Meng-Si Niu

Dual Förster resonance energy transfer effects in non-fullerene ternary organic solar cells with the third component embedded in the donor and acceptor

Non-fullerene ternary organic solar cells (OSCs) are new promising candidates for future applications in the area of organic photovoltaics. However, their low short-circuit current (JSC) values impede efforts at increasing their power conversion efficiency (PCE) levels. Maximizing the JSC is one of the critical elements for enabling high performances of OSCs. To improve the JSC of the non-fullerene ternary OSCs based on poly[[2,6′-4,8-di(5-ethylhexylthienyl)benzo[1,2-b:3,3-b]dithiophene][3-fluoro-2[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophenediyl]]:3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone))-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]-dithiophene (PTB7-Th:ITIC), a polymer of poly[N-9′′-hepta-decanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)] (PCDTBT) was added to the binary system. The PCDTBT was shown to embed in both PTB7-Th and ITIC, and introduced dual Forster resonance energy transfer (FRET) effects in the resulting ternary system. In addition, the PCDTBT may have decreased the molecular coherence lengths of PTB7-Th and ITIC and influenced the charge transport. Furthermore, the PCDTBT apparently also decreased the d-spacing of the π–π stacking of PTB7-Th and ITIC, which likely increased the intermolecular charge hopping efficiency. Doping an appropriate amount of PCDTBT in the system yielded an increase in the JSC from 13.89 to 16.71 mA cm−2. The increased JSC resulted in a 15% enhancement of the PCE, which indicated that introducing dual FRET effects is an effective way to enhance the JSC and thus the performance of the OSCs.

Structural and optical properties of conjugated polymer and carbon-based non-fullerene material blend films for photovoltaic applications

In this work, the structural and optical properties of bulk heterojunctions (BHJ) composed of MEH-PPV and carbon-based non-fullerene nanodiamond (ND) have been investigated. The steady-state absorption, temperature-dependent fluorescence and Raman spectroscopy demonstrate the conjugated length is increased and more ordered crystalline domains are formed in MEH-PPV films with the increment of ND content. The time-resolved fluorescence spectroscopy and 2D microscopy indicate that the BHJs with higher concentrations of ND may enhance the donor/acceptor interfacial contact which favors the dissociation of excitons into free charge carriers. Solar cells based on MEH-PPV:ND BHJs were fabricated to explore the interplay between structural, photophysical properties, and ultimately, device performances. The results show that optimization of blend composition and structures with ND may improve the efficiency of the thin film photovoltaic devices.

Efficient photoinduced charge transfer in chemically-linked organic-metal Ag-P3HT nanocomposites

A novel nanocomposite of P3HT and Ag nanoparticles (Ag-P3HT) has been synthesized by laser ablation. The fluorescence wavelength of the nanocomposite can be tuned by varying the ablation duration. The steady-state emission maximum at 580 nm for pristine P3HT shows significant blueshift to wavelengths ranging from 520 to 550 nm for Ag-P3HT. NMR, FTIR and XPS spectroscopy confirm that chemical links are formed between P3HT and silver nanoparticles (NPs) in the nanocomposite. For the sample with an emission maximum at 530 nm, 1H NMR spectra indicate that 66% of the P3HT thiophene ring protons are replaced by Ag NPs. Time-resolved spectroscopy demonstrates that charge transfer efficiency increases for Ag-P3HT and this is attributed to the enhanced intimate interfacial contact between the chemically-bonded metal NPs and polymer chains. The synthetic route outlined provides a one-pot and green strategy for producing metal-organic polymeric materials, with controlled luminescence wavelengths and efficient photoinduced charge transfer that meet the requirement for developing high-performance organic light-emitting and photovoltaic devices.

Improved compatibility of DDAB-functionalized graphene oxide with a conjugated polymer by isocyanate treatment

2-Chlorophenyl isocyanate (CI) reacts with didodecyl dimethyl ammonium bromide (DDAB) functionalized graphene oxide (DDAB-GO) dispersed in ortho-dichlorobenzene under mild conditions. The CI treatment complements DDAB functionalization to further decrease the hydrophilicity of pristine GO sheets. The resulting CI–DDAB-GO exhibits improved compatibility with the conjugated polymer poly(3-hexylthiophene) (P3HT), compared to DDAB-GO. CI–DDAB-GO sheets can be homogeneously dispersed when blended with P3HT, resulting in an improved morphology compared to P3HT:DDAB-GO composites. The incorporation of CI–DDAB-GO can effectively reduce the dark current of photo-diodes based on P3HT composites, showing potential to enhance the performance of electronic devices based on conjugated polymer composites.

Recent Advances of Plasmonic Organic Solar Cells: Photophysical Investigations

The surface plasmon resonance (SPR) of metallic nanomaterials, such as gold (Au) and silver (Ag), has been extensively exploited to improve the optical absorption, the charge carrier transport, and the ultimate device performances in organic photovoltaic cells (OPV). With the incorporation of diverse metallic nanostructures in active layers, buffer layers, electrodes, or between adjacent layers of OPVs, multiple plasmonic mechanisms may occur and need to be distinguished to better understand plasmonic enhancement. Steady-state photophysics is a powerful tool for unraveling the plasmonic nature and revealing plasmonic mechanisms such as the localized surface plasmon resonance (LSPR), the propagating plasmon-polariton (SPP), and the plasmon-gap mode. Furthermore, the charge transfer dynamics in the organic semiconductor materials can be elucidated from the transient photophysical investigations. In this review article, the basics of the plasmonic mechanisms and the related metallic nanostructures are briefly introduced. We then outline the recent advances of the plasmonic applications in OPVs emphasizing the linkage between the photophysical properties, the nanometallic geometries, and the photovoltaic performance of the OPV devices.

Femtosecond laser processing induced low loss waveguides in multicomponent glasses

We have investigated that femtosecond laser induced optical waveguides in AF32 and in Borofloat-33 glasses. Type-I positive and type-II negative refractive index change mechanisms were established in AF32 and in Borofloat-33 glass waveguides, respectively. Lowest propagation loss of 1.1 ± 0.31 dB/cm could be attained in AF32 glass, which has a typically higher index change than in Borofloat-33 glass. Resultant losses are directly correlated with densification and non-bridging oxygen hole centers, which can be authenticated by Raman and photoluminescence studies.