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11% efficiency solid-state dye-sensitized solar cells with copper(II/I) hole transport materials

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-se...

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Detalles Bibliográficos
Autores principales: Cao, Yiming, Saygili, Yasemin, Ummadisingu, Amita, Teuscher, Joël, Luo, Jingshan, Pellet, Norman, Giordano, Fabrizio, Zakeeruddin, Shaik Mohammed, Moser, Jacques -E., Freitag, Marina, Hagfeldt, Anders, Grätzel, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472710/
https://www.ncbi.nlm.nih.gov/pubmed/28598436
http://dx.doi.org/10.1038/ncomms15390
Descripción
Sumario: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.