One-dimensional crystals of fluorinated perylene diimides were achieved by the self-assembly of them via solvent-nonsolvent exchanging.The π-conjugated fluorinated perylene diimides were assembled into highly-ordered nanostructures of well-defined morphologies in organic solvents due to the π-π interaction between the aromatic cores.It was found that with more introduced F atoms,perylene diimides showed remarkably improved solubility and thus were much easier to grow into crystals,due to the increased polarity induced by the strong electron-withdrawing F group.More importantly,single crystal of N,N＇-diperfluorophenyl-3,4,9,10-perylenetetracarboxylic diimide（DPFPP）was obtained,and the unit cell-dimensions of triclinic structure were determined by the selected area electron diffraction（SAED） pattems to be a=0.712 nm,b=1.072 nm,c=2.914 nm,a=97.0°,β=89.6°,γ=93.4°.Owing to most of the longest c-axis orienting nearly vertically to the long axis of the needle crystal,the molecular planes are expected to be vertical to the needle axis.
HUANG Jiachi LI Hanying MO Xiong SHI Minmin WANG Mang CHEN Hongzheng
Improved hybrid solar cells consisting of vertical aligned cadmium sulfide （CdS） nanorod arrays and interpenetrating polythiophene （P3HT） have been achieved via modification of CdS nanorod surface by using conjugated N719 dye. The complete infiltration of P3HT between CdS nanorods interspacing was verified by scanning electron microscopy. By employing absorption and photoluminescence spectra, and current-voltage characterization the interaction between N719 molecules and CdS nanorods/P3HT interface was explored, and the role of N719 dye on the improvement of device performance was discussed.
Stable aqueous amino-grafted silicon nanoparticles （SiNPs-NH2） were prepared via one-pot solution method. By grafting amino groups on the particle surface, the dispersion of SiNPs in water became very stable and clear aqueous solutions could be obtained. By incorporating SiNPs-NH2 into the hole transport layer of poly（3,4- ethylenedioxythiophene）/polystyrene sulfonic acid （PEDOT＇PSS）, the performance of polymer solar cells composed of poly[2-methoxy,5-（2＇-ethylhexyloxy）-1,4-phenylene vinylene] （MEH-PPV）：[6,6]-phenyl-C61-butyric acid methyl ester （PCBM） as active layer can be improved. SiNPs-NH2 are dispersed uniformly in the PEDOT：PSS solution and help form morphologies with small-sized domains in the PEDOT：PSS film. SiNPs-NH2 serve as screens between conducting polymer PEDOT and ionomer PSS to improve the phase separation and charge transport of the hole transport layer. As a result, the sheet resistance of PEDOT：PSS thin films is decreased from （93 ±5） × 10^5 to （13 ± 3） × 10^5 Ω/□. The power conversion efficiency （PCE） of polymer solar cells was thus improved by 9.8% for devices fabricated with PEDOT＇PSS containing 1 wt% of SiNPs-NH2, compared with the devices fabricated by original PEDOT：PSS.
Light trapping based on the localized surface-plasmon resonance(LSPR)effect of metallic nanostructures is a promising strategy to improve the device performance of organic solar cells(OSCs).We review recent advances in plasmonic-enhanced OPVs with solution-processed metallic nanoparticles(NPs).The different types of metallic NPs(sizes,shapes,and hybrids),incorporation positions,and NPs with tunable resonance wavelengths toward broadband enhancement are systematically summarized to give a guideline for the realization of highly efficient plasmonic photovoltaics.
