METHOD FOR SINGLE CRYSTAL GROWTH OF PHOTOVOLTAIC PEROVSKITE MATERIAL AND DEVICES

Systems and methods for perovskite single crystal growth include using a low temperature solution process that employs a temperature gradient in a perovskite solution in a container , also including at least one small perovskite single crystal , and a substrate in the solution upon which substrate a perovskite crystal nucleates and grows , in part due to the temperature gradient in the solution and in part due to a temperature gradient in the substrate . For example , a top portion of the substrate external to the solution may be cooled

SYSTEMS AND METHODS FOR SCALABLE PEROVSKITE DEVICE FABRICATION

Continuous processes for fabricating a perovskite device are described that include forming a perovskite layer or film on a substrate using a linear deposition device , and optionally using a conductive tape lamination process to form an anode or a cathode layer on the perovskite device

Chloride Incorporation Process in CH\u3csub\u3e3\u3c/sub\u3eNH\u3csub\u3e3\u3c/sub\u3ePbI\u3csub\u3e3-x\u3c/sub\u3eCl\u3csub\u3ex\u3c/sub\u3e Perovskites via Nanoscale Bandgap Maps

CH3NH3PbI3-xClx perovskites enable fabrication of highly efficient solar cells. Chloride ions benefit the morphology, carrier diffusion length and stability of perovskite films; however, whether those benefits stem from the presence of Cl− in the precursor solution or from their incorporation in annealed films is debated. In this work, the photothermal induced resonance (PTIR), an in situ technique with nanoscale resolution, is leveraged to measure the bandgap of CH3NH3PbI3-xClx films obtained by a multicycle coating process that produces high efficiency (≈16 %) solar cells. Because chloride ions modify the perovskite lattice, thereby widening the bandgap, measuring the bandgap locally yields the local chloride content. After a mild annealing (60 min, 60°C) the films consist of Cl-rich (x \u3c 0.3) and Cl-poor phases that, upon further annealing (110 °C), evolve into a homogenous Cl-poorer (x \u3c 0.06) phase, suggesting that methylammonium-chrloride is progressively expelled from the film. Despite the small chloride content, CH3NH3PbI3-xClx films show better thermal stability up to 140 °C with respect CH3NH3PbI3 films fabricated with the same methodology

Thumb function and appearance following treatment of Wassel type III duplication thumbs

AbstractObjectiveThe purpose of our study is to evaluate thumb function and appearance after surgical correction of Wassel type III thumbs polydactyly.MethodsWe have reconstructed 28 cases of Wassel type III duplication thumbs, in which the duplicated digits were equal or almost equal in size by ablation of a radial digit. The extra thumb is osteotomized at the bifurcation level and excised except for the distal bone fragment supporting the nail bed and fillet flap. Meanwhile, the nail of the retained thumb should be reserved completely, and if the nail has relatively poor appearance it should be repaired by nail lengthening surgery. Eighteen cases were followed up for more than 3 years and were available for assessment using the Japanese Society for Surgery of the Hand evaluation form. The average age at follow-up was 5 years. The size of the nail and distal phalanx was measured to assess the growth of the thumb.ResultsAn average functional point was 12 points (maximum 14 points) and the cosmetic score averaged 3.6 (maximum 4 points) after the assessment. Slightly small nails without a central ridge were deemed acceptable. Second revision surgery is seldom. Long-term results after surgical reconstruction for duplication thumbs were excellent, and all patients and parents were satisfied with the cosmetic and functional results.ConclusionsThis procedure is a helpful and effective way to provide functional and aesthetical thumb for Wassel type III duplication thumbs

INSULATING TUNNELING CONTACT FOR EFFICIENT AND STABLE PEROVSKITE SOLAR CELLS

Perovskite-based photoactive devices, such as solar cells, include an insulating tunneling layer inserted between the perovskite photoactive material and the electron collection layer to reduce charge recombination and concomitantly provide water resistant properties to the device

Improving the sensitivity of a near-infrared nanocomposite photodetector by enhancing trap induced hole injection

We report the enhancement of the photoconductive gain of nanocomposite near-infrared photodetectors by a zinc oxide nanoparticles (ZnO NPs) rich surface at the nanocomposite/cathode interface. An argon plasma etching process was used to remove polymer at the surface of nanocomposite films, which resulted in a ZnO NPs rich surface. The other way is to spin-coat a thin layer of ZnO NPs onto the nanocomposite layer. The ZnO NPs rich surface, which acts as electron traps to induce secondary hole injection under reverse bias, increased hole injection, and thus the external quantum efficiency by 2–3 times. The darkcurrent declined one order of magnitude simultaneously as a result of etching the top nanocomposite layer. The specific detectivity at 800 nm was increased by 7.4 times to 1.11x1010 Jones due to the simultaneously suppressed noise and enhanced gain

Unraveling the hidden function of a stabilizer in a precursor in improving hybrid perovskite film morphology for high efficiency solar cells

The morphology of the organometal trihalide perovskite (OTP) plays a critical role in the performance of solar cell devices. Nevertheless it has been frequently reported that the morphology of OTP films tends to be different in different laboratories even with the same film preparation procedure, which makes it very difficult to compare and understand the material and device physics. Here, we unravel a critical role of the H3PO2 stabilizer in HI, which has been largely ignored, in controlling the morphology of the perovskite films. The H3PO2 stabilizer in HI solution introduces MAH2PO2 impurities into the synthesized MAI (non-purified MAI) by reacting with methylamine (MA) aqueous solution. MAH2PO2 impurities can slow down the overall crystallization process of perovskite by forming an intermediate phase of Pb(H2PO2)2. Both MAH2PO2 and Pb(H2PO2)2 impede the fast reaction of PbI2 and MAI, resulting in highly uniform and smooth perovskite films with larger grain sizes. The recrystallization of non-purified MAI can remove the MAH2PO2 impurity and form purified MAI, which however results in rough and non-uniform perovskite films. Uniform and smooth perovskite films can also be obtained by directly adding artificially synthesized MAH2PO2 into the purified MAI precursor. This study also suggests Pb(H2PO2)2 to be a new precursor to formhigh quality perovskite films

Fast Growth of Thin MAPbI\u3csub\u3e3\u3c/sub\u3e Crystal Wafers on Aqueous Solution Surface for Efficient Lateral-Structure Perovskite Solar Cells

Solar-grade single or multiple crystalline wafers are needed in large quantities in the solar cell industry, and are generally formed by a top-down process from crystal ingots, which causes a significant waste of materials and energy during slicing, polishing, and other processing. Here, a bottom-up technique that allows the growth of wafer-size hybrid perovskite multiple crystals directly from aqueous solution is reported. Single-crystalline hybrid perovskite wafers with centimeter size are grown at the top surface of a perovskite precursor solution. As well as saving raw materials, this method provides unprecedented advantages such as easily tunable thickness and rapid growth of the crystals. These crystalline wafers show high crystallinity, broader light absorption, and a long carrier recombination lifetime, comparable with those of bulk single crystals. Lateral-structure perovskite solar cells made of these crystals demonstrate a record power conversion efficiency of 5.9%. Includes supplementary materials