Abstract:The content and ratio of two stacking styles, namely H-aggregation and J-aggregation, of 5,5'-bis{(4-(7-hexylthiophen-2-yl)thiophen-2-yl)- [1,2,5]thiadiazolo [3,4-c]pyridine}-3 ,3'-di-2-ethylhexylsilylene-2,2'-bithiophene, DTS(PTTh 2 ) 2 had a profound influence on performance of solar cells based on DTS(PTTh 2 ) 2 /[6,6]-phenyl-C71-butyric acid methyl ester (PC 70 BM) (7/3, w/w) blend films. It was found that the H/J ratio could be tuned from 0.30 to 1.40 by controlling boiling point of main solvent, content … Show more
“…It was proved that a balance between the H and J aggregation is need for device to obtain best performance [43]. SVA was found to improve H-aggregation effectively as described above and offered a chance to enhance PCE.…”
Section: To Enhance Pce By Increasing H/j Ratiomentioning
“…It was proved that a balance between the H and J aggregation is need for device to obtain best performance [43]. SVA was found to improve H-aggregation effectively as described above and offered a chance to enhance PCE.…”
Section: To Enhance Pce By Increasing H/j Ratiomentioning
“…The thin film absorption spectra of M1 and M2 are presented in Figure S3, Supporting Information. Interestingly, M1 and M2 demonstrate different aggregation behaviors, that is, H‐like and J‐like, in the film state, according to the absorption band shift . For M1 , a blue‐shifted absorption band (≈10 nm) is observed from solution state to film state, indicating the formation of H‐like aggregation.…”
So far, squaraine‐based polymer donors have been less explored for the bulk heterojunction (BHJ) polymer solar cells. In this work, two new p–π conjugated polysquaraines (PASQ‐BDT1 and PASQ‐BDT2) with different electron‐rich subunits on the squaraine skeleton are rationally developed as new polymer donors based on the 2D structure design concept. PASQ‐BDT2 with N,N‐diisobutylaniline subunits shows superior device performances in both fullerene and nonfullerene PSCs compared to PASQ‐BDT1 containing triphenylamine subunits, with power conversion efficiencies (PCEs) of 4.34% and 3.72%, respectively, owing to increased light‐harvesting ability and more favorable nanoscale morphology in the BHJ films. Moreover, its demonstrated that solvent effects can play an effective role in elevating the device performance. For the PASQ‐BDT2/PC71BM blend, the PCE is improved from 3.19% to 4.34% after solvent vapor annealing treatment, mainly attributed to the optimized film morphology and increased hole mobility. More interestingly, when the processing solvent for nonfullerene devices is changed from chlorobenzene to chloroform, a significant enhancement on PCE from 1.96% to 3.72% is yielded for the PASQ‐BDT2/ITIC blend, due to suppressed charge recombination and enhanced crystallinity in the chloroform‐processed BHJ films.
“…In dilute chloroform solutions, o-4TBC-2F and m-4TBC-2F exhibited wide absorption in the ranges of 300-800 and 300-700 nm with maximum absorption peaks located at 671 and 595 nm, respectively.The absorption spectra of the o-4TBC-2F and m-4TBC-2F films were similar to their corresponding solution spectra with as light broadening and redshift. After thermal annealing of the o-4TBC-2F film at 100 8 8C for 5min, its absorption spectrum dramatically broadened and red-shifted, which indicated that the molecules probably form J-aggregates in the solid state; [12] while the absorption spectrum of m-4TBC-2F remained nearly unchanged before and after thermal annealing. According to the previously reported literature,t he formation of J-aggregates can help construct efficient charge transport channels.…”
Fused‐ring electron acceptors have made significant progress in recent years, while the development of fully non‐fused ring acceptors has been unsatisfactory. Here, two fully non‐fused ring acceptors, o‐4TBC‐2F and m‐4TBC‐2F, were designed and synthesized. By regulating the location of the hexyloxy chains, o‐4TBC‐2F formed planar backbones, while m‐4TBC‐2F displayed a twisted backbone. Additionally, the o‐4TBC‐2F film showed a markedly red‐shifted absorption after thermal annealing, which indicated the formation of J‐aggregates. For fabrication of organic solar cells (OSCs), PBDB‐T was used as a donor and blended with the two acceptors. The o‐4TBC‐2F‐based blend films displayed higher charge mobilities, lower energy loss and a higher power conversion efficiency (PCE). The optimized devices based on o‐4TBC‐2F gave a PCE of 10.26 %, which was much higher than those based on m‐4TBC‐2F at 2.63 %, and it is one of the highest reported PCE values for fully non‐fused ring electron acceptors.
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