Engineering of Efficient Panchromatic Sensitizers for Nanocrystalline TiO2-Based Solar Cells
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- 1 February 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 123 (8) , 1613-1624
- https://doi.org/10.1021/ja003299u
Abstract
A new series of panchromatic ruthenium(II) sensitizers derived from carboxylated terpyridyl complexes of tris-thiocyanato Ru(II) have been developed. Black dye containing different degrees of protonation {(C2H5)3NH}[Ru(H3tcterpy)(NCS)3] 1, {(C4H9)4N}2[Ru(H2tcterpy)(NCS)3] 2, {(C4H9)4N}3[Ru(Htcterpy)(NCS)3] 3, and {(C4H9)4N}4[Ru(tcterpy)(NCS)3] 4 (tcterpy = 4,4‘,4‘ ‘-tricarboxy-2,2‘:6‘,2‘ ‘-terpyridine) have been synthesized and fully characterized by UV−vis, emission, IR, Raman, NMR, cyclic voltammetry, and X-ray diffraction studies. The crystal structure of complex 2 confirms the presence of a RuIIN6 central core derived from the terpyridine ligand and three N-bonded thiocyanates. Intermolecular H-bonding between carboxylates on neighboring terpyridines gives rise to 2-D H-bonded arrays. The absorption and emission maxima of the black dye show a bathochromic shift with decreasing pH and exhibit pH-dependent excited-state lifetimes. The red-shift of the emission maxima is due to better π-acceptor properties of the acid form that lowers the energy of the CT excited state. The low-energy metal-to-ligand charge-transfer absorption band showed marked solvatochromism due to the presence of thiocyanate ligands. The Ru(II)/(III) oxidation potential of the black dye and the ligand-based reduction potential shifted cathodically with decreasing number of protons and showed more reversible character. The adsorption of complex 3 from methoxyacetonitrile solution onto transparent TiO2 films was interpreted by a Langmuir isotherm yielding an adsorption equilibrium constant, Kads, of (1.0 ± 0.3) × 105 Μ-1. The amount of dye adsorbed at monolayer saturation was (nα = 6.9 ± 0.3) × 10-8 mol/mg of TiO2, which is around 30% less than that of the cis-di(thiocyanato)bis(2,2‘-bipyridyl-4,4‘-dicarboxylate)ruthenium(II) complex. The black dye, when anchored to nanocrystalline TiO2 films achieves very efficient sensitization over the whole visible range extending into the near-IR region up to 920 nm, yielding over 80% incident photon-to-current efficiencies (IPCE). Solar cells containing the black dye were subjected to analysis by a photovoltaic calibration laboratory (NREL, U.S.A.) to determine their solar-to-electric conversion efficiency under standard AM 1.5 sunlight. A short circuit photocurrent density obtained was 20.5 mA/cm2, and the open circuit voltage was 0.72 V corresponding to an overall conversion efficiency of 10.4%.Keywords
This publication has 61 references indexed in Scilit:
- Electron Injection Dynamics of RuII(4,4‘-dicarboxy-2,2‘-bipyridine)2cis(NCS)2 Adsorbed on MoS2 NanoclustersThe Journal of Physical Chemistry B, 1999
- Visible Region Photooxidation on TiO2 with a Chromophore−Catalyst Molecular AssemblyInorganic Chemistry, 1999
- EQCM Investigations of Dye-Functionalized Nanocrystalline Titanium Dioxide Electrode/Solution Interfaces: Does Luminescence Report Directly on Interfacial Electron Transfer Kinetics?The Journal of Physical Chemistry B, 1999
- Photoelectrochemical Properties of a Porous Nb2O5 Electrode Sensitized by a Ruthenium DyeChemistry of Materials, 1998
- Efficient Photosensitization of Nanocrystalline TiO2 Films by a New Class of Sensitizer: cis-Dithiocyanato bis(4,7-dicarboxy-1,10-phenanthroline)ruthenium(II)Chemistry Letters, 1998
- One‐Pot Synthesis of Tetrahydronium Tris(4,4′‐Dicarboxylato‐2,2′‐Bipyridine)‐Ruthenium(II) DihydratePublished by Wiley ,1998
- Picosecond Raman investigation of interligand electron transfer in ruthenium(II) complexesThe Journal of Physical Chemistry, 1990
- Physics Considerations of Solar Energy ConversionJournal of Solar Energy Engineering, 1984
- An electrode-supported oxidation catalyst based on ruthenium(IV). pH "encapsulation" in a polymer filmJournal of the American Chemical Society, 1981
- The synthesis of some 4,4′,4″‐trialkyl‐2,2′:6′,2″‐terpyridylsJournal of Heterocyclic Chemistry, 1971