In2O3 thin films were deposited by the sol gel dip coating method adopting the following procedure. Clean ITO substrates were used for the deposition of the films. 10 ml of 0.33 M solution of Indium (III) nitrate was taken in a clean glass beaker. The solution was heated to 70˚C and the pH was brought to 9 by the addition of ammonia, then 1 gm of Acrylamide was added followed by the addition of 0.25 gm of N,N,bis methylene acrylamide. After 20 min, 5 mg ammonium persulphate initiator was added to this mixture. The solution became viscous. Cleaned microglass slides (2.5 cm x 7.5 cm) were immersed into the viscous solution and withdrawn at the rate of 1cm min-1. The film formed on the surface was dried in an air oven for about 15 min followed by annealing in air at different temperatures in the range of 350 - 500˚C for different durations in the range of 15 min to 90 min. Doping with Tm and Yb was done by adding 0.1 g of Yb(NO3)3 and 0.1 g of Tm(NO3)3 to the Indium nitrate solution before gelling. The doped and undoped films were dipped in N719 dye for 24 hours. a sandwich structure was formed by bonding the FTO substrate with dye coated In2O3 and a Pt counter electrode together through a hot-melt spacer, and a drop of electrolyte (0.60 M 1-butyl-3-methylimidazolium iodide (BMII), 0.03 M I2 was injected into the device through predrilled holes on the Pt counter electrode. DSSCs based on In2O3:Yb and In2O3:Tm were also fabricated via the same process. The XRD patterns of the In2O3, In2O3:Tm and In2O3:Yb. . All the patterns can be assigned to cubic phase standard card (JCPDS 06-0416) without any additional diffraction peaks. The UV–vis absorption spectra of the doped and undoped In2O3 exhibit the absorption peak of the pure In2O3 about 3.85 eV, which is consistent with the results published, and it icreases to 3.93 eV and 4.00 eV respectively as Tm and Yb are doped into In2O3. The J-V characteristics of the doped and undoped Indium oxide films indiacted that the Voc increased from 410 mV for undoped films increased to 530 mV and 630 mV for Tm and Yb doped films respectively. The Jsc increased from 2.45 mA cm-2 for the undoped films increased to 3.50 mA cm-2 and 4.25 mA cm-2 for Tm and Yb doping respectively.IPCE measurements indicated that for doped films the PCE was higher than that of undoped films. The fill factor of the films increased by doping with Tm and Yb. The larger Voc obtained with Yb doping can be explained on theb basis that the conduction band edge of Yb doped films is higher than that of undoped and Tm doped Indium oxide.
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