165 research outputs found

    The effect of rotational disorder on the microwave transmission of checkerboard metal square arrays

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    Published onlineJournal ArticleResearch Support, Non-U.S. Gov'tThe effect of rotational disorder on the microwave transmission through thin metallic checkerboard arrays has been experimentally studied. Broad resonant features below the onset of diffraction, attributed to electromagnetic radiation coupling through the structure via the evanescent fields of bound surface waves, are found to be strongly dependent on the electrical connectivity of the surface. By applying rotational disorder to the elements comprising the arrays, with the lattice constant and element size unchanged, the electrical connectivity of the structure can be controlled whilst maintaining periodicity. The results show that rotational disorder can significantly affect transmission only when it changes the structure's connectivity. When the initial structure is just above the connectivity threshold (where the metallic occupancy is 50%), increasing disorder causes the resonant features in transmission to invert as the structure switches from a predominantly connected array to a disconnected array. When approximately half of the connections are broken, the resonant features are suppressed, with scattering loss shown to dramatically increase to as much as 40% of the incident power over a broad frequency range. The result is a thin, highly effective scatterer of microwaves.The authors acknowledge the financial support of DSTL. APH and JRS also acknowledge the support of EPSRC through the QUEST programme grant

    Ferromagnetic resonance of patterned chromium dioxide thin films grown by selective area chemical vapour deposition

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    This is the final version of the article. Available from the American Institute of Physics via the DOI in this record.A selective area chemical vapour deposition technique has been used to fabricate continuous and patterned epitaxial CrO2 thin films on (100)-oriented TiO2 substrates. Precessional magnetization dynamics were stimulated both electrically and optically, and probed by means of time-resolved Kerr microscopy and vector network analyser ferromagnetic resonance techniques. The dependence of the precession frequency and the effective damping parameter upon the static applied magnetic field were investigated. All films exhibited a large in-plane uniaxial anisotropy. The effective damping parameter was found to exhibit strong field dependence in the vicinity of the hard axis saturation field. However, continuous and patterned films were found to possess generally similar dynamic properties, confirming the suitability of the deposition technique for fabrication of future spintronic devices

    High-efficiency and air-stable P3HT-based polymer solar cells with a new non-fullerene acceptor

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    We thank BASF for partial financial support, as well as EPSRC Projects EP/G037515/1 and EP/M023532/1, EC FP7 Project SC2 (610115), EC FP7 Project ArtESun (604397), EC FP7 Project POLYMED (612538), Project Synthetic carbon allotropes project SFB 953 and the King Abdullah University of Science and Technology (KAUST)

    Influence of climatic variables on crown condition in pine forests of Northern Spain

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    Producción CientíficaThe aim of this study was to find relationships between crown condition and some climatic parameters to identify which are those having a main influence on crown condition, and how this influence is shown in the tree (crown transparency), and to contribute to the understanding of how these parameters will affect under future climate change scenarios

    The Influence of Polymer Purification on Photovoltaic Device Performance of a Series of Indacenodithiophene Donor Polymers

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    A series of low bandgap indacenodithiophene polymers is purified by recycling SEC in order to isolate narrow polydispersity fractions. This additional purification step is found to have a significant beneficial influence on the solar cell performance and the reasons for this performance increase are investigated

    Molecular dynamics simulations and drug discovery

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    This review discusses the many roles atomistic computer simulations of macromolecular (for example, protein) receptors and their associated small-molecule ligands can play in drug discovery, including the identification of cryptic or allosteric binding sites, the enhancement of traditional virtual-screening methodologies, and the direct prediction of small-molecule binding energies. The limitations of current simulation methodologies, including the high computational costs and approximations of molecular forces required, are also discussed. With constant improvements in both computer power and algorithm design, the future of computer-aided drug design is promising; molecular dynamics simulations are likely to play an increasingly important role

    Ultraviolet Radiation Induced Dopant Loss in a TiO2 Photocatalyst

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    Doped TiO2 has been studied with intense interest in recent decades because of its ability to utilize visible wavelengths and enhance the efficiency of photocatalytic processes. Thus, as a class of materials, it is of significant interest for use in environmental ambient energy utilization applications. Using a popular and well-studied form of doped TiO2 (nitrogen doped) as an example, we show how 28 days of UVA irradiation which is identical in intensity with solar conditions is sufficient to cause the UV induced surface segregation and eventual loss of nitrogen dopant species in TiO2. This is evidenced by X-ray photoelectron spectroscopy and transient absorption spectroscopy. The loss of interstitial nitrogen dopants correlates with the eventual permanent loss of photocatalytic activity and visible light absorption. The UV induced loss of dopants in a metal oxide is unprecedented and represents a potential problem where the environmental use of doped metal oxides in applications is concerned

    Water Oxidation Kinetics of Accumulated Holes on the Surface of a TiO2 Photoanode: A Rate Law Analysis

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    It has been more than 40 years since Fujishima and Honda demonstrated water splitting using TiO2, yet there is still no clear mechanism by which surface holes on TiO2 oxidize water. In this paper, we use a range of complementary techniques to study this reaction that provide a unique insight into the reaction mechanism. Using transient photocurrent and transient absorption spectroscopy, we measure both the kinetics of electron extraction (t50% ≈ 200 μs, 1.5VRHE) and the kinetics of hole oxidation of water (t50% ≈ 100 ms, 1.5VRHE) as a function of applied potential, demonstrating the water oxidation by TiO2 holes is the kinetic bottleneck in this water-splitting system. Photoinduced absorption spectroscopy measurements under 5 s LED irradiation are used to monitor the accumulation of surface TiO2 holes under conditions of photoelectrochemical water oxidation. Under these conditions, we find that the surface density of these holes increases nonlinearly with photocurrent density. In alkali (pH 13.6), this corresponded to a rate law for water oxidation that is third order with respect to surface hole density, with a rate constant kWO = 22 ± 2 nm4·s–1. Under neutral (pH = 6.7) and acidic (pH = 0.6) conditions, the rate law was second order with respect to surface hole density, indicative of a change in reaction mechanism. Although a change in reaction order was observed, the rate of reaction did not change significantly over the wide pH range examined (with TOFs per surface hole in the region of 20–25 s–1 at ∼1 sun irradiance). This showed that the rate-limiting step does not involve OH– nucleophilic attack and demonstrated the versatility of TiO2 as an active water oxidation photocatalyst over a wide range of pH
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