Photovoltaic and optoelectronic device group

Abstract:

A simple strategy is presented to determine the pore-filling fraction of the hole-conductor 2,2-7,7-tetrakis-N,N-di-pmethoxyphenylamine-9,9- spirobifluorene (spiro-OMeTAD) into mesoporous photoanodes in solid-state dye-sensitized solar cells (ss-DSCs). Based on refractive index determination by the film's reflectance spectra and using effective medium approximations the volume fractions of the constituent materials can be extracted, hence the pore-filling fraction quantified. This non-destructive method can be used with complete films and does not require detailed model assumptions. Pore-filling fractions of up to 80% are estimated for optimized solid-state DSC photoanodes, which is higher than that previously estimated by indirect methods. Additionally, transport and recombination lifetimes as a function of the pore-filling fraction are determined using photovoltage and photocurrent decay measurements. While extended electron lifetimes are observed with increasing pore-filling fractions, no trend is found in the transport kinetics. The data suggest that a pore-filling fraction of greater than 60% is necessary to achieve optimized performance in ss-DSCs. This degree of pore-filling is even achieved in 5 μm thick mesoporous photoanodes. It is concluded that pore-filling is not a limiting factor in the fabrication of "thick" ss-DSCs with spiro-OMeTAD as the hole-conductor. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Abstract:

Device optimization and ultrafast absorption spectroscopic investigations on the role of semiconducting polymer as hole-transport layer in solid-state dye sensitized solar cells suggest their dual role of dye-regeneration and light-antenna assisting in improved photoconversionefficiencies.© 2012 OSA.

Abstract:

Device optimization and ultrafast absorption spectroscopic investigations on the role of semiconducting polymer as hole-transport layer in solid-state dye sensitized solar cells suggest their dual role of dye-regeneration and light-antenna assisting in improved photoconversion-efficiencies. © 2012 OSA.

Abstract:

The energy costs associated with separating tightly bound excitons (photoinduced electron-hole pairs) and extracting free charges from highly disordered low-mobility networks represent fundamental losses for many low-cost photovoltaic technologies. We report a low-cost, solution-processable solar cell, based on a highly crystalline perovskite absorber with intense visible to near-infrared absorptivity, that has a power conversion efficiency of 10.9% in a single-junction device under simulated full sunlight. This "meso- superstructured solar cell" exhibits exceptionally few fundamental energy losses; it can generate open-circuit photovoltages of more than 1.1 volts, despite the relatively narrow absorber band gap of 1.55 electron volts. The functionality arises from the use of mesoporous alumina as an inert scaffold that structures the absorber and forces electrons to reside in and be transported through the perovskite.

Abstract:

The energy costs associated with separating tightly bound excitons (photoinduced electron-hole pairs) and extracting free charges from highly disordered low-mobility networks represent fundamental losses for many low-cost photovoltaic technologies. We report a low-cost, solution-processable solar cell, based on a highly crystalline perovskite absorber with intense visible to near-infrared absorptivity, that has a power conversion efficiency of 10.9% in a single-junction device under simulated full sunlight. This "meso-superstructured solar cell" exhibits exceptionally few fundamental energy losses; it can generate open-circuit photovoltages of more than 1.1 volts, despite the relatively narrow absorber band gap of 1.55 electron volts. The functionality arises from the use of mesoporous alumina as an inert scaffold that structures the absorber and forces electrons to reside in and be transported through the perovskite.