Already, several technologies of polycrystalline thin-film photovoltaic materials have achieved certified record small-cell power conversion efficiencies exceeding 22%. They are CdTe, Cu(In,Ga)(S,Se)2 (CIGS), and metal halide perovskite (PSC), each named after the light-absorbing semiconductor material. Thin-film solar cells and modules require very little active material due to their very high absorption coefficient. Efficient production methods with low materials waste, moderate temperatures, attractive cost structures, and favorable energy payback times will play a strong role in market development as thin-film technologies reach full maturity, including mass production and the standardization of production machineries. In fact, the first two technologies have already been developed up to the industrial scale with a market share of several GW. In this review article, we outline similarities and differences between these high-efficiency thin-film technologies from both the materials and the industrial point of view. We address the materials characteristics and device concepts for each technology, including a description of recent developments that have led to very high efficiency achievements. We provide an overview of the CIGS industry players and their current status. The newcomer PSC has demonstrated its potential in the laboratory, and initial efforts in industrial production are underway. A large number of laboratories are experimenting through a wide range of options in order to optimize not only the efficiency but also stability, environmental aspects, and manufacturability of PSC. Its high efficiency and its high bandgap make PSC particularly attractive for tandem applications. An overview of all these topics is included here along with a list of materials configurations.
Wide-bandgap perovskite solar cells (PSCs) with optimal bandgap (E g ) and high power conversion efficiency (PCE) are key to high-performance perovskite-based tandem photovoltaics. A 2D/3D perovskite heterostructure passivation is employed for double-cation wide-bandgap PSCs with engineered bandgap (1.65 eV ≤ E g ≤ 1.85 eV), which results in improved stabilized PCEs and a strong enhancement in open-circuit voltages of around 45 mV compared to reference devices for all investigated bandgaps. Making use of this strategy, semitransparent PSCs with engineered bandgap are developed, which show stabilized PCEs of up to 25.7% and 25.0% in fourterminal perovskite/c-Si and perovskite/CIGS tandem solar cells, respectively. Moreover, comparable tandem PCEs are observed for a broad range of perovskite bandgaps. For the first time, the robustness of the four-terminal tandem configuration with respect to variations in the perovskite bandgap for two state-of-the-art bottom solar cells is experimentally validated.
Window integrated photovoltaics for automotive and building applications are a promising market segment for organic solar modules. Besides semi‐transparency, window integrated applications require a reasonable transparency perception and good color rendering properties in order to be suitable for realistic scene illumination. Here, the transmitted light through semi‐transparent organic solar cells comprising the polymer/fullerene blend poly[(4,4'‐bis(2‐ethylhexyl)dithieno[3,2‐b:2',3'‐d]silole)‐2,6‐diyl‐alt‐(2,1,3‐benzothiadiazole)‐4,7‐diyl]: [6,6]‐phenyl C71‐butric acid methyl ester (PSBTBT:PC70BM) as active layer and a sputtered aluminum doped zinc oxide cathode were found to exhibit a color neutral perception for the human eye and very good color rendering properties. Moreover, the electrical cell properties allow for efficient energy harvesting with an overall power conversion efficiency η ≈ 3%.
Based on the well-known beneficial effect of a thin LiF layer underneath Al contacts for organic solar cells, a comparative study of interlayers made from the alkaline fluorides LiF, NaF, and KF is presented for polymer bulk heterojunction solar cells. The overall suitability of these materials and the underlying mechanisms are discussed. While an improvement in cell efficiency up to a factor of 2 can be reached with all three fluorides, the necessary thickness of the interlayer for maximum improvement is smallest for NaF and largest for LiF, suggesting the alternative use of NaF instead of LiF.
provide good solubility in organic solvents and processability, we attached branched alkyl substituents at the DTP-nitrogen (ethylhexyl (EH) 1 , 4 , octylnonyl (ON) 2 , 5 , hexyldecyl (HD) 3 , 6 ) and hexyl side chains to each thiophene unit in a regioregular fashion as a mimic of the well-known and frequently used regioregular poly(3-hexylthiophene). [ 26 ] Thereby, the hexyl chains were attached either at the outer ( 1 -3 ) or inner ( 4 -6 ) positions thus yielding three isomeric pairs, which only differ in the positioning of the side chains. As a result, excellent solubilities of ≥120 mg mL −1 in chloroform for molecules 5 and 6 have been obtained. First solar cell results of oligomer pair 1 and 4 have recently been published and we discovered a striking difference between the photovoltaic behavior of the two isomers. [ 16 ] Whereas the so far highest PCE of 4.8% for any DTP-based oligomer has been obtained for oligothiophene 1 and PC 61 BM in BHJSCs, isomer 4 showed a lower performance (0.8%), which we attributed to the different blend morphologies and phase separation probed by atomic force microscopy (AFM) and X-ray diffraction (XRD) techniques. [ 16 ] The detailed photovoltaic behavior, further optimization, and characterization of the photoactive layers of the whole series of soluble DTP-oligothiophenes 1 -6 is now described. Signifi cant improvement of the oligomer BHJSC performance was obtained by SVA, which was investigated by absorption spectroscopy, grazing incidence XRD (GI-XRD), and AFM. After extensive optimization, power conversion effi ciencies up to 6.1% and fi ll factors greater than 70% were achieved.
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