PSS are demonstrated in the optimized device due to the incorporation of an MoO3 layer.

The lead-free perovskite solar cells (PSCs) have drawn a great deal of research interest due to the Pb toxicity of the lead halide perovskite. CH 3 NH 3 SnI 3 is a viable alternative to CH 3 NH 3 PbX 3 , because it has a narrower band gap of 1.3 eV and a wider visible absorption spectrum than the lead halide perovskite. The progress of fabricating tin iodide PSCs with good stability has stimulated the studies of these CH 3 NH 3 SnI 3 based cells greatly. In the paper, we study the influences of various parameters on the solar cell performance through theoretical analysis and device simulation. It is found in the simulation that the solar cell performance can be improved to some extent by adjusting the doping concentration of the perovskite absorption layer and the electron affinity of the buffer and HTM, while the reduction of the defect density of the perovskite absorption layer significantly improves the cell performance. By further optimizing the parameters of the doping concentration (1.3 × 10 16 cm −3 ) and the defect density (1 × 10 15 cm −3 ) of perovskite absorption layer, and the electron affinity of buffer (4.0 eV) and HTM (2.6 eV), we finally obtain some encouraging results of the J sc of 31.59 mA/cm 2 , V oc of 0.92 V, FF of 79.99%, and PCE of 23.36%. The results show that the lead-free CH 3 NH 3 SnI 3 PSC is a potential environmentally friendly solar cell with high efficiency. Improving the Sn 2+ stability and reducing the defect density of CH 3 NH 3 SnI 3 are key issues for the future research, which can be solved by improving the fabrication and encapsulation process of the cell.

We demonstrate a cascade-energy-level alignment based organic photovoltaic cell by using stacking three materials with appropriate energy levels. A cell with a structure of ITO/4,4′,4″-tris[N,(3-methylphenyl)-N-phenylamino]-triphenylamine (m-MTDATA)/copper phthalocyanine (CuPc)/fullerene (C60)/4,4′-N,N′-dicarubreneazolebiphenyl (BCP)/LiF/Al was shown to have a power efficiency enhancement in more than 30% over that of a standard reference cell (ITO/CuPc/C60/BCP/LiF/Al), which has only one exciton-dissociation interface. The efficiency improvement was mainly ascribed to the ingenious cascade-energy-level alignment and the application of the bipolar carrier transporting property.

The authors demonstrate high response organic ultraviolet (UV) photodetector (PD) using 4,4′,4″-tri-(2-methylphenyl phenylamino) triphenylaine (m-MTDATA) and tris-(8-hydroxyquinoline) gallium (Gaq3) to act as the electron donor and acceptor, respectively. The m-MTDATA:Gaq3 blend device shows a photocurrent of 405μA∕cm−2 at −8V, corresponding to a response of 338mA∕W under an illumination of 365nm UV light with an intensity of 1.2mW∕cm2. The high response is attributed to the enhanced dissociation of geminate hole-electron pairs in the distributed heterojunction of the blend and suppression of radiative decay. Photophysics of the PD involved is also discussed in terms of the performance and device structures.