Co(III) Complexes as p-Dopants in Solid-State Dye-Sensitized Solar Cells

Following our recent work on the use of Co(III) complexes as p-type dopants for triarylamine-based organic hole-conductors, we herein report on two new Co(III) complexes for doping applications. With the aim of ameliorating the dopant's suitability for its use in solid-state dye-sensitized solar cells, we show how the properties of the dopant can be easily adjusted by a slight modification of the molecular structure. We prove the eligibility of the two new dopants by characterizing their optical and electrochemical properties and give evidence that both of them can be used to oxidize the molecular hole-transporter spiro-MeOTAD. Finally, we fabricate high-performance solid-state dye-sensitized solar cells using a state-of-the-art metal-free organic sensitizer in order to elucidate the influence of the type of dopant on device performance

Metal complexes for use as dopants and other uses

The invention relates to electrochemical devices comprising complexes of cobalt comprising at least one ligand with a 5- or six membered, N- containing heteroring. The complex are useful as p- and n- dopants, as over of electrochemical devices, in particular in organic semiconductors. The complexes are further useful as over- discharge prevention and overvoltage protection agents

Influence of the interfacial charge-transfer resistance at the counter electrode in dye-sensitized solar cells employing cobalt redox shuttles

We highlight the effect of the interfacial charge-transfer resistance at the counter electrode in dye-sensitized solar cells based on two cobalt redox shuttles, namely cobalt(III/II) tris(2,2'-bipyridine) and cobalt(III/II) tris(1,10-phenanthroline). Highly porous counter electrodes based on poly(3,4-ethylenedioxythiophene) (PEDOT) prepared by electro-oxidative polymerization are compared to the typically employed platinized FTO glass, with the former showing much lower charge transfer resistances for both cobalt complexes, leading to improved fill factors and to linear response of the short circuit photo-current density to light intensity up to one sun. Based on these findings, an excellent power conversion efficiency of 10.3% was achieved with a recently reported organic sensitizer and PEDOT as counter electrode

Co(III) Complexes as p‑Dopants in Solid-State Dye-Sensitized Solar Cells

Following our recent work on the use of Co­(III) complexes as p-type dopants for triarylamine-based organic hole-conductors, we herein report on two new Co­(III) complexes for doping applications. With the aim of ameliorating the dopant’s suitability for its use in solid-state dye-sensitized solar cells, we show how the properties of the dopant can be easily adjusted by a slight modification of the molecular structure. We prove the eligibility of the two new dopants by characterizing their optical and electrochemical properties and give evidence that both of them can be used to oxidize the molecular hole-transporter spiro-MeOTAD. Finally, we fabricate high-performance solid-state dye-sensitized solar cells using a state-of-the-art metal-free organic sensitizer in order to elucidate the influence of the type of dopant on device performance

Protic ionic liquid assisted solution processing of lead halide perovskites with water, alcohols and acetonitrile

A major obstacle and persisting challenge towards safe and sustainable industrial scale processing and commercialization of perovskite based (opto) electronic devices including solar cells lies in the essential need of strongly coordinating toxic solvents such as N, N-dimethylformamide (DMF) in the preparation of perovskite precursor inks. In this work, we present novel ink systems for perovskite precursors composed of protic ionic liquids (PILs) based on methylammonium cation and carboxylate anion and their binary blends with water, alcohols and acetonitrile for solution processing of CH3NH3PbX3 (X = I, Br). Among the investigated ink-systems, new PIL methylammonium propionate and its blends were identified as the most promising candidates in terms of chemical stability and compatibility for single- and two-step solution processing of the perovskite materials. Multi-cation mixed halide perovskites solar cells prepared with PIL/acetonitrile solvent system showed power conversion efficiency in excess of 15%

Sequential deposition as a route to high-performance perovskite-sensitized solar cells

Following pioneering work(1), solution-processable organic-inorganic hybrid perovskites-such as CH3NH3PbX3 (X = Cl, Br, I)-have attracted attention as light-harvesting materials for mesoscopic solar cells(2-15). So far, the perovskite pigment has been deposited in a single step onto mesoporous metal oxide films using a mixture of PbX2 and CH3NH3X in a common solvent. However, the uncontrolled precipitation of the perovskite produces large morphological variations, resulting in a wide spread of photovoltaic performance in the resulting devices, which hampers the prospects for practical applications. Here we describe a sequential deposition method for the formation of the perovskite pigment within the porous metal oxide film. PbI2 is first introduced from solution into a nanoporous titanium dioxide film and subsequently transformed into the perovskite by exposing it to a solution of CH3NH3I. We find that the conversion occurs within the nanoporous host as soon as the two components come into contact, permitting much better control over the perovskite morphology than is possible with the previously employed route. Using this technique for the fabrication of solid-state mesoscopic solar cells greatly increases the reproducibility of their performance and allows us to achieve a power conversion efficiency of approximately 15 per cent (measured under standard AM1.5G test conditions on solar zenith angle, solar light intensity and cell temperature). This two-step method should provide new opportunities for the fabrication of solution-processed photovoltaic cells with unprecedented power conversion efficiencies and high stability equal to or even greater than those of today's best thin-film photovoltaic devices

Molecular Engineering of Organic Dyes for Improved Recombination Lifetime in Solid-State Dye-Sensitized Solar Cells

A major limitation of solid-state dye-sensitized solar cells is a short electron diffusion length, which is due to fast recombination between electrons in the TiO2 electron-transporting layer and holes in the 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenylamine)-9,9'-spirobifluorene (Spiro-OMeTAD) hole-transporting layer. In this report, the sensitizing dye that separates the TiO2 from the Spiro-OMeTAD was engineered to slow recombination and increase device performance. Through the synthesis and characterization of three new organic D-pi-A sensitizing dyes (WN1, WN3, and WN3.1), the quantity and placement of alkyl chains on the sensitizing dye were found to play a significant role in the suppression of recombination. In solid-state devices using Spiro-OMeTAD as the hole-transport material, these dyes achieved the following efficiencies: 4.9% for WN1, 5.9% for WN3, and 6.3% for WN3.1, compared to 6.6% achieved with Y123 as a reference dye. Of the dyes investigated in this study, WN3.1 is shown to be the most effective at suppressing recombination in solid-state dye-sensitized solar cells, using transient photovoltage and photocurrent measurements