Increasing inequalities in what we do online: A longitudinal cross sectional analysis of Internet activities among the Dutch population (2010 to 2013) over gender,age, education,and income

We investigate types of Internet activities among a representative sample of the Dutch population from 2010 to 2013. We examined usage patterns of seven types of Internet activities (i.e., information, news, personal development, commercial transaction, social interaction, leisure, and gaming) and related these patterns with gender, age, education, and income. Activities related to news, personal development, commercial transaction, and social interaction increased in popularity. For most capital enhancing activities, men, younger people, higher educated people, and people with higher than average incomes were prominent. These observations, however, are subject to change. The Internet seems to provide increasingly more capital-enhancing opportunities for those with higher education and income, which would accordingly reinforce their already strong positions in society.     

Vapor Phase Growth of Functional Pentacene Films at Atmospheric Pressure

Compared to traditional vacuum evaporation techniques for small organic molecules, organic vapor phase deposition (OVPD) possesses a extra processing parameter: the pressure of process gas P_ch. Here, the influence of large P_ch variations (from 0.1 mbar to atmospheric pressure) on pentacene thin film growth is explored. OVPD operation at higher P_ch is characterized by lower carrier gas velocities and lower organic diffusivities. These result in an invariance of the material utilization efficiency over the entire pressure span and in an advantageous equilibrium evaporation regime in the source. An increase in P_ch yields rough pentacene layers. Classical nucleation theory is applied to demonstrate how the pressure rise triggers homogeneous nucleation in the gas phase, causing the observed roughening. The use of lower deposition rates, higher dilution flow rates, and higher substrate temperatures result in the suppression of gas phase nucleation and the growth of smooth pentacene films at atmospheric pressure. Using these optimized conditions, state‐of‐the‐art pentacene thin film transistors with saturation mobilities above 0.9 cm²/Vs are reproducibly fabricated. p‐Type circuits are also made and a 19‐stage ring oscillator with a stage delay of 51 μs at a supply voltage of 15 V is demonstrated.     

Highly Utilized Active Sites on Pt@Cu/C for Ethanol Electrocatalytic Oxidation in Alkali Metal Hydroxide Solutions

Using ethanol electrocatalytic oxidation reaction (EOR) with a lower reaction potential to replace oxygen evolution reaction (OER) and integrating hydrogen evolution reaction (HER) have a promising development prospect for more energy-saving electrolytic hydrogen production. However, the main challenges of EOR are insufficient catalytic activity, high overpotential, and slow kinetics. Active sites on the electrocatalysts surface are occupied by alkali metal ion hydrate clusters by noncovalent interactions, which is considered to be one of the major causes of these challenges. To reduce the effect of the noncovalent interactions on the catalytic activity of the electrocatalyst, copper is chosen and doped in the form of a single atom in the electrocatalyst (Pt@Cu/C) to increase the electrocatalyst conductivity and make the anode contain more positive charge in this study. Then, alkali metal ion hydrate clusters are difficult to adsorb at the active site of Pt@Cu/C. The EOR electrocatalytic activity of Pt@Cu/C is up to 8184 mA mg_Pt⁻¹, which is ≈4.8 times as high as that of Pt/C. The two-electrode hydrogen production device using Pt@Cu/C as anode for coupled EOR&HER requires a smaller voltage of 0.60 V to reach 10 mA cm⁻² compared with that of Pt/C (0.76 V).     

Influence of the underneath cavity on buoyant‐forced cooling of the integrated photovoltaic panels in building roof: a thermography study

Airflow around building‐integrated photovoltaics (BIPV) has a significant impact on their hygrothermal behavior and degradation. The potential of reducing the temperature of BIPV using an underneath cavity is experimentally and numerically investigated in literature. Most of the models are oversimplified in terms of modeling the impact of 3D flow over/underneath of PV modules, which can result in a non‐uniform surface temperature and consequently a non‐homogenous thermal degradation. Moreover, the simultaneous presence of radiation and convection related to upstream wind, in addition to the combined impact of back‐ventilation and surface convection, is barely addressed in literature. However, these simplifications can result in the unrealistic loading climate conditions. This paper aims to present a unique experimental setup to provide more realistic climate conditions for investigating the ventilation potential of the underneath. The setup consists of a solar simulator and a building prototype with installed PV, placed inside an atmospheric wind tunnel to control upstream wind velocity. Thermography is performed using an infrared camera to monitor the surface temperature of the BIPV. The potential of an underneath cavity with various cavity heights and PV arrangement is further investigated in this paper. The outcome would be eventually useful in the development of practical guidelines for BIPV installation. Copyright © 2013 John Wiley & Sons, Ltd.     

Demonstration of the monolithic interconnection on CIS solar cells by picosecond laser structuring on 30 by 30 cm2 modules

In this paper, we present the selective structuring of all three patterns (P1, P2 and P3) of a monolithic interconnection of CIS (Cu(In,Ga)(S,Se)₂) thin film solar cells by picosecond laser pulses at a wavelength of 1064 nm. We show results for single pulse ablation threshold values and line scribing of molybdenum films on glass (P1), CIS on molybdenum (P2) and zinc oxide on CIS (P3). The purposes of these processes are the p‐type isolation (P1), cell interconnect (P2) and n‐type isolation (P3), which are required for complete cell architecture. The half micron thick molybdenum back electrode can be structured with a process speed of more than 15 m/s at about 15 W average power without detectable residues and damage by direct induced laser ablation from the back side (P1). The CIS layer can be structured selectively down to the molybdenum at process speeds up to 1 m/s at about 15 W average power, due to the precision of direct laser ablation in the ultrashort pulse regime (P2). The ZnO front electrode layer is separated by clean trenches with straight side walls at process speeds of up to 15 m/s at about 10 W average power, as a result of indirect induced laser ablation (P3). A validation of functionality of all processes is demonstrated on CIS solar cell modules (30 × 30 cm²). By replacing one state‐of‐the‐art process by a picosecond laser process at a time, solar efficiencies could be increased for P1 and P2 and stayed on a similar level for P3. After an optimization of the patterning processes in the R&D pilot line of AVANCIS, we achieved a new record efficiency for an all‐laser‐patterned CIS solar module: 14.7% as best value for the aperture area efficiency of a 30 × 30 cm² sized CIS module was reached. Copyright © 2014 John Wiley & Sons, Ltd.     

Carbon‐Based Anodes for Lithium Sulfur Full Cells with High Cycle Stability

The lithium sulfur battery system has been studied since the late 1970s and has seen renewed interest in recent years. However, even after three decades of intensive research, prolonged cycling can only be achieved when a large excess of electrolyte and lithium is used. Here, for the first time, a balanced and stable lithium sulfur full cell is demonstrated with silicon–carbon as well as all‐carbon anodes. More than 1000 cycles, a specific capacity up to 1470 mAh g^?1 _sulfur (720 mAh g^?1 _cathode), and a high coulombic efficiency of over 99% even with a low amount of electrolyte are achieved. The alternative anodes do not suffer from electrolyte depletion, which is found to be the main cause of cell failure when using metallic lithium anodes.     

Normally Oriented Adhesion versus Friction Forces in Bacterial Adhesion to Polymer‐Brush Functionalized Surfaces Under Fluid Flow

Bacterial adhesion is problematic in many diverse applications. Coatings of hydrophilic polymer chains in a brush configuration reduce bacterial adhesion by orders of magnitude, but not to zero. Here, the mechanism by which polymer‐brush functionalized surfaces reduce bacterial adhesion from a flowing carrier fluid by relating bacterial adhesion with normally oriented adhesion and friction forces on polymer (PEG)‐brush coatings of different softness is studied. Softer brush coatings deform more than rigid ones, which yields extensive bond‐maturation and strong, normally oriented adhesion forces, accompanied by irreversible adhesion of bacteria. On rigid brushes, normally oriented adhesion forces remain small, allowing desorption and accordingly lower numbers of adhering bacteria result. Friction forces, generated by fluid flow and normally oriented adhesion forces, are required to oppose fluid shear forces and cause immobile adhesion. Summarizing, inclusion of friction forces and substratum softness provides a more complete mechanism of bacterial adhesion from flowing carrier fluids than available hitherto.     

Identifying peer‐to‐peer communities in the network by connection graph analysis

In this paper we present a unified solution to identify peer‐to‐peer (P2P) communities operating in the network. We propose an algorithm that is able to progressively discover nodes cooperating in a P2P network and to identify that P2P network. Starting from a single known node, we can easily identify other nodes in the P2P network, through the analysis of widely available and standardized IPFIX (NetFlow) data. Instead of relying on the analysis of content characteristics or packet properties, we monitor connections of known nodes in the network and then progressively discover other nodes through the analysis of their mutual contacts. We show that our method is able to discover cooperating nodes in many P2P networks and present the real computational requirements of the algorithm on a large network. The use of standardized input data allows for easy deployment onto real networks. Copyright © 2014 John Wiley & Sons, Ltd.     

Renoprotective Angiographic Polymersomes

Computed tomography (CT) angiography is powerful for the diagnosis of vascular diseases. Unfortunately, this method usually requires a high dosage of iodinated contrast agents, which can lead to severe elevation of reactive oxygen species (ROS) levels within kidneys. This causes oxidative stress, apoptosis, and hence contrast-induced nephropathy (CIN), a leading cause of iatrogenic renal failure, especially for patients with renal insufficiency. Herein, a route is shown to circumvent such problems with the usage of rationally designed renoprotective angiographic polymersomes (RAPs) as blood pool CT contrast agents. RAPs are biodegradable nanoparticles prepared via self-assembly of poly(ethylene oxide)-block-poly(triiodobenzoic chloride-conjugated polylysine-stat-phenylboronic acid pinacol ester-conjugated polylysine) (PEO₄₅-b-P[(Lys-IBC)₄₅-stat-(Lys-PAPE)₁₅]). The key to the efficiency of such nanoparticles as renoprotective contrast agents arises from the rationally chosen repeat units: Lys-IBC exhibits a concentration-dependent X-ray attenuation capability and Lys-PAPE introduces an ROS-scavenging ability to the polymersome. The study shows that RAPs can reduce the risk of CIN in mice with kidney injury. Additionally, a 5-fold increase in angiographic live time is observed using RAPs, compared to commonly used iodinated small molecule contrast agents. In summary, a new strategy is proposed for the design of a renoprotective angiographic contrast agent that is capable of reducing the risk of CIN.     

Robust Single Molecule Magnet Monolayers on Graphene and Graphite with Magnetic Hysteresis up to 28 K

The chemical functionalization of fullerene single molecule magnet Tb₂@C₈₀(CH₂Ph) enables the facile preparation of robust monolayers on graphene and highly oriented pyrolytic graphite from solution without impairing their magnetic properties. Monolayers of endohedral fullerene functionalized with pyrene exhibit magnetic bistability up to a temperature of 28 K. The use of pyrene terminated linker molecules opens the way to devise integration of spin carrying units encapsulated by fullerene cages on graphitic substrates, be it single-molecule magnets or qubit candidates.