arXiv subjects

Syed Arshad Hussain

Publications and source records attributed to Syed Arshad Hussain.

30 records · Page 2Linked to original sources

arXiv2011

Reaction-kinetics of organo-clay hybrid films: in-situ IRRAS and AFM studies

In this paper we have reported the reaction kinetics of nano dimensional clay saponite and hectorite with an amphiphilic cation octadecyl rhodamine B (RhB) in hybrid Langmuir monolayer at the air-water interface. The surface pressure-molecular area (pi-A) isotherms were strongly influenced by the presence of clay with the lift-off area of the cationic amphiphile shifted to progressively larger area. In-situ infrared reflection absorption spectroscopy (IRRAS) was used to demonstrate the reaction kinetics. Time taken to complete the reaction kinetics for RhB-hectorite hybrid films is larger than RhB-saponite hybrid films. Atomic force microscopic images of hybrid Langmuir-Blodgett films give compelling visual evidence of the incorporation of clay platelets into the hybrid films and density of which increases with the progress of reaction kinetics.

cond-mat.mtrl-sci↗

arXiv2011

Langmuir-Blodgett Monolayers of Cationic Dyes in the Presence and Absence of Clay Mineral Layers: N,N'-Dioctadecyl Thiacyanine, Octadecyl Rhodamine B and Laponite

Langmuir-Blodgett (LB) films of N,N'-dioctadecyl thiacyanine perchlorate (NK) and octadecyl rhodamine B chloride (RhB18) and their mixtures in the presence and absence of clay mineral layers were investigated by recording surface pressure - area isotherms and by UV-Vis and fluorescence spectroscopies. The isotherms of NK, RhB18 and their mixtures are characteristic for liquid expanded state behaviour with repulsive interactions between the two cationic dyes. In the presence of laponite the isotherms show liquid expanded and condensed state behaviour. In laponite dispersions and in monolayers, NK has a strong tendency to aggregate with formation of H- and J- aggregates. The absorption and fluorescence maxima of the monomers in the films are at 435 nm and at 480 nm; H-dimer have an absorption maximum around 410 nm and do not fluoresce. J-dimers are present in all the films with absorption maximum at 461 nm and fluorescence at 463 nm. RhB18 is mainly present as monomers in the LB films with an absorption maximum at 576 nm and fluorescence at 595 nm. Fluorescence resonance energy transfer from NK to RhB18 has been observed in clay dispersions and in films with and without laponite. The optimum condition for NK RhB18 fluorescence energy transfer in the films is 90 mol% NK + 10 mol% RhB18.

cond-mat.mtrl-sci↗

arXiv2011

Fluorescence resonance energy transfer between organic dyes adsorbed onto nano-clay and Langmuir-Blodgett (LB) films

In this communication we investigate two dyes N,N' -dioctadecyl thiacyanine perchlorate (NK) and octadecyl rhodamine B chloride (RhB) in Langmuir and Langmuir-Blodgett (LB) films with or with out a synthetic clay laponite. Observed changes in isotherms of RhB in absence and presence of nano-clay platelets indicate the incorporation of clay platelets onto RhB-clay hybrid films. AFM image confirms the incorporation of clay in hybrid films. FRET was observed in clay dispersion and LB films with and without clay. Efficiency of energy transfer was maximum in LB films with clay.

cond-mat.mtrl-sci↗

arXiv2009

Langmuir-Blodgett Films a unique tool for molecular electronics

Molecular electronics is a new, exciting and interdisciplinary field of research. The main concern of the subject is to exploit the organic materials in electronic and optoelectronic devices. On the other hand Langmuir-Blodgett (LB) film deposition technique is one of the best among few methods used to manipulate materials in molecular level. In this article LB film preparation technique has been discussed briefly with an emphasize of its application towards molecular electronics.

physics.gen-ph↗

arXiv2009

An Introduction to Fluorescence Resonance Energy Transfer (FRET)

Recent advances in Fluorescence Resonance Energy Transfer (FRET) provides a way to measure and understand different biological systems and molecular interactions in nanometer order. In this report the introduction and principle of the FRET process have been explained.

physics.gen-ph↗

arXiv2008

Formation of complex Langmuir and Langmuir-Blodgett films of water soluble rosebengal

This communication reports the formation of complex Langmuir monolayer at the air-water interface by charge transfer types of interaction with the water soluble N- cetyl N, N, N trimethyl ammonium bromide (CTAB) molecules doped with rosebengal (RB), with the stearic acid (SA) molecules of a preformed SA Langmuir monolayer. The reaction kinetics of the formation of RB-CTAB-SA complex monolayer was monitored by observing the increase in surface pressure with time while the barrier was kept fixed. Completion of interaction kinetics was confirmed by FTIR study. This complex Langmuir films at the air-water interface was transferred onto solid substrates at a desired surface pressure to form multilayered Langmuir-Blodgett films. Spectroscopic characterizations reveal some molecular level interactions as well as formation of microcrystalline aggregates depending upon the molar ratios of CTAB and RB within the complex LB films. Presence of two types of species in the complex LB films was confirmed by fluorescence spectroscopy.

cond-mat.mtrl-sci↗

arXiv2008

Formation of complex films with water-soluble CTAB molecules

This communication reports the formation of complex Langmuir monolayer at the air-water interface with the water-soluble -trimethyl ammonium bromide (CTAB) molecules when interacted with the stearic acid (SA) molecules. The reaction kinetics of the formation of the CTAB-SA complex was monitored by observing the surface pressure versus time graph. Multilayered LB films of this complex doped with congo red was successfully formed onto a quartz substrate. UV-Vis absorption and steady state fluorescence spectroscopic characteristics of this doped LB films confirms the successful incorporation of congo red molecules in to the CTAB-SA complex films.

cond-mat.mtrl-sci↗

arXiv2008

Preparation of ODA-clay hybrid films by Langmuir-Blodgett technique

Hybrid monolayers of clay minerals (hectorite) and Octadecyamine (ODA) were prepared using the Langmuir-Blodgett (LB) technique. Surface pressure-area per molecule isotherm, FTIR and atomic force microscopy were used to confirm and analyze the ODA-hectorite hybrid films. The monolayer thickness is 2 nm and average height, length and width of individual clay platelets ranges between 1.5 to 2 nm, 500 to 1250 nm and 100 to 115 nm respectively. The surface coverage was more than 80%.

cond-mat.mtrl-sci↗

arXiv2008

Preparation and characterization of an anionic dye-polycation molecular films by electrostatic Layer-by-Layer adsorption process

This communication reports the formation and characterization of self assembled films of a low molecular weight anionic dye amaranth and polycation Poly (allylamine hydrochloride) (PAH) by electrostatic alternating Layer-by-Layer (LBL) adsorption. It was observed that there was almost no material loss occurred during adsorption process. The UV-Vis absorption and fluorescence spectra of amaranth solution reveal that with the increase in amaranth concentration in solution, the aggregated species starts to dominate over the monomeric species. New aggregated band at 600 nm was observed in amaranth-PAH mixture solution absorption spectrum. A new broad low intense band at the longer wavelength region, in the amaranth-PAH mixture solution fluorescence spectrum was observed due to the closer association of amaranth molecule while tagged into the polymer backbone of PAH and consequent formation of aggregates. The broad band system in the 650-750 nm region in the fluorescence spectra of different layered LBL films changes in intensity distribution among various bands within itself, with changing layer number and at 10 bilayer LBL films the longer wavelength band at 710 nm becomes prominent. Existence of dimeric or higher order n-meric species in the LBL films was confirmed by excitation spectroscopic studies. Almost 45 minute was required to complete the interaction between amaranth and PAH molecules in the 1-bilayer LBL film.

cond-mat.mtrl-sci↗

arXiv2008

Aggregation of P-terphenyl along with PMMA/SA at the Langmuir and Langmuir-Blodgett Films

Molecular aggregation and monolayer characteristics of non-amphiphilic p-terphenyl (TP) mixed with either polymethyl methacrylate (PMMA) or stearic acid (SA) at the air-water interface were investigated. The miscibility of the two components was evaluated by measuring and analyzing surface pressure versus area per molecule (pi-A) isotherm. Both attractive and repulsive interactions between the sample (TP) and the matrix (PMMA or SA) were observed depending on the composition and microenvironment. TP and PMMA/SA were not completely miscible in the mixed monolayer. Aggregation and phase separation between sample TP and matrix molecule was revealed by UV-Vis absorption spectroscopic studies and confirmed by scanning electron micrograpgh of LB films.

cond-mat.mtrl-sci↗

arXiv2008

Immobilization of single strand DNA on solid substrate

Thin films based on Layer-by-Layer (LbL) self assembled technique are useful for immobilization of DNA onto solid support. This communication reports the immobilization of DNA onto a solid support by electrostatic interaction with a polycation Poly (allylamine hydrochloride) (PAH). UV-Vis absorption and steady state fluorescence spectroscopic studies exhibit the characteristics of DNA organized in LbL films. The most significant observation is that single strand DNA are immobilized on the PAH backbone of LbL films when the films are fabricated above the melting temperature of DNA. DNA immobilized in this way on LbL films remains as such when the temperature is restored at room temperature and the organization remains unaffected even after several days. UV-Vis absorption spectroscopic studies confirm this finding.

cond-mat.mtrl-sci↗

arXiv2008

Monolayer Characteristics of Pyrene Mixed with Stearic Acid at the Air-Water Interface

In the present communication we report the monolayer characteristics of pyrene mixed with stearic acid (SA) at the air-water interface. The monolayer properties are investigated by recording and analyzing the surface pressure-area per molecule isotherm (pi-A) of the pyrene-SA mixed films. It is observed that the pyrene and SA are miscible in the mixed monolayer. This miscibility/nonideality leads to phase separation between the constituent components (pyrene and SA). BAM image of the mixed monolayer confirms the miscibility or nonideal mixing at the mixed monolayer.

cond-mat.mtrl-sci↗