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http://hdl.handle.net/10266/5165
Title: | Influence of Ag-Cu Binary Metal Photo Deposition Over TiO2 on its Photocatalytic Activity under Sunlight Irradiation |
Authors: | Deeksha |
Supervisor: | Pal, Bonamali Singh, Satnam |
Keywords: | Photodeposition;Ag-Cu-TiO2;Neutral red;Photocatalytical activity |
Issue Date: | 6-Aug-2018 |
Abstract: | The present work demonstrates the preparation and photocatalytic activity of mono (Ag/Cu) and binary (Ag-Cu) metal deposited TiO2 photocatalysts using photo-deposition method. Various properties of catalysts were studied by DRS, PL, DLS and SEM-EDS analysis. Ag-Cu@TiO2 catalysts were found to display considerable red shift of plasmon band (460-700 nm) enhancement in a broad visible region in the absorption spectra. The effects of different amount (1-5) wt % of Ag-Cu binary metal and by varying photo-deposition time (15 - 90 min.) time on the photodegradation of Neutral red dye have been evaluated under solar light irradiation. DLS measurements showed that with increase in photo-deposition time, hydrodynamic size of various photocatalysts increase (from 72 nm of bare TiO2to 386 nm for Ag/Cu deposited TiO2) due to continuous growth of deposited Ag-Cu on TiO2 surface. From the SEM-EDS analysis it was also confirmed that during the photo-deposition of binary metal (Ag-Cu), Ag metal with higher reduction potential gets deposited first followed by Cu. Further, the photocatalytic activity of various catalysts under solar irradiations revealed that binary metal deposited Ag3- Cu3@TiO2always showed considerable increase in the photodegradation rate of dye relative to mono metal Ag/Cu-TiO2 catalysts. It has been realized that the appropriate metal NP distribution and their growth control onto TiO2 plays an important role for the effectiveness of a photocatalytic process. |
Description: | Master of Science- Chemistry |
URI: | http://hdl.handle.net/10266/5165 |
Appears in Collections: | Masters Theses@SCBC |
Files in This Item:
File | Description | Size | Format | |
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Deeksha Dogra Thesis.pdf | 2.61 MB | Adobe PDF | ![]() View/Open |
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