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Register a new userRole of microenvironment in the mixed Langmuir-Blodgett films
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Syed Arshad Hussain
Publication date
2008
fields
Physics
and research's language is
English
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This paper reports the pi-A isotherms and spectroscopic characteristics of mixed Langmuir and Langmuir-Blodgett (LB) films of non-amphiphilic carbazole (CA) molecules mixed with polymethyl methacrylate (PMMA) and stearic acid (SA). pi-A isotherm studies of mixed monolayer and as well as also the collapse pressure study of isotherms definitely conclude that CA is incorporated into PMMA and SA matrices. However CA is stacked in the PMMA/SA chains and forms microcrystalline aggregates as is evidenced from the scanning electron micrograph picture. Nature of these aggregated species in the mixed LB films has been revealed by UV-Vis absorption and fluorescence spectroscopic studies. The presence of two different kinds of band systems in the fluorescence spectra of the mixed LB films have been observed. This may be due to the formation of low dimensional aggregates in the mixed LB films. Intensity distribution of different band system is highly sensitive to the microenvironment of two different matrices as well as also on the film thickness
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Although a considerable number of solvent based methodologies have been developed for exfoliating black phosphorus, so far there are no reports on controlled organization of these exfoliated nanosheets on substrates. Here, for the first time to the best of our knowledge, a mixture of N-Methyl-2-pyrrolidone (NMP) and deoxygenated water is employed as a subphase in Langmuir Blodgett (LB) trough for assembling the nanosheets followed by their deposition on substrates and studied its field effect transistor (FET) characteristics. Electron microscopy reveals the presence of densely aligned, crystalline, ultra-thin sheets of pristine phosphorene having lateral dimensions larger than hundred of microns. Furthermore, these assembled nanosheets retain their electronic properties and show a high current modulation of 10^4 at room temperature in FET devices. The proposed technique provides semiconducting phosphorene thin films that are amenable for large area applications.
Single walled carbon nanotubes exhibit advanced electrical and surface properties useful for high performance nanoelectronics. Important to future manufacturing of nanotube circuits is large scale assembly of SWNTs into aligned forms. Despite progress in assembly and oriented synthesis, pristine SWNTs in aligned and close-packed form remain elusive and needed for high current, speed and density devices through collective operations of parallel SWNTs. Here, we develop a Langmuir Blodgett method achieving monolayers of aligned SWNTs with dense packing, central to which is a non covalent polymer functionalization by PmPV imparting high solubility and stability of SWNTs in an organic solvent DCE. Pressure cycling or annealing during LB film compression reduces hysteresis and facilitates high degree alignment and packing of SWNTs characterized by microscopy and polarized Raman spectroscopy. The monolayer SWNTs are readily patterned for device integration by microfabrication, enabling the highest currents 3mA through the narrowest regions packed with aligned SWNTs thus far.
A plethora of different morphologies are fabricated by the self assembly of molybdenum disulphide (MoS2) exfoliated flakes with the help of Langmuir-Blodgett (LB) technique at the liquid/air interface. The MoS2 flakes are chemically exfoliated in various solvents but their stable sheet like assembly on substrate is achieved only in case of the flakes exfoliated in dimethylformamide. The density of the monolayer sheets is finely controlled by the surface pressure while the stabilization of MoS2 LB film onto the water subphase results in its self assembly into diffusion limited cluster aggregates and fractals. We further demonstrate the effect of excitation on the emission of LB assembled MoS2 sheets which reveals the existence of a new exciton corresponding to 2.43 eV apart from the direct bandgap emission at 1.86 eV. Finally, field effect transistors are fabricated on SiO2/Si and a mobility of 7.4 cm2V-1s-1 with a current on-off ratio of 10^5 is obtained. This work provides a new approach for the systematic deposition of the solution processed exfoliated flakes on large scale as well as formation of pattern structures in a natural way.
Ferrimagnetic TbFe or TbFeCo amorphous alloy thin films have been grown by co-evaporation in ultra-high vacuum. They exhibit an out-of-plane magnetic anisotropy up to their Curie temperature with a nucleation and propagation reversal mechanism suitable for current induced domain wall motion. Rutherford back scattering experiments confirmed a fine control of the Tb depth-integrated composition within the evaporation process. However, a large set of experimental techniques were used to evidence an interface related contribution in such thin films as compared to much thicker samples. In particular, scanning transmission electron microscopy experiments evidence a depth dependent composition and perturbed top and bottom interfaces with preferential oxidation and diffusion of terbium. Despite of that, amorphous and homogeneous alloy film remains in a bulk-like part. The composition of that bulk-like part of the magnetic layer, labeled as effective composition, is biased when compared with the depth-integrated composition. The magnetic properties of the film are mostly dictated by this effective composition, which we show changes with different top and bottom interfaces.
Epitaxial thin films have been utilised to investigate the radiolytic dissolution of uranium dioxide interfaces. Thin films of UO$_2$ deposited on single crystal yttria stabilised zirconia substrates have been exposed to water in the presence of a high flux, monochromatic, synchrotron x-ray source. In particular, this technique was applied to induce dissolution of three UO$_2$ thin films, grown along the principle UO$_2$ crystallographic orientations: (001), (110) and (111). Dissolution of each film was induced for 9 accumulative corrosion periods, totalling 270s, after which XRR spectra were recorded to observe the change in morphology of the films as a function of exposure time. While the (001) and (110) oriented films were found to corrode almost linearly and at comparable rates, the (111) film was found to be significantly more corrosion resistant, with no loss of UO$_2$ material being observed after the initial 90s corrosion period. These results distinctly show the effect of crystallographic orientation on the rate of x-ray induced UO$_2$ dissolution. This result may have important consequences for theoretical dissolution models, as it is evident that orientation dependence must be taken into consideration to obtain accurate predictions of the dissolution behaviour of UO$_2$.
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