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Gradual chlorination at different positions of D-π-A copolymers based on benzodithiophene and isoindigo for organic solar cells 被引量:1
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作者 Jialing Zhou Bao Zhang +3 位作者 Yanfang Geng Qing Guo Qiang Guo Erjun Zhou 《Materials Reports(Energy)》 2021年第4期68-76,共9页
Isoindigo(IID)has been widely used as strong acceptor unit(A)to construct narrow bandgap polymers in organic field effect transistors(OFETs)and organic solar cells(OSCs).Combing with IID,we chose benzodithiophene(BDT)... Isoindigo(IID)has been widely used as strong acceptor unit(A)to construct narrow bandgap polymers in organic field effect transistors(OFETs)and organic solar cells(OSCs).Combing with IID,we chose benzodithiophene(BDT)as the donor unit(D)and thieno[3,2-b]thiophene(TT)as theπbridge to construct a new type of D-π-A polymer PE70.Based on PE70,we adopt the chlorination strategy to fine-tune photoelectric characteristics and film morphology,and then developed PE74 and PE75.By blending with non-fullerene acceptor(NFA)Y6,device based on PE74 with chloride substitution on the BDT unit showed increasing photovoltaic performance.In addition,further chlorine substitution on the IID(PE75)would greatly reduce the non-radiative voltage loss(ΔV3),and the distorted molecular conformation also took responsible for the excessive recombination.As results,PE74:Y6-based device achieves a power conversion efficiency(PCE)of 11.06%with open-circuit voltage(VOC)of 0.76 V,which are higher than those of PE70:Y6(PCE of 10.40%and VOC of 0.72 V)and PE75:Y6-based device(PCE of 6.24%and VOC of 0.84 V).This work demonstrates the regularity of the photovoltaic performance caused by chlorination strategy in polymer in the non-fullerene OSC devices,which provide important insights into highperformance photovoltaic materials. 展开更多
关键词 Isoindigo polymer donor materials D-π-A polymer Chlorination strategy Non-fullerene acceptor Voltage loss
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Non-equivalent D-A copolymerization strategy towards highly efficient polymer donor for polymer solar cells 被引量:1
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作者 Ziya Shang Liuyang Zhou +5 位作者 Chenkai Sun Lei Meng Wenbin Lai Jinyuan Zhang Wenchao Huang Yongfang Li 《Science China Chemistry》 SCIE EI CSCD 2021年第6期1031-1038,共8页
D-A copolymerization is a broadly utilized molecular design strategy to construct high efficiency photovoltaic materials for polymer solar cells(PSCs),and all the D-A copolymer donors reported till now are the alterna... D-A copolymerization is a broadly utilized molecular design strategy to construct high efficiency photovoltaic materials for polymer solar cells(PSCs),and all the D-A copolymer donors reported till now are the alternate D-A copolymers with equal D-and A-units.Here,we first propose a non-equivalent D-A copolymerization strategy with unequal D-and A-units,and develop three novel non-equivalent D-A copolymer donors(PM6-D1,PM6-D2 and PM6-D3 with D/A unit ratio of 1.1:0.9,1.2:0.8 and1.3:0.7,respectively)by inserting more D units into the alternate D-A copolymer PM6 backbone to finely tune the physicochemical and photovoltaic properties of the polymers.The three non-equivalent D-A copolymers show the down-shifted highest occupied molecular orbital(HOMO)energy levels,higher hole mobility,higher degree of molecular self-assembly and higher molecular crystallinity with the increase of D-unit ratio in comparison with the alternate D-A copolymer PM6.As a result,all the three non-equivalent D-A copolymer-based PSCs with Y6 as acceptor achieve improved power conversion efficiency(PCE)with higher V_(oc),larger J_(sc)and higher FF simultaneously.Particularly,the PM6-D1:Y6 based PSC achieved a high PCE of17.71%,which is significantly higher than that(15.82%)of the PM6:Y6 based PSC and is one of the highest performances in the binary PSCs. 展开更多
关键词 polymer solar cells conjugated polymer donor materials donor-acceptor copolymers non-equivalent D-A copolymerization
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