| In recent years,organic solar cells have been a hot topic due to its advantage of light weight,low cost,flexibility and solution-processable capabilities.The design and synthesis of non-fullerene acceptors and molecular donors is very effective in improving the photovoltaic properties of the organic solar cells and now is a research hotspot in this field.Accordingly,our main work is as followed.1.A non-fullerene electron acceptor with a spirobifluorene(SF)core and four diketopyrrolopyrrole(DPP)arms end capped by 4-fluorobenzene(FB),is designed and synthesized.Comparing to its non-fluorination analogue,the introduction of fluorine reduces the lowest unoccupied molecular orbital(LUMO)energy levels of SF(DPPFB)4 and improves the electron mobility of the poly(3-hexylthiophene)(P3HT)and SF(DPPFB)4 blends.The highest power conversion efficiency obtained by the OSCs based on P3HT:SF(DPPFB)4 is 4.42%,with a lifted short current density of 8.48 mA cm-2.2.An organic small molecule with a fluorene(F)core and two diketopyrrolopyrrole(DPP)arms end capped by ethyl thiophene-2-carboxylate(CT),F(DPPCT)2,which can serve as both the acceptor and the donor,is designed and synthesized.The optical energy gap is 1.65 eV,with a LUMO of-3.68 eV and HOMO of-5.28 eV.The resulting devices based on P3HT:F(DPPCT)2 and F(DPPCT)2:PC7iBM can give a highest power conversion efficiency of 2.14%and 2.50%,respectively.3.An organic molecular donor with a benzodithiophene(BDT)core and two diketopyrrolopyrrole(DPP)arms end capped by ethyl thiophene-2-carboxylate(CT),BDT(DPPCT)2,is designed and synthesized.It shows intense absorptions in the range of 500 nm-800 nm.The optical energy gap is 1.54 eV,with a LUMO of-3.40 eV and HOMO of-5.03 eV,suggesting a typical p type semiconductor.From the 1H NMR spectrum,we know that BDT(DPPCT)2 is strongly aggregated and π-π stacked even in solution,which contributes to high electron mobility.However,BDT(DPPCT)2 is too aggregated to be soluble in the hot solutions of common solvents,and we can’t get a uniform film with the hot-spin-coating method.The resulting device based on BDT(DPPCT)2:PC71BM can give a highest power conversion efficiency of only 0.835%. |