Subnanometer Cobalt-Hydroxide-Anchored N-Doped Carbon Nanotube Forest for Bifunctional Oxygen Catalyst
Source abstract
Abstract
Electrochemical oxygen redox reactions are the crucial elements for energy conversion and storage including fuel cells and metal air batteries. Despite tremendous research efforts, developing high-efficient, low-cost, and durable bifunctional oxygen catalysts remains a major challenge. We report a new class of hybrid material consisting of subnanometer thick amorphous cobalt hydroxide anchored on NCNT as a durable ORR/OER bifunctional catalyst. Although amorphous cobalt species-based catalysts are known as good OER catalysts, hybridizing with NCNT successfully enhanced ORR activity by promoting a 4e reduction pathway. Abundant charge carriers in amorphous cobalt hydroxide are found to trigger the superior OER activity with high current density and low Tafel slope as low as 36 mV/decade. A remarkably high OER turnover frequency (TOF) of 2.3 s(-1) at an overpotential of 300 mV was obtained, one of the highest values reported so far. Moreover, the catalytic activity was maintained over 120 h of cycling. The unique subnanometer scale morphology of amorphous hydroxide cobalt species along with intimate cobalt species-NCNT interaction minimizes the deactivation of catalyst during prolonged repeated cycles.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Advanced Memory and Neural Computing
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Creative Research Initiative (CRI) Center for Multi-Dimensional Directed Nanoscale Assembly, Department of Material Science and Engineering, KAIST, Daejeon 34141, Republic of Korea
Pohang Accelerator Laboratory (PAL), Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea
Funding
National Research Foundation of Korea
References (32)
Show source-provided references
1. 10.1016/j.jelechem.2010.10.00410.1016/j.jelechem.2010.10.004 ↗
2. 10.1039/C4CY00669K10.1039/C4CY00669K ↗
3. 10.1021/ar300359w10.1021/ar300359w ↗
4. 10.1039/c2ee03590a10.1039/c2ee03590a ↗
5. 10.1021/jz201650710.1021/jz2016507 ↗
6. 10.1016/j.jpowsour.2005.05.09810.1016/j.jpowsour.2005.05.098 ↗
7. 10.1021/ja308992310.1021/ja3089923 ↗
8. 10.1021/cr500356310.1021/cr5003563 ↗
9. 10.1039/C4CY00669K10.1039/C4CY00669K ↗
10. 10.1021/am507744y10.1021/am507744y ↗
11. 10.1002/smll.20130371510.1002/smll.201303715 ↗
12. 10.1002/adfm.20140365710.1002/adfm.201403657 ↗
13. 10.1039/C5TA00661A10.1039/C5TA00661A ↗
14. 10.1021/acsami.5b0267010.1021/acsami.5b02670 ↗
15. 10.1002/aenm.20130138910.1002/aenm.201301389 ↗
16. 10.1126/science.123363810.1126/science.1233638 ↗
17. 10.1007/s12274-014-0591-z10.1007/s12274-014-0591-z ↗
18. 10.1103/PhysRevLett.106.17550210.1103/PhysRevLett.106.175502 ↗
19. Kaye M. H. · 2011 · 11110.1002/9780470872864.ch9 ↗
20. 10.1021/nn204504h10.1021/nn204504h ↗
21. 10.1038/srep0164810.1038/srep01648 ↗
22. 10.1021/am100724v10.1021/am100724v ↗
23. 10.1149/1.363570210.1149/1.3635702 ↗
24. Sato N. · 1998 · 23510.1016/B978-044482806-4/50008-8 ↗
25. 10.1021/ja503557x10.1021/ja503557x ↗
26. 10.1038/nmat308710.1038/nmat3087 ↗
27. 10.1039/b815338h10.1039/b815338h ↗
28. Sato N. · 1998 · 11910.1016/B978-044482806-4/50005-2 ↗
29. Sudakar C. · 2012 · 3710.1007/978-1-4419-9931-3_3 ↗
30. 10.1038/ncomms281210.1038/ncomms2812 ↗
31. 10.1002/aenm.20130138910.1002/aenm.201301389 ↗
32. 10.1021/nl404108a10.1021/nl404108a ↗