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Journal ArticleDOI

An Iron‐Based Photosensitizer with Extended Excited‐State Lifetime: Photophysical and Photovoltaic Properties

TLDR
In this article, a homoleptic iron complex bearing tridentate bis-carbene (CNC) ligands was designed for sensitization of TiO2 photoanodes.
Abstract
Herein, we report a homoleptic iron complex bearing tridentate bis-carbene (CNC) ligands designed for sensitization of TiO2 photoanodes. Its excited state has been characterized by ultra-fast transient spectroscopy and time-dependent density functional theory (TD-DFT) computations, which reveal a record triplet metal-to-ligand charge-transfer ((MLCT)-M-3) excited-state lifetime (16 ps). The new dye was efficiently chemisorbed on TiO2 and promoted electron injection and photocurrent generation in a dye-sensitized solar cell upon solar irradiation.

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Citations
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Journal ArticleDOI

Photoactive Complexes with Earth-Abundant Metals

TL;DR: The focus is on conceptually new, structurally well-characterized complexes with excited-state lifetimes between 10 ps and 1 ms in fluid solution for possible applications in photosensitizing, light-harvesting, luminescence and catalysis.
Journal ArticleDOI

Ultrafast Electron Dynamics in Solar Energy Conversion

TL;DR: The light-induced electron processes underlying the function of several molecular and hybrid materials currently under development for solar energy applications in dye or quantum dot-sensitized solar cells, polymer-fullerene polymer solar cells," organometal halide perovskite solar cells", and finally some photocatalytic systems are discussed.
Journal ArticleDOI

Luminescence and reactivity of a charge-transfer excited iron complex with nanosecond lifetime.

TL;DR: It is shown that octahedral coordination of iron(III) by two mono-anionic facial tris-carbene ligands can markedly suppress such deactivation through low-lying metal-centered states, extending iron’s photoactivity to a nanosecond time frame.
Journal ArticleDOI

Iron sensitizer converts light to electrons with 92% yield

TL;DR: This work describes the development of an iron-nitrogen-heterocyclic-carbene sensitizer with an excited-state lifetime that is nearly a thousand-fold longer than that of traditional iron polypyridyl complexes and opens up possibilities to develop solar energy-converting materials based on abundant elements.
References
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Journal ArticleDOI

A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films

TL;DR: In this article, the authors describe a photovoltaic cell, created from low-to medium-purity materials through low-cost processes, which exhibits a commercially realistic energy-conversion efficiency.
Journal ArticleDOI

Long-range corrected hybrid density functionals with damped atom–atom dispersion corrections

TL;DR: The re-optimization of a recently proposed long-range corrected hybrid density functional, omegaB97X-D, to include empirical atom-atom dispersion corrections yields satisfactory accuracy for thermochemistry, kinetics, and non-covalent interactions.
Journal Article

Long-Range Corrected Hybrid Density Functionals with Damped Atom-Atom Dispersion Corrections

TL;DR: Chai and Head-Gordon as discussed by the authors proposed a long-range corrected (LC) hybrid density functional with Damped Atom-Atom Dispersion corrections, which is called ωB97X-D.
Journal ArticleDOI

Conversion of light to electricity by cis-X2bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) charge-transfer sensitizers (X = Cl-, Br-, I-, CN-, and SCN-) on nanocrystalline titanium dioxide electrodes

TL;DR: Cis-X 2 Bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) complexes were prepared and characterized with respct to their absorption, luminescence, and redox behavior.
Journal ArticleDOI

Solar energy conversion by dye-sensitized photovoltaic cells

TL;DR: Developing solar cells that are based on the sensitization of mesoscopic oxide films by dyes or quantum dots, and the examples for the first outdoor application of such solar cells will be provided.
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