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DC Field | Value | Language |
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dc.contributor.author | Mukurala, Nagaraju | en_US |
dc.contributor.author | Kushwaha, Ajay Kumar | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-21T11:11:39Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:11:39Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Mukurala, N., Mokurala, K., Kumar, A., Kushwaha, A. K., & Jin, S. H. (2021). Synthesis process dependent physico-chemical and opto-electronic properties of Cu2FeSnS4 nanoparticle films. Ceramics International, 47(19), 27898-27907. doi:10.1016/j.ceramint.2021.06.220 | en_US |
dc.identifier.issn | 0272-8842 | - |
dc.identifier.other | EID(2-s2.0-85109185600) | - |
dc.identifier.uri | https://doi.org/10.1016/j.ceramint.2021.06.220 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/7435 | - |
dc.description.abstract | The present work reports a comparative study of synthesis process-dependent physicochemical, optical, electrical, and photodetective properties of earth-abundant quaternary Cu2FeSnS4 (CFTS) nanoparticle-based films. CFTS nanoparticles are synthesized via solvothermal and monoethanolamine-assisted hydrothermal processes. X-ray diffraction (XRD) and Raman spectroscopy analyses confirm the phase purity of the synthesized particles. FE-TEM, FE-SEM, and energy-dispersive X-ray spectroscopy (EDS) results demonstrate the formation of smaller particles (~5–10 nm) with stoichiometric chemical composition and larger particles (~100 nm) with Cu-deficient chemical composition in hydrothermal and solvothermal processes, respectively. The optical bandgaps of the hydrothermal and solvothermal-processed CFTS nanocrystalline-based films are calculated to be 1.56 and 1.48 eV, respectively. The temperature-dependent electrical properties of the CFTS nanocrystalline films are analyzed by the transfer length method. The electrical conductivity of hydrothermally and solvothermally synthesized CFTS nanoparticle-based films increased from 31.02 ± 4.04 and 3.12 ± 0.69 mS/cm to 67.73 ± 5.84 and 17.62 ± 2.62 mS/cm, respectively, with an increase in the measuring temperature from 298 to 373 K. The temperature-dependent charge transport properties are attributed to the thermal activation of defects in the CFTS films. The hydrothermally synthesized CFTS nanoparticle-based visible photodetectors exhibited photoinactive properties. The solvothermally synthesized CFTS nanoparticle-based devices exhibited maximum photosensitivity of (21 ± 4) %, photoresponsivity of 128 ± 6 mA/W, and detectivity of 4.68 ± 0.86 × 109 Jones. The present study shows that the synthesis process significantly affects the morphology, chemical composition, optical properties, electrical properties, and performance of CFTS nanoparticle-based visible photodetectors. © 2021 Elsevier Ltd and Techna Group S.r.l. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Ltd | en_US |
dc.source | Ceramics International | en_US |
dc.subject | Copper compounds | en_US |
dc.subject | Electric conductivity | en_US |
dc.subject | Electronic properties | en_US |
dc.subject | Energy dispersive spectroscopy | en_US |
dc.subject | Iron compounds | en_US |
dc.subject | Nanocrystals | en_US |
dc.subject | Nanoparticles | en_US |
dc.subject | Photodetectors | en_US |
dc.subject | Photons | en_US |
dc.subject | Synthesis (chemical) | en_US |
dc.subject | Tin compounds | en_US |
dc.subject | Chemical compositions | en_US |
dc.subject | Cu2FeSnS4 particle | en_US |
dc.subject | Energy | en_US |
dc.subject | Hydrothermal process | en_US |
dc.subject | Photodetective property | en_US |
dc.subject | Property | en_US |
dc.subject | Solvothermal process | en_US |
dc.subject | Synthesis process | en_US |
dc.subject | Synthesised | en_US |
dc.subject | Temperature-dependent electrical conductivity | en_US |
dc.subject | Activation energy | en_US |
dc.title | Synthesis process dependent physico-chemical and opto-electronic properties of Cu2FeSnS4 nanoparticle films | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Metallurgical Engineering and Materials Sciences |
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