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Charge Recombination Dynamics in Sensitized SnO2/TiO2 Core/Shell Photoanodes
Studies have been conducted to examine the mechanisms of charge recombination in dye-sensitized SnO2/TiO2 core/shell films. Nanostructured SnO2/TiO2 core/shell films varying in TiO2 shell thicknesses were prepared via atomic layer deposition and sensitized with a phosphonate-derivatized ruthenium ch...
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Published in: | Journal of physical chemistry. C 2015-12, Vol.119 (51), p.28353-28360 |
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creator | Knauf, Robin R Kalanyan, Berç Parsons, Gregory N Dempsey, Jillian L |
description | Studies have been conducted to examine the mechanisms of charge recombination in dye-sensitized SnO2/TiO2 core/shell films. Nanostructured SnO2/TiO2 core/shell films varying in TiO2 shell thicknesses were prepared via atomic layer deposition and sensitized with a phosphonate-derivatized ruthenium chromophore [Ru(bpy)2(4,4′-(PO3H2)2bpy)]2+. Transient absorption spectroscopy was used to study the interfacial charge recombination dynamics for these core/shell materials. Charge recombination for sensitized, as-deposited SnO2/TiO2 core/shell systems is dominated by a tunneling mechanism for shell thicknesses between 0 and 3.2 nm, with β = 0.25 Å–1. For shell thicknesses greater than 3.2 nm, recombination primarily proceeds directly via electrons localized in the relatively thick TiO2 shell. Annealing the SnO2/TiO2 core/shell structure at 450 °C affects the recombination dynamics substantially; charge recombination dynamics for the annealed films do not show a dependence on shell thickness and are comparable to ZrO2/TiO2 control samples, suggesting the annealing process perturbs the core/shell interface. This analysis of charge recombination dynamics indicates that there is an optimum shell thickness to maximize charge separation lifetimes in dye-sensitized core/shell photoanodes and that the nature of the core/shell interface influences the efficacy of these materials. |
doi_str_mv | 10.1021/acs.jpcc.5b10574 |
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Center for Solar Fuels (UNC EFRC)</creatorcontrib><description>Studies have been conducted to examine the mechanisms of charge recombination in dye-sensitized SnO2/TiO2 core/shell films. Nanostructured SnO2/TiO2 core/shell films varying in TiO2 shell thicknesses were prepared via atomic layer deposition and sensitized with a phosphonate-derivatized ruthenium chromophore [Ru(bpy)2(4,4′-(PO3H2)2bpy)]2+. Transient absorption spectroscopy was used to study the interfacial charge recombination dynamics for these core/shell materials. Charge recombination for sensitized, as-deposited SnO2/TiO2 core/shell systems is dominated by a tunneling mechanism for shell thicknesses between 0 and 3.2 nm, with β = 0.25 Å–1. For shell thicknesses greater than 3.2 nm, recombination primarily proceeds directly via electrons localized in the relatively thick TiO2 shell. Annealing the SnO2/TiO2 core/shell structure at 450 °C affects the recombination dynamics substantially; charge recombination dynamics for the annealed films do not show a dependence on shell thickness and are comparable to ZrO2/TiO2 control samples, suggesting the annealing process perturbs the core/shell interface. This analysis of charge recombination dynamics indicates that there is an optimum shell thickness to maximize charge separation lifetimes in dye-sensitized core/shell photoanodes and that the nature of the core/shell interface influences the efficacy of these materials.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/acs.jpcc.5b10574</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>catalysis (heterogeneous) ; catalysis (homogeneous) ; charge transport ; electrodes - solar ; hydrogen and fuel cells ; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY ; materials and chemistry by design ; photosynthesis (natural and artificial) ; solar (fuels) ; solar (photovoltaic) ; synthesis (novel materials) ; synthesis (self-assembly)</subject><ispartof>Journal of physical chemistry. 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Center for Solar Fuels (UNC EFRC)</creatorcontrib><title>Charge Recombination Dynamics in Sensitized SnO2/TiO2 Core/Shell Photoanodes</title><title>Journal of physical chemistry. C</title><addtitle>J. Phys. Chem. C</addtitle><description>Studies have been conducted to examine the mechanisms of charge recombination in dye-sensitized SnO2/TiO2 core/shell films. Nanostructured SnO2/TiO2 core/shell films varying in TiO2 shell thicknesses were prepared via atomic layer deposition and sensitized with a phosphonate-derivatized ruthenium chromophore [Ru(bpy)2(4,4′-(PO3H2)2bpy)]2+. Transient absorption spectroscopy was used to study the interfacial charge recombination dynamics for these core/shell materials. Charge recombination for sensitized, as-deposited SnO2/TiO2 core/shell systems is dominated by a tunneling mechanism for shell thicknesses between 0 and 3.2 nm, with β = 0.25 Å–1. For shell thicknesses greater than 3.2 nm, recombination primarily proceeds directly via electrons localized in the relatively thick TiO2 shell. Annealing the SnO2/TiO2 core/shell structure at 450 °C affects the recombination dynamics substantially; charge recombination dynamics for the annealed films do not show a dependence on shell thickness and are comparable to ZrO2/TiO2 control samples, suggesting the annealing process perturbs the core/shell interface. This analysis of charge recombination dynamics indicates that there is an optimum shell thickness to maximize charge separation lifetimes in dye-sensitized core/shell photoanodes and that the nature of the core/shell interface influences the efficacy of these materials.</description><subject>catalysis (heterogeneous)</subject><subject>catalysis (homogeneous)</subject><subject>charge transport</subject><subject>electrodes - solar</subject><subject>hydrogen and fuel cells</subject><subject>INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY</subject><subject>materials and chemistry by design</subject><subject>photosynthesis (natural and artificial)</subject><subject>solar (fuels)</subject><subject>solar (photovoltaic)</subject><subject>synthesis (novel materials)</subject><subject>synthesis (self-assembly)</subject><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNo9kM1LAzEUxIMoWKt3j8Gz2yZ5G7M9yvoJhYrtPaRvX9yUNpEmHvSvd7XiaYZhGIYfY5dSTKRQcuowTzbviBO9lkKb-oiN5AxUZWqtj_99bU7ZWc4bITQICSM2b3u3fyP-Sph26xBdCSnyu8_odgEzD5EvKeZQwhd1fBkXaroKC8XbtKfpsqftlr_0qSQXU0f5nJ14t8108adjtnq4X7VP1Xzx-NzeziunZk2pCITwN9R0TkoF0nggo9eInhCUJnLUea81EorG0czXBK5RSmvwtagVjNnVYTblEmzGUAh7TDESFiuhMQrMULo-lAYwdpM-9nF4ZKWwP7TsbzjQsn-04BvxSl9G</recordid><startdate>20151224</startdate><enddate>20151224</enddate><creator>Knauf, Robin R</creator><creator>Kalanyan, Berç</creator><creator>Parsons, Gregory N</creator><creator>Dempsey, Jillian L</creator><general>American Chemical Society</general><scope>OIOZB</scope><scope>OTOTI</scope></search><sort><creationdate>20151224</creationdate><title>Charge Recombination Dynamics in Sensitized SnO2/TiO2 Core/Shell Photoanodes</title><author>Knauf, Robin R ; Kalanyan, Berç ; Parsons, Gregory N ; Dempsey, Jillian L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a298t-e300f6e8da112317f3e75bccfec325eeaedff55cec08ae9f4e3a822553f40423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>catalysis (heterogeneous)</topic><topic>catalysis (homogeneous)</topic><topic>charge transport</topic><topic>electrodes - solar</topic><topic>hydrogen and fuel cells</topic><topic>INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY</topic><topic>materials and chemistry by design</topic><topic>photosynthesis (natural and artificial)</topic><topic>solar (fuels)</topic><topic>solar (photovoltaic)</topic><topic>synthesis (novel materials)</topic><topic>synthesis (self-assembly)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Knauf, Robin R</creatorcontrib><creatorcontrib>Kalanyan, Berç</creatorcontrib><creatorcontrib>Parsons, Gregory N</creatorcontrib><creatorcontrib>Dempsey, Jillian L</creatorcontrib><creatorcontrib>Energy Frontier Research Centers (EFRC) (United States). Center for Solar Fuels (UNC EFRC)</creatorcontrib><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Knauf, Robin R</au><au>Kalanyan, Berç</au><au>Parsons, Gregory N</au><au>Dempsey, Jillian L</au><aucorp>Energy Frontier Research Centers (EFRC) (United States). Center for Solar Fuels (UNC EFRC)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Charge Recombination Dynamics in Sensitized SnO2/TiO2 Core/Shell Photoanodes</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2015-12-24</date><risdate>2015</risdate><volume>119</volume><issue>51</issue><spage>28353</spage><epage>28360</epage><pages>28353-28360</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>Studies have been conducted to examine the mechanisms of charge recombination in dye-sensitized SnO2/TiO2 core/shell films. Nanostructured SnO2/TiO2 core/shell films varying in TiO2 shell thicknesses were prepared via atomic layer deposition and sensitized with a phosphonate-derivatized ruthenium chromophore [Ru(bpy)2(4,4′-(PO3H2)2bpy)]2+. Transient absorption spectroscopy was used to study the interfacial charge recombination dynamics for these core/shell materials. Charge recombination for sensitized, as-deposited SnO2/TiO2 core/shell systems is dominated by a tunneling mechanism for shell thicknesses between 0 and 3.2 nm, with β = 0.25 Å–1. For shell thicknesses greater than 3.2 nm, recombination primarily proceeds directly via electrons localized in the relatively thick TiO2 shell. Annealing the SnO2/TiO2 core/shell structure at 450 °C affects the recombination dynamics substantially; charge recombination dynamics for the annealed films do not show a dependence on shell thickness and are comparable to ZrO2/TiO2 control samples, suggesting the annealing process perturbs the core/shell interface. This analysis of charge recombination dynamics indicates that there is an optimum shell thickness to maximize charge separation lifetimes in dye-sensitized core/shell photoanodes and that the nature of the core/shell interface influences the efficacy of these materials.</abstract><cop>United States</cop><pub>American Chemical Society</pub><doi>10.1021/acs.jpcc.5b10574</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | catalysis (heterogeneous) catalysis (homogeneous) charge transport electrodes - solar hydrogen and fuel cells INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY materials and chemistry by design photosynthesis (natural and artificial) solar (fuels) solar (photovoltaic) synthesis (novel materials) synthesis (self-assembly) |
title | Charge Recombination Dynamics in Sensitized SnO2/TiO2 Core/Shell Photoanodes |
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