822
(Invited) Inverted Planar Perovskite Solar Cells Using Coordination Fullerene Polymers As Acceptor Layer

Thursday, 17 May 2018: 11:00
Room 204 (Washington State Convention Center)
K. Winkler, E. Gradzka, M. Wysocka-Zolopa (Institute of Chemistry, University of Bialystok), M. Enachescu, C. Moise, and A. Pumnea (University POLITEHNICA of Bucharest)
Perovskite solar cells can be composed of thin film of perovskite donor and fullerene derivative acceptor sandwiched between a PEDOT:PSS coated ITO positive electrode and a low work function metal negative electrode. So far, [6,6]-phenyl-C61-butrilic acid methyl ester (PC60BM) and its corresponding C70 derivative (PC70BM) have been dominantly used as the acceptors in these solar cells.1 Fullerenes and fullerene derivatives can be incorporated into polymeric structure with transition metal atoms (Pd, Pt) or metal complexes units (-Ir(CO)2-, -Rh(CF3CO2)2-, -Ni[P(CH3)3]-).2 They can be formed under chemical and electrochemical conditions. Coordination polymers of fullerene and palladium, C60Pdx (x = 1-3), have been investigated most intensively. The chemical synthesis of this material is carried out in benzene solution containing fullerene and zero-valent palladium complex as precursors for polymerization process. The same procedure has been applied for the formation of coordination polymers of fullerene derivatives, PC60BM and PC70BM. These polymers formed regularly sized spherical particles with diameter of about 120 nm (Fig. 1). They also exhibit electrochemical activity in the potential range of fullerene cage reduction (Fig. 2). Electron transfer on the polymeric backbone results in the significant increase of the conductivity of the polymeric material.3 Coordination polymers containing PC60BM and PC70BM can be used as an acceptor layer in perovskite solar cells. We anticipate an improvement in power conversion efficiency and stability of the devices in comparison to the solar cells based on tin crystalline films of PC60BM and PC70BM.
  1. Meng, L.; You, J.; Guo, T.F.; Yang, Y. Chem. Res. 2016, 49, 155-165.
  2. Balch, A.L.; Winkler, K. Chem. Rev. 2016, 116, 3812-3882.
  3. Gradzka, E.; Wysocka-Zolopa, M.; Winkler, K. Phys. Chem. C 2014, 118, 14061-14072.