An organosilane self-assembled monolayer incorporated into polymer solar cells enabling interfacial coherence to improve charge transport

The reproducible silylation of titanium oxide (TiO2) with small molecular (dichloromethyl) dimethylchlorosilane (DCS) as the cathode buffer layer was developed to improve electron extraction. Through incorporating the DCS capping layer into polymer solar cells (PSCs), the interfacial coherence of devices could be enhanced, leading to a shift in nanocrystallite size and a smaller internal charge transport resistance. Furthermore, a TiO2/DCS combined interfacial layer could serve as both an exciton dissociation center and a charge transfer channel, which results in a reduction in the energy barrier and electron loss, improving hole-blocking and surface-state passivation in the TiO2 interfacial layer. The Kelvin probe measurements demonstrate that the employment of the DCS nanolayer decreases conduction band energy of TiO2 via forming a dipole layer at the interface of TiO2 and the DCS nanolayer, which tunes the work-function of the device and ulteriorly enhances charge carrier transfer between the electrode and the active layer. As a result, the photocurrent and the fill factor of the PSCs are both increased, resulting in an increased power conversion efficiency (PCE) of 6.959%

An organosilane self-assembled monolayer incorporated into polymer solar cells enabling interfacial coherence to improve charge transport

The reproducible silylation of titanium oxide (TiO2) with small molecular (dichloromethyl) dimethylchlorosilane (DCS) as the cathode buffer layer was developed to improve electron extraction. Through incorporating the DCS capping layer into polymer solar cells (PSCs), the interfacial coherence of devices could be enhanced, leading to a shift in nanocrystallite size and a smaller internal charge transport resistance. Furthermore, a TiO2/DCS combined interfacial layer could serve as both an exciton dissociation center and a charge transfer channel, which results in a reduction in the energy barrier and electron loss, improving hole-blocking and surface-state passivation in the TiO2 interfacial layer. The Kelvin probe measurements demonstrate that the employment of the DCS nanolayer decreases conduction band energy of TiO2 via forming a dipole layer at the interface of TiO2 and the DCS nanolayer, which tunes the work-function of the device and ulteriorly enhances charge carrier transfer between the electrode and the active layer. As a result, the photocurrent and the fill factor of the PSCs are both increased, resulting in an increased power conversion efficiency (PCE) of 6.959%

The operation mechanism of poly(9,9-dioctylfluorenyl-2,7-diyl) dots in high efficiency polymer solar cells

The highly efficient polymer solar cells were realized by doping poly(9,9-dioctylfluorenyl-2,7-diyl) (PFO) dots into active layer. The dependence of doping amount on devices performance was investigated and a high efficiency of 7.15% was obtained at an optimal concentration, accounting for a 22.4% enhancement. The incorporation of PFO dots (Pdots) is conducted to the improvement of Jsc and fill factor mainly due to the enhancement of light absorption and charge transport property. Pdots blended in active layer provides an interface for charge transfer and enables the formation of percolation pathways for electron transport. The introduction of Pdots was proven an effective way to improve optical and electrical properties of solar cells

Enhanced electron extraction capability of polymer solar cells \u3ci\u3evia\u3c/i\u3e modifying the cathode buffer layer with inorganic quantum dots

Enhanced performance of polymer solar cells (PSCs) based on the blend of poly[N-9 -hepta-decanyl- 2,7-carbazole-alt-5,5-(4\u27,7\u27-di-2-thienyl-2\u27,1\u27,3\u27-benzothiadiazole)] (PCDTBT):[6,6]-phenyl-C70-butyric acid methyl ester (PC71BM) is demonstrated by titanium dioxide (TiO2) interface modification via CuInS2/ZnS quantum dots (CZdots). Devices with a TiO2/CZdots composite buffer layer exhibit both a high shortcircuit current density (Jsc) and fill factor (FF), leading to a power conversion efficiency (PCE) up to 7.01%. The charge transport recombination mechanisms are investigated by an impedance behavior model, which indicates that TiO2 interfacial modification results in not only increasing the electron extraction but also reducing impedance. This study provides an important and beneficial approach to develop high efficiency PSCs

Erratum: “The operation mechanism of poly (9,9-dioctylfluorenyl-2,7-diyl) dots in high efficiency polymer solar cells” [Appl. Phys. Lett. 106, 193904 (2015)]

We have noticed an error in Fig. 7 of the original article. Figs. 7(a) and 7(b) should be exchanged and the revised figure is shown below. We apologize for this error.

High-power mid-infrared femtosecond master oscillator power amplifier Er:ZBLAN fiber laser system

High-power femtosecond mid-infrared (MIR) lasers are of vast importance to both fundamental research and applications. We report a high-power femtosecond master oscillator power amplifier laser system consisting of a single-mode Er:ZBLAN fiber mode-locked oscillator and pre-amplifier followed by a large-mode-area Er:ZBLAN fiber main amplifier. The main amplifier is actively cooled and bidirectionally pumped at 976 nm, generating a slope efficiency of 26.9%. Pulses of 8.12 W, 148 fs at 2.8 μm with a repetition rate of 69.65 MHz are achieved. To the best of our knowledge, this is the highest average power ever achieved from a femtosecond MIR laser source. Such a compact ultrafast laser system is promising for a wide range of applications, such as medical surgery and material processing

The operation mechanism of poly(9,9-dioctylfluorenyl-2,7-diyl) dots in high efficiency polymer solar cells

The highly efficient polymer solar cells were realized by doping poly(9,9-dioctylfluorenyl-2,7-diyl) (PFO) dots into active layer. The dependence of doping amount on devices performance was investigated and a high efficiency of 7.15% was obtained at an optimal concentration, accounting for a 22.4% enhancement. The incorporation of PFO dots (Pdots) is conducted to the improvement of Jsc and fill factor mainly due to the enhancement of light absorption and charge transport property. Pdots blended in active layer provides an interface for charge transfer and enables the formation of percolation pathways for electron transport. The introduction of Pdots was proven an effective way to improve optical and electrical properties of solar cells

Erratum: “The operation mechanism of poly (9,9-dioctylfluorenyl-2,7-diyl) dots in high efficiency polymer solar cells” [Appl. Phys. Lett. 106, 193904 (2015)]

We have noticed an error in Fig. 7 of the original article. Figs. 7(a) and 7(b) should be exchanged and the revised figure is shown below. We apologize for this error.