STUDIES ON SOLAR ENERGY CONVERSION DEVICES BASED ON DYESENSITIZED NANO-POROUS TI02 ELECTRODES AND PHOTOCATALYTIC HEAVY METAL REMOVAL FROM AQUEOUS MEDIA USING TI02 PHOTOCATALYSTS

Show simple item record

dc.contributor.author Wijayantha, Kahagala Gamage Upul
dc.date.accessioned 2020-01-25T06:50:04Z
dc.date.available 2020-01-25T06:50:04Z
dc.date.issued 1997-03
dc.identifier.citation Wijayantha, Kahagala Gamage Upul (1997). STUDIES ON SOLAR ENERGY CONVERSION DEVICES BASED ON DYESENSITIZED NANO-POROUS TI02 ELECTRODES AND PHOTOCATALYTIC HEAVY METAL REMOVAL FROM AQUEOUS MEDIA USING TI02 PHOTOCATALYSTS. Matara, Department of Chemistry, University of Ruhuna, Matara. en_US
dc.identifier.other 111787
dc.identifier.uri http://ir.lib.ruh.ac.lk/xmlui/handle/iruor/111
dc.description.abstract This study was undertaken to identify a more convenient prototype dye, compared to the earlier reported cyanidin, for the fabrication of the dye-sensitized nano-porous solid-state photovoltaic device and to further investigate the performance of the device. It was found that copper chlorophyllin can be successfully employed for the fabrication of the n-Ti02/copper chlorophyllin/p-Cul cell. The photo-excited pigment is found to inject electrons into n-Ti02 and holes into p-Cul generating photocurrent and photovoltage that are significant for a solid-state dye-sensitized cell. However, in the presence of oxygen, moisture and UV light the cell exhibits a rapid decay in photocurrent and photovoltage. It was found that the decay of the photocurrent and photovoltage in n-Ti02/copper chlorophyllin/p-Cul cell is almost completely suppressed, provided oxygen, moisture and UV-light (X < 348 nm) are excluded. It was also observed that the peak at 360 nm originating from bandgap excitation of Ti02 in the photocurrent action spectrum of the n-Ti02/cyanidin/p-CuI of n-type semiconductor/dye/p-type semiconductor (NDP) cell, attains a maximum for a certain critical surface concentration of cyanidin. Inorganic heavy metal ions form complex anions with sacrificial oxidizing agents such as citrate ions and tartarate ions. In the oxidative photodegradation of these complexes with TiO^, metals are found to become deposited on Ti02. The reactions are sufficiently sensitive to sunlight and, for practical application, Ti02 can be confined in a transparent dialysis bag to facilitate the disposal of extracted metals. Photocatalytic removal of Cu2+ from aqueous media in the presence of tartarate ions was carried out as a model system by this method. As an alternative method, It was found that Ti02 particles affixed to the surface of polypropylene films can be conveniently utilized to extract metals such as Cd, Pb, Hg, Ag, Bi and Cu in the presence of citric acid which acts as a sacrificial and complexing agent. As an example, photoextraction of lead from aqueous solution is described. en_US
dc.description.sponsorship Institute of Fundamental Studies Physical & Chemical Sciences Group Kandy, Sri Lanka. en_US
dc.language.iso en en_US
dc.publisher University of Ruhuna en_US
dc.relation.ispartofseries ;111787
dc.subject solar energy en_US
dc.subject dyesensitized nano-porous en_US
dc.subject electrodes en_US
dc.subject photocatalytic en_US
dc.title STUDIES ON SOLAR ENERGY CONVERSION DEVICES BASED ON DYESENSITIZED NANO-POROUS TI02 ELECTRODES AND PHOTOCATALYTIC HEAVY METAL REMOVAL FROM AQUEOUS MEDIA USING TI02 PHOTOCATALYSTS en_US
dc.type Masters Thesis en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Browse

My Account