Unique Size of Co Nanoparticles Encapsulated in N-Rich Carbon Structure Derived from Electrochemical Etching for Enhanced Electrocatalytic Hydrogen Evolution
Source abstract
Abstract
Co nanoparticles with uniform size distribution are promising electrocatalysts for hydrogen evolution reaction. Herein, we synthesize Co nanoparticles encapsulated in in situ formed N-doped carbon and carbon nanotubes (CNTs) named as Co–N/C(CNTs) by low-temperature carbonization the organic–inorganic hybrid precursors. The as-prepared 4.55% Co–N/C(CNTs) shows the better hydrogen evolution reaction (HER) performance. As demonstrated in electrochemical measurements, 4.55% Co–N/C(CNTs) composite can achieve 10 mA cm–2 at the overpotential of 263 mV in 0.5 M H2SO4 at the first LSV curve. After electrochemical etching, which is carried out through the cyclic voltammetry (CV) cycle with different laps, a uniform Co nanoparticle with a diameter of around 7 nm encapsulated in N-doped carbon is obtained. The overpotential is 168 mV after 4000 times CV cycles and stabilizes at 180 mV after 6000 times cycles. Therefore, this work may provide an idea for the design of high activity HER electrocatalysts in acid solution.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081, P.R. China
School of Materials and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081, P.R. China
Funding
Natural Science Foundation of Hubei Province · National Natural Science Foundation of China
References (21)
Show source-provided references
1. 10.1002/anie.20180799610.1002/anie.201807996 ↗
2. 10.1002/adfm.20160091510.1002/adfm.201600915 ↗
3. 10.1021/acsnano.6b0608910.1021/acsnano.6b06089 ↗
4. 10.1039/C7TA10202J10.1039/C7TA10202J ↗
5. 10.1002/adfm.20180564110.1002/adfm.201805641 ↗
6. 10.1021/jacs.6b0585110.1021/jacs.6b05851 ↗
7. 10.1039/C4CS00448E10.1039/C4CS00448E ↗
8. 10.1016/j.nanoen.2017.11.06310.1016/j.nanoen.2017.11.063 ↗
9. 10.1002/smll.20170009210.1002/smll.201700092 ↗
10. 10.1021/acs.nanolett.6b0333210.1021/acs.nanolett.6b03332 ↗
11. 10.1016/j.electacta.2018.11.12910.1016/j.electacta.2018.11.129 ↗
12. 10.1002/aenm.20180098010.1002/aenm.201800980 ↗
13. 10.1038/nmat441010.1038/nmat4410 ↗
14. 10.1007/s10934-019-00772-410.1007/s10934-019-00772-4 ↗
15. 10.1002/adfm.20170416910.1002/adfm.201704169 ↗
16. 10.1016/j.apcatb.2018.03.09310.1016/j.apcatb.2018.03.093 ↗
17. 10.1021/acs.jpcc.6b1178210.1021/acs.jpcc.6b11782 ↗
18. 10.1002/adma.20180288010.1002/adma.201802880 ↗
19. 10.1002/adma.20180201110.1002/adma.201802011 ↗
20. Eliezer G. · 2011
21. 10.1021/acssuschemeng.8b0219410.1021/acssuschemeng.8b02194 ↗