Single-walled carbon nanotubes (SWCNTs) have highly desirable attributes for solution-processable thin-film photovoltaics (TFPVs), such as broadband absorption, high carrier mobility, and environmental stability. However, previous TFPVs incorporating photoactive SWCNTs have utilized architectures that have limited current, voltage, and ultimately power conversion efficiency (PCE). Here, we report a solar cell geometry that maximizes photocurrent using polychiral SWCNTs while retaining high photovoltage, leading to record-high efficiency SWCNT-fullerene solar cells with average NREL certified and champion PCEs of 2.5% and 3.1%, respectively. Moreover, these cells show significant absorption in the near-infrared portion of the solar spectrum that is currently inaccessible by many leading TFPV technologies.

Noble metal/semiconductor nanocomposites play an important role in high efficient photocatalysis. Herein, we demonstrate a facile strategy for fabrication of hollow Pt-ZnO nanocomposite microspheres with hierarchical structure under mild solvothermal conditions using Zn (CH(3)COO)(2)·2H(2)O and HPtCl(4) as the precursors, and polyethylene glycol-6000 (PEG-6000) and ethylene glycol as the reducing agent and solvent, respectively. The as-synthesized ZnO and Pt-ZnO composite nanocrystals were well characterized by powder X-ray diffraction (XRD), nitrogen-physical adsorption, scanning electron microscopy (SEM), energy dispersive X-ray (EDX), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectra (DRS), and photoluminescence (PL) emission spectroscopy. It was found that Pt content greatly influences the morphology of Pt-ZnO composite nanocrystals. Suitable concentration of HPtCl(4) in the reaction solution system can produce well hierarchically hollow Pt-ZnO nanocomposite microspheres, which are composed of an assembly of fine Pt-ZnO nanocrystals. Photocatalytic tests of the Pt-ZnO microspheres for the degradation of the dye acid orange II revealed extremely high photocatalytic activity and stability compared with those of pure ZnO and corresponding Pt deposited ZnO. The remarkable photocatalytic performance of hollow Pt-ZnO microspheres mainly originated from their unique nanostructures and the low recombination rate of the e(-)/h(+) pairs by the platinum nanoparticles embedded in ZnO nanocrystals.

In order to understand the dependence of photoinduced initial processes on thermal annealing, the femtosecond time-resolved fluorescence dynamics of regioregular poly(3-hexylthiophene) (P3HT) in (thermally) annealed P3HT/[6,6]-phenyl-C61 butyric acid methyl ester (PCBM) blend films has been studied by using the fluorescence up-conversion technique. For comparison, a P3HT solution, pristine P3HT, and unannealed P3HT/PCBM blend films have been investigated as well. The fluorescence dynamics of the P3HT solution showed wavelength dependence. Excitation energy transfer between the segments and torsional relaxation possibly occurred in a time scale of several ps in the solution. Observed rise times at longer wavelength emission suggested the formation of these relatively lower emission states (at 650 and 700 nm). Charge transfer (or excitonic quenching) was the dominant process in the fs time scale with emission at 650 nm in the unannealed blend film. In the annealed blend film, the charge transfer (334 fs) and downhill relaxation (942 fs) of self-trapped (dynamic localized) excitons were competitive processes due to the well aligned nanodomains in the P3HT/PCBM blend films. There were different charge transfer rates at different excited states (650 and 700 nm) in the annealed film. The charge transfer process occurred faster at a lower excited state, and a stronger electronic and vibrational coupling in the annealed P3HT/PCBM films was revealed within these measurements as well. The ultrafast anisotropy decays suggested that a strong and ultrafast reorientation of the molecular dipole moments occurred at excited states. The anisotropy decay was mainly determined by the ultrafast process, whereas the energy could continuously migrate along or between P3HT chains in a time scale of ∼100 ps. The ultrafast process suggested that there was an excitation delocalization associated with vibrational modes, as was consistent with the observation from steady-state measurements. On the basis of the understanding of the mechanisms above, the optimized cell performance has been established.

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High‐performance broad‐spectrum nanocarbon bulk‐heterojunction photovoltaic photodetectors are reported. These reported photodetectors consist of a semiconducting single‐walled carbon nanotube (s‐SWCNT) and a PC71BM blended active layer. Magnetic‐field effects and the chirality of the s‐SWCNTs play an important role in controlling the photoresponse time and photocurrent improvement.

A series of pincer-type compounds possessing an N-heterocyclic carbene precursor and a carboxyl group as proton transfer agent were synthesized and used as organocatalysts for the cycloaddition of epoxides with CO 2 . In this context, we have demonstrated the high activity of these one-component organocatalysts in the CO 2 transformation to cyclic carbonates under ambient conditions (room temperature, 1 bar of CO 2 ). The catalytic potential of these multifunctional organocatalysts on challenging internal epoxides is particularly deserving of mention because organocatalysts that are able to mediate the cycloaddition reaction of internal epoxides with CO 2 under mild conditions remain scarce. The intramolecular synergistic activation mechanism was elucidated by control experiments and DFT calculations.

An efficient method for palladium-catalyzed homocoupling reaction of terminal alkynes in the synthesis of symmetric diynes is presented. The results showed that both Pd(OAc)(2) and CuI played crucial roles in the reaction. In the presence of 2 mol % Pd(OAc)(2), 2 mol % CuI, 3 equiv of Dabco, and air, homocoupling of various terminal alkynes afforded the corresponding symmetrical diynes in moderate to excellent yields, whereas low yields were obtained without either Pd(OAc)(2) or CuI. Moreover, high TONs (turnover numbers; up to 940 000 for the reaction of phenylacetylene) for the homocoupling reaction were observed. Under similar reaction conditions, cross-coupling of 1-iodo-4-nitrobenzene with phenylacetylene was also carried out smoothly in quantitative yield. However, the presence of CuI disfavored the palladium-catalyzed Sonogashira cross-coupling reactions of the less active aryl iodides and bromides. In the presence of 0.01-2 mol % Pd(OAc)(2), a number of aryl iodides and bromides were coupled with terminal alkynes in good to excellent yields. It is noteworthy that this protocol employs mild, efficient, aerobic, copper-free, and ligand-free conditions.

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