Controllable synthesis of hollow NiSe2 spheres as an active electrocatalyst for hydrogen evolution reaction
Source abstract
Abstract
The design of electrocatalysts with excellent performance and low cost is of great significance for the electrocatalytic water splitting. NiSe2 has been widely concerned because of its suitable adsorption energy and adjustable electronic structure for hydrogen evolution reaction (HER). Here, a hollow spherical NiSe2 catalyst was designed and prepared by the hydrothermal method. Thanks to the unique three-dimensional (3D) open configuration and favorable active components, it exhibits superior catalytic activity for HER. It delivers an overpotential of 330[Formula: see text]mV at the current density of 10[Formula: see text]mA[Formula: see text]cm[Formula: see text], corresponding to the Tafel slope of 128[Formula: see text]mV[Formula: see text]dec[Formula: see text]. This work demonstrates that the 3D hollow structure with large specific surface and rich internal space can effectively improve the mass transfer efficiency and electron transfer. This work may provide a controllable way for the design of hollow structure catalysts.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced Photocatalysis Techniques · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Henan Institutes of Advanced Technology, Zhengzhou University, Zhengzhou 450003, P. R. China
Wuhan University of Technology, College of Resources and Environmental Engineering, Wuhan 430070, P. R. China
Funding
Postdoctoral Science Foundation · National Natural Science Foundation of China
References (21)
Show source-provided references
1. Wu X. · Funct. Mater. Lett. · 2017 · 5 · 7001
2. Aroua S. · Chem. Cat. Chem. · 2017 · 12 · 2099
3. Wang X. · Int. J. Hydrog. Energy · 2020 · 45 · 1223710.1016/j.ijhydene.2020.02.173 ↗
4. Li M. · Appl. Surf. Sci. · 2019 · 496 · 14367210.1016/j.apsusc.2019.143672 ↗
5. Mahmood J. · Nat. Nanotechnol. · 2017 · 12 · 44110.1038/nnano.2016.304 ↗
6. 10.1142/S179360471950021810.1142/S1793604719500218 ↗
7. Voiry D. · Adv. Mater. · 2016 · 28 · 619710.1002/adma.201505597 ↗
8. Lin J. · J. Colloid Interface Sci. · 2020 · 571 · 26010.1016/j.jcis.2020.03.053 ↗
9. Ullah N. · Electrochim. Acta · 2019 · 298 · 16310.1016/j.electacta.2018.12.053 ↗
10. Yang Y. · Small · 2020 · 16 · e190508310.1002/smll.201905083 ↗
11. Peng Z. · J. Mater. Chem. A · 2019 · 7 · 667610.1039/C8TA09136F ↗
12. Wu X. · Appl. Catal. B, Environ. · 2013 · 142 · 45010.1016/j.apcatb.2013.05.052 ↗
13. Yin S. · Tungsten · 2019 · 1 · 15
14. Chen W. · J. Catal. · 2017 · 381 · 36310.1016/j.jcat.2019.11.013 ↗
15. Wang H. · ACS Sustain. Chem. Eng. · 2019 · 7 · 1874410.1021/acssuschemeng.9b02126 ↗
16. Lonkar S. · Int. J. Hydrog. Energy · 2020 · 45 · 1047510.1016/j.ijhydene.2019.03.195 ↗
17. Wang G. · J. Mater. Chem. A · 2018 · 6 · 1776310.1039/C8TA06827E ↗
18. Chen T. · Nano Res. · 2018 · 11 · 133110.1007/s12274-017-1748-3 ↗
19. Tian Y. · Inorg. Chem. · 2020 · 59 · 601810.1021/acs.inorgchem.0c00012 ↗
20. Dubouis N. · Chem. Sci. · 2018 · 10 · 916510.1039/C9SC03831K ↗
21. Askari M. · Chem. Phys. Lett. · 2019 · 711 · 3210.1016/j.cplett.2018.09.025 ↗