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Eco-friendly green synthesis of Fe-doped WS2 using neem leaf extract: unlocking large interlayer spacing for improved capacitance and rapid ion transport
Iron-doped tungsten disulfide (Fe-WS2) nanoparticles were synthesized via a green method using neem leaf extract. X-ray diffraction (XRD) confirmed structural changes, with the formation of a hexagonal structure. The d-spacing is increased by Fe doping (6.05–6.08 Å). Fourier-transform infrared (FTIR...
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Published in: | RSC advances 2024-12, Vol.14 (53), p.39727-39739 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Iron-doped tungsten disulfide (Fe-WS2) nanoparticles were synthesized via a green method using neem leaf extract. X-ray diffraction (XRD) confirmed structural changes, with the formation of a hexagonal structure. The d-spacing is increased by Fe doping (6.05–6.08 Å). Fourier-transform infrared (FTIR) spectroscopy identified W–S and S–S bond vibrations, crucial for material integrity. The Brunauer–Emmett–Teller (BET) analysis confirmed the increased surface area and pore radius as a result of enhanced ions diffusion. The morphology study through Scanning Electron Microscopy (SEM) revealed enhanced porosity of Fe-WS2, as evidenced by the more granular and disordered structure. UV-vis spectroscopy (UV-vis) showed a blue shift and an increased energy band gap from 2.48 eV to 2.64 eV, indicating improved optical properties. Methyl blue (MB) dye adsorption spectra showed that the Fe-WS2 is porous, and as a result, more electrolyte adsorbs within the electrode. Cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) revealed enhanced specific capacitance and energy density. Electrochemical impedance spectroscopy (EIS) demonstrated a significant reduction in charge transfer resistance and a substantial increase in the ion diffusion coefficient. These findings underscore the potential of Fe-WS2 for high-performance energy storage devices. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/d4ra07012g |