.1039/C6CS00230G ↗
50. 10.1007/BF0020202610.1007/BF00202026 ↗
51. 10.1107/S090904959900169710.1107/S0909049599001697 ↗
52. 10.1103/PhysRevB.42.545910.1103/PhysRevB.42.5459 ↗
53. 10.1143/JPSJ.63.278810.1143/JPSJ.63.2788 ↗
54. 10.1016/0368-2048(93)02041-J10.1016/0368-2048(93)02041-J ↗
55. 10.1088/0953-8984/4/16/01910.1088/0953-8984/4/16/019 ↗
56. 10.1103/PhysRevB.84.01443610.1103/PhysRevB.84.014436 ↗
57. 10.1021/jacs.5b0354510.1021/jacs.5b03545 ↗
58. 10.1103/PhysRevLett.90.01740110.1103/PhysRevLett.90.017401 ↗
59. 10.1103/PhysRevB.74.24511110.1103/PhysRevB.74.245111 ↗
60. 10.1103/PhysRevLett.102.11640110.1103/PhysRevLett.102.116401 ↗
61. 10.1039/c2ee23844f10.1039/c2ee23844f ↗
62. 10.1021/ja210924t10.1021/ja210924t ↗
63. 10.1209/0295-5075/80/3700310.1209/0295-5075/80/37003 ↗
64. 10.1021/nl201821j10.1021/nl201821j ↗
65. 10.1063/1.34321110.1063/1.343211 ↗