Scinovex
article Open AccessTop 1% cited

Molecular Photovoltaics

Accounts of Chemical Research · 2000 · Vol. 33(5) · pp. 269–277
Anders HagfeldtMichaël Grätzel

Abstract

The dye-sensitized nanocrystalline injection solar cell employs transition metal complexes for spectral sensitization of mesoporous TiO(2) films together with suitable redox electrolytes or amorphous organic hole conductors. Light harvesting occurs efficiently over the whole visible and near-IR range due to the very large internal surface area of the films. Judicious molecular engineering allows the photoinduced charge separation to occur quantitatively within a few femtoseconds. The certified overall power conversion efficiency of the new solar cell for AM 1.5 solar radiation stands presently at 10.4%.

TiO2 Photocatalysis and Solar CellsAdvanced Photocatalysis TechniquesQuantum Dots Synthesis And PropertiesMaterials scienceSolar cellNanocrystalline materialFemtosecondPhotovoltaicsOrganic solar cellEnergy conversion efficiencyOptoelectronicsAmorphous solidPhotoinduced charge separation

MeSH terms

Coloring AgentsElectrochemistryKineticsMicroscopy, Electron, ScanningModels, MolecularPhotochemistryQuantum TheorySolar EnergyTitaniumMolecular Structure
Citations
2,597
FWCI
110.26
field-weighted impact
References
39
Percentile
100%
vs. same field & year
Citations per year
Cited by
A 5% efficient photoelectrochemical solar cell based on nanostructured ZnO electrodes
Solar Energy Materials and Solar Cells · 2002 · 618 citations
Solar Energy Conversion by Dye-Sensitized Photovoltaic Cells
Inorganic Chemistry · 2005 · 3,357 citations
Hybrid solar cells
Inorganica Chimica Acta · 2007 · 306 citations
Molecular Design of Coumarin Dyes for Efficient Dye-Sensitized Solar Cells
The Journal of Physical Chemistry B · 2002 · 1,053 citations
Charge Transfer on the Nanoscale:  Current Status
The Journal of Physical Chemistry B · 2003 · 1,010 citations
Conjugated Polymer Photovoltaic Cells
Chemistry of Materials · 2004 · 2,124 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.