Emad Oveisi

High‐Performance Perovskite Solar Cells with Enhanced Environmental Stability Based on Amphiphile‐Modified CH3NH3PbI3

A new aliphatic fluorinated amphiphilic additive is added to CH3 NH3 PbI3 perovskite to tune the morphology and enhance the environmental stability without sacrificing the performance of the devices. Judicious screening of the perovskite precursor solution realizes a power conversion efficiency of 18.0% for mesoporous perovskite solar cells as a result of improved surface coverage. A slower degradation in ambient air is observed with this modified perovskite.

Dopant-Free Hole-Transporting Materials for Stable and Efficient Perovskite Solar Cells

Molecularly engineered novel dopant-free hole-transporting materials for perovskite solar cells (PSCs) combined with mixed-perovskite (FAPbI3 )0.85 (MAPbBr3 )0.15 (MA: CH3 NH3+ , FA: NH=CHNH3+ ) that exhibit an excellent power conversion efficiency of 18.9% under AM 1.5 conditions are investigated. The mobilities of FA-CN, and TPA-CN are determined to be 1.2 × 10-4 cm2 V-1 s-1 and 1.1 × 10-4 cm2 V-1 s-1 , respectively. Exceptional stability up to 500 h is measured with the PSC based on FA-CN. Additionally, it is found that the maximum power output collected after 1300 h remained 65% of its initial value. This opens up new avenue for efficient and stable PSCs exploring new materials as alternatives to Spiro-OMeTAD.

Enhanced charge collection with passivation of the tin oxide layer in planar perovskite solar cells

Tin oxide is an excellent candidate to replace mesoporous TiO2 electron transport layers (ETLs) in perovskite solar cells. Here, we introduced a SnO2 layer by a low-temperature solution process, and investigated its morphology, opto-physical and electrical properties affecting the device performance. We reveal that low-temperature processed SnO2 is self-passivating in nature, which leads to a high efficiency. To further enhance the blocking effect, we combined a compact TiO2 underlayer with the SnO2 contact layer, and found that the bi-layered ETL is superior compared to single layers. The best device shows photovoltaic values in a planar structure with a short-circuit current density (Jsc) of 22.58 mA cm−2, an open-circuit voltage (Voc) of 1.13 V, a fill factor (FF) of 0.78, and a power conversion efficiency (PCE) of 19.80% under 1 sunlight illumination.

Selective growth of layered perovskites for stable and efficient photovoltaics

Perovskite solar cells (PSCs) are promising alternatives toward clean energy because of their high-power conversion efficiency (PCE) and low materials and processing cost. However, their poor stability under operation still limits their practical applications. Here we design an innovative approach to control the surface growth of a low dimensional perovskite layer on top of a bulk three-dimensional (3D) perovskite film. This results in a structured perovskite interface where a distinct layered low dimensional perovskite is engineered on top of the 3D film. Structural and optical properties of the stack are investigated and solar cells are realized. When embodying the low dimensional perovskite layer, the photovoltaic cells exhibit an enhanced PCE of 20.1% on average, when compared to pristine 3D perovskite. In addition, superior stability is observed: the devices retain 85% of the initial PCE stressed under one sun illumination for 800 hours at 50 °C in an ambient environment.

Rapid, Selective Heavy Metal Removal from Water by a Metal–Organic Framework/Polydopamine Composite

Drinking water contamination with heavy metals, particularly lead, is a persistent problem worldwide with grave public health consequences. Existing purification methods often cannot address this problem quickly and economically. Here we report a cheap, water stable metal–organic framework/polymer composite, Fe-BTC/PDA, that exhibits rapid, selective removal of large quantities of heavy metals, such as Pb2+ and Hg2+, from real world water samples. In this work, Fe-BTC is treated with dopamine, which undergoes a spontaneous polymerization to polydopamine (PDA) within its pores via the Fe3+ open metal sites. The PDA, pinned on the internal MOF surface, gains extrinsic porosity, resulting in a composite that binds up to 1634 mg of Hg2+ and 394 mg of Pb2+ per gram of composite and removes more than 99.8% of these ions from a 1 ppm solution, yielding drinkable levels in seconds. Further, the composite properties are well-maintained in river and seawater samples spiked with only trace amounts of lead, illustrating unprecedented selectivity. Remarkably, no significant uptake of competing metal ions is observed even when interferents, such as Na+, are present at concentrations up to 14u202f000 times that of Pb2+. The material is further shown to be resistant to fouling when tested in high concentrations of common organic interferents, like humic acid, and is fully regenerable over many cycles.

Trash into Treasure: δ‐FAPbI3 Polymorph Stabilized MAPbI3 Perovskite with Power Conversion Efficiency beyond 21%

Effective passivation and stabilization of both the inside and interface of a perovskite layer are crucial for perovskite solar cells (PSCs), in terms of efficiency, reproducibility, and stability. Here, the first formamidinium lead iodide (δ-FAPbI3 ) polymorph passivated and stabilized MAPbI3 PSCs are reported. This novel MAPbI3 /δ-FAPbI3 structure is realized via treating a mixed organic cation MA x FA1-x PbI3 perovskite film with methylamine (MA) gas. In addition to the morphology healing, MA gas can also induce the formation of δ-FAPbI3 phase within the perovskite film. The in situ formed 1D δ-FAPbI3 polymorph behaves like an organic scaffold that can passivate the trap state, tunnel contact, and restrict organic-cation diffusion. As a result, the device efficiency is easily boosted to 21%. Furthermore, the stability of the MAPbI3 /δ-FAPbI3 film is also obviously improved. This δ-FAPbI3 phase passivation strategy opens up a new direction of perovskite structure modification for further improving stability without sacrificing efficiency.

Stereo-vision three-dimensional reconstruction of curvilinear structures imaged with a TEM

Deriving accurate three-dimensional (3-D) structural information of materials at the nanometre level is often crucial for understanding their properties. Tomography in transmission electron microscopy (TEM) is a powerful technique that provides such information. It is however demanding and sometimes inapplicable, as it requires the acquisition of multiple images within a large tilt arc and hence prolonged exposure to electrons. In some cases, prior knowledge about the structure can tremendously simplify the 3-D reconstruction if incorporated adequately. Here, a novel algorithm is presented that is able to produce a full 3-D reconstruction of curvilinear structures from stereo pair of TEM images acquired within a small tilt range that spans from only a few to tens of degrees. Reliability of the algorithm is demonstrated through reconstruction of a model 3-D object from its simulated projections, and is compared with that of conventional tomography. This method is experimentally demonstrated for the 3-D visualization of dislocation arrangements in a deformed metallic micro-pillar.

MOF-Derived Cobalt Phosphide/Carbon Nanocubes for Selective Hydrogenation of Nitroarenes to Anilines

Transition-metal phosphides have received tremendous attention during the past few years because they are earth-abundant, cost-effective, and show outstanding catalytic performance in several electrochemically driven conversions including hydrogen evolution, oxygen evolution, and water splitting. As one member of the transition-metal phosphides, Cox P-based materials have been widely explored as electrocatalyts; however, their application in the traditional thermal catalysis are rarely reported. In this work, cobalt phosphide/carbon nanocubes are designed and their catalytic activity for the selective hydrogenation of nitroarenes to anilines is studied. A high surface area metal-organic framework (MOF), ZIF-67, is infused with red phosphorous, and then pyrolysis promotes the facile production of the phosphide-based catalysts. The resulting composite, consisting of Co2 P/CNx nanocubes, is shown to exhibit excellent catalytic performance in the selective hydrogenation of nitroarenes to anilines. To the best of our knowledge, this is the first report showing catalytic activity of a cobalt phosphide in nitroarenes hydrogenation.

Tilt-less 3-D electron imaging and reconstruction of complex curvilinear structures

The ability to obtain three-dimensional (3-D) information about morphologies of nanostructures elucidates many interesting properties of materials in both physical and biological sciences. Here we demonstrate a novel method in scanning transmission electron microscopy (STEM) that gives a fast and reliable assessment of the 3-D configuration of curvilinear nanoufeffstructures, all without needing to tilt the sample through an arc. Using one-dimensional crystalline defects known as dislocations as a prototypical example of a complex curvilinear object, we demonstrate their 3-D reconstruction two orders of magnitude faster than by standard tilt-arc TEM tomographic techniques, from data recorded by selecting different ray paths of the convergent STEM probe. Due to its speed and immunity to problems associated with a tilt arc, the tilt-less 3-D imaging offers important advantages for investigations of radiation-sensitive, polycrystalline, or magnetic materials. Further, by using a segmented detector, the total electron dose is reduced to a single STEM raster scan acquisition; our tilt-less approach will therefore open new avenues for real-time 3-D electron imaging of dynamic processes.

Single-layer graphene membranes by crack-free transfer for gas mixture separation

The single-layer graphene film, when incorporated with molecular-sized pores, is predicted to be the ultimate membrane. However, the major bottlenecks have been the crack-free transfer of large-area graphene on a porous support, and the incorporation of molecular-sized nanopores. Herein, we report a nanoporous-carbon-assisted transfer technique, yielding a relatively large area (1u2009mm2), crack-free, suspended graphene film. Gas-sieving (H2/CH4 selectivity up to 25) is observed from the intrinsic defects generated during the chemical-vapor deposition of graphene. Despite the ultralow porosity of 0.025%, an attractive H2 permeance (up to 4.1u2009×u200910−7u2009molu2009m−2u2009s−1u2009Pa−1) is observed. Finally, we report ozone functionalization-based etching and pore-modification chemistry to etch hydrogen-selective pores, and to shrink the pore-size, improving H2 permeance (up to 300%) and H2/CH4 selectivity (up to 150%). Overall, the scalable transfer, etching, and functionalization methods developed herein are expected to bring nanoporous graphene membranes a step closer to reality.Graphene shows great promise for gas separation applications, but obtaining large membranes that are free of cracks and tears remains highly challenging. Here, the authors realize monolayer, crack-free, millimeter-scale graphene membranes that exhibit selective gas permeation solely thanks to their intrinsic defects