Autor: |
Lejda K; Faculty of Energy and Fuels, AGH University, al. Mickiewicza 30, 30-059 Krakow, Poland., Ziąbka M; Faculty of Materials Science and Ceramics, AGH University, al. Mickiewicza 30, 30-059 Krakow, Poland., Olejniczak Z; Institute of Nuclear Physics, Polish Academy of Sciences, ul. Radzikowskiego 152, 31-342 Krakow, Poland., Janik JF; Faculty of Energy and Fuels, AGH University, al. Mickiewicza 30, 30-059 Krakow, Poland. |
Jazyk: |
angličtina |
Zdroj: |
Materials (Basel, Switzerland) [Materials (Basel)] 2023 Sep 11; Vol. 16 (18). Date of Electronic Publication: 2023 Sep 11. |
DOI: |
10.3390/ma16186160 |
Abstrakt: |
The often overlooked and annoying aspects of the propensity of no-oxygen semiconductor kesterite, Cu 2 ZnSnS 4 , to oxidation during manipulation and storage in ambient air prompted the study on the prolonged exposure of kesterite nanopowders to air. Three precursor systems were used to make a large pool of the cubic and tetragonal polytypes of kesterite via a convenient mechanochemical synthesis route. The systems included the starting mixtures of (i) constituent elements (2Cu + Zn + Sn + 4S), (ii) selected metal sulfides and sulfur (Cu 2 S + ZnS + SnS + S), and (iii) in situ made copper alloys (from the high-energy ball milling of the metals 2Cu + Zn + Sn) and sulfur. All raw products were shown to be cubic kesterite nanopowders with defunct semiconductor properties. These nanopowders were converted to the tetragonal kesterite semiconductor by annealing at 500 °C under argon. All materials were exposed to the ambient air for 1, 3, and 6 months and were suitably analyzed after each of the stages. The characterization methods included powder XRD, FT-IR/UV-Vis/Raman/NMR spectroscopies, SEM, the determination of BET/BJH specific surface area and helium density (d He ), and direct oxygen and hydrogen-content analyses. The results confirmed the progressive, relatively fast, and pronounced oxidation of all kesterite nanopowders towards, mainly, hydrated copper(II) and zinc(II) sulfates, and tin(IV) oxide. The time-related oxidation changes were reflected in the lowering of the energy band gap E g of the remaining tetragonal kesterite component. |
Databáze: |
MEDLINE |
Externí odkaz: |
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