Preserved crystal phase and morphology: Improving the magnetic and electrochemical performance of sulfur doped tin oxide nanoparticles synthesized via the hydrothermal method
Mohd Arif Dar, Nazir Ahmad Mala, Md. Yasir Bhat and 4 more
Applied Surface Science Advances · 2023
doi:10.1016/j.apsadv.2022.100360 (opens in a new tab)
We email you when a new notice or a question about this paper appears.
Abstract
Herein, we report synthesis of bare and Sulfur (S) doped SnO2 nanoparticles (NPs) using simple and low cost hydrothermal method. S with different concentration (0, 2, 4 and 6) were doped in SnO2 and named as bare SnO2, 2%S:SnO2, 4%S:SnO2 and 6%S:SnO2, respectively. The synthesized NPs were characterized for structural, functional, optical, morphological, electrochemical and magnetic properties. XRD confirms the tetragonal structure of bare SnO2 2%S:SnO2, 4%S:SnO2 and 6%S:SnO2 NPs. The crystallite size and microstrain was calculated using the Scherrer equation, W-H plot, SSP plot, and H-W plot and are in well agreement with each other. The FTIR confirmed formation of S-O and Sn-O bonding. The direct energy band gap values of bare SnO2, 2%S:SnO2, 4%S:SnO2 and 6%S:SnO2 are 3.8 eV, 3.6 eV, 3.1 eV and 2.2 eV, respectively. The electrochemical performance (ECP) of bare SnO2 and 2%S:SnO2 NPs were studied by making their electrodes through CV, GCDs, and EIS measurements. The bare SnO2 and 2%S:SnO2 electrodes show the specific capacitance of 125 F/g and 225 F/g at a current density of 3 A/g proves S doping enhances the capacitive performance of SnO2 NPs. The VSM shows paramagnetic behavior changes into ferromagnetic behavior with S doping.
Abstract licence: CC BY-NC-ND
References84
84 more references, whose wording the paper’s licence keeps private.
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.