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Standing Wave Enhancement of Red Absorbance and Photocurrent in Dye-Sensitized Titanium Dioxide Photoelectrodes Coupled to Photonic Crystals
595
Citations
32
References
2003
Year
EngineeringPhoto-electrochemical CellChemistryPhotoelectrochemistryPhotonic CrystalsChemical EngineeringOptical PropertiesDielectric MirrorPhotocatalysisPhotophysical PropertyMaterials SciencePhotonicsPhotochemistryPhotonic MaterialsUpconversion LuminescenceApplied PhysicsWave EnhancementRed AbsorbanceLight AbsorptionPhotonic Crystal Layer
The enhancement arises from slow light near the photonic crystal stop band, localizing intensity in the voids (blue) or dye‑sensitized TiO₂ (red) regions. Coupling a TiO₂ photonic crystal to a conventional TiO₂ nanoparticle film increases light‑harvesting efficiency, shifts dye absorbance with the stop‑band position—suppressing shorter wavelengths and enhancing longer ones—and boosts short‑circuit photocurrent by ~26% across 400–750 nm compared to ordinary dye‑sensitized TiO₂ electrodes.
The light harvesting efficiency of dye-sensitized photoelectrodes was enhanced by coupling a TiO(2) photonic crystal layer to a conventional film of TiO(2) nanoparticles. In addition to acting as a dielectric mirror, the inverse opal photonic crystal caused a significant change in dye absorbance which depended on the position of the stop band. Absorbance was suppressed at wavelengths shorter than the stop band maximum and was enhanced at longer wavelengths. This effect arises from the slow group velocity of light in the vicinity of the stop band, and the consequent localization of light intensity in the voids (to the blue) or in the dye-sensitized TiO(2) (to the red) portions of the photonic crystal. By coupling a photonic crystal to a film of TiO(2) nanoparticles, the short circuit photocurrent efficiency across the visible spectrum (400-750 nm) could be increased by about 26%, relative to an ordinary dye-sensitized nanocrystalline TiO(2) photoelectrode.
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