{"id":{"repo_id":"cambridge","oai_identifier":"oai:www.repository.cam.ac.uk:1810/286026"},"canonical_url":"https://search.dev.ndltd.org/etd/cambridge/oai:www.repository.cam.ac.uk:1810/286026","repository":{"repo_id":"cambridge","name":"Cambridge University","base_url":"https://api.repository.cam.ac.uk/server/oai/request"},"display":{"title":"Spatially Resolved Charge Transport and Recombination in Metal-Halide Perovskite Films and Solar Cells","abstract":"Metal-halide perovskites show great promise as solution-processable semiconductors for efficient solar cells and LEDs. In particular, the diffusion range of photogenerated carriers is unexpectedly long and the luminescence yield is remarkably high. While much effort has been made to improve device performance, the barriers to improving charge transport and recombination properties remain unidentified. I first explore charge transport by investigating a back-contact architecture for measurement. In collaboration with the Snaith group at Oxford, we develop a new architecture to isolate charge carriers. We prepare thin films of perovskite semiconductors over laterally-separated electron- and hole-selective materials of SnO$_{x}$ and NiO$_{x}$, respectively. Upon illumination, electrons (holes) generated over SnO$_{x}$ (NiO$_{x}$) rapidly transfer to the buried collection electrode, leaving holes (electrons) to diffuse laterally as majority carriers in the perovskite layer. We characterise charge transport parameters of electrons and holes, separately, and demonstrate that grain boundaries do not prevent charge transport. Our results show that the low mobilities found in applied-field techniques do not reflect charge diffusivity in perovskite solar cells at operating conditions. We then use the back-contact architecture to investigate recombination under large excess of one charge carrier type. Recombination velocities under these conditions are found to be below 2 cm s$^{-1}$, approaching values of high quality silicon and an order of magnitude lower than under common bipolar conditions. Similarly, diffusion lengths of electrons and holes exceed 12 $\\mu$m, an order of magnitude higher than reported in perovskite devices to date. We report back-contact solar cells with short-circuit currents as high as 18.4 mA cm$^{-2}$, giving 70% external charge-collection efficiency. We then explore the behaviour of charge carriers in continuously illuminated metal-halide perovskite devices. We show that continuous illumination of perovskite devices gives rise to a segregated charge carrier population, and we find that the distance photo-induced charges travel increases significantly under these conditions. Finally, we examine intermittancy in the photoluminescence intensity of metal-halide perovskite films.","abstract_html":"Metal-halide perovskites show great promise as solution-processable semiconductors for efficient solar cells and LEDs. In particular, the diffusion range of photogenerated carriers is unexpectedly long and the luminescence yield is remarkably high. While much effort has been made to improve device performance, the barriers to improving charge transport and recombination properties remain unidentified. I first explore charge transport by investigating a back-contact architecture for measurement. In collaboration with the Snaith group at Oxford, we develop a new architecture to isolate charge carriers. We prepare thin films of perovskite semiconductors over laterally-separated electron- and hole-selective materials of SnO<span class=\"etd-inline-math\"><sub>x</sub></span> and NiO<span class=\"etd-inline-math\"><sub>x</sub></span>, respectively. Upon illumination, electrons (holes) generated over SnO<span class=\"etd-inline-math\"><sub>x</sub></span> (NiO<span class=\"etd-inline-math\"><sub>x</sub></span>) rapidly transfer to the buried collection electrode, leaving holes (electrons) to diffuse laterally as majority carriers in the perovskite layer. We characterise charge transport parameters of electrons and holes, separately, and demonstrate that grain boundaries do not prevent charge transport. Our results show that the low mobilities found in applied-field techniques do not reflect charge diffusivity in perovskite solar cells at operating conditions. We then use the back-contact architecture to investigate recombination under large excess of one charge carrier type. Recombination velocities under these conditions are found to be below 2 cm s<span class=\"etd-inline-math\"><sup>-1</sup></span>, approaching values of high quality silicon and an order of magnitude lower than under common bipolar conditions. Similarly, diffusion lengths of electrons and holes exceed 12 <span class=\"etd-inline-math\">&mu;</span>m, an order of magnitude higher than reported in perovskite devices to date. We report back-contact solar cells with short-circuit currents as high as 18.4 mA cm<span class=\"etd-inline-math\"><sup>-2</sup></span>, giving 70% external charge-collection efficiency. We then explore the behaviour of charge carriers in continuously illuminated metal-halide perovskite devices. We show that continuous illumination of perovskite devices gives rise to a segregated charge carrier population, and we find that the distance photo-induced charges travel increases significantly under these conditions. Finally, we examine intermittancy in the photoluminescence intensity of metal-halide perovskite films.","abstract_has_math":true,"creators":["Tainter, Gregory Demaray"],"institution":"University of Cambridge","degree_name":"Doctor of Philosophy (PhD)","degree_level":"Doctoral","degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Joyce, Hannah","Deschler, Felix","Friend, Richard","Phillips, Richard"],"committee_chairs":[],"committee_members":[],"year":2018,"date_issued":"2018-12-08","date_published":"2018-12-08","updated_at":"2026-07-22T22:24:18Z","subjects":["Perovskite solar cells","photoluminescence spectroscopy","photocurrent spectroscopy","hybrid perovskites","charge transport","charge recombination"],"languages":["en"],"rights":[],"rights_urls":["https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/12e305ee-0cf4-4583-b7d4-f5a0801bcbc9/download","https://creativecommons.org/licenses/by-nc-nd/4.0/"],"identifier_entries":[{"key":"dc:creator.authoridentifier","label":"Author Identifier","values":["0000000302726940","000000029737680X","0000000207713324"],"render_values":[{"text":"0000-0003-0272-6940","href":"https://orcid.org/0000-0003-0272-6940","code":true},{"text":"0000-0002-9737-680X","href":"https://orcid.org/0000-0002-9737-680X","code":true},{"text":"0000-0002-0771-3324","href":"https://orcid.org/0000-0002-0771-3324","code":true}]}]},"links":{"outbound_url":"https://doi.org/10.17863/CAM.33347","outbound_label":"DOI","outbound_source":"dc:identifier.doi"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Joyce, Hannah","Deschler, Felix","Friend, Richard","Phillips, Richard"]},{"key":"dc:contributor.sponsor","label":"Sponsor","values":["I principally benefited from joint funding between the Nanotechnology Doctoral Training Centre and the Cambridge Overseas Trusts. In addition, I received some support from Robinson College and my supervisor, Dr Hannah Joyce."]},{"key":"dc:creator","label":"Author","values":["Tainter, Gregory Demaray"]},{"key":"dc:creator.authoridentifier","label":"Author Identifier","values":["0000000302726940","000000029737680X","0000000207713324"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.issued","label":"Date","values":["2018-12-08"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["University of Cambridge"]},{"key":"dc:relation.isreferencedby.uri","label":"Dc Relation Isreferencedby URI","values":["https://www.repository.cam.ac.uk/handle/1810/286026"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["Doctoral"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["Doctor of Philosophy (PhD)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Perovskite solar cells","photoluminescence spectroscopy","photocurrent spectroscopy","hybrid perovskites","charge transport","charge recombination"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/12e305ee-0cf4-4583-b7d4-f5a0801bcbc9/download","https://creativecommons.org/licenses/by-nc-nd/4.0/"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.doi","label":"DOI","values":["10.17863/CAM.33347"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/ab90209f-4abe-4cdd-a7ed-9f7ca20e3b4f/download"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Metal-halide perovskites show great promise as solution-processable semiconductors for efficient solar cells and LEDs. In particular, the diffusion range of photogenerated carriers is unexpectedly long and the luminescence yield is remarkably high. While much effort has been made to improve device performance, the barriers to improving charge transport and recombination properties remain unidentified. I first explore charge transport by investigating a back-contact architecture for measurement. In collaboration with the Snaith group at Oxford, we develop a new architecture to isolate charge carriers. We prepare thin films of perovskite semiconductors over laterally-separated electron- and hole-selective materials of SnO$_{x}$ and NiO$_{x}$, respectively. Upon illumination, electrons (holes) generated over SnO$_{x}$ (NiO$_{x}$) rapidly transfer to the buried collection electrode, leaving holes (electrons) to diffuse laterally as majority carriers in the perovskite layer. We characterise charge transport parameters of electrons and holes, separately, and demonstrate that grain boundaries do not prevent charge transport. Our results show that the low mobilities found in applied-field techniques do not reflect charge diffusivity in perovskite solar cells at operating conditions. We then use the back-contact architecture to investigate recombination under large excess of one charge carrier type. Recombination velocities under these conditions are found to be below 2 cm s$^{-1}$, approaching values of high quality silicon and an order of magnitude lower than under common bipolar conditions. Similarly, diffusion lengths of electrons and holes exceed 12 $\\mu$m, an order of magnitude higher than reported in perovskite devices to date. We report back-contact solar cells with short-circuit currents as high as 18.4 mA cm$^{-2}$, giving 70% external charge-collection efficiency. We then explore the behaviour of charge carriers in continuously illuminated metal-halide perovskite devices. We show that continuous illumination of perovskite devices gives rise to a segregated charge carrier population, and we find that the distance photo-induced charges travel increases significantly under these conditions. Finally, we examine intermittancy in the photoluminescence intensity of metal-halide perovskite films."]},{"key":"dc:format.checksum.md5","label":"Dc Format Checksum Md5","values":["0663b881853687e4612156d3b06ab484","87eda9de84448d1f82354d60eee3eb5f"]},{"key":"dc:title","label":"Title","values":["Spatially Resolved Charge Transport and Recombination in Metal-Halide Perovskite Films and Solar Cells"]}]}],"canonical_facts":{"dc:contributor.advisor":["Joyce, Hannah","Deschler, Felix","Friend, Richard","Phillips, Richard"],"dc:contributor.sponsor":["I principally benefited from joint funding between the Nanotechnology Doctoral Training Centre and the Cambridge Overseas Trusts. In addition, I received some support from Robinson College and my supervisor, Dr Hannah Joyce."],"dc:creator":["Tainter, Gregory Demaray"],"dc:creator.authoridentifier":["0000000302726940","000000029737680X","0000000207713324"],"dc:date.issued":["2018-12-08"],"dc:description.abstract":["Metal-halide perovskites show great promise as solution-processable semiconductors for efficient solar cells and LEDs. In particular, the diffusion range of photogenerated carriers is unexpectedly long and the luminescence yield is remarkably high. While much effort has been made to improve device performance, the barriers to improving charge transport and recombination properties remain unidentified. I first explore charge transport by investigating a back-contact architecture for measurement. In collaboration with the Snaith group at Oxford, we develop a new architecture to isolate charge carriers. We prepare thin films of perovskite semiconductors over laterally-separated electron- and hole-selective materials of SnO$_{x}$ and NiO$_{x}$, respectively. Upon illumination, electrons (holes) generated over SnO$_{x}$ (NiO$_{x}$) rapidly transfer to the buried collection electrode, leaving holes (electrons) to diffuse laterally as majority carriers in the perovskite layer. We characterise charge transport parameters of electrons and holes, separately, and demonstrate that grain boundaries do not prevent charge transport. Our results show that the low mobilities found in applied-field techniques do not reflect charge diffusivity in perovskite solar cells at operating conditions. We then use the back-contact architecture to investigate recombination under large excess of one charge carrier type. Recombination velocities under these conditions are found to be below 2 cm s$^{-1}$, approaching values of high quality silicon and an order of magnitude lower than under common bipolar conditions. Similarly, diffusion lengths of electrons and holes exceed 12 $\\mu$m, an order of magnitude higher than reported in perovskite devices to date. We report back-contact solar cells with short-circuit currents as high as 18.4 mA cm$^{-2}$, giving 70% external charge-collection efficiency. We then explore the behaviour of charge carriers in continuously illuminated metal-halide perovskite devices. We show that continuous illumination of perovskite devices gives rise to a segregated charge carrier population, and we find that the distance photo-induced charges travel increases significantly under these conditions. Finally, we examine intermittancy in the photoluminescence intensity of metal-halide perovskite films."],"dc:format.checksum.md5":["0663b881853687e4612156d3b06ab484","87eda9de84448d1f82354d60eee3eb5f"],"dc:identifier.doi":["10.17863/CAM.33347"],"dc:identifier.uri":["https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/ab90209f-4abe-4cdd-a7ed-9f7ca20e3b4f/download"],"dc:language":["en"],"dc:publisher.institution":["University of Cambridge"],"dc:relation.isreferencedby.uri":["https://www.repository.cam.ac.uk/handle/1810/286026"],"dc:rights":["https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/12e305ee-0cf4-4583-b7d4-f5a0801bcbc9/download","https://creativecommons.org/licenses/by-nc-nd/4.0/"],"dc:subject":["Perovskite solar cells","photoluminescence spectroscopy","photocurrent spectroscopy","hybrid perovskites","charge transport","charge recombination"],"dc:title":["Spatially Resolved Charge Transport and Recombination in Metal-Halide Perovskite Films and Solar Cells"],"dc:type":["Thesis"],"dc:type.qualificationlevel":["Doctoral"],"dc:type.qualificationname":["Doctor of Philosophy (PhD)"]},"updated_at":"2026-07-22T22:24:18Z"}