Source abstract
Abstract
Dye-sensitized solar cells (DSSCs) are a strong contender for next-generation photovoltaic technology with niche applications as solar-powered windows. The performance of a DSSC is particularly susceptible to the dye sensitizer, which is adsorbed onto the surface of a wide-band-gap semiconductor such as TiO2, to form the working electrode. The nature by which such surfaces are sensitized stands to influence the resulting dye···TiO2 interfacial structure and thence the operational performance of the DSSC working electrode. In particular, a nanoscopic understanding of the sensitization process would ultimately help to improve DSSC device function. In this study, atomic force microscopy (AFM) is used to image the nanoscopic formation of dye···TiO2 interfacial structures. This employs, as case studies, four well-known DSSC dyes adsorbed onto amorphous TiO2 substrates: two ruthenium-based dyes, N3 and the Black Dye (N749); and two organic dyes, the thiophenylcarbazole, MK-2, and the zwitterionic squaraine, SQ-2. We discover that all four dyes present some form of aggregation upon sensitization of TiO2, whose spatial distributions show distinct nanoaggregate particle characteristics. These particle clusters of N749, N3, and MK-2 are found to assemble in lines of nanoaggregates, while clusters of SQ-2 dye chromophores distribute themselves randomly on the amorphous TiO2 substrates. This nanoparticle structural assembly persists even when these dye···TiO2 interfaces are fabricated using hundred-fold diluted dye sensitization concentrations. The formation of dye aggregates in N749 is further studied as a function of dye sensitization time. This tracks the pattern formation of aggregates of N749 and reveals that dye aggregation begins within the first hour and has completed within a 5 h period. The large expanse of dye nanoaggregates observed shows that dye···dye interactions are much more important than previously envisaged, while the nature of their spatial distribution can be related to different aggregation modes of the dye molecules. These nanostructural features will undoubtedly impact the performance of DSSCs.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Cavendish Laboratory, Department of Physics, University of Cambridge, J. J. Thomson Avenue, Cambridge CB3 0HE, United Kingdom
Research Complex at Harwell, Rutherford Appleton Laboratory, Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0FA, United Kingdom
ISIS Neutron and Muon Source, Rutherford Appleton Laboratory, Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0QX, United Kingdom
Department of Chemical Engineering and Biotechnology, University of Cambridge, West Cambridge Site, Philippa Fawcett Drive, Cambridge CB3 0AS, United Kingdom
Argonne National Laboratory, 9700 South Cass Avenue, Argonne, Illinois 60439, United States
Funding
BASF · Royal Commission for the Exhibition of 1851