Open-Microcolumn Array: A Novel Approach for Enhanced Electrocatalytic Bubble Desorption in Microreactors
Source abstract
Abstract
High-efficiency electrocatalytic water splitting requires high intrinsic activity of catalysts and even more importantly favorable mass transfer. However, gas bubbles adhering to the surface of catalysts limit the re-expose of catalytic active sites to the electrolyte and reduce the catalytic activities. The efficient desorption of bubbles can be facilitated by a hierarchical multiscale structure of the electrode surface. Herein, we report an opened periodic three-dimensional electrode composed of iron (Fe)-cobalt (Co)-nickel (Ni) (oxy)hydroxide nanorods (NRs) grown in situ on a high aspect ratio nickel microcolumn array (NCA) for electrocatalytic water splitting. Compared with the flat nickel plate, the NCA not only increases the surface area for catalyst loading but also improves the wettability of the electrolyte on the electrode surface, exhibiting superhydrophilicity/superaerophobicity (the electrolyte and the bubble contact angles were about ∼0 and 163°, respectively), which accelerates the bubble evolution and desorption process. The X-ray photoelectron spectroscopy indicates that the synergy of Fe–Co–Ni could enhance the ratio of Co 3+ /Co 2+ and Ni 3+ /Ni 2+ and promote the electrocatalytic activity. Benefiting from the microstructure design and synergistic effects, the Co 4 Fe 0.5 Ni 0.5 OOH-NR@NCA electrode achieves a superior OER performance with an overpotential of 199 mV at 10 mA·cm –2 .
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, Jiangsu Key Laboratory of Artificial Functional Materials, College of Engineering and Applied Sciences, Nanjing University, Nanjing 210093, P. R. China
National Laboratory of Solid State Microstructures, Nanjing 210093, China
Funding
National Natural Science Foundation of China · Jiangsu Science and Technology Department
References (52)
Show source-provided references
1. 10.1016/j.cej.2021.13106210.1016/j.cej.2021.131062 ↗
2. 10.1039/D1EN00529D10.1039/D1EN00529D ↗
3. 10.1002/admt.20220057210.1002/admt.202200572 ↗
4. 10.1039/D1TA05332A10.1039/D1TA05332A ↗
5. 10.1002/adma.20220950010.1002/adma.202209500 ↗
6. 10.1002/aenm.20210236110.1002/aenm.202102361 ↗
7. 10.1016/j.apcatb.2021.12060010.1016/j.apcatb.2021.120600 ↗
8. 10.1021/acscatal.7b0359410.1021/acscatal.7b03594 ↗
9. 10.1039/C7SC05033J10.1039/C7SC05033J ↗
10. 10.1002/aenm.20210255610.1002/aenm.202102556 ↗
11. 10.1038/s41929-022-00753-y10.1038/s41929-022-00753-y ↗
12. 10.1021/acs.nanolett.1c0158110.1021/acs.nanolett.1c01581 ↗
13. 10.1002/anie.20160052510.1002/anie.201600525 ↗
14. 10.1039/C5RA26748J10.1039/C5RA26748J ↗
15. 10.1002/adma.20180554110.1002/adma.201805541 ↗
16. 10.1021/acscatal.0c0465610.1021/acscatal.0c04656 ↗
17. 10.1039/D2EE03936B10.1039/D2EE03936B ↗
18. 10.1002/adma.20230310910.1002/adma.202303109 ↗
19. 10.1021/acsami.1c0750410.1021/acsami.1c07504 ↗
20. 10.1002/aenm.20160008710.1002/aenm.201600087 ↗
21. 10.1007/s12274-022-4701-z10.1007/s12274-022-4701-z ↗
22. 10.1021/acssuschemeng.1c0651410.1021/acssuschemeng.1c06514 ↗
23. 10.1557/mrs.2020.16610.1557/mrs.2020.166 ↗
24. 10.1016/j.apcatb.2015.08.00710.1016/j.apcatb.2015.08.007 ↗
25. 10.1038/s41467-020-18891-x10.1038/s41467-020-18891-x ↗
26. 10.1039/d1ta10519a10.1039/d1ta10519a ↗
27. 10.1021/acsami.1c2260110.1021/acsami.1c22601 ↗
28. 10.1016/j.apcatb.2021.12091310.1016/j.apcatb.2021.120913 ↗
29. 10.1021/acsnano.2c1193910.1021/acsnano.2c11939 ↗
30. 10.1002/cctc.20120022910.1002/cctc.201200229 ↗
31. 10.1021/accountsmr.1c0000910.1021/accountsmr.1c00009 ↗
32. 10.1039/C6CS00567E10.1039/C6CS00567E ↗
33. 10.1002/aenm.20200295510.1002/aenm.202002955 ↗
34. 10.1021/acsnano.0c0297310.1021/acsnano.0c02973 ↗
35. 10.1021/acsami.2c1939610.1021/acsami.2c19396 ↗
36. 10.1002/slct.20180270910.1002/slct.201802709 ↗
37. 10.1016/j.apcatb.2021.12058710.1016/j.apcatb.2021.120587 ↗
38. 10.1016/j.apcatb.2017.09.04710.1016/j.apcatb.2017.09.047 ↗
39. 10.1016/j.cej.2021.13273310.1016/j.cej.2021.132733 ↗
40. 10.1016/j.jcis.2019.09.01210.1016/j.jcis.2019.09.012 ↗
41. 10.1021/acs.nanolett.0c0395010.1021/acs.nanolett.0c03950 ↗
42. 10.1039/C9NR09959J10.1039/C9NR09959J ↗
43. 10.1002/anie.20191161710.1002/anie.201911617 ↗
44. 10.1209/0295-5075/79/5600510.1209/0295-5075/79/56005 ↗
45. 10.1149/1.164614810.1149/1.1646148 ↗
46. 10.1002/adma.20130475910.1002/adma.201304759 ↗
47. 10.1038/s41467-022-33590-510.1038/s41467-022-33590-5 ↗
48. 10.1016/j.scib.2023.06.00110.1016/j.scib.2023.06.001 ↗
49. 10.1016/j.apcatb.2019.05.03510.1016/j.apcatb.2019.05.035 ↗
50. 10.1039/C7EE01571B10.1039/C7EE01571B ↗
51. 10.1002/adma.20210184510.1002/adma.202101845 ↗
52. 10.1016/j.apcatb.2020.11937510.1016/j.apcatb.2020.119375 ↗