2D Co6Mo6C Nanosheets as Robust Hydrogen Evolution Reaction Electrocatalyst
Source abstract
Abstract
Abstract Hydrogen production by electrochemical water splitting via nonprecious metal catalysts is still a great challenge due to sluggish kinetics and poor electrochemical durability toward hydrogen evolution reaction (HER). In this work, the fabrication of two dimensional (2D) bimetallic carbide nanosheets on graphene hybrid (Co6Mo6C NSs/G) is first reported, which exhibits excellent HER performance with a nearly zero onset overpotential, a small overpotential of 73 mV at current densities of 10 mA cm−2, a small Tafel slope of 43 mV dec−1, and an outstanding electrochemical durability. The density functional theoretical calculations suggest that the Gibbs free energy of hydrogen bonding of Co6Mo6C is −0.12 eV, which is very close to Pt (−0.09 eV).
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · MXene and MAX Phase Materials · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Dongguan Neutron Science Center Dongguan 523803 China
Institute of High Energy Physics Chinese Academy of Sciences (CAS) Beijing 100049 China
Funding
Natural Science Foundation of Guangdong Province · Chinese Academy of Sciences
References (50)
Show source-provided references
1. 10.1126/science.110319710.1126/science.1103197 ↗
2. 10.1039/C6TA02334G10.1039/C6TA02334G ↗
3. 10.1039/C6NR09893B10.1039/C6NR09893B ↗
4. 10.1038/nchem.14110.1038/nchem.141 ↗
5. 10.1021/cr100232610.1021/cr1002326 ↗
6. 10.1039/C6EE03768B10.1039/C6EE03768B ↗
7. 10.1126/science.121193410.1126/science.1211934 ↗
8. 10.1002/anie.20150871510.1002/anie.201508715 ↗
9. 10.1126/science.181.4099.54710.1126/science.181.4099.547 ↗
10. 10.1002/anie.20080323310.1002/anie.200803233 ↗
11. 10.1039/C5CC01240F10.1039/C5CC01240F ↗
12. 10.1039/C6CC03876J10.1039/C6CC03876J ↗
13. 10.1039/C5TA02908B10.1039/C5TA02908B ↗
14. 10.1039/c3ta12984e10.1039/c3ta12984e ↗
15. 10.1021/ja209305310.1021/ja2093053 ↗
16. 10.1039/C3CC48240E10.1039/C3CC48240E ↗
17. 10.1016/j.apcatb.2014.10.07010.1016/j.apcatb.2014.10.070 ↗
18. 10.1039/C4NR06295G10.1039/C4NR06295G ↗
19. 10.1016/j.jcat.2017.01.00710.1016/j.jcat.2017.01.007 ↗
20. 10.1039/c3cs60407a10.1039/c3cs60407a ↗
21. 10.1038/nmat437410.1038/nmat4374 ↗
22. 10.1016/j.nanoen.2017.01.05710.1016/j.nanoen.2017.01.057 ↗
23. 10.1021/acs.nanolett.6b0126510.1021/acs.nanolett.6b01265 ↗
24. 10.1016/j.apcata.2006.10.01310.1016/j.apcata.2006.10.013 ↗
25. 10.1016/j.jpowsour.2008.03.08410.1016/j.jpowsour.2008.03.084 ↗
26. 10.1039/C4EE00957F10.1039/C4EE00957F ↗
27. 10.1039/C6RA12456A10.1039/C6RA12456A ↗
28. 10.1039/C5RA25367E10.1039/C5RA25367E ↗
29. 10.1016/j.apcata.2012.04.03510.1016/j.apcata.2012.04.035 ↗
30. 10.1038/srep0214410.1038/srep02144 ↗
31. 10.1039/C7EE00388A10.1039/C7EE00388A ↗
32. 10.1021/nn501214410.1021/nn5012144 ↗
33. 10.1039/C3EE42441C10.1039/C3EE42441C ↗
34. 10.1038/ncomms751210.1038/ncomms7512 ↗
35. 10.1039/C6TA01601D10.1039/C6TA01601D ↗
36. 10.1002/adfm.20140363310.1002/adfm.201403633 ↗
37. 10.1021/ja501497n10.1021/ja501497n ↗
38. 10.1016/j.nanoen.2015.12.00810.1016/j.nanoen.2015.12.008 ↗
39. 10.1021/nn500959v10.1021/nn500959v ↗
40. 10.1016/j.apcatb.2014.02.02010.1016/j.apcatb.2014.02.020 ↗
41. Ma R. · Angew. Chem., Int. Ed. · 2015 · 74 · 718
42. 10.1039/c2ee23891h10.1039/c2ee23891h ↗
43. 10.1002/anie.20130752710.1002/anie.201307527 ↗
44. 10.1039/C6TA00596A10.1039/C6TA00596A ↗
45. 10.1039/C6TA05838H10.1039/C6TA05838H ↗
46. 10.1039/C6TA01328G10.1039/C6TA01328G ↗
47. 10.1016/S0360-3199(03)00096-X10.1016/S0360-3199(03)00096-X ↗
48. 10.1039/c3cc45416a10.1039/c3cc45416a ↗
49. 10.1039/C5CS00434A10.1039/C5CS00434A ↗
50. 10.1021/acs.nanolett.6b0333210.1021/acs.nanolett.6b03332 ↗