Magnetic Field-Enhanced Performance of Superparamagnetic LiMn2 O4 -Based Composite Slurry Electrode for Semisolid Flow Battery.

Semisolid flow batteries are expected to be applied to large-scale energy storage fields due to the combination of the high energy density of rechargeable batteries and the flexible design of flow batteries. However, electronic conductivity, specific capacity, and viscosity of slurry electrodes are generally mutually restrictive. Here, a new concept of semisolid flow batteries based on magnetic modification slurry electrode is proposed and the electrochemical performance of the semisolid electrode is expected to be improved by close contact and enhanced electronic conductivity between the active particles with the aid of external magnetic field. This concept is further demonstrated using superparamagnetic LiMn2 O4 -Fe3 O4 -carbon nanotube composite as semisolid cathode. It achieves a capacity of 113.7 mAh g-1 at a current density of 0.5 mA cm-2 with the aid of external magnetic field (about 0.4 T), which is about 21% higher than that without external magnetic field. Simulation study also reveals this improvement mainly resulted from the increase of the conductive paths of electrons after the rearrangement of the active particles under the external magnetic field. It is believed that this strategy gives a new and effective method for controlling the viscosity and electronic conductivity of the slurry electrodes and related flowable electrochemical energy storage systems.

Potassium Iodide-Modified Lead-Free Cs3Bi2I9 Perovskites for Enhanced High-Efficiency Solar Cells.

Lead-free, bismuth-based perovskite solar cells (PSCs) are promising, non-toxic, and stable alternatives to lead-based PSCs, which are environmentally harmful and highly unstable under deprived air conditions. However, bismuth-based PSCs still suffer from low-power-conversion efficiency (PCE) due to their large bandgap and poor film morphology. Their poor film-forming ability is the greatest obstacle to Cs3Bi2I9 progress in thin-film solar cell technology. This study synthesizes novel, lead-free perovskites with a small bandgap, excellent stability, and highly improved photovoltaic performance by integrating different amounts of potassium iodide (KI) into a perovskite precursor solution. KI incorporation improves the crystallinity of the perovskite, increases the grain size, and decreases the potential contact distribution, which is demonstrated by X-ray diffraction, electronic scanning microscopy, atomic force microscopy, and ultraviolet-visible spectroscopy. The Cs3Bi2I9 PSC device with 2 vol. % incorporation of KI shows the highest PCE of 2.81% and Voc of 1.01 V as far as all the Bi-based cells fabricated for this study are concerned. The study demonstrates that incorporating KI in the Cs3Bi2I9 perovskite layer highly stabilizes the resultant PSC device against humidity to the extent that it maintains 98% of the initial PCE after 90 days, which is suitable for solar cell applications. The devices also demonstrate greater resistance to airborne contaminants and high temperatures without encapsulation, opening up new possibilities for lead-free Cs3Bi2I9 PSCs in future commercialization.

Layer-by-Layer Fabrication of PAH/PAMAM/Nano-CaCO3 Composite Films and Characterization for Enhanced Biocompatibility.

Nanoparticle production and functionalization for various biomedical uses are still challenging. Polymer composites constituted of poly(amidoamine) (PAMAM), polyallylamine hydrochloride (PAH), and calcium carbonate (CaCO3) nanoparticles have good biocompatibility with physiological tissue and fluids, making them excellent candidates for biomedical applications. This study investigated the characteristics of polymeric/nano-CaCO3 composite films based on a PAH/PAMAM matrix, which were fabricated through layer-by-layer synthesis on quartz glass substrates. It was found that the as-prepared elastic moduli of the resultant (PAH/PAMAM) n -CaCO3 (where n represents the number of bilayers) composite films varied from 1.40 to 23.70 GPa for different degrees of cross-linking when 0.1 M nano-CaCO3 particles were incorporated into the polymer matrix. The highly cross-linked (PAH/PAMAM)15-CaCO3 composite film had the highest recorded elastic modulus of 23.70 GPa, while it was observed that for all the composite films fabricated for the present study, the addition of the nano-CaCO3 particles approximately doubled the elastic modulus regardless of the degree of polymerization. Live/Dead assays were used to determine whether the produced composite films were compatible with human lung fibroblast cells. The findings indicate that the (PAH/PAMAM)7.5-CaCO3 composite film had the most positive effect on cell growth and proliferation, with the (PAH/PAMAM)15-CaCO3 composite film demonstrating significant ion transport behavior with low impedance, which was considered good for in vivo rapid cell-to-cell communication. Therefore, the (PAH/PAMAM)7.5-CaCO3 and (PAH/PAMAM)15-CaCO3 composite films are potential tissue engineering biomaterials, but further studies are essential to generate more data to evaluate the suitability of these composites for this and other biomedical functions.

Solvent Engineering for Intermediates Phase, All-Ambient-Air-Processed in Organic-Inorganic Hybrid Perovskite Solar Cells.

Intermediate phase is considered an important aspect to deeply understand the crystallization procedure in the growth of high-quality perovskite layers by an anti-solvent technique. However, the moisture influence on the intermediate phase formation is not clear in air conditions as yet. In this work, pure (FA0.2MA1.8)Pb3X8(DMSO·DMF) intermediate phase was obtained in as-prepared perovskite film by spin-coating the precursor of co-solvent (DMSO and DMF) in an ambient air (RH20-30%). Moreover, the appropriate quantity of ethyl acetate (C4H8O2, EA) also controls the formation of pure intermediate phase. The uniform and homogeneous perovskite film was obtained after annealing this intermediate film. Therefore, the best power conversion efficiency (PCE) of perovskite solar cells (PSCs) is 16.24% with an average PCE of 15.53%, of which almost 86% of its initial PCE was preserved after 30 days in air conditions. Besides, the steady-state output efficiency ups to 15.38% under continuous illumination. In addition, the PCE of large area device (100 mm2) reaches 11.11% with a little hysteresis effect. This work would give an orientation for PSCs production at the commercial level, which could lower the cost of fabricating the high efficiency PSCs.

SnSe2 Field-Effect Transistor with High On/Off Ratio and Polarity-Switchable Photoconductivity.

SnSe2 field-effect transistor was fabricated based on exfoliated few-layered SnSe2 flake, and its electrical and photoelectric properties have been investigated in detail. With the help of a drop of de-ionized (DI) water, the SnSe2 FET can achieve an on/off ratio as high as ~ 104 within 1 V bias, which is ever extremely difficult for SnSe2 due to its ultrahigh carrier density (1018/cm3). Moreover, the subthreshold swing and mobility are both improved to ∼ 62 mV/decade and ~ 127 cm2 V-1 s-1 at 300 K, which results from the efficient screening by the liquid dielectric gate. Interestingly, the SnSe2 FET exhibits a gate bias-dependent photoconductivity, in which a competition between the carrier concentration and the mobility under illumination plays a key role in determining the polarity of photoconductivity.

Light Trapping Effect in Perovskite Solar Cells by the Addition of Ag Nanoparticles, Using Textured Substrates.

In this contribution, the efficiencies of perovskite solar cells have been further enhanced, based on optical optimization studies. The photovoltaic devices with textured perovskite film can be obtained and a power conversion efficiency (PCE) of the textured fluorine-doped tin oxide (FTO)/Ag nanoparticles (NPs) embedded in c-TiO2/m-TiO2/CH3NH3PbI3/Spiro-OMeTAD/Au showed 33.7% enhancement, and a maximum of up to 14.01% was achieved. The efficiency enhancement can be attributed to the light trapping effect caused by the textured FTO and the incorporated Ag NPs, which can enhance scattering to extend the optical pathway in the photoactive layer of the solar cell. Interestingly, aside from enhanced light absorption, the charge transport characteristics of the devices can be improved by optimizing Ag NPs loading levels, which is due to the localized surface plasmon resonance (LSPR) from the incorporated Ag NPs. This light trapping strategy helps to provide an appropriated management for optical optimization of perovskite solar cells.

Fabrication of Efficient Organic-Inorganic Perovskite Solar Cells in Ambient Air.

Although many groups have been trying to prepare perovskite solar cells (PSCs) in ambient air, the power conversion efficiency (PCE) is still low. Besides, the effect of moisture on the formation of perovskite films is still controversial. In this paper, we studied the effect of moisture on the formation of perovskite films in detail, and found that moisture can speed up the crystallizing process of PbI2 films to form poor-quality films with large grain size and surface roughness, while, for the conversion of PbI2 to perovskite films, a small amount of moisture is not adverse, and even beneficial. On this basis, we report the successful fabrication of efficient mesoporous PSCs with PCE of 16.00% under ambient air conditions at 25% relative humidity by adding a small amount of n-butyl amine into the solution of PbI2 to enhance the quality of PbI2 films and thus to achieve high-quality perovskite films with smooth surface, large crystal grains, and high crystal quality.

Ultrathin Si/CNTs Paper-Like Composite for Flexible Li-Ion Battery Anode With High Volumetric Capacity.

Thin and lightweight flexible lithium-ion batteries (LIBs) with high volumetric capacities are crucial for the development of flexible electronic devices. In the present work, we reported a paper-like ultrathin and flexible Si/carbon nanotube (CNT) composite anode for LIBs, which was realized by conformal electrodeposition of a thin layer of silicon on CNTs at ambient temperature. This method was quite simple and easy to scale up with low cost as compared to other deposition techniques, such as sputtering or CVD. The flexible Si/CNT composite exhibited high volumetric capacities in terms of the total volume of active material and current collector, surpassing the most previously reported Si-based flexible electrodes at various rates. In addition, the poor initial coulombic efficiency of the Si/CNT composites can be effectively improved by prelithiation treatment and a commercial red LED can be easily lighted by a full pouch cell using a Si/CNT composite as a flexible anode under flat or bent states. Therefore, the ultrathin and flexible Si/CNT composite is highly attractive as an anode material for flexible LIBs.

Large-Area WS2 Film with Big Single Domains Grown by Chemical Vapor Deposition.

High-quality WS2 film with the single domain size up to 400 µm was grown on Si/SiO2 wafer by atmospheric pressure chemical vapor deposition. The effects of some important fabrication parameters on the controlled growth of WS2 film have been investigated in detail, including the choice of precursors, tube pressure, growing temperature, holding time, the amount of sulfur powder, and gas flow rate. By optimizing the growth conditions at one atmospheric pressure, we obtained tungsten disulfide single domains with an average size over 100 µm. Raman spectra, atomic force microscopy, and transmission electron microscopy provided direct evidence that the WS2 film had an atomic layer thickness and a single-domain hexagonal structure with a high crystal quality. And the photoluminescence spectra indicated that the tungsten disulfide films showed an evident layer-number-dependent fluorescence efficiency, depending on their energy band structure. Our study provides an important experimental basis for large-area, controllable preparation of atom-thick tungsten disulfide thin film and can also expedite the development of scalable high-performance optoelectronic devices based on WS2 film.

Synthesis of ZnO Nanocrystals and Application in Inverted Polymer Solar Cells.

Controllable synthesis of various ZnO nanocrystals was achieved via a simple and cost-effective hydrothermal process. The morphology evolution of the ZnO nanostructures was well monitored by tuning hydrothermal growth parameters, such as solution concentration, reaction temperature, and surfactant. As-obtained ZnO nanocrystals with different morphologies, e.g., ZnO nanorods, nanotetrapods, nanoflowers, and nanocubes, were further introduced into the organic bulk heterojunction solar cells as the electron transport channel. It was found that the device performance was closely related to the morphology of the ZnO nanocrystals.

Electroluminescence of ordered ZnO nanorod array/p-GaN light-emitting diodes with graphene current spreading layer.

Ordered ZnO nanorod array/p-GaN heterojunction light-emitting diodes (LEDs) have been fabricated by introducing graphene as the current spreading layer, which exhibit improved electroluminescence performance by comparison to the LED using a conventional structure (indium-tin-oxide as the current spreading layer). In addition, by adjusting the diameter of ZnO nanorod array in use, the light emission of the ZnO nanorod array/p-GaN heterojunction LEDs was enhanced further. This work has great potential applications in solid-state lighting, high performance optoelectronic devices, and so on. PACS: 78.60.Fi; 85.60.Jb; 78.67.Lt; 81.10.Dn.

Controllable synthesis of ZnO nanostructures on the Si substrate by a hydrothermal route.

In this paper, controllable synthesis of various ZnO nanostructures was achieved via a simple and cost-effective hydrothermal process on the Si substrate. The morphology evolution of the ZnO nanostructures was well monitored by tuning hydrothermal growth parameters, such as the seed layer, solution concentration, reaction temperature, and surfactant. X-ray diffraction and photoluminescence measurements reveal that crystal quality and optical properties crucially depend on the morphology of the ZnO nanostructures. The ease of synthesis and convenience to tune morphology and optical properties bring this approach great potential for nanoscale applications.