DOI:
Authors:
Yiming Cao, Yasemin Saygılı, Amita Ummadisingu, Joël Teuscher, Jingshan Luo, Norman Pellet, Fabrizio Giordano, Shaik M. Zakeeruddin, Jacques‐E. Moser, Marina Freitag, Anders Hagfeldt, Michaël Grätzel
Abstract:
Abstract Solid-state dye-sensitized solar cells currently suffer from issues such as inadequate nanopore filling, low conductivity and crystallization of hole-transport materials infiltrated in the mesoscopic TiO 2 scaffolds, leading to low performances. Here we report a record 11% stable solid-state dye-sensitized solar cell under standard air mass 1.5 global using a hole-transport material composed of a blend of [Cu (4,4′,6,6′-tetramethyl-2,2′-bipyridine) 2 ](bis(trifluoromethylsulfonyl)imide) 2 and [Cu (4,4′,6,6′-tetramethyl-2,2′-bipyridine) 2 ](bis(trifluoromethylsulfonyl)imide). The amorphous Cu(II/I) conductors that conduct holes by rapid hopping infiltrated in a 6.5 μm-thick mesoscopic TiO 2 scaffold are crucial for achieving such high efficiency. Using time-resolved laser photolysis, we determine the time constants for electron injection from the photoexcited sensitizers Y123 into the TiO 2 and regeneration of the Y123 by Cu(I) to be 25 ps and 3.2 μs, respectively. Our work will foster the development of low-cost solid-state photovoltaic based on transition metal complexes as hole conductors.