Abstract
We report a new approach for fabricating pyrite (cubic FeS2) thin films via a non-vacuum direct solution coating route using iron-acetate dissolved in ethanol as a precursor solution. The precursor ink is deposited by spin coating and annealed in air at 300 °C to produce amorphous iron oxide films. Subsequent heat treatment of the iron oxide films in a sulfur environment at 450 °C results in the formation of phase-pure, carbon-free, large-grained pyrite films. In particular, the phase evolution during sulfurization is systematically investigated, focusing on the effects of the principal experimental variables such as temperature and pressure. As the temperature increases, iron oxide first begins to transform into marcasite (orthorhombic FeS2) and then is completely converted to pyrite. Further increasing the temperature above 500 °C induces the decomposition of pyrite into pyrrhotite (Fe1-xS) and sulfur vapor. The decomposition is also strongly dependent on the partial pressure of sulfur: as the pressure decreases, the decomposition occurs at lower temperature. The synthesized single-phase pyrite films show an indirect band gap of 0.94 eV, a strong anodic photocurrent based on photo-electrochemical measurements, and n-type semiconducting properties based on Mott-Schottky analysis. Thus, the films demonstrate great potential for use as absorbing layers in solar cells. This journal is
| Original language | English |
|---|---|
| Pages (from-to) | 17779-17786 |
| Number of pages | 8 |
| Journal | Journal of Materials Chemistry A |
| Volume | 2 |
| Issue number | 42 |
| DOIs | |
| Publication status | Published - 2014 Nov 14 |
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All Science Journal Classification (ASJC) codes
- Chemistry(all)
- Renewable Energy, Sustainability and the Environment
- Materials Science(all)
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Iron pyrite thin films deposited via non-vacuum direct coating of iron-salt/ethanol-based precursor solutions. / Ahn, Sejin; Moon, Dong Gwon; Cho, Ara; Park, Joo Hyung; Ahn, Soohoon; Kwon, Hyuksang; Cho, Yong Soo.
In: Journal of Materials Chemistry A, Vol. 2, No. 42, 14.11.2014, p. 17779-17786.Research output: Contribution to journal › Article
TY - JOUR
T1 - Iron pyrite thin films deposited via non-vacuum direct coating of iron-salt/ethanol-based precursor solutions
AU - Ahn, Sejin
AU - Moon, Dong Gwon
AU - Cho, Ara
AU - Park, Joo Hyung
AU - Ahn, Soohoon
AU - Kwon, Hyuksang
AU - Cho, Yong Soo
PY - 2014/11/14
Y1 - 2014/11/14
N2 - We report a new approach for fabricating pyrite (cubic FeS2) thin films via a non-vacuum direct solution coating route using iron-acetate dissolved in ethanol as a precursor solution. The precursor ink is deposited by spin coating and annealed in air at 300 °C to produce amorphous iron oxide films. Subsequent heat treatment of the iron oxide films in a sulfur environment at 450 °C results in the formation of phase-pure, carbon-free, large-grained pyrite films. In particular, the phase evolution during sulfurization is systematically investigated, focusing on the effects of the principal experimental variables such as temperature and pressure. As the temperature increases, iron oxide first begins to transform into marcasite (orthorhombic FeS2) and then is completely converted to pyrite. Further increasing the temperature above 500 °C induces the decomposition of pyrite into pyrrhotite (Fe1-xS) and sulfur vapor. The decomposition is also strongly dependent on the partial pressure of sulfur: as the pressure decreases, the decomposition occurs at lower temperature. The synthesized single-phase pyrite films show an indirect band gap of 0.94 eV, a strong anodic photocurrent based on photo-electrochemical measurements, and n-type semiconducting properties based on Mott-Schottky analysis. Thus, the films demonstrate great potential for use as absorbing layers in solar cells. This journal is
AB - We report a new approach for fabricating pyrite (cubic FeS2) thin films via a non-vacuum direct solution coating route using iron-acetate dissolved in ethanol as a precursor solution. The precursor ink is deposited by spin coating and annealed in air at 300 °C to produce amorphous iron oxide films. Subsequent heat treatment of the iron oxide films in a sulfur environment at 450 °C results in the formation of phase-pure, carbon-free, large-grained pyrite films. In particular, the phase evolution during sulfurization is systematically investigated, focusing on the effects of the principal experimental variables such as temperature and pressure. As the temperature increases, iron oxide first begins to transform into marcasite (orthorhombic FeS2) and then is completely converted to pyrite. Further increasing the temperature above 500 °C induces the decomposition of pyrite into pyrrhotite (Fe1-xS) and sulfur vapor. The decomposition is also strongly dependent on the partial pressure of sulfur: as the pressure decreases, the decomposition occurs at lower temperature. The synthesized single-phase pyrite films show an indirect band gap of 0.94 eV, a strong anodic photocurrent based on photo-electrochemical measurements, and n-type semiconducting properties based on Mott-Schottky analysis. Thus, the films demonstrate great potential for use as absorbing layers in solar cells. This journal is
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U2 - 10.1039/c4ta03397c
DO - 10.1039/c4ta03397c
M3 - Article
AN - SCOPUS:84907801205
VL - 2
SP - 17779
EP - 17786
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
SN - 2050-7488
IS - 42
ER -