Atomic Layer Deposition-Based Synthesis of Photoactive TiO2 Nanoparticle Chains by Using Carbon Nanotubes as Sacrificial Templates

Highly ordered and self supported anatase TiO2 nanoparticle chains were fabricated by calcining conformally TiO2 coated multi-walled carbon nanotubes (MWCNTs). During annealing, the thin tubular TiO2 coating that was deposited onto the MWCNTs by atomic layer deposition (ALD) was transformed into chains of TiO2 nanoparticles (~12 nm diameter) with an ultrahigh surface area (137 cm2 per cm2 of substrate), while at the same time the carbon from the MWCNTs was removed. Photocatalytic tests on the degradation of acetaldehyde proved that these forests of TiO2 nanoparticle chains are highly photo active under UV light because of their well crystallized anatase phase

Hot Carrier extraction with plasmonic broadband absorbers

Hot charge carrier extraction from metallic nanostructures is a very promising approach for applications in photo-catalysis, photovoltaics and photodetection. One limitation is that many metallic nanostructures support a single plasmon resonance thus restricting the light-to-charge-carrier activity to a spectral band. Here we demonstrate that a monolayer of plasmonic nanoparticles can be assembled on a multi-stack layered configuration to achieve broad-band, near-unit light absorption, which is spatially localised on the nanoparticle layer. We show that this enhanced light absorbance leads to $\sim$ 40-fold increases in the photon-to-electron conversion efficiency by the plasmonic nanostructures. We developed a model that successfully captures the essential physics of the plasmonic hot-electron charge generation and separation in these structures. This model also allowed us to establish that efficient hot carrier extraction is limited to spectral regions where the photons possessing energies higher than the Schottky junctions and the localised light absorption of the metal nanoparticles overlap.Comment: submitte

Hierarchical DSSC structures based on single walled TiO2 nanotube arrays reach back-side illumination solar light conversion efficiency of 8%

In the present work we introduce a path to the controlled construction of DSSCs based on hierarchically structured single walled, self-organized TiO2 layers. In a first step we describe a simple approach to selectively remove the inner detrimental shell of anodic TiO2 nanotubes (NTs). This then allows controlled well-defined layer-by-layer decoration of these TiO2-NT walls with TiO2 nanoparticles (this in contrast to conventional TiO2 nanotubes). We show that such defined multiple layered decoration can be optimized to build dye sensitized solar cells that (under back-side illumination conditions) can yield solar light conversion efficiencies in the range of 8 %. The beneficial effects observed can be ascribed to a combination of three factors : 1) improved electronic properties of the single walled tubes themselves, 2) a further improvement of the electronic properties by the defined TiCl4 treatment, and 3) a higher specific dye loading that becomes possible for the layer-by-layer decorated single walled tubes.Comment: arXiv admin note: text overlap with arXiv:1610.0643

How mobile are dye adsorbates and acetonitrile molecules on the surface of TiO2 nanoparticles? A quasi-elastic neutron scattering study

Motions of molecules adsorbed to surfaces may control the rate of charge transport within monolayers in systems such as dye sensitized solar cells. We used quasi-elastic neutron scattering (QENS) to evaluate the possible dynamics of two small dye moieties, isonicotinic acid (INA) and bis-isonicotinic acid (BINA), attached to TiO2 nanoparticles via carboxylate groups. The scattering data indicate that moieties are immobile and do not rotate around the anchoring groups on timescales between around 10 ps and a few ns (corresponding to the instrumental range). This gives an upper limit for the rate at which conformational fluctuations can assist charge transport between anchored molecules. Our observations suggest that if the conformation of larger dye molecules varies with time, it does so on longer timescales and/or in parts of the molecule which are not directly connected to the anchoring group. The QENS measurements also indicate that several layers of acetonitrile solvent molecules are immobilized at the interface with the TiO2 on the measurement time scale, in reasonable agreement with recent classical molecular dynamics results

Effect of nanomaterial properties on thermal conductivity of heat transfer fluids and nanomaterial suspension

This paper was presented at the 4th Micro and Nano Flows Conference (MNF2014), which was held at University College, London, UK. The conference was organised by Brunel University and supported by the Italian Union of Thermofluiddynamics, IPEM, the Process Intensification Network, the Institution of Mechanical Engineers, the Heat Transfer Society, HEXAG - the Heat Exchange Action Group, and the Energy Institute, ASME Press, LCN London Centre for Nanotechnology, UCL University College London, UCL Engineering, the International NanoScience Community, www.nanopaprika.eu.Energy has been rated as the single most important issue facing humanity in the current as well as next 50 years. Securing clean energy has become the top priority of most developed countries. Considering the rapid increase in energy demand worldwide, intensifying the heat transfer process and reducing energy loss due to ineffective use have become an increasingly important task. Fundamentally, energy conversion and transportation occur at atomic or molecular levels, Nanoscience and nanotechnology are expected to play a significant role in revitalizing the traditional energy industries and stimulating the emerging renewable energy industries. Nanofluid is a modern engineering heat transfer fluid with superior potential for enhancing the heat transfer performance of conventional fluids such as water, ethylene glycol and oils. It is consisting of solid nanoparticles with sizes typically of 1–100 nm suspended in base fluids. Many attempts have been made to investigate its important thermal properties, i.e. thermal conductivity; however, no definitive agreements and idea have emerged about this property. This article reports the effect of different nanomaterial on the thermal conductivity enhancement of nanofluids experimentally. TiO2, Fe3O4 and Al2O3 nanoparticles dispersed in water and ethylene glycol with volume concentration of 1 – 7.5 vol. % is used in the present study. A transient hot-wire apparatus (KD2 pro) is used for measuring the thermal conductivity of nanofluids. The results show that all the heat transfer fluids show an increase in thermal conductivity with the addition of nanoparticles in it. The measured thermal conductivity of nanofluids increased as the particle concentrations increased and are higher than the values of the base liquids. This confirms the effect of volume concentration of nanoparticles on the thermal conductivity enhancement

Informing Selection of Nanomaterial Concentrations for ToxCast In Vitro Testing based on Occupational Exposure Potential

Background: Little justification is generally provided for selection of in vitro assay testing concentrations for engineered nanomaterials (ENMs). Selection of concentration levels for hazard evaluation based on real-world exposure scenarios is desirable. Objectives: Our goal is to use estimates of lung deposition following occupational exposure to nanomaterials to recommend in vitro testing concentrations for the U.S. Environmental Protection Agency’s ToxCastTM program. We provide testing concentrations for carbon nanotubes (CNTs), titanium dioxide (TiO2) and silver (Ag) nanoparticles. Methods: We reviewed published ENM concentrations measured in air in manufacturing and R&D labs to identify input levels for estimating ENM mass retained in the human lung using the Multiple-Path Particle Dosimetry (MPPD) model. Model input parameters were individually varied to estimate alveolar mass retained for different particle sizes (5-1000 nm), aerosol concentrations (0.1, 1 mg/m3), aspect ratios (2, 4, 10, 167), and exposure durations (24 hours and a working lifetime). The calculated lung surface concentrations were then converted to in vitro solution concentrations. Results: Modeled alveolar mass retained after 24 hours is most affected by activity level and aerosol concentration. Alveolar retention for Ag and TiO2 nanoparticles and CNTs for a working lifetime (45 years) exposure duration is similar to high-end concentrations (~ 30-400 μg/mL) typical of in vitro testing reported in the literature. Conclusions: Analyses performed are generally applicable to provide ENM testing concentrations for in vitro hazard screening studies though further research is needed to improve the approach. Understanding the relationship between potential real-world exposures and in vitro test concentrations will facilitate interpretation of toxicological results

Antibacterial Properties of Nanoparticles in Dental Restorative Materials. A Systematic Review and Meta-Analysis

Background and Objectives: Nanotechnology has become a significant area of research focused mainly on increasing the antibacterial and mechanical properties of dental materials. The aim of the present systematic review and meta-analysis was to examine and quantitatively analyze the current evidence for the addition of different nanoparticles into dental restorative materials, to determine whether their incorporation increases the antibacterial/antimicrobial properties of the materials. Materials and Methods: A literature search was performed in the Pubmed, Scopus, and Embase databases, up to December 2018, following PRISMA (Preferred Reporting Items for Systematic Review and Meta-Analysis) guidelines for systematic reviews and meta-analyses. Results: A total of 624 papers were identified in the initial search. After screening the texts and applying inclusion criteria, only 11 of these were selected for quantitative analysis. The incorporation of nanoparticles led to a significant increase (p-value < 0.01) in the antibacterial capacity of all the dental materials synthesized in comparison with control materials. Conclusions: The incorporation of nanoparticles into dental restorative materials was a favorable option; the antibacterial activity of nanoparticle-modified dental materials was significantly higher compared with the original unmodified materials, TiO2 nanoparticles providing the greatest benefits. However, the high heterogeneity among the articles reviewed points to the need for further research and the application of standardized research protocols

Evidence of diffusive fractal aggregation of TiO2 nanoparticles by femtosecond laser ablation at ambient conditions

The specific mechanisms which leads to the formation of fractal nanostructures by pulsed laser deposition remain elusive despite intense research efforts, motivated mainly by the technological interest in obtaining tailored nanostructures with simple and scalable production methods. Here we focus on fractal nanostructures of titanium dioxide, $TiO_2$, a strategic material for many applications, obtained by femtosecond laser ablation at ambient conditions. We model the fractal formation through extensive Monte Carlo simulations based on a set of minimal assumptions: irreversible sticking and size independent diffusion. Our model is able to reproduce the fractal dimensions and the area distributions of the nanostructures obtained in the experiments for different densities of the ablated material. The comparison of theory and experiment show that such fractal aggregates are formed after landing of the ablated material on the substrate surface by a diffusive mechanism. Finally we discuss the role of the thermal conductivity of the substrate and the laser fluence on the properties of the fractal nanostructures. Our results represent an advancement towards controlling the production of fractal nanostructures by pulsed laser deposition.Comment: 21 page

Structure – Property relationships for nanofluids

This paper was presented at the 3rd Micro and Nano Flows Conference (MNF2011), which was held at the Makedonia Palace Hotel, Thessaloniki in Greece. The conference was organised by Brunel University and supported by the Italian Union of Thermofluiddynamics, Aristotle University of Thessaloniki, University of Thessaly, IPEM, the Process Intensification Network, the Institution of Mechanical Engineers, the Heat Transfer Society, HEXAG - the Heat Exchange Action Group, and the Energy Institute.Nanofluids refer to dilute liquid suspensions of nanoparticles in commonly used heat transfer liquids. They triggered much excitement since mid 1990s mainly owing to the claims of anomalous enhancement of thermal conductivity even at very low nanoparticle concentrations. There have been numerous attempts to interpret the mechanism(s) that drive the displayed enhancement. A long debate within the research community supported by experimental and theoretical evidence has highlighted the nanoparticle structuring as the dominant underlying mechanism. On the other hand the viscosity increase as a result of nanoparticle structuring raises concerns about their suitability for certain applications. This paper mainly discusses the structure – property relationship for nanofluids in microscopically static conditions