Investigation of pulsed non-melt laser annealing on the film properties and performance of Cu(In,Ga)Se2 solar cells

Pulsed non-melt laser annealing (NLA) has been used for the first time to modify near-surface defects and related junction properties in Cu(In,Ga)Se₂ (CIGS) solar cells. CIGS films deposited on Mo/glass substrates were annealed using a 25 ns pulsed 248 nm laser beam at selected laser energy density in the range 20–60 mJ/cm² and pulse number in the range 5–20 pulses. XRD peak narrowing and SEM surface feature size increase suggest near-surface structure changes. Dual-beam optical modulation (DBOM) and Hall-effect measurements indicate NLA treatment increases the effective carrier lifetime and mobility along with the sheet resistance. In addition, several annealed CdS/CIGS films processed by NLA were fabricated into solar cells and characterized by photo- and dark-J–V and quantum efficiency (QE) measurements. The results show significant improvement in the overall cell performance when compared to unannealed cells. The results suggest that an optimal NLA energy density and pulse number for a 25 ns pulse width are approximately 30 mJ/cm² and 5 pulses, respectively. The NLA results reveal that overall cell efficiency of a cell processed from an unannealed film increased from 7.69% to 13.41% and 12.22% after annealing 2 different samples at the best condition prior to device processing.     

Effect of surface modification of TiO2 on the photovoltaic performance of the quasi solid state dye sensitized solar cells using a benzothiadiazole-based dye

We report the preparation of nanoporous TiO₂ electrode modified with an insulating material—BaCO₃ and used as electrode for quasi solid state dye sensitized solar cells (DSSCs), with a benzothiadiazole-based dye (BTDR2) as sensitizer and PEDOT:PSS coated FTO as counter electrode. We found that the BaCO₃ modification significantly increases the dye adsorption, resulting from the fact that the surface of BaCO₃ is more basic than TiO₂. The performance of the DSSCs with and without BaCO₃ modified TiO₂ electrodes were analyzed by cyclic voltammograms, optical absorption spectra, current-voltage characteristics in dark and under illumination and electrochemical impedance spectra. The photovoltaic performance has been significantly improved for the BaCO₃ modified electrode as compared to bare TiO₂ electrode having the same other components in the DSSCs. The value of the overall power conversion efficiency (η) improves from 2.42% to 4.38% under illumination intensity, when BaCO₃ modified electrode is used instead of bare TiO₂ electrode. The improvement in η has been attributed to the increased dye adsorption, reduction in recombination rate and enhancement in the electron lifetime when the modified TiO₂ electrode is used.     

Synthesis and photovoltaic properties of an alternating phenylenevinylene copolymer with substituted-triphenylamine units along the backbone for bulk heterojunction and dye-sensitized solar cells

We have fabricated bulk heterojunction (BHJ) photovoltaic devices based on the as cast and thermally annealed P:[6,6]-phenyl-C-61-butyric acid methyl ester (PCBM) blends and found that these devices gave power conversion efficiency (PCE) of about 1.15 and 1.60% respectively. P is a novel alternating phenylenevinylene copolymer which contains 2-cyano-3-(4-(diphenylamino)phenyl)acrylic acid units along the backbone and was synthesized by Heck coupling. This copolymer was soluble in common organic solvents and showed long-wavelength absorption maximum at 390-420 nm with optical band gap of 1.94 eV. The improvement of PCE after thermal annealing of the device based on the P:PCBM blend was attributed to the increase in hole mobility due to the enhanced crystallinity of P induced by thermal treatment. In addition, we have fabricated BHJ photovoltaic devices based on the as cast and thermally annealed PB:P:PCBM ternary blend. PB is a low band gap alternating phenylenevinylene copolymer with BF₂-azopyrrole complex units, which has been previously synthesized in our laboratory. We found that the device based on this ternary blend exhibited higher PCE (2.56%) as compared to either P:PCBM (1.15%) or PB:PCBM (1.57%) blend. This feature was associated with the well energy level alignment of P, PB and PCBM, the higher donor-acceptor interfaces for the exciton dissociation and the improved light harvesting property of the ternary blend. The further increase in the PCE with thermally annealed ternary blend (3.48%) has been correlated with the increase in the crystallinity of both P and PB. Finally, we used copolymer P as sensitizer for quasi solid state dye-sensitized solar cell and we achieved PCE of approximately 3.78%.