The cost-effective organic semiconductors are strongly needed in organic photovoltaics(OPVs). Herein,two medium bandgap(MBG) electron acceptors, TPT4F and TPT4Cl are developed via the new design of multi-noncovalent i...The cost-effective organic semiconductors are strongly needed in organic photovoltaics(OPVs). Herein,two medium bandgap(MBG) electron acceptors, TPT4F and TPT4Cl are developed via the new design of multi-noncovalent interaction assisted unfused core, flanked with two electron withdrawing end groups. These fullly non-fused MBG acceptors adapt the planar and rigid conformation in solid, therefore exhibiting the ordered face-on stacking and strong photoluminescence in films. As results, TPT4Cl^(-)based OPVs, upon blending with the PBDB-TF polymer donor, have achieved a power conversion efficiency of 10.16% with a low non-radiative loss of 0.27 e V, representing one of the best fullly non-fused medium bandgap acceptors with desirable cost-efficiency balance.展开更多
The recent evolution of active components yielded brilliant progresses for organic solar cells(OSCs),yet the mechanism is needed to be clearly understood.In this wo rk,two electron acceptors,a linear SN6-2Br and a V-s...The recent evolution of active components yielded brilliant progresses for organic solar cells(OSCs),yet the mechanism is needed to be clearly understood.In this wo rk,two electron acceptors,a linear SN6-2Br and a V-shaped BTP-2Br,are developed with nitrogen atoms introduced to replace the traditional sp3-hybridized carbon in the fused ring.BTP-2Br possesses an electron-de ficient central core,which exhibits slightly blue-shifted absorption as well as deepened HOMO-level compared with SN6-2Br.The corresponding photovoltaic performance from V-shaped BTP-2Br based devices exhibit superior performance especially in short-circuit current(Jsc),despite an enhanced absorption and charge carrier mobilities for SN6-2Br.The primary reason for the higher JSC from BTP-2Br is faster exciton diffusion and dissociation in ble nds,than those of SN6-2Br.As a result,PBDB-TF:BTP-2Br based devices achieve a power conversion efficiency(PCE)of 13.84%with an voltage-loss of only 0.46 V,which is one of the lowest values ever reported.Moreover,we fabricated semitransparent OSCs that exhibit an excellent PCE of 9.62%with average visible transparency of 20.1%.展开更多
基金funded by the National Natural Science Foundation of China(22125901 and 21722404)the Research Grants Council(RGC)of Hong Kong(General Research Fund(14303519)+3 种基金the Joint Laboratory Funding Scheme Project(JLFS/P-102/18)the NSFC/RGC Joint Research Scheme Grant(NCUHK418/17))the CUHK direct grant(4442384)the beam time and technical support provided by Chun-Jen Su and U-Ser Jeng form Synchrotron Radiation Research Center,Hsinchu Science Park,Taiwan,China。
文摘The cost-effective organic semiconductors are strongly needed in organic photovoltaics(OPVs). Herein,two medium bandgap(MBG) electron acceptors, TPT4F and TPT4Cl are developed via the new design of multi-noncovalent interaction assisted unfused core, flanked with two electron withdrawing end groups. These fullly non-fused MBG acceptors adapt the planar and rigid conformation in solid, therefore exhibiting the ordered face-on stacking and strong photoluminescence in films. As results, TPT4Cl^(-)based OPVs, upon blending with the PBDB-TF polymer donor, have achieved a power conversion efficiency of 10.16% with a low non-radiative loss of 0.27 e V, representing one of the best fullly non-fused medium bandgap acceptors with desirable cost-efficiency balance.
基金National Natural Science Foundation of China(Nos.21722404,21674093 and 21734008)International Science and Technology Cooperation Program of China(ISTCP)(No.2016YFE0102900)+3 种基金supported by the Fundamental Research Funds for the Central Universities(No.2018XZZX002-16)the support by Zhejiang Natural Science Fund for Distinguished Young Scholars(No.LR17E030001)the support by the China Postdoctoral Science Foundation Funded Project(No.2018M632448)Postdoctoral Science Foundation Funded Project of Zhejiang Province(No.zj2017131)。
文摘The recent evolution of active components yielded brilliant progresses for organic solar cells(OSCs),yet the mechanism is needed to be clearly understood.In this wo rk,two electron acceptors,a linear SN6-2Br and a V-shaped BTP-2Br,are developed with nitrogen atoms introduced to replace the traditional sp3-hybridized carbon in the fused ring.BTP-2Br possesses an electron-de ficient central core,which exhibits slightly blue-shifted absorption as well as deepened HOMO-level compared with SN6-2Br.The corresponding photovoltaic performance from V-shaped BTP-2Br based devices exhibit superior performance especially in short-circuit current(Jsc),despite an enhanced absorption and charge carrier mobilities for SN6-2Br.The primary reason for the higher JSC from BTP-2Br is faster exciton diffusion and dissociation in ble nds,than those of SN6-2Br.As a result,PBDB-TF:BTP-2Br based devices achieve a power conversion efficiency(PCE)of 13.84%with an voltage-loss of only 0.46 V,which is one of the lowest values ever reported.Moreover,we fabricated semitransparent OSCs that exhibit an excellent PCE of 9.62%with average visible transparency of 20.1%.
