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Beilstein J. Nanotechnol. 2013, 4, 680–689, doi:10.3762/bjnano.4.77
Scheme 1: Alternative synthetic routes used to yield DCV5T-Bu4.
Figure 1: (a) Absorption spectrum of DCV5T-Bu4 measured in chloroform and as thin film, spin-coated from chlo...
Figure 2: Diagram showing the HOMO and LUMO energy levels of DCV5T-Bu4, PCBM derivatives [34,35], and C60.
Figure 3: J–V curve of DCV5T-Bu4:PC61BM solution-processed solar cells made from 1:1 blends spin-coated from ...
Figure 4: Power conversion efficiency of DCV5T-Bu4:PC61BM solution-processed solar cells as a function of CN ...
Figure 5: (a) Normalized absorption spectra of DCV5T-Bu4:PC61BM blends spin-coated from CB, CB:CN (0.375% wt....
Figure 6: AFM phase images of samples spin-coated on ITO|PEDOT:PSS| with (a) DCV5T-Bu4:PC61BM from CB, (b) DC...
Beilstein J. Nanotechnol. 2011, 2, 802–808, doi:10.3762/bjnano.2.88
Figure 1: General formula of carboxylic acid functionalized oligothiophenes HnTCOOH.
Figure 2: Left: STM image of H4TCOOH on HOPG (100 × 100 nm2, U = −120 mV, I = 50 pA). The letters label the d...
Figure 3: STM image of H6TCOOH. Left: 70 × 70 nm2, U = −360 mV, I = 50 pA. Center: 20 × 20 nm2, U = −361 mV, I...
Figure 4: STM images of H8TCOOH. Left: 60 × 60 nm2, U = −640 mV, I = 44 pA. Center: 30 × 30 nm2, U = −725 mV, ...
Figure 5: STM images of H10TCOOH. Left: 50 × 50 nm2, U = −200 mV, I = 73 pA. Center: 24 × 19 nm2, U = −100 mV...
Figure 6: STM images of H12TCOOH. Left: 80 × 80 nm2, U = −200 mV, I = 73 pA. Center: 20 × 20 nm2, U = −750 mV...