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4 th Hybrid and Organic Photovoltaic Conference -Uppsala 2012 93<br />

B47- Consistent physics-based modeling of DC and small-signal behavior of dyesensitized<br />

solar cells under different illumination conditions<br />

Shuai Ma a , Federica Cappelluti a , Giovanni Ghione a , Adriano Sacco b , Diego Pugliese b , Andrea<br />

Lamberti b , Elena Tresso c<br />

a, Department of Electronics and Telecommunications, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino, 10129, IT<br />

b, Center for Space Human Robotics @PoliTo, Istituto Italiano di Tecnologia, Corso Trento 21, Torino, 10129, IT<br />

c, Applied Science and Technology Department, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino, 10129, IT<br />

The development of physics-based tools able to consistently predict the cell behavior under<br />

different operating conditions is a key issue toward the technological development of dyesensitized<br />

solar cells (DSSCs), since it may provide deeper understanding of the many physical<br />

mechanisms involved in the cell operation and their interplay [1-3]. In this contribution we<br />

investigate through experiments and device-level numerical simulations, the static and<br />

dynamic small-signal behavior of DSSCs with different architectures and under different<br />

illumination conditions.<br />

The adopted model exploits a mixed-mode approach where electron transport through the<br />

nanoporous dyed TiO2 film is described by a diffusion transport model, including non-uniform<br />

optical generation [1-2], electron trapping mechanisms [4] and recombination with iodine<br />

species in the electrolyte and/or oxidized dye molecules [3], while electrical loss induced by<br />

contacts, electrolyte, and series parasitic paths are modeled by compact equivalent circuit<br />

elements.<br />

The cells analyzed in this study were fabricated following a standard procedure, with a layer<br />

of dye sensitized TiO2 nanoparticles as photoanode, a counter electrode constituted by a FTOcovered<br />

glass coated with a thermally evaporated Pt thin layer, I3-/I- redox electrolyte, and a<br />

thermoplastic polymer as sealing material. The devices were characterized through I-V<br />

measurements under AM1.5G solar simulator, Electrochemical Impedance Spectra (EIS) under<br />

AM1.5G illumination and in dark condition (bias voltages from 0 to 0.8 V, frequency range 10 -1<br />

– 10 5 Hz), and Incident Photon-to-electron Conversion Efficiency (IPCE) spectra acquired in DC<br />

mode using a 150W Xenon halogen lamp and a dual grating Czerny Turner monochromator.<br />

Figure 1 Comparison between measured and simulated performance. Left: IPCE for photoelectrode-side (PE) and<br />

counter-electrode-side (CE) illumination; Center: I-V under AM1.5G sun simulator; Right: Small-signal impedance of<br />

the TiO2 film under AM1.5G sun simulator for PE illumination at bias voltage from 0.55 to 0.8 V with 0.05 V step<br />

(parasitic series resistance, electrolyte and counter electrode contribution have been de-embedded).<br />

The model is applied to analyze the impact of different technological parameters (TiO2 layer<br />

thickness, used dye, cell total thickness) on the cell operation. As an example, Fig. 1 shows a<br />

comparison between experiments and simulations of a cell with 7 um thick TiO2 film and N719<br />

dye. All the reported simulations (I-V, IPCE, and EIS) exploit the same set of physical<br />

parameters, and predict the overall cell behavior consistently and with good accuracy, under<br />

both directions of illumination. The cell shows a comparatively low IPCE with respect to the<br />

photovoltaic performance. This has been attributed to low collection efficiency under weak<br />

© SEFIN 2012

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