Pollution generated by synthetic polymers,particularly plastics,has become a significant global environmental problem.However,when compared to polymer-derived products like microplastics,oligomers have not received th...Pollution generated by synthetic polymers,particularly plastics,has become a significant global environmental problem.However,when compared to polymer-derived products like microplastics,oligomers have not received the attention they deserve.Oligomers are by-products of polymer production and intermediates of degradation.Despite the industrial advancements leading to an exponential increase in the production of new polymers,a majority of oligomers have remained inadequately researched.While the exposure and toxic effects of polylactic acid oligomers have been documented,the structures and fundamental properties of oligomers derived from most polymers are still poorly understood.This knowledge gap presents challenges in establishing effective analytical methods.Considering the potential of oligomers to act as new pollutants,it is imperative to investigate their environmental behavior,as well as their absorption,distribution,metabolism,excretion,and toxicity(ADMET)properties.This perspective highlights the research gap concerning oligomers.展开更多
A series of donor-acceptor oligomer OBTThn （n = 1- 7） and polymer PBTThl and PBTTh2 composed of al- ternative 2,1,3-benzothiadiazole and 3-hexylthiophene have been designed and synthesized for the purpose of in- ves...A series of donor-acceptor oligomer OBTThn （n = 1- 7） and polymer PBTThl and PBTTh2 composed of al- ternative 2,1,3-benzothiadiazole and 3-hexylthiophene have been designed and synthesized for the purpose of in- vestigation on the effect of chain length and side-chain regioregularity on their basic properties and photovoltaic performance. In the OBTThn oligomers and PBTThl polymer, all the hexyl side chains on thienyl units orient to- ward the same direction. Upon elongation of the chain length, the intramolecular charge transfer （ICT） absorption band in solution gradually redshifts from 398 nm for OBTThl to 505 nm for OBTThT, then to 512 nm for PBTThl polymer. Meanwhile, the HOMO energy level increases from -5.45 eV （OBTTh0 to -5.08 eV （OBTThT） and -5.09 eV （PBTThl）, and the LUMO energy level decreases from -3.11 eV （OBTTh0 to -3.30 eV （OBTThT） and -3.33 eV （PBTThl）, thus giving a smaller and smaller energy bandgap for higher oligomers and polymers. Theo- retical calculation suggests straight line-like backbone geometry for this series of oligomers and polymer. On the other hand, polymer PBTTh2 possesses a different side-chain regioregularity, in which every two neighbor hexyl side chains are arranged in different orienting direction. It is theoretically suggested to have curved line-like back- bone geometry. In solution, it shows similar photophysical and electrochemical properties as PBTThl. However in film state, it displays a less redshift in the ICT band as refer to that in solution than PBTThl. In combination with [6,6]-phenyl-C61-butyric acid methyl ester （PC61BM）, these oligomers and polymers were used as donor material to fabricate organic bulk heterojunction solar cells. Again, chain length-dependent device photovoltaic performance was observed. The device based on OBTTh4 showed a power conversion efficiency of 0.16%, while it increased to 0.36% and 0.49% for the devices based on OBTTh6 and PBTThb respectively. However, the side-chain regio- regularity has less influence on the device photovoltaic output since the device based on PBTTh~ displayed an effi- ciency of 0.52%, comparable to that of PBTThl.展开更多
We assembled a ternary blend bulk heterojunction polymer solar cell(PSCs) containing P3HT(donor) and PC61BM(acceptor) incorporated with a small molecule oligomer, dihexyl-quaterthiophene(DH4T) as a third component. By...We assembled a ternary blend bulk heterojunction polymer solar cell(PSCs) containing P3HT(donor) and PC61BM(acceptor) incorporated with a small molecule oligomer, dihexyl-quaterthiophene(DH4T) as a third component. By optimizing the contents of DH4 T, we increased the power conversion efficiency of ternary P3HT:DH4T:PC61BM PSCs to 4.17% from 3.44% of binary P3HT:PC61BM PSCs under AM 1.5 G of 100 m W/cm2 intensity. The major improvement is from the increase of the short circuit current and fill factor that is due to the increased light absorption at short wavelength, the balanced charge carrier transportation and the enhanced hole evacuation by a DH4T-enriched layer at the anode interface. In this work, we demonstrated that the efficiency of the PSCs can be enhanced by using low-bandgap conjugated polymer and its oligomer as donors and fullerene derivatives as acceptors.展开更多
基金supported by the National Key R&D Program(Nos.2022YFC3702600 and 2022YFC3702601)Startup Grant of Fudan University(No.JIH 1829010Y).
文摘Pollution generated by synthetic polymers,particularly plastics,has become a significant global environmental problem.However,when compared to polymer-derived products like microplastics,oligomers have not received the attention they deserve.Oligomers are by-products of polymer production and intermediates of degradation.Despite the industrial advancements leading to an exponential increase in the production of new polymers,a majority of oligomers have remained inadequately researched.While the exposure and toxic effects of polylactic acid oligomers have been documented,the structures and fundamental properties of oligomers derived from most polymers are still poorly understood.This knowledge gap presents challenges in establishing effective analytical methods.Considering the potential of oligomers to act as new pollutants,it is imperative to investigate their environmental behavior,as well as their absorption,distribution,metabolism,excretion,and toxicity(ADMET)properties.This perspective highlights the research gap concerning oligomers.
基金the National Natural Science Foundation of China，Chinese Academy of Sciences,and Shanghai Science and Technology Commission
文摘A series of donor-acceptor oligomer OBTThn （n = 1- 7） and polymer PBTThl and PBTTh2 composed of al- ternative 2,1,3-benzothiadiazole and 3-hexylthiophene have been designed and synthesized for the purpose of in- vestigation on the effect of chain length and side-chain regioregularity on their basic properties and photovoltaic performance. In the OBTThn oligomers and PBTThl polymer, all the hexyl side chains on thienyl units orient to- ward the same direction. Upon elongation of the chain length, the intramolecular charge transfer （ICT） absorption band in solution gradually redshifts from 398 nm for OBTThl to 505 nm for OBTThT, then to 512 nm for PBTThl polymer. Meanwhile, the HOMO energy level increases from -5.45 eV （OBTTh0 to -5.08 eV （OBTThT） and -5.09 eV （PBTThl）, and the LUMO energy level decreases from -3.11 eV （OBTTh0 to -3.30 eV （OBTThT） and -3.33 eV （PBTThl）, thus giving a smaller and smaller energy bandgap for higher oligomers and polymers. Theo- retical calculation suggests straight line-like backbone geometry for this series of oligomers and polymer. On the other hand, polymer PBTTh2 possesses a different side-chain regioregularity, in which every two neighbor hexyl side chains are arranged in different orienting direction. It is theoretically suggested to have curved line-like back- bone geometry. In solution, it shows similar photophysical and electrochemical properties as PBTThl. However in film state, it displays a less redshift in the ICT band as refer to that in solution than PBTThl. In combination with [6,6]-phenyl-C61-butyric acid methyl ester （PC61BM）, these oligomers and polymers were used as donor material to fabricate organic bulk heterojunction solar cells. Again, chain length-dependent device photovoltaic performance was observed. The device based on OBTTh4 showed a power conversion efficiency of 0.16%, while it increased to 0.36% and 0.49% for the devices based on OBTTh6 and PBTThb respectively. However, the side-chain regio- regularity has less influence on the device photovoltaic output since the device based on PBTTh~ displayed an effi- ciency of 0.52%, comparable to that of PBTThl.
基金financially supported by the National Natural Science Foundation of China(21374120)support by 100 Talents Program of the Chinese Academy of Sciences
文摘We assembled a ternary blend bulk heterojunction polymer solar cell(PSCs) containing P3HT(donor) and PC61BM(acceptor) incorporated with a small molecule oligomer, dihexyl-quaterthiophene(DH4T) as a third component. By optimizing the contents of DH4 T, we increased the power conversion efficiency of ternary P3HT:DH4T:PC61BM PSCs to 4.17% from 3.44% of binary P3HT:PC61BM PSCs under AM 1.5 G of 100 m W/cm2 intensity. The major improvement is from the increase of the short circuit current and fill factor that is due to the increased light absorption at short wavelength, the balanced charge carrier transportation and the enhanced hole evacuation by a DH4T-enriched layer at the anode interface. In this work, we demonstrated that the efficiency of the PSCs can be enhanced by using low-bandgap conjugated polymer and its oligomer as donors and fullerene derivatives as acceptors.
