CoIr Nanoalloy/N-Doped Ti3C2Tx MXene 0D/2D Heterojunction as a Catalyst for the Electrochemical Oxygen Evolution Reaction
Source abstract
Abstract
Developing high-efficiency oxygen evolution reaction (OER) electrocatalysts is essential for industrial application of sustainable energy conversion and storage systems, which can address energy and environmental challenges. We herein use an ultrasonic-assisted reduction strategy to design an efficient 0D/2D heterojunction by strongly coupling CoIr nanoalloys and N-doped Ti 3 C 2 T x MXenes for the alkaline OER. The resulting CoIr/N-Ti 3 C 2 T x heterojunction not only modifies the electronic structure of Ir sites but also enhances the exposure of active sites, thereby optimizing the adsorption strength of oxygen-related intermediates and significantly lowering the reaction energy barrier for the OER. The CoIr/N-Ti 3 C 2 T x catalyst with a low Ir content (5.12 wt %) only requires a low activation energy of 30.66 kJ mol –1 and a small OER overpotential of 260 mV RHE at 10 mA cm –2, outperforming the commercial IrO 2 catalyst. The as-made OER electrocatalyst also shows high catalytic stability for at least 30 h of testing, highlighting that constructing MXene-based heterojunctions is a promising route to achieve high-performance OER electrocatalysts.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: MXene and MAX Phase Materials · Electrocatalysts for Energy Conversion · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Applied Technology and Sustainable Development
Nguyen Tat Thanh University
Future Materials & Devices Lab., Institute of Fundamental and Applied Sciences
Duy Tan University
The Faculty of Environmental and Chemical Engineering
Ho Chi Minh City University of Natural Resources and Environment (HCMUNRE)
References (59)
Show source-provided references
1. 10.1021/acsenergylett.4c0141210.1021/acsenergylett.4c01412 ↗
2. 10.1021/acsnano.3c0494510.1021/acsnano.3c04945 ↗
3. 10.1016/j.cej.2021.13357710.1016/j.cej.2021.133577 ↗
4. 10.1039/D3IM00034F10.1039/D3IM00034F ↗
5. 10.1016/j.jallcom.2022.16711510.1016/j.jallcom.2022.167115 ↗
6. 10.1016/j.ccr.2023.21514310.1016/j.ccr.2023.215143 ↗
7. 10.1021/acssuschemeng.3c0430410.1021/acssuschemeng.3c04304 ↗
8. 10.1016/j.jechem.2023.08.03910.1016/j.jechem.2023.08.039 ↗
9. 10.1016/j.jechem.2023.10.05510.1016/j.jechem.2023.10.055 ↗
10. 10.1039/D0NR06601J10.1039/D0NR06601J ↗
11. 10.1002/aenm.20220416910.1002/aenm.202204169 ↗
12. 10.1016/j.cjsc.2023.10019710.1016/j.cjsc.2023.100197 ↗
13. 10.1039/D0TA05189F10.1039/D0TA05189F ↗
14. 10.1039/D2TA03496D10.1039/D2TA03496D ↗
15. 10.1002/cjoc.20220020010.1002/cjoc.202200200 ↗
16. 10.1039/D3TA07803E10.1039/D3TA07803E ↗
17. 10.1016/j.jallcom.2022.16481310.1016/j.jallcom.2022.164813 ↗
18. 10.1002/cssc.20190322210.1002/cssc.201903222 ↗
19. 10.1002/smtd.20240144910.1002/smtd.202401449 ↗
20. 10.1002/adsu.20240099510.1002/adsu.202400995 ↗
21. 10.1002/adfm.20230834510.1002/adfm.202308345 ↗
22. 10.1016/j.jcis.2023.02.11310.1016/j.jcis.2023.02.113 ↗
23. 10.1016/j.ccr.2024.21603910.1016/j.ccr.2024.216039 ↗
24. 10.1016/j.jssc.2021.12252910.1016/j.jssc.2021.122529 ↗
25. 10.1016/j.ijhydene.2024.08.46110.1016/j.ijhydene.2024.08.461 ↗
26. 10.1016/j.ijhydene.2022.11.17810.1016/j.ijhydene.2022.11.178 ↗
27. 10.1016/j.jcat.2019.11.01410.1016/j.jcat.2019.11.014 ↗
28. 10.1016/j.cej.2023.14418710.1016/j.cej.2023.144187 ↗
29. 10.1039/C9NA00706G10.1039/C9NA00706G ↗
30. 10.1016/j.cej.2024.15546310.1016/j.cej.2024.155463 ↗
31. 10.1002/smll.20230524710.1002/smll.202305247 ↗
32. 10.1002/admi.20200144910.1002/admi.202001449 ↗
33. 10.1016/j.cej.2021.13386510.1016/j.cej.2021.133865 ↗
34. 10.1016/j.jechem.2024.02.03810.1016/j.jechem.2024.02.038 ↗
35. 10.1039/D0TA09538A10.1039/D0TA09538A ↗
36. 10.1002/advs.20190005310.1002/advs.201900053 ↗
37. 10.1002/smll.20240359610.1002/smll.202403596 ↗
38. 10.1002/advs.20230156610.1002/advs.202301566 ↗
39. 10.1002/adma.20200710010.1002/adma.202007100 ↗
40. 10.1021/acsenergylett.1c0060810.1021/acsenergylett.1c00608 ↗
41. 10.1039/D0TA05908K10.1039/D0TA05908K ↗
42. 10.1016/j.cjsc.2023.10020610.1016/j.cjsc.2023.100206 ↗
43. 10.1016/j.cjsc.2023.10019110.1016/j.cjsc.2023.100191 ↗
44. 10.1038/s41467-021-26416-310.1038/s41467-021-26416-3 ↗
45. 10.1002/cctc.20190092610.1002/cctc.201900926 ↗
46. 10.1039/D4NJ02733G10.1039/D4NJ02733G ↗
47. 10.1039/D4TA02888K10.1039/D4TA02888K ↗
48. 10.1016/j.cej.2024.15233810.1016/j.cej.2024.152338 ↗
49. 10.1002/smll.20220472310.1002/smll.202204723 ↗
50. 10.1016/j.apcatb.2024.12399010.1016/j.apcatb.2024.123990 ↗
51. 10.1016/j.jcis.2024.03.04410.1016/j.jcis.2024.03.044 ↗
52. 10.1016/j.apcatb.2023.12357810.1016/j.apcatb.2023.123578 ↗
53. 10.1016/j.jallcom.2023.17057110.1016/j.jallcom.2023.170571 ↗
54. 10.1039/D4GC01788A10.1039/D4GC01788A ↗
55. 10.1016/j.jechem.2024.06.01010.1016/j.jechem.2024.06.010 ↗
56. 10.1038/s41467-023-41036-910.1038/s41467-023-41036-9 ↗
57. 10.1002/smll.20231117210.1002/smll.202311172 ↗
58. 10.1021/acsnano.3c0295610.1021/acsnano.3c02956 ↗
59. 10.1016/j.cej.2021.12983210.1016/j.cej.2021.129832 ↗