Ultrafast spectroscopy of charge separation, transport and recombination processes in functional materials for thin-film photovoltaics
<p>Dye-sensitized solar cells (DSSCs) and perovskite solar cells are emerging as promising potential low-cost alternatives to established crystalline silicon photovoltaics. Of the employed functional materials, however, many fundamental optoelectronic properties governing photovoltaic device o...
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| Format: | Thesis |
| Language: | English |
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2014
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| _version_ | 1817932188051570688 |
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| author | Wehrenfennig, C |
| author2 | Herz, L |
| author_facet | Herz, L Wehrenfennig, C |
| author_sort | Wehrenfennig, C |
| collection | OXFORD |
| description | <p>Dye-sensitized solar cells (DSSCs) and perovskite solar cells are emerging as promising potential low-cost alternatives to established crystalline silicon photovoltaics. Of the employed functional materials, however, many fundamental optoelectronic properties governing photovoltaic device operation are not sufficiently well understood. This thesis reports on a series of studies using ultrafast THz and photoluminescence spectroscopy on two classes of such materials, providing insight into the dynamics of charge-transport and recombination processes following photoexcitation.</p> <p>For TiO<sub>2</sub>-nanotubes, which have been proposed as easy-to-fabricate electron transporters for DSSCs, fast, shallow electron trapping is identified as a limiting factor for efficient charge collection. Trapping lifetimes are found to be about an order of magnitude shorter than in the prevalently employed sintered nanoparticles under similar excitation conditions and trap saturation effects are not observed, even at very high excitation densities.</p> <p>In organo-lead halide perovskites - specifically CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> and CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3-x</sub>Cl<sub>x</sub>, which have only recently emerged as highly efficient absorbers and charge transporters for thin-film solar cells, carrier mobilities and fundamental recombination dynamics are revealed. Extremely low bi-molecular recombination rates at least four orders of magnitude below the prediction of Langevin's model are found as well as relatively high charge-carrier mobilities in comparison to other solution-processable materials. Furthermore a very low influence of trap-mediated recombination channels was observed. Due to a combination of these factors, diffusion lengths reach hundreds of nanometres for CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> and several microns for CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3-x</sub>Cl<sub>x</sub>. These results are shown to hold for both, solution processed and vapour-deposited CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3-x</sub>Cl<sub>x</sub> and underline the superb suitability of the materials as absorbers in solar cells, even in planar heterojunction architectures.</p> <p>The THz-frequency spectrum of the conductivity of the investigated perovskites is consistent with Drude-like charge transport additionally exhibiting weak signatures of phonon coupling. These coupling effects are also reflected in the luminescence of CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3-x</sub>Cl<sub>x</sub>, where they are believed to be the cause of the observed homogeneous spectral broadening. Further photoluminescence measurements were performed at temperatures between 4 K and room temperature to study the nature of recombination pathways in the material.</p> |
| first_indexed | 2024-03-06T19:37:25Z |
| format | Thesis |
| id | oxford-uuid:1f812413-4a2f-418f-a7fd-d749e88cc2e1 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-12-09T03:33:56Z |
| publishDate | 2014 |
| record_format | dspace |
| spelling | oxford-uuid:1f812413-4a2f-418f-a7fd-d749e88cc2e12024-12-01T17:30:07ZUltrafast spectroscopy of charge separation, transport and recombination processes in functional materials for thin-film photovoltaicsThesishttp://purl.org/coar/resource_type/c_db06uuid:1f812413-4a2f-418f-a7fd-d749e88cc2e1Condensed Matter PhysicsEnglishOxford University Research Archive - Valet2014Wehrenfennig, CHerz, L<p>Dye-sensitized solar cells (DSSCs) and perovskite solar cells are emerging as promising potential low-cost alternatives to established crystalline silicon photovoltaics. Of the employed functional materials, however, many fundamental optoelectronic properties governing photovoltaic device operation are not sufficiently well understood. This thesis reports on a series of studies using ultrafast THz and photoluminescence spectroscopy on two classes of such materials, providing insight into the dynamics of charge-transport and recombination processes following photoexcitation.</p> <p>For TiO<sub>2</sub>-nanotubes, which have been proposed as easy-to-fabricate electron transporters for DSSCs, fast, shallow electron trapping is identified as a limiting factor for efficient charge collection. Trapping lifetimes are found to be about an order of magnitude shorter than in the prevalently employed sintered nanoparticles under similar excitation conditions and trap saturation effects are not observed, even at very high excitation densities.</p> <p>In organo-lead halide perovskites - specifically CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> and CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3-x</sub>Cl<sub>x</sub>, which have only recently emerged as highly efficient absorbers and charge transporters for thin-film solar cells, carrier mobilities and fundamental recombination dynamics are revealed. Extremely low bi-molecular recombination rates at least four orders of magnitude below the prediction of Langevin's model are found as well as relatively high charge-carrier mobilities in comparison to other solution-processable materials. Furthermore a very low influence of trap-mediated recombination channels was observed. Due to a combination of these factors, diffusion lengths reach hundreds of nanometres for CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> and several microns for CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3-x</sub>Cl<sub>x</sub>. These results are shown to hold for both, solution processed and vapour-deposited CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3-x</sub>Cl<sub>x</sub> and underline the superb suitability of the materials as absorbers in solar cells, even in planar heterojunction architectures.</p> <p>The THz-frequency spectrum of the conductivity of the investigated perovskites is consistent with Drude-like charge transport additionally exhibiting weak signatures of phonon coupling. These coupling effects are also reflected in the luminescence of CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3-x</sub>Cl<sub>x</sub>, where they are believed to be the cause of the observed homogeneous spectral broadening. Further photoluminescence measurements were performed at temperatures between 4 K and room temperature to study the nature of recombination pathways in the material.</p> |
| spellingShingle | Condensed Matter Physics Wehrenfennig, C Ultrafast spectroscopy of charge separation, transport and recombination processes in functional materials for thin-film photovoltaics |
| title | Ultrafast spectroscopy of charge separation, transport and recombination processes in functional materials for thin-film photovoltaics |
| title_full | Ultrafast spectroscopy of charge separation, transport and recombination processes in functional materials for thin-film photovoltaics |
| title_fullStr | Ultrafast spectroscopy of charge separation, transport and recombination processes in functional materials for thin-film photovoltaics |
| title_full_unstemmed | Ultrafast spectroscopy of charge separation, transport and recombination processes in functional materials for thin-film photovoltaics |
| title_short | Ultrafast spectroscopy of charge separation, transport and recombination processes in functional materials for thin-film photovoltaics |
| title_sort | ultrafast spectroscopy of charge separation transport and recombination processes in functional materials for thin film photovoltaics |
| topic | Condensed Matter Physics |
| work_keys_str_mv | AT wehrenfennigc ultrafastspectroscopyofchargeseparationtransportandrecombinationprocessesinfunctionalmaterialsforthinfilmphotovoltaics |