Synthesis of Ni3S4/NiS2/FeS2 nanoparticles for hydrogen and oxygen evolution reaction
- 1. Key Laboratory of Biobased Polymer Materials, Shandong Provincial Education Department, School of Polymer Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China)
- 2. Key Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, MOE, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China)
Description
Highlights: • Ni3S4/NiS2/FeS2 nanoparticles are constructed by a facile hydrothermal method. • Ni3S4/NiS2/FeS2 nanoparticles expose the interfacial structures. • Ni3S4/NiS2/FeS2 nanoparticles show the outstanding overall water splitting activity. • Interfacial structures between Ni-S and Fe-S are accounting for the high activity. Construction of bi-functional noble metal-free catalysts with low cost and high efficiency is greatly desired for hydrogen and oxygen evolution reactions. It is of vital importance to regulate the surface electron state of pyrite to improve the electrocatalytic performance towards overall water splitting. In this work, we provide a simple one-pot interface-regulated strategy to synthesize Ni3S4/NiS2/FeS2 nanoparticles with exposed interfacial structures between Ni-S and Fe-S, which can then affect the conductivity and activity of pyrite. Notably, Ni3S4/NiS2/FeS2 nanoparticles are highly active in the hydrogen evolution reaction with 197 mV at 10 mA/cm2. Superior oxygen evolution activity is observed for Ni3S4/NiS2/FeS2 nanoparticles with 1.46 V at 10 mA/cm2, outperforming RuO2 with 1.54 V. Impressively, Ni3S4/NiS2/FeS2 nanoparticles could efficiently drive water splitting into hydrogen and oxygen at a voltage of 1.68 V at 10 mA/cm2 in a two-electrode configuration and robust long-term stability was verified by continuous 20 h i-t tests without apparent loss in the current density. The outstanding catalytic activity could be traced back to the presence of interfacial structures between Ni-S and Fe-S. This work highlights that engineering heteroatoms into pyrite that can trigger the generation of interfacial structures, which beneficially accelerates electron transfer during the water splitting process.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apsusc.2021.149985Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2021.149985;
- PII
- S0169433221010618;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 560
- Journal Page Range
- vp.
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54079342
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- CURRENT DENSITY; ELECTRIC POTENTIAL; ELECTRON TRANSFER; EVOLUTION; HYDROGEN; HYDROTHERMAL SYNTHESIS; IRON SULFIDES; NANOPARTICLES; OXYGEN; PYRITE; RUTHENIUM OXIDES
- Descriptors DEC
- CHALCOGENIDES; ELEMENTS; IRON COMPOUNDS; MINERALS; NONMETALS; OXIDES; OXYGEN COMPOUNDS; PARTICLES; REFRACTORY METAL COMPOUNDS; RUTHENIUM COMPOUNDS; SULFIDE MINERALS; SULFIDES; SULFUR COMPOUNDS; SYNTHESIS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier B.V. All rights reserved.