scispace - formally typeset
Search or ask a question

Showing papers on "Thin film published in 2013"


Journal ArticleDOI
21 Jun 2013-Science
TL;DR: A number of methods have been developed to exfoliate layered materials in order to produce monolayer nanosheets, which are ideal for applications that require surface activity.
Abstract: Background Since at least 400 C.E., when the Mayans first used layered clays to make dyes, people have been harnessing the properties of layered materials. This gradually developed into scientific research, leading to the elucidation of the laminar structure of layered materials, detailed understanding of their properties, and eventually experiments to exfoliate or delaminate them into individual, atomically thin nanosheets. This culminated in the discovery of graphene, resulting in a new explosion of interest in two-dimensional materials. Layered materials consist of two-dimensional platelets weakly stacked to form three-dimensional structures. The archetypal example is graphite, which consists of stacked graphene monolayers. However, there are many others: from MoS 2 and layered clays to more exotic examples such as MoO 3 , GaTe, and Bi 2 Se 3 . These materials display a wide range of electronic, optical, mechanical, and electrochemical properties. Over the past decade, a number of methods have been developed to exfoliate layered materials in order to produce monolayer nanosheets. Such exfoliation creates extremely high-aspect-ratio nanosheets with enormous surface area, which are ideal for applications that require surface activity. More importantly, however, the two-dimensional confinement of electrons upon exfoliation leads to unprecedented optical and electrical properties. Liquid exfoliation of layered crystals allows the production of suspensions of two-dimensional nanosheets, which can be formed into a range of structures. (A) MoS 2 powder. (B) WS 2 dispersed in surfactant solution. (C) An exfoliated MoS 2 nanosheet. (D) A hybrid material consisting of WS 2 nanosheets embedded in a network of carbon nanotubes. Advances An important advance has been the discovery that layered crystals can be exfoliated in liquids. There are a number of methods to do this that involve oxidation, ion intercalation/exchange, or surface passivation by solvents. However, all result in liquid dispersions containing large quantities of nanosheets. This brings considerable advantages: Liquid exfoliation allows the formation of thin films and composites, is potentially scaleable, and may facilitate processing by using standard technologies such as reel-to-reel manufacturing. Although much work has focused on liquid exfoliation of graphene, such processes have also been demonstrated for a host of other materials, including MoS 2 and related structures, layered oxides, and clays. The resultant liquid dispersions have been formed into films, hybrids, and composites for a range of applications. Outlook There is little doubt that the main advances are in the future. Multifunctional composites based on metal and polymer matrices will be developed that will result in enhanced mechanical, electrical, and barrier properties. Applications in energy generation and storage will abound, with layered materials appearing as electrodes or active elements in devices such as displays, solar cells, and batteries. Particularly important will be the use of MoS 2 for water splitting and metal oxides as hydrogen evolution catalysts. In addition, two-dimensional materials will find important roles in printed electronics as dielectrics, optoelectronic devices, and transistors. To achieve this, much needs to be done. Production rates need to be increased dramatically, the degree of exfoliation improved, and methods to control nanosheet properties developed. The range of layered materials that can be exfoliated must be expanded, even as methods for chemical modification must be developed. Success in these areas will lead to a family of materials that will dominate nanomaterials science in the 21st century.

3,127 citations


Journal ArticleDOI
12 Apr 2013-Science
TL;DR: The observation of the quantum anomalous Hall (QAH) effect in thin films of chromium-doped (Bi,Sb)2Te3, a magnetic topological insulator shows a plateau in the Hall resistance as a function of the gating voltage without any applied magnetic fields, signifying the achievement of the QAH state.
Abstract: The quantized version of the anomalous Hall effect has been predicted to occur in magnetic topological insulators, but the experimental realization has been challenging. Here, we report the observation of the quantum anomalous Hall (QAH) effect in thin films of chromium-doped (Bi,Sb)2Te3, a magnetic topological insulator. At zero magnetic field, the gate-tuned anomalous Hall resistance reaches the predicted quantized value of h/e2, accompanied by a considerable drop in the longitudinal resistance. Under a strong magnetic field, the longitudinal resistance vanishes, whereas the Hall resistance remains at the quantized value. The realization of the QAH effect may lead to the development of low-power-consumption electronics.

2,972 citations


Journal ArticleDOI
TL;DR: This communication presents a synthesis process to grow MoS2 and MoSe2 thin films with vertically aligned layers, thereby maximally exposing the edges on the film surface, and confirmed their catalytic activity in a hydrogen evolution reaction (HER), in which the exchange current density correlates directly with the density of the exposed edge sites.
Abstract: Layered materials consist of molecular layers stacked together by weak interlayer interactions. They often crystallize to form atomically smooth thin films, nanotubes, and platelet or fullerene-like nanoparticles due to the anisotropic bonding. Structures that predominately expose edges of the layers exhibit high surface energy and are often considered unstable. In this communication, we present a synthesis process to grow MoS2 and MoSe2 thin films with vertically aligned layers, thereby maximally exposing the edges on the film surface. Such edge-terminated films are metastable structures of MoS2 and MoSe2, which may find applications in diverse catalytic reactions. We have confirmed their catalytic activity in a hydrogen evolution reaction (HER), in which the exchange current density correlates directly with the density of the exposed edge sites.

1,976 citations


Journal ArticleDOI
TL;DR: In this paper, the bulk absorber layer of CH3NH3PbI3−xClx perovskite solar cells was reduced from 500 to <150 °C and achieved power conversion efficiency up to 12.3%.
Abstract: We have reduced the processing temperature of the bulk absorber layer in CH3NH3PbI3−xClx perovskite solar cells from 500 to <150 °C and achieved power conversion efficiencies up to 12.3%. Remarkably, we find that devices with planar thin-film architecture, where the ambipolar perovskite transports both holes and electrons, convert the absorbed photons into collected charge with close to 100% efficiency.

1,524 citations


Journal ArticleDOI
TL;DR: Puurunen et al. as discussed by the authors summarized the two-reactant ALD processes to grow inorganic materials developed to-date, updating the information of an earlier review on ALD.
Abstract: Atomic layer deposition (ALD) is gaining attention as a thin film deposition method, uniquely suitable for depositing uniform and conformal films on complex three-dimensional topographies. The deposition of a film of a given material by ALD relies on the successive, separated, and self-terminating gas–solid reactions of typically two gaseous reactants. Hundreds of ALD chemistries have been found for depositing a variety of materials during the past decades, mostly for inorganic materials but lately also for organic and inorganic–organic hybrid compounds. One factor that often dictates the properties of ALD films in actual applications is the crystallinity of the grown film: Is the material amorphous or, if it is crystalline, which phase(s) is (are) present. In this thematic review, we first describe the basics of ALD, summarize the two-reactant ALD processes to grow inorganic materials developed to-date, updating the information of an earlier review on ALD [R. L. Puurunen, J. Appl. Phys. 97, 121301 (2005)], and give an overview of the status of processing ternary compounds by ALD. We then proceed to analyze the published experimental data for information on the crystallinity and phase of inorganic materials deposited by ALD from different reactants at different temperatures. The data are collected for films in their as-deposited state and tabulated for easy reference. Case studies are presented to illustrate the effect of different process parameters on crystallinity for representative materials: aluminium oxide, zirconium oxide, zinc oxide, titanium nitride, zinc zulfide, and ruthenium. Finally, we discuss the general trends in the development of film crystallinity as function of ALD process parameters. The authors hope that this review will help newcomers to ALD to familiarize themselves with the complex world of crystalline ALD films and, at the same time, serve for the expert as a handbook-type reference source on ALD processes and film crystallinity.

1,160 citations


Journal ArticleDOI
TL;DR: A new sequential post-deposition treatment of the CIGS layer with sodium and potassium fluoride is presented that enables fabrication of flexible photovoltaic devices with a remarkable conversion efficiency due to modified interface properties and mitigation of optical losses in the CdS buffer layer.
Abstract: Thin-film photovoltaic devices based on chalcopyrite Cu(In,Ga)Se2 (CIGS) absorber layers show excellent light-to-power conversion efficiencies exceeding 20%. This high performance level requires a small amount of alkaline metals incorporated into the CIGS layer, naturally provided by soda lime glass substrates used for processing of champion devices. The use of flexible substrates requires distinct incorporation of the alkaline metals, and so far mainly Na was believed to be the most favourable element, whereas other alkaline metals have resulted in significantly inferior device performance. Here we present a new sequential post-deposition treatment of the CIGS layer with sodium and potassium fluoride that enables fabrication of flexible photovoltaic devices with a remarkable conversion efficiency due to modified interface properties and mitigation of optical losses in the CdS buffer layer. The described treatment leads to a significant depletion of Cu and Ga concentrations in the CIGS near-surface region and enables a significant thickness reduction of the CdS buffer layer without the commonly observed losses in photovoltaic parameters. Ion exchange processes, well known in other research areas, are proposed as underlying mechanisms responsible for the changes in chemical composition of the deposited CIGS layer and interface properties of the heterojunction.

1,124 citations


Journal ArticleDOI
TL;DR: An approach--termed fluid-enhanced crystal engineering (FLUENCE)--that allows for a high degree of morphological control of solution-printed thin films and may find use in the fabrication of high-performance, large-area printed electronics.
Abstract: Solution coating of organic semiconductors offers great potential for achieving low-cost manufacturing of large-area and flexible electronics. However, the rapid coating speed needed for industrial-scale production poses challenges to the control of thin-film morphology. Here, we report an approach—termed fluid-enhanced crystal engineering (FLUENCE)—that allows for a high degree of morphological control of solution-printed thin films. We designed a micropillar-patterned printing blade to induce recirculation in the ink for enhancing crystal growth, and engineered the curvature of the ink meniscus to control crystal nucleation. Using FLUENCE, we demonstrate the fast coating and patterning of millimetre-wide, centimetre-long, highly aligned single-crystalline organic semiconductor thin films. In particular, we fabricated thin films of 6,13-bis(triisopropylsilylethynyl) pentacene having non-equilibrium single-crystalline domains and an unprecedented average and maximum mobilities of 8.1±1.2 cm2 V−1 s−1 and 11 cm2 V−1 s−1. FLUENCE of organic semiconductors with non-equilibrium single-crystalline domains may find use in the fabrication of high-performance, large-area printed electronics. Solution printing of organic semiconductors could in principle be scaled to industrial needs, yet attaining aligned single-crystals directly with this method has been challenging. By using a micropillar-patterned printing blade designed to enhance the control of crystal nucleation and growth, thin films of macroscopic, highly aligned single crystals of organic semiconductors can now be fabricated.

876 citations


Journal ArticleDOI
TL;DR: It is shown that under appropriate conditions interference can instead persist in ultrathin, highly absorbing films of a few to tens of nanometres in thickness, and a new type of optical coating comprising such a film on a metallic substrate, which selectively absorbs various frequency ranges of the incident light is demonstrated.
Abstract: Optical coatings usually consist of many multilayers of thin films to achieve the desired properties A new approach using interference effects between an absorbing dielectric film and a metallic substrate now enables ultrathin optical coatings that could also find applications as thin solar cells or photodetectors

861 citations


Journal ArticleDOI
TL;DR: A new kind of transparent conducting electrode is produced that exhibits both superior optoelectronic performances and remarkable mechanical flexibility under both stretching and bending stresses.
Abstract: Transparent conducting electrodes are essential components for numerous flexible optoelectronic devices, including touch screens and interactive electronics. Thin films of indium tin oxide-the prototypical transparent electrode material-demonstrate excellent electronic performances, but film brittleness, low infrared transmittance and low abundance limit suitability for certain industrial applications. Alternatives to indium tin oxide have recently been reported and include conducting polymers, carbon nanotubes and graphene. However, although flexibility is greatly improved, the optoelectronic performance of these carbon-based materials is limited by low conductivity. Other examples include metal nanowire-based electrodes, which can achieve sheet resistances of less than 10Ω □(-1) at 90% transmission because of the high conductivity of the metals. To achieve these performances, however, metal nanowires must be defect-free, have conductivities close to their values in bulk, be as long as possible to minimize the number of wire-to-wire junctions, and exhibit small junction resistance. Here, we present a facile fabrication process that allows us to satisfy all these requirements and fabricate a new kind of transparent conducting electrode that exhibits both superior optoelectronic performances (sheet resistance of ~2Ω □(-1) at 90% transmission) and remarkable mechanical flexibility under both stretching and bending stresses. The electrode is composed of a free-standing metallic nanotrough network and is produced with a process involving electrospinning and metal deposition. We demonstrate the practical suitability of our transparent conducting electrode by fabricating a flexible touch-screen device and a transparent conducting tape.

842 citations


Journal ArticleDOI
27 Jun 2013-Langmuir
TL;DR: Chemical and physical characterization of polydopamine films deposited on gold surfaces from stirred basic solutions at times ranging from 2 to 60 min are reported, with a focus on times ≤10 min.
Abstract: Current interest in melanin films derived from the autoxidation of dopamine stems from their use as a universal adhesion layer. Here we report chemical and physical characterization of polydopamine films deposited on gold surfaces from stirred basic solutions at times ranging from 2 to 60 min, with a focus on times ≤10 min. Data from Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), and electrochemical methods suggest the presence of starting (dopamine) and intermediate (C=N-containing tautomers of quinone and indole) species in the polydopamine films at all deposition times. A uniform overlayer analysis of the XPS data indicates that film thickness increased linearly at short deposition times of ≤10 min. At deposition times ≥10 min, the films appeared largely continuous with surface roughness ≈ ≤ 2 nm, as determined by atomic force microscopy (AFM). Pinhole-free films, as determined by anionic redox probe measurements, required deposition times of 60 min or greater.

702 citations


Journal ArticleDOI
13 Aug 2013-Sensors
TL;DR: A comprehensive review on the state-of-the-art research activities in the UV photodetection field, including not only semiconductor thin films, but also 1D nanostructured materials, which are attracting more and more attention in the detection field are provided.
Abstract: Ultraviolet (UV) photodetectors have drawn extensive attention owing to their applications in industrial, environmental and even biological fields. Compared to UV-enhanced Si photodetectors, a new generation of wide bandgap semiconductors, such as (Al, In) GaN, diamond, and SiC, have the advantages of high responsivity, high thermal stability, robust radiation hardness and high response speed. On the other hand, one-dimensional (1D) nanostructure semiconductors with a wide bandgap, such as β-Ga2O3, GaN, ZnO, or other metal-oxide nanostructures, also show their potential for high-efficiency UV photodetection. In some cases such as flame detection, high-temperature thermally stable detectors with high performance are required. This article provides a comprehensive review on the state-of-the-art research activities in the UV photodetection field, including not only semiconductor thin films, but also 1D nanostructured materials, which are attracting more and more attention in the detection field. A special focus is given on the thermal stability of the developed devices, which is one of the key characteristics for the real applications.

Journal ArticleDOI
TL;DR: It is demonstrated that an anode consisting of a Sn thin film deposited on a hierarchical wood fiber substrate simultaneously addresses all the challenges associated with Sn anodes.
Abstract: Sodium (Na)-ion batteries offer an attractive option for low cost grid scale storage due to the abundance of Na. Tin (Sn) is touted as a high capacity anode for Na-ion batteries with a high theoretical capacity of 847 mAh/g, but it has several limitations such as large volume expansion with cycling, slow kinetics, and unstable solid electrolyte interphase (SEI) formation. In this article, we demonstrate that an anode consisting of a Sn thin film deposited on a hierarchical wood fiber substrate simultaneously addresses all the challenges associated with Sn anodes. The soft nature of wood fibers effectively releases the mechanical stresses associated with the sodiation process, and the mesoporous structure functions as an electrolyte reservoir that allows for ion transport through the outer and inner surface of the fiber. These properties are confirmed experimentally and computationally. A stable cycling performance of 400 cycles with an initial capacity of 339 mAh/g is demonstrated; a significant improvement over other reported Sn nanostructures. The soft and mesoporous wood fiber substrate can be utilized as a new platform for low cost Na-ion batteries.

Journal ArticleDOI
TL;DR: In this paper, the second harmonic of an 810-nm pulse is generated in a mechanically exfoliated monolayer, with a nonlinear susceptibility on the order of 10{}^{\ensuremath{-}7}$ m/V.
Abstract: We show that the lack of inversion symmetry in monolayer MoS${}_{2}$ allows strong optical second harmonic generation. The second harmonic of an 810-nm pulse is generated in a mechanically exfoliated monolayer, with a nonlinear susceptibility on the order of 10${}^{\ensuremath{-}7}$ m/V. The susceptibility reduces by a factor of seven in trilayers, and by about two orders of magnitude in even layers. A proof-of-principle second harmonic microscopy measurement is performed on samples grown by chemical vapor deposition, which illustrates potential applications of this effect in the fast and noninvasive detection of crystalline orientation, thickness uniformity, layer stacking, and single-crystal domain size of atomically thin films of MoS${}_{2}$ and similar materials.

Journal ArticleDOI
15 May 2013-ACS Nano
TL;DR: A controlled thermal reduction-sulfurization method is used to synthesize large-area WS2 sheets with thicknesses ranging from monolayers to a few layers, thus shedding light on the controlled production of heterolayered devices from transition metal chalcogenides.
Abstract: The isolation of few-layered transition metal dichalcogenides has mainly been performed by mechanical and chemical exfoliation with very low yields. In this account, a controlled thermal reduction–sulfurization method is used to synthesize large-area (∼1 cm2) WS2 sheets with thicknesses ranging from monolayers to a few layers. During synthesis, WOx thin films are first deposited on Si/SiO2 substrates, which are then sulfurized (under vacuum) at high temperatures (750–950 °C). An efficient route to transfer the synthesized WS2 films onto different substrates such as quartz and transmission electron microscopy (TEM) grids has been satisfactorily developed using concentrated HF. Samples with different thicknesses have been analyzed by Raman spectroscopy and TEM, and their photoluminescence properties have been evaluated. We demonstrated the presence of single-, bi-, and few-layered WS2 on as-grown samples. It is well known that the electronic structure of these materials is very sensitive to the number of la...

Journal ArticleDOI
TL;DR: When mixed Ag and Au nanoparticles are incorporated into the anode buffer layer, dual nanoparticles show superior behavior on enhancing light absorption in comparison with single nanoparticles, which led to the realization of a polymer solar cell with a power conversion efficiency of 8.67%, accounting for a 20% enhancement.
Abstract: This article describes a cooperative plasmonic effect on improving the performance of polymer bulk heterojunction solar cells. When mixed Ag and Au nanoparticles are incorporated into the anode buffer layer, dual nanoparticles show superior behavior on enhancing light absorption in comparison with single nanoparticles, which led to the realization of a polymer solar cell with a power conversion efficiency of 8.67%, accounting for a 20% enhancement. The cooperative plasmonic effect aroused from dual resonance enhancement of two different nanoparticles. The idea was further unraveled by comparing Au nanorods with Au nanoparticles for solar cell application. Detailed studies shed light into the influence of plasmonic nanostructures on exciton generation, dissociation, and charge recombination and transport inside thin film devices.

Journal ArticleDOI
TL;DR: The performance of perovskite solar cells recently exceeded 15% solar-to-electricity conversion efficiency for small-area devices as mentioned in this paper, and the fundamental properties of the active absorber layers, hybrid organic-inorganic perovsites formed from mixing metal and organic halides, are largely unknown.
Abstract: The performance of perovskite solar cells recently exceeded 15% solar-to-electricity conversion efficiency for small-area devices. The fundamental properties of the active absorber layers, hybrid organic-inorganic perovskites formed from mixing metal and organic halides [e.g., (NH4)PbI3 and (CH3NH3)PbI3], are largely unknown. The materials are semiconductors with direct band gaps at the boundary of the first Brillouin zone. The calculated dielectric constants and band gaps show an orientation dependence, with a low barrier for rotation of the organic cations. Due to the electric dipole of the methylammonium cation, a photoferroic effect may be accessible, which could enhance carrier collection.

Journal ArticleDOI
TL;DR: This review will cover the whole field of the intersection between electrochemistry and ordered mesoporous materials, which includes the generation of mesostructured solids by electro-assisted deposition using appropriate templates and the application of these novel materials for electrochemical purposes.
Abstract: Ordered mesoporous materials prepared by the template route have attracted increasing interest from the electrochemists community due to their plenty of unique properties and functionalities that can be effectively exploited in electrochemical devices. This review will cover the whole field of the intersection between electrochemistry and ordered mesoporous materials. The latter are either electronically insulating (silica and some other metal oxides, as well as silica-based organic–inorganic hybrid materials), semi-conducting (metal oxides), or conducting (metals, carbons). The three main intersection areas are: (1) the development/use of electrochemical methods to characterize the properties of mesoporous materials (i.e., charge and mass transfer processes); (2) the generation of mesostructured solids by electro-assisted deposition using appropriate templates; and (3) the application of these novel materials for electrochemical purposes. The most common devices to date are based on a bulk composite or thin film configuration and the resulting electrodes modified with such mesoporous materials have been successfully applied in various fields, including mainly electrochemical sensing and biosensing as well as energy conversion and storage (620 references).

Journal ArticleDOI
TL;DR: The reasons for cracking in thin films is explored as well as various methods to minimize its effect, including the physical reason for enhanced evaporation at the edge of droplets.
Abstract: When thin films of colloidal fluids are dried, a range of transitions are observed and the final film profile is found to depend on the processes that occur during the drying step. This article describes the drying process, initially concentrating on the various transitions. Particles are seen to initially consolidate at the edge of a drying droplet, the so-called coffee-ring effect. Flow is seen to be from the centre of the drop towards the edge and a front of close-packed particles passes horizontally across the film. Just behind the particle front the now solid film often displays cracks and finally the film is observed to de-wet. These various transitions are explained, with particular reference to the capillary pressure which forms in the solidified region of the film. The reasons for cracking in thin films is explored as well as various methods to minimize its effect. Methods to obtain stratified coatings through a single application are considered for a one-dimensional drying problem and this is then extended to two-dimensional films. Different evaporative models are described, including the physical reason for enhanced evaporation at the edge of droplets. The various scenarios when evaporation is found to be uniform across a drying film are then explained. Finally different experimental techniques for examining the drying step are mentioned and the article ends with suggested areas that warrant further study.

Journal ArticleDOI
TL;DR: In this paper, the anomalous photovoltaic (PV) effect in BiFeO3 (BFO) thin films, which resulted in open circuit voltages considerably larger than the band gap of the material, has generated a revival of the entire field of photoferroelectrics.
Abstract: Recently, the anomalous photovoltaic (PV) effect in BiFeO3 (BFO) thin films, which resulted in open circuit voltages (Voc) considerably larger than the band gap of the material, has generated a revival of the entire field of photoferroelectrics. Here, via temperature-dependent PV studies, we prove that the bulk photovoltaic (BPV) effect, which has been studied in the past for many non-centrosymmetric materials, is at the origin of the anomalous PV effect in BFO films. Moreover, we show that irrespective of the measurement geometry, Voc as high as 50 V can be achieved by controlling the conductivity of domain walls (DW). We also show that photoconductivity of the DW is markedly higher than in the bulk of BFO.

Journal ArticleDOI
TL;DR: Using a simple integration scheme, it is found that the electrical conductivity of MoS2 films is highly sensitive to NH3 adsorption, consistent with n-type semiconducting behavior.
Abstract: High-performance sensors based on molybdenum disulfide (MoS2 ) grown by sulfurization of sputtered molybdenum layers are presented. Using a simple integration scheme, it is found that the electrical conductivity of MoS2 films is highly sensitive to NH3 adsorption, consistent with n-type semiconducting behavior. A sensitivity of 300 ppb at room temperature is achieved, showing the high potential of 2D transition metal-dichalcogenides for sensing.

Journal ArticleDOI
TL;DR: In this article, a two-step deposition technique was used for preparing CH3NH3PbI3 perovskite solar cells using ZrO2 and TiO2 as a mesoporous layer, achieving an efficiency of 10.8% and 9.5% under 1000 W m−2 illumination.
Abstract: A two-step deposition technique is used for preparing CH3NH3PbI3 perovskite solar cells. Using ZrO2 and TiO2 as a mesoporous layer, we obtain an efficiency of 10.8% and 9.5%, respectively, under 1000 W m−2 illumination. The ZrO2 based solar cell shows higher photovoltage and longer electron lifetime than the TiO2 based solar cell.

Journal ArticleDOI
TL;DR: This work combines low-temperature shadow deposition with nanoscale patterning to realize nanocolloids with anisotropic three-dimensional shapes, feature sizes down to 20 nm and a wide choice of materials.
Abstract: Tuning the optical, electromagnetic and mechanical properties of a material requires simultaneous control over its composition and shape. This is particularly challenging for complex structures at the nanoscale because surface-energy minimization generally causes small structures to be highly symmetric. Here we combine low-temperature shadow deposition with nanoscale patterning to realize nanocolloids with anisotropic three-dimensional shapes, feature sizes down to 20 nm and a wide choice of materials. We demonstrate the versatility of the fabrication scheme by growing three-dimensional hybrid nanostructures that contain several functional materials with the lowest possible symmetry, and by fabricating hundreds of billions of plasmonic nanohelices, which we use as chiral metafluids with record circular dichroism and tunable chiroptical properties.

Journal ArticleDOI
TL;DR: Super gas barrier thin films, fabricated with layer-by-layer assembly of polyethylenimine and graphene oxide, exhibit significantly reduced oxygen and carbon dioxide transmission rates and provide high gas selectivity for hydrogen.
Abstract: Super gas barrier thin films, fabricated with layer-by-layer assembly of polyethylenimine and graphene oxide, exhibit significantly reduced oxygen and carbon dioxide transmission rates. This thin film's nanobrick wall structure also provides high gas selectivity for hydrogen.

Journal ArticleDOI
TL;DR: X-ray diffraction measurements show that synthesized Cu( 2)O thin films grow on c-sapphire substrate with preferred (111) orientation, and the performance of Cu(2)O films is poorer compared to that ofCu(2),O using RF power of 0.1 V.
Abstract: Cuprous oxide (Cu2O) films synthesis by radical oxidation with nitrogen (N2) plasma treatment and different RF power at low temperature (500°C) are studied in this paper. X-ray diffraction measurements show that synthesized Cu2O thin films grow on c-sapphire substrate with preferred (111) orientation. With nitrogen (N2) plasma treatment, the optical bandgap energy is increased from 1.69 to 2.42 eV, when N2 plasma treatment time is increased from 0 min to 40 min. Although the hole density is increased from 1014 to 1015 cm−3 and the resistivity is decreased from 1879 to 780Ωcm after N2 plasma treatment, the performance of Cu2O films is poorer compared to that of Cu2O using RF power of 0. The fabricated ZnO/Cu2O solar cells based on Cu2O films with RF power of 0 W show a good rectifying behavior with a efficiency of 0.02%, an open-circuit voltage of 0.1 V, and a fill factor of 24%.

Journal ArticleDOI
TL;DR: Lasers with ultrashort pulses are shown to be particularly useful tools for the production of nanocluster films and the important question of the film stoichiometry relative to that of the target will be thoroughly discussed in relation to the films reported in the literature.
Abstract: Laser ablation of dielectrics by ultrashort laser pulses is reviewed. The basic interaction between ultrashort light pulses and the dielectric material is described, and different approaches to the modeling of the femtosecond ablation dynamics are reviewed. Material excitation by ultrashort laser pulses is induced by a combination of strong-field excitation (multi-photon and tunnel excitation), collisional excitation (potentially leading to an avalanche process), and absorption in the plasma consisting of the electrons excited to the conduction band. It is discussed how these excitation processes can be described by various rate-equation models in combination with different descriptions of the excited electrons. The optical properties of the highly excited dielectric undergo a rapid change during the laser pulse, which must be included in a detailed modeling of the excitations. The material ejected from the dielectric following the femtosecond-laser excitation can potentially be used for thin-film deposition. The deposition rate is typically much smaller than that for nanosecond lasers, but film production by femtosecond lasers does possess several attractive features. First, the strong-field excitation makes it possible to produce films of materials that are transparent to the laser light. Second, the highly localized excitation reduces the emission of larger material particulates. Third, lasers with ultrashort pulses are shown to be particularly useful tools for the production of nanocluster films. The important question of the film stoichiometry relative to that of the target will be thoroughly discussed in relation to the films reported in the literature.

Journal ArticleDOI
TL;DR: In this article, the transport properties of lithium ion conducting glass ceramics represented by the general composition Li1+x−yAlx3+My5+M2−x-y4+(PO4)3 with NASICON-type structure and their stability in contact with lithium metal were investigated.
Abstract: We report on the transport properties of lithium ion conducting glass ceramics represented by the general composition Li1+x–yAlx3+My5+M2–x–y4+(PO4)3 with NASICON-type structure and their stability in contact with lithium metal. In particular, solid electrolyte phases with M = Ge, M = Ti, Ge, and M = Ti, Ta were investigated. AC impedance spectroscopy and DC polarization measurements were applied to determine the conductivity as a function of temperature, and to extract the partial electronic conductivity. The maximum total conductivity at room temperature was found to be about 4 × 10–4 S/cm for the solely Ge containing sample. We demonstrate that the combination of vacuum-based lithium thin film deposition and X-ray photoelectron spectroscopy (XPS) is well suited to study the reactivity of the solid electrolyte membranes in contact with lithium. As a major result, we show that none of the materials investigated is stable in contact with lithium metal, and we discuss the reactive interaction between solid ...

Journal ArticleDOI
TL;DR: In this paper, the electronic structures of epitaxial Sr2IrO4 thin-films were studied as a function of lattice-strains and it was shown that the electronic correlation energy is also affected by in-plane latticestrains.
Abstract: We have synthesized epitaxial Sr2IrO4 thin-films on various substrates and studied their electronic structures as a function of lattice-strains. Under tensile (compressive) strains, increased (decreased) Ir-O-Ir bond-angles are expected to result in increased (decreased) electronic bandwidths. However, we have observed that the two optical absorption peaks near 0.5 eV and 1.0 eV are shifted to higher (lower) energies under tensile (compressive) strains, indicating that the electronic-correlation energy is also affected by in-plane lattice-strains. The effective tuning of electronic structures under lattice-modification provides an important insight into the physics driven by the coexisting strong spin-orbit coupling and electronic correlation.

Journal ArticleDOI
TL;DR: One of the tenets of the SQ limit, that photons only produce one electron-hole pair at the electrodes of a solar cell, can be overcome is shown, showing an external quantum efficiency for photocurrent of greater than 100% and an internal quantum efficiency reached 130%.
Abstract: Improving the primary photoconversion process in a photovoltaiccell by utilizing the excess energy that is otherwise lost as heat can lead to an increase in the overall power conversion efficiency (PCE). Semiconductor nanocrystals (NCs) with at least one dimension small enough to produce quantum confinement effects provide new ways of controlling energy flow not achievable in thin film or bulk semiconductors. Researchers have developed various strategies to incorporate these novel structures into suitable solar conversion systems. Some of these methods could increase the PCE past the Shockley–Queisser (SQ) limit of ∼33%, making them viable “third generation photovoltaic” (TGPV) cell architectures. Surpassing the SQ limit for single junction solar cells presents both a scientific and a technological challenge, and the use of semiconductor NCs to enhance the primary photoconversion process offers a promising potential solution.The NCs are synthesized via solution phase chemical reactions prod-ucing stable c...

Journal ArticleDOI
TL;DR: It is shown that smooth neat PVDF films can be made at elevated substrate temperature, and the replacement of P(VDF-TrFE) by the commodity polymer PVDF may boost large-scale industrial applications.
Abstract: Although poly(vinylidene fluoride) is a well-known organic ferroelectric, its utilization in microelectronics has been hampered by the difficulty in obtaining uniform thin films. By exploiting a high-temperature deposition approach, smooth and thin films of the ferroelectric δ-phase polymorph of this material are now obtained, showing their potential for capacitors and non-volatile memories.

Journal ArticleDOI
TL;DR: Greiner et al. as mentioned in this paper provided a rational guide to process engineers in selecting the best suitable electrode/oxide structures for a targeted applications, which can be used as a buffer layer to modify the electrode work function.
Abstract: Thin-film metal oxides are among the key materials used in organic semiconductor devices. As there are no intrinsic charge carriers in a typical organic semiconductor, all charges in the device must be injected from electrode/organic interfaces, whose energetic structure consequentially dictates the performance of devices. The energy barrier at the interface depends critically on the work function of the electrode. For this reason, various types of thin-film metal oxides can be used as a buffer layer to modify the electrode work function. This paper provides a review on recent progress in metal oxide/organic interface energetics, oxide valence structure and work function, as well as the impact of defects and interfacial reactions on oxide work functions. This review provides a rational guide to process engineers in selecting the best suitable electrode/oxide structures for a targeted applications. Organic semiconductors offer an attractive alternative to the traditional, silicon-based components of electronic devices. Cheaper to produce and more sustainable, they can also introduce different attributes, such as flexibility, to these devices. However, as organic materials do not typically possess intrinsic charge carriers — electrons or holes — all charges in the device must originate from the electrode and pass through the electrode-organic material interface, a process hindered by an energy barrier. Mark Greiner and Zheng-Hong Lu review recent achievements in a versatile class of buffer layer — thin films of transition metal oxides — that can be positioned between the two materials to reduce the energy barrier that limits charge injection. The researchers discuss how to select the most suitable metal oxide for a specific purpose, and then tune the thin film's properties by adjusting the thickness of the metal oxide layer, the oxidation state of its cations and the concentration of its defects. Over the last decade, metal oxides have proven to be important materials for organic electronics. Oxides are often used as charge-injection and charge-selective interlayers to engineer the electrical resistance at electrode/organic interfaces in organic devices. An oxide’s behavior as an interlayer depends strongly on the oxide’s electronic properties—such as its band structure and work function. The numerous degrees of freedom in an oxide’s electronic properties allow these characteristics to be easily modified. The present review outlines the use of metal oxides in organic electronics, and discusses the factors that affect the oxide’s properties that are relevant to oxide/organic interfaces.