Potassium-doped organometal halide perovskite solar cells (PSCs) of more than 20% power conversion efficiency (PCE) without I-V hysteresis were constructed. The crystal lattice of the organometal halide perovskite was expanded with increasing of the potassium ratio, where both absorption and photoluminescence spectra shifted to the longer wavelength, suggesting that the optical band gap decreased. In the case of the perovskite with the 5% K+, the conduction band minimum (CBM) became similar to the CBM level of the TiO2-Li. In this situation, the electron transfer barrier at the interface between TiO2-Li and the perovskite was minimised. In fact, the transient current rise at the maximum power voltages of PSCs with 5% K+ was faster than that without K+. It is concluded that stagnation-less carrier transportation could minimise the I-V hysteresis of PSCs.
An efficient metal-free formulation of a hole transport material (HTM) based on an ionic liquid polymer is developed for n-i-p perovskite solar cells (PSCs), to address reproducibility issues related to the use of complex dopant mixtures based on lithium salts and cobalt coordination complexes. The conductivity of the HTM is thus significantly improved by 4 orders of magnitude, up to 1.9 x 10 -3 S.cm -1 , using poly(1-butyl-3-vinylimidazolium bis(trifluoromethylsulfonyl)imide) (PVBI-TFSI) as dopant.Introduced in the FTO/c-TiO 2 /mp-TiO2/K0.05(MA0.15FA0.85)0.95PbI2.55Br0.45/HTM/Au PSC configuration, PVBI-TFSI-HTM formulation shows power conversion efficiency as high as 20.3 %, versus 18.4 % for the standard lithium salt-HTM formulation, with considerably reduced hysteresis and excellent reproducibility. Mechanistic investigations suggest that PVBI-TFSI acts as a source of protons promoting the HTM oxidation.
AgBiS 2 nanocrystals (NCs) are nontoxic, lead-free, and near-infrared absorbing materials. Eco-friendly solar cells were constructed using interdigitated layers of ZnO nanowires (NWs) and AgBiS 2 NCs, with the aim of elongating the otherwise short carrier diffusion length of the AgBiS 2 NC assembly. AgBiS 2 NCs were uniformly infiltrated into the ZnO NW layers using a low-cost and easily scalable dip coating method. The resulting ZnO NW/AgBiS 2 NC interdigitated structures provided efficient carrier pathways in constructed nanowire solar cells (NWSCs), composed of a transparent electrode/ZnO NW/AgBiS 2 NC interdigitated layer/P3HT hole transport layer/Au. The photocurrent external quantum efficiency (EQE) in the visible to nearinfrared regions was enhanced compared to those of the control solar cells made with ZnO/AgBiS 2 tandem layered structures. The maximum EQE for the NWSCs reached 82% in the visible region, which is higher than the EQE values previously reported for solar cells fabricated with ZnO/AgBiS 2 NCs. Air stability tests on unsealed NWSCs demonstrated that 90% or more of the initial power conversion efficiency was maintained even after 6 months.
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