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Quantum Dot Solar Cells. Harvesting Light Energy with CdSe Nanocrystals Molecularly Linked to Mesoscopic TiO<sub>2</sub> Films

István RobelContribution from the Notre Dame Radiation Laboratory, Department of Chemistry and Biochemistry, Department of Chemical and Biomolecular Engineering, and Department of Physics, University of Notre Dame, Notre Dame, Indiana 46556-5674Vaidyanathan SubramanianContribution from the Notre Dame Radiation Laboratory, Department of Chemistry and Biochemistry, Department of Chemical and Biomolecular Engineering, and Department of Physics, University of Notre Dame, Notre Dame, Indiana 46556-5674Masaru KunoContribution from the Notre Dame Radiation Laboratory, Department of Chemistry and Biochemistry, Department of Chemical and Biomolecular Engineering, and Department of Physics, University of Notre Dame, Notre Dame, Indiana 46556-5674Prashant V. KamatContribution from the Notre Dame Radiation Laboratory, Department of Chemistry and Biochemistry, Department of Chemical and Biomolecular Engineering, and Department of Physics, University of Notre Dame, Notre Dame, Indiana 46556-5674
2006en
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By using bifunctional surface modifiers (SH-R-COOH), CdSe quantum dots (QDs) have been assembled onto mesoscopic TiO(2) films. Upon visible light excitation, CdSe QDs inject electrons into TiO(2) nanocrystallites. Femtosecond transient absorption as well as emission quenching experiments confirm the injection from the excited state of CdSe QDs into TiO(2) nanoparticles. Electron transfer from the thermally relaxed s-state occurs over a wide range of rate constant values between 7.3 x 10(9) and 1.95 x 10(11) s(-1). The injected charge carriers in a CdSe-modified TiO(2) film can be collected at a conducting electrode to generate a photocurrent. The TiO(2)-CdSe composite, when employed as a photoanode in a photoelectrochemical cell, exhibits a photon-to-charge carrier generation efficiency of 12%. Significant loss of electrons occurs due to scattering as well as charge recombination at TiO(2)/CdSe interfaces and internal TiO(2) grain boundaries.

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