RESUMO
Air-stable and solution-processable fluorene-based bipolar charge transporting materials (CTMs) were designed, synthesized, and analyzed. These CTMs feature anthraquinone, 9-fluorenone, and 9-dicyanofluorenylidine groups and exhibit good film formation properties for solvent processing. Quantum chemistry simulations and optical absorption measurements proved that several stable conformers and charge transfer complexes form inside the molecules. Hole mobilities in CTMs were around 10-4 to 10-5 cm2 V-1 s-1, while electron mobility in compounds with anthraquinone and 9-dicyanofluorenylidine groups was approximately one order of magnitude lower.
RESUMO
Fluorene-based hole transport materials (HTMs) with terminating thiophene units are explored, for the first time, for antimony sulfide (Sb2S3) solar cells. These HTMs possess largely simplified synthesis processes and high yields compared to the conventional expensive hole conductors making them reasonably economical. The thiophene unit-linked HTMs have been successfully demonstrated in ultrasonic spray-deposited Sb2S3 solar cells resulting in efficiencies in the range of 4.7-4.9% with an average visible transmittance (AVT) of 30-33% (400-800 nm) for the cell stack without metal contact, while the cells fabricated using conventional P3HT have yielded an efficiency of 4.7% with an AVT of 26%. The study puts forward cost-effective and transparent HTMs that avoid a post-coating activation at elevated temperatures like P3HT, devoid of parasitic absorption losses in the visible region and are demonstrated to be well aligned for the band edges of Sb2S3 thereby ascertaining their suitability for Sb2S3 solar cells and are potential candidates for semitransparent applications.
RESUMO
A group of small-molecule hole-transporting materials (HTMs) that are based on fluorenylidene fragments were synthesized and tested in perovskite solar cells (PSCs). The investigated compounds were synthesized by a facile two-step synthesis, and their properties were measured using thermoanalytical, optoelectronic, and photovoltaic methods. The champion PSC device that was doped with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) reached a power conversion efficiency of 22.83%. The longevity of the PSC device with the best performing HTM, V1387, was evaluated in different conditions and compared to that of 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenylamine)-9,9'-spirobifluorene (spiro-MeOTAD), showing improved stability. This work provides an alternative HTM strategy for fabricating efficient and stable PSCs.