Synthesis and characterization of TiO2/poly(methyl methacrylate) nanocomposites via surface thiol-lactam initiated radical polymerization

An approach to the surface modification of TiO2 nanoparticles was described based on the thiol functionalization of TiO2 followed by thiol-lactam initiated radical polymerization (TLIRP) of methyl methacrylate (MMA). FT-IR, XRD and XPS analyses confirmed the grafting of the polymer on the TiO2 surface. TGA analysis revealed superior thermal stability of PMMA-g-TiO2 compared with PMMA. TEM measurements and time-dependent phase monitoring suggested much higher colloidal stability of PMMA-g-TiO2 than TiO2 in toluene. The controlled nature of the TLIRP of MMA from the surface of TiO2 was determined by GPC analysis.     

Fatigue characteristics of SAE52100 steel via ultrasonic nanocrystal surface modification technology

Ultrasonic nanocrystal surface modification (UNSM) technology is a novel surface modification technology that can improve the mechanical and tribological properties of interacting surfaces in relative motion. UNSM treatment was utilized to improve the wear resistance fatigue strength of slim bearing rings made of SAE52100 bearing steel without damaging the raceway surfaces. In this study, wear and fatigue results that were subjected to different impact loads of the UNSM treatment were investigated and compared with those of the untreated specimen. The microhardness of the UNSM-treated specimens increased by about 20%, higher than that of the untreated specimens. The X-ray diffraction analysis showed that a compressive residual stress of more than 1,000 MPa was induced after the UNSM treatment. Also, electron backscatter diffraction analysis was used to study the surface structure and nanograin refinement. The results showed that the rolling contact fatigue life and the rotary bending fatigue strength of the UNSM-treated specimens increased by about 80% and 31%, respectively, compared to those of the untreated specimen. These results might be attributed to the increased microhardness, the induced compressive residual stress, and the nanocrystal structure modification after the UNSM treatment. In addition, the fracture surface analysis showed that the fish eye crack initiation phenomenon was observed after the UNSM treatment.     

Plasma treatment effect on dye-sensitized solar cell efficiency of hydrothermal-processed TiO2 nanorods

Atmospheric plasma (AP) treatment was carried out on TiO2 nanorods (NRs) that were hydrothermally grown on F-doped SnO2 (FTO)/glass. The effects of AP treatment on the surface of the TiO2 NRs were investigated, where the treatment involved the use of the reactive gases H2, N2, and O2. The surface energy of AP-treated TiO2 NRs was about 1.5 times higher than that of untreated TiO2 NRs (364.3 mJ/m2). After AP treatment, the increase of the peak area ratios of the Ti2O3 and TiO2 peaks in the XPS spectra resulted in a decrease in the number of oxygen vacancies in the TiO2 NRs. The efficiency of a dye-sensitized solar cell (DSSC) based on the N2-plasma-treated TiO2 NRs, which was approximately 1.11%, was about 79% higher than that of a DSSC based on the untreated TiO2 NRs.     

Interface modification of cathode electrode using dimmethyldicyanoquinonediimine as a charge transfer layer in organic photovoltaic cell

Various metals for the cathode electrode of organic electronic devices have been used in order to improve carrier injection and contact resistance etc. However, metal electrodes have some disadvantages such as rough surfaces, inadequate interfacial durability and unsuitable work functions. In the present work, we have fabricated an organic photovoltaic cell consisting of ITO/PEDOT:PSS/P3HT:PCBM/DMDCNQI/Al. The dimmethyldicyanoquinonediimine (DMDCNQI) compound was used as an organic n-type charge transfer complex between the cathode electrode and an organic active layer to improve contact resistance and electron transport ability. The prepared device shows a high short-circuit current density of 10.39 mA/cm2 and a maximum power conversion efficiency of 3.10%.     

Dimension-controlled synthesis of CdS nanocrystals: from 0D quantum dots to 2D nanoplates

The dimension-controlled synthesis of CdS nanocrystals in the strong quantum confinement regime is reported. Zero-, one-, and two-dimensional CdS nanocrystals are selectively synthesized via low-temperature reactions using alkylamines as surface-capping ligands. The shape of the nanocrystals is controlled systematically by using different amines and reaction conditions. The 2D nanoplates have a uniform thickness as low as 1.2 nm. Furthermore, their optical absorption and emission spectra show very narrow peaks indicating extremely uniform thickness. It is demonstrated that 2D nanoplates are generated by 2D assembly of CdS magic-sized clusters formed at the nucleation stage, and subsequent attachment of the clusters. The stability of magic-sized clusters in amine solvent strongly influences the final shapes of the nanocrystals. The thickness of the nanoplates increases in a stepwise manner while retaining their uniformity, similar to the growth behavior of inorganic clusters. The 2D CdS nanoplates are a new type of quantum well with novel nanoscale properties in the strong quantum confinement regime.     

Metastable Ge1-xCx alloy nanowires

Carbon-containing alloy materials such as Ge(1-x)C(x) are attractive candidates for replacing silicon (Si) in the semiconductor industry. The addition of carbon to diamond lattice not only allows control over the lattice dimensions, but also enhances the electrical properties by enabling variations in strain and compositions. However, extremely low carbon solubility in bulk germanium (Ge) and thermodynamically unfavorable Ge-C bond have hampered the production of crystalline Ge(1-x)C(x) alloy materials in an equilibrium growth system. Here we successfully synthesized high-quality Ge(1-x)C(x) alloy nanowires (NWs) by a nonequilibrium vapor-liquid-solid (VLS) method. The carbon incorporation was controlled by NW growth conditions and the position of carbon atoms in the Ge matrix (at substitutional or interstitial sites) was determined by the carbon concentration. Furthermore, the shrinking of lattice spacing caused by substitutional carbon offered the promising possibility of band gap engineering for photovoltaic and optoelectronic applications.     

The effect of a concentration graded cathode for organic solar cells

We present the effects of a concentration graded Li:Al cathode when it is made by one-step evaporation method using single alloy sources on the performance of organic solar cells. The concentration profile of the Li:Al cathode and related interface energy levels were investigated by means of secondary ion mass spectroscopy and ultraviolet photoelectron spectroscopy, in comparison with those of a common Al cathode. The results indicate that interfacial lithium accumulation introduces a cascade decrease of the work function (WF) of the cathode. The WF graded cathode applied to bulk heterojunction solar cells resulted in increased short circuit current and power conversion efficiency. Furthermore, the Li:Al cathode avoids the formation of interface Al-C complex, which may cause disruption of electron transport.     

Filtration performance at high temperatures and analysis of ceramic filter elements during biomass gasification

During the CHRISGAS project, various experimental campaigns were performed with the aim to study the hot gas filtration process during steam-O₂ biomass gasification at Delft University of Technology. The test-rig consists of a 100 kW thermal atmospheric circulating fluidized-bed gasifier and a high temperature filter unit which contains 3 rigid ceramic candles with an outer diameter of 60 mm, 10 mm wall thickness and a length of 1520 mm. This paper gives an overview of tests performed with different fuels (A-wood, B-wood, miscanthus) and with sand and magnesite used as bed materials. Dia-Schumalith¹ candles were operated in the temperature range between 600 °C and 800 °C for more than 50 h. The filtration performance was studied through continuous observation of the increasing differential pressure while the filter cake formed on the surface of the candles. Gas face velocities ranged between 3 cm s^?1 and 5 cm s^?1. Stable filtration was achieved during some tests. Dust cake analysis indicated formation of calcium phosphates and silicates and potassium silicates.     

Enrichment of (8,4) Single‐Walled Carbon Nanotubes Through Coextraction with Heparin

Heparin sodium salt is investigated as a dispersant for dispersing single‐walled carbon nanotubes (SWNTs). Photoluminescence excitation (PLE) spectroscopy is used for identification and abundance estimation of the chiral species. It is found that heparin sodium salt preferentially disperses larger‐diameter Hipco SWNTs. When used to disperse CoMoCAT nanotube samples, heparin has a strong preference for (8,4) tubes, which have larger diameter than the predominant (6,5) in pristine CoMoCAT samples. PLE intensity due to (8,4) tubes increases from 7% to 60% of the total after threefold extractions. Computer modeling verifies that the complex of (8,4) SWNTs and heparin has the lowest binding energy amongst the four semiconducting species present in CoMoCAT. Network field‐effect transistors are successfully made with CoMoCAT/heparin and CoMoCAT/sodium dodecylbenzene sulfonate (SDBS)–heparin (x3), confirming the easy removability of heparin.