journal article·2026-01

Urea‐Assisted N‐Doping of Nickel Sulfide for Enhanced Oxygen Evolution Reaction Performance

Somnath Bali, Arnab Halder, Avijit Mondal

ChemNanoMat· Volume 12· Issue 1
Publisher page

Abstract

The oxygen evolution reaction (OER) limits the efficiency of electrochemical water splitting, making the development of low‐cost, stable, and efficient catalysts a key challenge. In this work, nickel sulfide (NiS 2 ) nanostructures are grown on cone‐shaped graphite electrodes and further modified via annealing in the presence of urea or NaH 2 PO 2 , introducing N or P element to alter the electronic environment around Ni 2+ centers. Comprehensive characterization (XRD, FE‐SEM, EDX, ICP‐AES, XPS, and electrochemical techniques) confirms successful doping. The OER activity follows the trend N‐NiS 2 > S‐NiS 2 > P‐NiS 2 , correlating with the elemental electronegativity order of N > S > P. N‐doped NiS 2 achieves a low overpotential of 260 mV at 10 mA cm −2 and a Tafel slope of 53 mV dec −1 in 1 M KOH. Urea‐derived ammonia treatment creates a porous, high‐surface‐area architecture that enhances easy mass transport and catalytic efficiency. This simple, scalable strategy presents a cost‐effective route to high‐performance OER electrocatalysts.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Ammonia Synthesis and Nitrogen Reduction · Advanced Photocatalysis Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry Presidency University Kolkata India

References (35)

Show source-provided references
1. 10.1038/nmat487610.1038/nmat4876 ↗
2. 10.1038/s41467-024-53310-510.1038/s41467-024-53310-5 ↗
3. 10.1016/j.pecs.2009.11.00210.1016/j.pecs.2009.11.002 ↗
4. 10.1002/adma.20230613810.1002/adma.202306138 ↗
5. 10.1016/j.chempr.2022.04.01310.1016/j.chempr.2022.04.013 ↗
6. Atkins P. W. · 2023
7. Castellan G. W. · 1983
8. 10.1007/s12034-021-02519-x10.1007/s12034-021-02519-x ↗
9. 10.1021/jz201650710.1021/jz2016507 ↗
10. 10.1039/C6SC04622C10.1039/C6SC04622C ↗
11. 10.1016/j.jcat.2021.02.00710.1016/j.jcat.2021.02.007 ↗
12. 10.1039/D1TA10103J10.1039/D1TA10103J ↗
13. 10.1038/s41467-019-13092-710.1038/s41467-019-13092-7 ↗
14. 10.1016/j.ijhydene.2022.04.21310.1016/j.ijhydene.2022.04.213 ↗
15. 10.3390/en1505160910.3390/en15051609 ↗
16. 10.1016/j.ijhydene.2024.02.10910.1016/j.ijhydene.2024.02.109 ↗
17. 10.1038/s41467-024-49015-410.1038/s41467-024-49015-4 ↗
18. 10.1021/acscatal.2c0100110.1021/acscatal.2c01001 ↗
19. 10.1002/chem.20240303010.1002/chem.202403030 ↗
20. 10.1016/j.apcatb.2020.11913710.1016/j.apcatb.2020.119137 ↗
21. 10.1002/cctc.20190168210.1002/cctc.201901682 ↗
22. 10.1021/acsenergylett.8b0098210.1021/acsenergylett.8b00982 ↗
23. 10.1039/C8NR09902B10.1039/C8NR09902B ↗
24. 10.1039/D0TA05797E10.1039/D0TA05797E ↗
25. 10.1002/smll.20200677010.1002/smll.202006770 ↗
26. 10.1039/C7TA02217D10.1039/C7TA02217D ↗
27. 10.1002/smll.20231032710.1002/smll.202310327 ↗
28. 10.1038/s41467-019-11600-310.1038/s41467-019-11600-3 ↗
29. 10.1007/s12274-016-1198-310.1007/s12274-016-1198-3 ↗
30. 10.1021/acs.inorgchem.3c0192510.1021/acs.inorgchem.3c01925 ↗
31. 10.1016/j.ijhydene.2018.11.17610.1016/j.ijhydene.2018.11.176 ↗
32. 10.1039/C5CY01111F10.1039/C5CY01111F ↗
33. 10.1039/C5NR04252F10.1039/C5NR04252F ↗
34. 10.1002/adfm.20190031510.1002/adfm.201900315 ↗
35. 10.1039/D2RA07340D10.1039/D2RA07340D ↗