Dimesso, L. ; Dimamay, M. ; Hamburger, M. ; Jaegermann, W. (2014):
Properties of CH3NH3PbX3 (X = I, Br, Cl) Powders as Precursors for Organic/Inorganic Solar Cells.
In: Chemistry of Materials, 26 (23), pp. 6762-6770. ACS Publications, ISSN 0897-4756,
[Article]
Abstract
CH3NH3PbX3 (X = Cl, Br, I) perovskites were prepared by a self-organization processes using different precursor solutions. The XRD analysis indicates the formation, at room temperature, of a tetragonal structure (space group I4/mcm) for X = I, of a cubic structure (space group Pm3̅m) for X = Br, and of centro-symmetric cubic structure (space group Pm3m) for X = Cl, respectively. The structural analysis revealed the formation of CH3NH3Cl as secondary phase in the Cl-containing system. The morphological investigation revealed the formation of rhombo-hexagonal dodecahedra crystallite for X = I, Br, whereas cube-like aggregates were observed for X = Cl. The thermogravimetric analysis performed in air did not reveal any loss until 250 °C for X = I and 300 °C for X = Br, respectively, whereas the differential thermal analysis (DTA) detected two endothermic thermal events (at 336 and 409 °C) for X = I and one only (379 °C) for X = Br, respectively. The infrared spectra (IR) of the powders conformed to the 3-fold symmetry of the methylammonium ion which rotates around the C–N axis. Optical absorption measurements indicated that the CH3NH3PbX3 systems behave as direct-gap semiconductors with energy band gaps of 1.53 eV for X = I, 2.20 eV for X = Br, and 3.00 eV for X = Cl, respectively, at room temperature. The direct-gap semiconductivity for X = I and X = Br was confirmed by the photoluminescence emission measurements, whereas the compound for X = Cl is inactive. I-containing powders were dissolved in an organic solvent (dimethyl-formamide, DMF). The dispersion (100–300 μL) was dropped on glassy substrates on which thick films were obtained by spin-coating and thermal treatment at 120 °C for ca. 5 min. The preparation of the layers was performed in air at room temperature.
| Item Type: | Article |
|---|---|
| Erschienen: | 2014 |
| Creators: | Dimesso, L. ; Dimamay, M. ; Hamburger, M. ; Jaegermann, W. |
| Title: | Properties of CH3NH3PbX3 (X = I, Br, Cl) Powders as Precursors for Organic/Inorganic Solar Cells |
| Language: | English |
| Abstract: | CH3NH3PbX3 (X = Cl, Br, I) perovskites were prepared by a self-organization processes using different precursor solutions. The XRD analysis indicates the formation, at room temperature, of a tetragonal structure (space group I4/mcm) for X = I, of a cubic structure (space group Pm3̅m) for X = Br, and of centro-symmetric cubic structure (space group Pm3m) for X = Cl, respectively. The structural analysis revealed the formation of CH3NH3Cl as secondary phase in the Cl-containing system. The morphological investigation revealed the formation of rhombo-hexagonal dodecahedra crystallite for X = I, Br, whereas cube-like aggregates were observed for X = Cl. The thermogravimetric analysis performed in air did not reveal any loss until 250 °C for X = I and 300 °C for X = Br, respectively, whereas the differential thermal analysis (DTA) detected two endothermic thermal events (at 336 and 409 °C) for X = I and one only (379 °C) for X = Br, respectively. The infrared spectra (IR) of the powders conformed to the 3-fold symmetry of the methylammonium ion which rotates around the C–N axis. Optical absorption measurements indicated that the CH3NH3PbX3 systems behave as direct-gap semiconductors with energy band gaps of 1.53 eV for X = I, 2.20 eV for X = Br, and 3.00 eV for X = Cl, respectively, at room temperature. The direct-gap semiconductivity for X = I and X = Br was confirmed by the photoluminescence emission measurements, whereas the compound for X = Cl is inactive. I-containing powders were dissolved in an organic solvent (dimethyl-formamide, DMF). The dispersion (100–300 μL) was dropped on glassy substrates on which thick films were obtained by spin-coating and thermal treatment at 120 °C for ca. 5 min. The preparation of the layers was performed in air at room temperature. |
| Journal or Publication Title: | Chemistry of Materials |
| Volume of the journal: | 26 |
| Issue Number: | 23 |
| Publisher: | ACS Publications |
| Divisions: | 11 Department of Materials and Earth Sciences > Material Science > Surface Science 11 Department of Materials and Earth Sciences > Material Science 11 Department of Materials and Earth Sciences |
| Date Deposited: | 27 Feb 2015 12:07 |
| URL / URN: | http://dx.doi.org/10.1021/cm503240k |
| Identification Number: | doi:10.1021/cm503240k |
| PPN: | |
| Funders: | The authors thank the Federal Ministry of Research and Development (BMBF) for the financial support during this work. |
| Export: | |
| Suche nach Titel in: | TUfind oder in Google |
 |
Send an inquiry |
Options (only for editors)
 |
Show editorial Details |
Drucken
Impressum