Szczegóły publikacji
Opis bibliograficzny
Thermogravimetric/thermal–mass spectroscopy insight into oxidation propensity of various mechanochemically made kesterite $Cu_{2}ZnSnS_{4}$ nanopowders / Katarzyna LEJDA, Janusz PARTYKA, Jerzy F. JANIK // Materials [Dokument elektroniczny]. — Czasopismo elektroniczne ; ISSN 1996-1944. — 2024 — vol. 17 iss. 6 art. no. 1232, s. 1-17. — Wymagania systemowe: Adobe Reader. — Bibliogr. s. 15-17, Abstr. — Publikacja dostępna online od: 2024-03-07
Autorzy (3)
Słowa kluczowe
Dane bibliometryczne
| ID BaDAP | 152319 |
|---|---|
| Data dodania do BaDAP | 2024-04-16 |
| Tekst źródłowy | URL |
| DOI | 10.3390/ma17061232 |
| Rok publikacji | 2024 |
| Typ publikacji | artykuł w czasopiśmie |
| Otwarty dostęp |  |
| Creative Commons | |
| Czasopismo/seria | Materials |
Abstract
Thermogravimetry coupled with thermal analysis and quadrupole mass spectroscopy TGA/DTA-QMS were primarily used to assess the oxidation susceptibility of a pool of nanocrystalline powders of the semiconductor kesterite Cu2ZnSnS4 for prospective photovoltaic applications, which were prepared via the mechanochemically assisted synthesis route from two different precursor systems. Each system, as confirmed by XRD patterns, yielded first the cubic polytype of kesterite with defunct semiconductor properties, which, after thermal annealing at 500 °C under neutral gas atmosphere, was converted to the tetragonal semiconductor polytype. The TGA/DTA-QMS determinations up to 1000 °C were carried out under a neutral argon Ar atmosphere and under a dry, oxygen-containing gas mixture of O2:Ar = 1:4 (vol.). The mass spectroscopy data confirmed that under each of the gas atmospheres, a distinctly different, multistep evolution of such oxygen-bearing gaseous compounds as sulfur oxides SO2/SO3, carbon dioxide CO2, and water vapor H2O was taking place. The TGA/DTA changes in correlation with the nature of evolving gases helped in the elucidation of the plausible chemistry linked to kesterite oxidation, both in the stage of nanopowder synthesis/storage at ambient air conditions and during forced oxidation up to 1000 °C in the dry, oxygen-containing gas mixture.