Single-Phase Perovskite SrIrO3 Nanofibers as a Highly Efficient Electrocatalyst for a pH-Universal Oxygen Evolution Reaction
Source abstract
Abstract
pH-universal electrocatalysts are desirable for high efficiency of water electrolysis. Herein, we report the facile synthesis of single-phase perovskite SrIrO3 nanofibers (NFs) and demonstrate that SrIrO3 NFs are promising electrocatalysts for the oxygen evolution reaction (OER) in a wide range of pH. Single-phase SrIrO3 NFs were synthesized by electrospinning and subsequent calcination processes, and the electrocatalytic performance of SrIrO3 NFs toward the OER was evaluated under acidic, neutral, and alkaline media. A large surface area due to the NF morphology with an average diameter of 105.5 (± 15.5) nm led to enhanced catalytic activity of SrIrO3 NFs, representing smaller overpotentials and Tafel slopes under pH-universal conditions than IrO2/Ir NFs and commercial Ir/C. SrIrO3 NFs also manifested remarkably stable activity for continuous OER operation in all three electrolytes, even though a considerable amount of Sr was leached out of them. The long-lasting high OER activity of SrIrO3 NFs could be ascribed to stable Ir cations taking B sites of the perovskite oxide structure, known as an active site for electrocatalysis. The initial perovskite crystal structure of SrIrO3 was maintained for a certain time even after significant Sr leaching. This work is the first application of SrIrO3 perovskite for pH-universal OER catalysis.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry & Nanoscience, Ewha Womans University, Seoul 03760, Korea
Funding
National Research Foundation of Korea
References (38)
Show source-provided references
1. 10.1039/c2ee22554a10.1039/c2ee22554a ↗
2. 10.1038/nature1147510.1038/nature11475 ↗
3. 10.1021/acs.chemmater.0c0014910.1021/acs.chemmater.0c00149 ↗
4. 10.1021/acsaem.9b0065810.1021/acsaem.9b00658 ↗
5. 10.1039/C9CS00607A10.1039/C9CS00607A ↗
6. 10.1038/s41467-019-08532-310.1038/s41467-019-08532-3 ↗
7. 10.1021/acsmaterialslett.1c0001810.1021/acsmaterialslett.1c00018 ↗
8. 10.1002/aenm.20160127510.1002/aenm.201601275 ↗
9. 10.1039/D0NR08034A10.1039/D0NR08034A ↗
10. 10.1016/j.jcis.2020.02.03010.1016/j.jcis.2020.02.030 ↗
11. 10.1016/j.jpowsour.2020.22873110.1016/j.jpowsour.2020.228731 ↗
12. 10.1016/j.jcis.2021.05.04110.1016/j.jcis.2021.05.041 ↗
13. 10.1021/acs.chemrev.7b0005110.1021/acs.chemrev.7b00051 ↗
14. 10.1002/aenm.20200242810.1002/aenm.202002428 ↗
15. 10.1021/acs.jpcc.8b0928710.1021/acs.jpcc.8b09287 ↗
16. 10.1016/j.apmt.2019.05.00410.1016/j.apmt.2019.05.004 ↗
17. 10.1002/aenm.20170066610.1002/aenm.201700666 ↗
18. 10.1021/acsami.9b1128710.1021/acsami.9b11287 ↗
19. 10.1126/sciadv.aap936010.1126/sciadv.aap9360 ↗
20. 10.1088/2053-1591/ab4f1c10.1088/2053-1591/ab4f1c ↗
21. 10.1038/s41467-018-07678-w10.1038/s41467-018-07678-w ↗
22. 10.1126/science.aaf505010.1126/science.aaf5050 ↗
23. 10.1016/j.chempr.2019.10.01110.1016/j.chempr.2019.10.011 ↗
24. 10.1039/C5TA09530A10.1039/C5TA09530A ↗
25. 10.1002/smtd.20180007110.1002/smtd.201800071 ↗
26. 10.1002/aenm.20160212210.1002/aenm.201602122 ↗
27. 10.1039/c1ee02201f10.1039/c1ee02201f ↗
28. 10.1002/anie.20200675610.1002/anie.202006756 ↗
29. 10.1016/j.snb.2014.02.03210.1016/j.snb.2014.02.032 ↗
30. 10.1021/acsenergylett.1c0060810.1021/acsenergylett.1c00608 ↗
31. 10.1038/s41929-018-0085-610.1038/s41929-018-0085-6 ↗
32. 10.1021/jacs.7b0707910.1021/jacs.7b07079 ↗
33. 10.1016/S0266-3538(03)00178-710.1016/S0266-3538(03)00178-7 ↗
34. 10.1021/jacs.0c0895910.1021/jacs.0c08959 ↗
35. 10.1126/sciadv.abc732310.1126/sciadv.abc7323 ↗
36. 10.1002/adfm.20210154210.1002/adfm.202101542 ↗
37. 10.1002/asia.20150064010.1002/asia.201500640 ↗
38. 10.1039/C8EE01574K10.1039/C8EE01574K ↗