Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV16)
Publication date: 28th March 2016
Solid-state dye-sensitized solar cells (ssDSCs) are of huge interest within the scientific community due to the growing need for renewable energy sources. Such technologies are compatible with robust and inexpensive manufacturing technologies like inkjet and role-to-role thin film printing. ssDSCs traditionally employ organic hole transport materials (HTMs) such as spiro-OMeTAD, however, its expensive synthesis route and poor conductivity has highlighted the need for new low-cost HTMs that are easy to be synthesised for application in thin film solar cells. Over the past few decades, research efforts have focussed mainly on organic small molecules, polymers and inorganic materials, however, the use of transition metal complexes as HTMs in ssDSCs remains largely unexplored.
Transition metal complexes are promising candidates to be considered as HTMs for solution processible thin film solar cells. The ligand structure can be manipulated to control the redox properties of the central metal atom as well as control solubility, morphology and electrical properties of the resulting metal complex. Here we report the synthesis and characterization of a new solution-processible HTM based on cobalt complex of a high denticity ligand. Solid-state thin films are largely amorphous and exhibit, surprisingly, a negative temperature coefficient of conductivity (dσ/dT) and non-Arrhenius behavior, having a solid-state conductivity of 3.0 S/m at room temperature and 7.4 S/m at 4.5 K. When applied as a HTM in a ssDSC, impressive solar energy conversion efficiencies of 5.7% were achieved. The lack of strong π – π interactions or high crystallinity as that seen in other organic-inorganic hybrid materials displaying negative temperature coefficients highlights this transition metal complex as a new class of charge transport material (CTM) with a unique charge transport mechanism that remains to be explored.