ABSTRACT
Four organic solar cell (OSC) devices with the bilayer heterojunction architecture were investigated, where carbon nanotubes (CNTs) were doped within the acceptor layer. The power conversion efficiency (PCE) of the CNT-incorporated device with a concentration of 0.004 wt% is approximately 20% point higher than that of the reference one. As the concentration of CNTs became higher, the PCE of the devices deteriorated; this could be caused by the percolative connection of CNTs within the layer. The voltage dependence on the effective lifetime of the charge carriers, determined by Cole-Cole curves of the impedance analysis, was different for the reference and CNT-incorporating devices-the lifetime of the CNT-incorporated ones was shorter, possibly owing to the high local electric field near the CNTs. Controlling the concentration of CNTs below the critical concentration of percolation is a key factor in achieving high photovoltaic performance.
ABSTRACT
A TiO2 with exposed (001) facets/Bi4O5Br2 nanosheets heterojunction (TNS/BOB) was fabricated via a hydrothermal and electrostatic self-assembly method. The photocatalytic activity for NO removal was evaluated under simulated solar light irradiation. Through optimizing the content of TNS nanosheets, the photo-oxidative NO removal rate of 15% TNS/BOB was increased by up to 54.3%. This value is much higher than that of the individual components TNS (31.1%) and BOB (37.7%). Through capturing experiments and electron spin resonance (ESR) measurements, the main active species in the photocatalytic process were identified as ·[Formula: see text] and ·OH. Discrete Fourier transform computation results and ESR tests revealed that the photo-induced electrons in TNS should recombine with the holes in BOB, leading to effectively promoted charge separation at the TNS/BOB interface through the Z-type charge transfer. This work showed that with appropriate facet control and heterojunction design TiO2 can be used as an effective visible-light photocatalyst material.
