Metal–Organic Framework-Derived NiS/Fe3O4 Heterostructure-Decorated Carbon Nanotubes as Highly Efficient and Durable Electrocatalysts for Oxygen Evolution Reaction
Source abstract
Abstract
Because of the sluggish oxygen evolution kinetics, it is extremely important but still challenging to develop low-cost, efficient, and stable electrocatalysts for oxygen evolution reaction (OER) to enhance the efficiency of water electrolysis. Herein, for the first time, we present a novel heterostructure catalyst, constructed by ultrafine NiS/Fe3O4 heterostructural nanoparticles decorated on a carbon nanotube (CNT) matrix (NiS/Fe3O4 HNPs@CNT), which is synthesized by a facile hydrothermal reaction and subsequent sulfurization process. The NiS/Fe3O4 HNPs@CNT hybrid delivers superior OER activity in alkaline medium: it delivers a current density of 10 mA cm–2 at an ultralow overpotential of 243 mV with a small Tafel slope of 44.2 mV dec–1, which outperforms the benchmark RuO2 electrocatalyst; moreover, it exhibits terrific long-term stability over 36 h without any noticeable performance decay. The exceptional OER performance can be attributed to the unique nanoarchitecture, high conductivity of the CNT matrix, and particularly, the interaction between the Ni and Fe species in NiS/Fe3O4 heterostructural nanoparticles. This work introduces a sensible nanoarchitecture design with a facile and novel fabrication strategy to attain nonprecious metal-based composite catalysts with high OER performance and outstanding long-term stability.
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
School of Electronic Science and Engineering, and State Key Laboratory of Electronic Thin Films and Integrated Devices, University of Electronic Science and Technology of China, Chengdu 610054, PR China
School of Science, and Institute of Oxygen Supply, Tibet University, Lhasa 850000, PR China
Funding
China Postdoctoral Science Foundation · National Natural Science Foundation of China · China Government
References (68)
Show source-provided references
1. Laughner J. · Nat. Gas Dev. · 2012 · 1 · 56
2. 10.1002/smtd.20180021110.1002/smtd.201800211 ↗
3. 10.1038/440295a10.1038/440295a ↗
4. 10.1002/adfm.20180703110.1002/adfm.201807031 ↗
5. 10.1002/adfm.20170251310.1002/adfm.201702513 ↗
6. 10.1021/acsenergylett.9b0034810.1021/acsenergylett.9b00348 ↗
7. 10.1039/c6cs00328a10.1039/c6cs00328a ↗
8. 10.1021/acs.chemrev.7b0005110.1021/acs.chemrev.7b00051 ↗
9. 10.1002/smtd.20190012910.1002/smtd.201900129 ↗
10. 10.1002/adma.20190051010.1002/adma.201900510 ↗
11. 10.1002/anie.20181426210.1002/anie.201814262 ↗
12. 10.1126/science.125830710.1126/science.1258307 ↗
13. 10.1126/science.aad499810.1126/science.aad4998 ↗
14. 10.1021/acs.chemrev.9b0022310.1021/acs.chemrev.9b00223 ↗
15. 10.1038/s41467-018-08208-410.1038/s41467-018-08208-4 ↗
16. 10.1021/jacs.8b0874410.1021/jacs.8b08744 ↗
17. 10.1002/anie.20180467310.1002/anie.201804673 ↗
18. 10.1021/acsami.8b1761210.1021/acsami.8b17612 ↗
19. 10.1021/jacs.7b1242010.1021/jacs.7b12420 ↗
20. 10.1002/anie.20160727110.1002/anie.201607271 ↗
21. 10.1016/j.jpowsour.2019.05.09410.1016/j.jpowsour.2019.05.094 ↗
22. 10.1021/jacs.8b0075210.1021/jacs.8b00752 ↗
23. 10.1002/adfm.20180155410.1002/adfm.201801554 ↗
24. 10.1002/anie.20171137610.1002/anie.201711376 ↗
25. 10.1002/eem2.1202410.1002/eem2.12024 ↗
26. 10.1021/acsami.7b1643010.1021/acsami.7b16430 ↗
27. 10.1021/acsaem.9b0031710.1021/acsaem.9b00317 ↗
28. 10.1002/adfm.20170045110.1002/adfm.201700451 ↗
29. 10.1039/c9ta03819a10.1039/c9ta03819a ↗
30. 10.1016/j.apsusc.2019.04.16510.1016/j.apsusc.2019.04.165 ↗
31. 10.1016/j.electacta.2016.01.16010.1016/j.electacta.2016.01.160 ↗
32. 10.1016/j.ijhydene.2018.12.03110.1016/j.ijhydene.2018.12.031 ↗
33. 10.1016/j.ijhydene.2018.11.17610.1016/j.ijhydene.2018.11.176 ↗
34. 10.1016/j.apsusc.2018.02.09710.1016/j.apsusc.2018.02.097 ↗
35. 10.1016/j.electacta.2017.02.08010.1016/j.electacta.2017.02.080 ↗
36. 10.1016/j.ijhydene.2017.08.04510.1016/j.ijhydene.2017.08.045 ↗
37. 10.1002/adfm.20180529810.1002/adfm.201805298 ↗
38. 10.1039/c2dt32073h10.1039/c2dt32073h ↗
39. 10.1007/s11783-019-1101-z10.1007/s11783-019-1101-z ↗
40. 10.1016/j.cej.2018.05.17710.1016/j.cej.2018.05.177 ↗
41. 10.1016/j.apt.2019.01.01610.1016/j.apt.2019.01.016 ↗
42. 10.1039/c7nj02985c10.1039/c7nj02985c ↗
43. 10.1016/j.apcatb.2018.02.04710.1016/j.apcatb.2018.02.047 ↗
44. 10.1021/am505378410.1021/am5053784 ↗
45. 10.1016/j.micromeso.2019.02.01210.1016/j.micromeso.2019.02.012 ↗
46. 10.1021/acs.iecr.9b0165310.1021/acs.iecr.9b01653 ↗
47. 10.1016/s0001-8686(98)00047-510.1016/s0001-8686(98)00047-5 ↗
48. 10.1016/j.mssp.2015.01.01210.1016/j.mssp.2015.01.012 ↗
49. 10.1039/c8cc03112f10.1039/c8cc03112f ↗
50. 10.1002/chem.20180515210.1002/chem.201805152 ↗
51. 10.1021/ic402948s10.1021/ic402948s ↗
52. 10.1016/j.ijhydene.2019.08.12710.1016/j.ijhydene.2019.08.127 ↗
53. 10.1016/j.ensm.2017.05.00610.1016/j.ensm.2017.05.006 ↗
54. 10.1038/srep3400410.1038/srep34004 ↗
55. 10.1038/ncomms1534110.1038/ncomms15341 ↗
56. 10.1021/acssuschemeng.9b0119910.1021/acssuschemeng.9b01199 ↗
57. 10.1002/adfm.20160067410.1002/adfm.201600674 ↗
58. 10.1021/acsami.6b0537510.1021/acsami.6b05375 ↗
59. 10.1016/j.nanoen.2017.11.07110.1016/j.nanoen.2017.11.071 ↗
60. 10.1039/d0nr00879f10.1039/d0nr00879f ↗
61. 10.1021/acsaem.8b0033810.1021/acsaem.8b00338 ↗
62. 10.1021/acssuschemeng.9b0718210.1021/acssuschemeng.9b07182 ↗
63. 10.1039/c6ta08149e10.1039/c6ta08149e ↗
64. 10.1002/ange.20161176710.1002/ange.201611767 ↗
65. 10.1016/j.apcatb.2019.11799610.1016/j.apcatb.2019.117996 ↗
66. 10.1002/adfm.20180529810.1002/adfm.201805298 ↗
67. 10.1016/j.electacta.2019.13498310.1016/j.electacta.2019.134983 ↗
68. 10.1039/c7ta04438k10.1039/c7ta04438k ↗