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Sarbajit Banerjee

Publications and source records attributed to Sarbajit Banerjee.

14 recordsLinked to original sources
PubMed2006

Imperfect surface order and functionalization in vertical carbon nanotube arrays probed by near edge X-ray absorption fine structure spectroscopy (NEXAFS).

Probing surface order as well as the degree of structural modification in carbon nanotube systems is of fundamental importance for incorporation of these materials into practical functional devices. The current study pertains to the analysis of the surface order of vertically-aligned single-walled and multi-walled carbon nanotube arrays of varying length and composition by means of near-edge X-ray fine structure spectroscopy (NEXAFS). Both NEXAFS and scanning electron microscopy (SEM) studies concluded that the nanotubes in these samples were oriented vertically to the plane of the surface. However, NEXAFS polarization analysis provided a more quantitative and nuanced description of the surface structure, indicative of far less localized surface order, an observation partially attributed to misalignment and bending of the tubes. Moreover, it was demonstrated by NEXAFS that the surface order of the arrays was imperfect and relatively independent of the height of the nanotube arrays. In addition, we have shown that NEXAFS can be used to correlate the extent of chemical functionalization and oxygenation with disruption of the electronic and physical structure of nanotubes embedded in array motifs.

Carbon↗
PubMed2006

Near-edge X-ray absorption fine structure spectroscopy as a tool for investigating nanomaterials.

We have demonstrated near-edge X-ray absorption fine structure (NEXAFS) spectroscopy as a particularly useful and effective technique for simultaneously probing the surface chemistry, surface molecular orientation, degree of order, and electronic structure of carbon nanotubes and related nanomaterials. Specifically, we employ NEXAFS in the study of single-walled carbon nanotube and multi-walled carbon nanotube powders, films, and arrays, as well as of boron nitride nanotubes. We have focused on the advantages of NEXAFS as an exciting, complementary tool to conventional microscopy and spectroscopy for providing chemical and structural information about nanoscale samples.

Crystallography↗
PubMed2006

Raman microprobe analysis of elastic strain and fracture in electrophoretically deposited CdSe nanocrystal films.

The mechanical stability of nanocrystal films is critical for applications, yet largely unexplored. Raman microprobe analysis used here to probe the nanocrystal cores of thick, fractured electrophoretically deposited films of 3.2 nm diameter CdSe nanocrystals measures approximately 2.5% in-plane tensile strain in cores of unfractured films. The crack dimensions determine the overall in-plane film strain, approximately 11.7%, and the film biaxial modulus, approximately 13.8 GPa, from which the biaxial modulus of the trioctylphosphine oxide ligand matrix is inferred, approximately 5.1 GPa.

Cadmium Compounds↗
PubMed2005

Near-edge X-ray absorption fine structure investigations of order in carbon nanotube-based systems.

Probing order in nanotube systems is of fundamental importance in devising applications of these tubes in field emission applications as well as for components of composite materials. We use near-edge X-ray absorption fine structure (NEXAFS) spectroscopy to qualitatively and quantitatively study the degree of order and alignment in a wide range of carbon nanotube-based systems, including single-walled carbon nanotube (SWNT) powder, SWNT films, and aligned multiwalled carbon nanotubes. The results are compared to analogous data obtained from a highly ordered pyrolytic graphite (HOPG) sample.

Journal Article↗
PubMed2005

Routes towards separating metallic and semiconducting nanotubes.

Separation of single-walled carbon nanotubes (SWNTs), according to their electronic characteristics, is essential to the development of molecular electronics, including field-effect transistors. Recent efforts by many groups have used non-covalent and covalent sidewall chemistry to probe differential reactivity in metallic and semiconducting nanotubes. These chemically based methods may more easily effect the bulk separation of tubes, as compared with physical techniques associated with (i) alternating current dielectrophoresis as well as (ii) the current-induced oxidation of metallic nanotubes, that have recently been reported as alternative methods of achieving chiral separations of nanotubes. Exploration of these types of reactions is critical for the development of interesting chemical and physical properties at the interface between molecules and materials as well as for establishing protocols for the selective functionalization of nanotubes.

Crystallization↗
PubMed2004

Surface chemistry and structure of purified, ozonized, multiwalled carbon nanotubes probed by NEXAFS and vibrational spectroscopies.

Understanding of oxidative processes such as solution-phase ozonolysis in multiwalled carbon nanotubes (MWNTs) is of fundamental importance in devising applications of these tubes as components in composite materials, as well as for development of cutting and filling protocols. We present here an evaluation of various spectroscopic tools to study the structure and composition of functionalized nanotubes. We demonstrate near-edge X-ray absorption fine structure (NEXAFS) spectroscopy as a particularly useful and effective technique for studying the surface chemistry of carbon nanotubes.

Journal Article↗
PubMed2004

Selective metallic tube reactivity in the solution-phase osmylation of single-walled carbon nanotubes.

Single-walled carbon nanotubes have been reacted with osmium tetroxide (OsO(4)) in solution in the presence of O(2) and UV irradiation at 254 nm. We observe one main structural motif, namely thickly coated nanotube structures, densely covered with OsO(2), consisting of multiple bundles of derivatized tubes. In a few instances, bridging uncoated tubes, connecting these thickly coated structures, incorporate a number of smaller nanotube bundles, projecting out from the larger functionalized aggregates of tubes. It is believed that OsO(2) (a) initially forms on the nanotubes by the preferential covalent sidewall functionalization of metallic nanotubes and (b) subsequently self-aggregates. The formation of an intermediate charge-transfer complex is likely the basis for the observed selectivity and reactivity of metallic tubes. Extensive characterization of these osmylated adducts has been performed using a variety of electron microscopy and optical spectroscopy techniques.

Journal Article↗
PubMed2003

Large-scale synthesis of single-crystalline perovskite nanostructures.

Single-crystalline perovskite nanostructures with reproducible shape have been prepared using a simple, readily scaleable solid-state reaction in the presence of NaCl and a nonionic surfactant. Pristine BaTiO3 nanowires have diameters ranging from 50 to 80 nm with an aspect ratio larger than 25. Single-crystalline SrTiO3 nanocubes with a mean edge length of 80 nm have been produced using a similar procedure.

Journal Article↗
PubMed2003

In situ quantum dot growth on multiwalled carbon nanotubes.

The generation of nanoscale interconnects and supramolecular, hierarchical assemblies enables the development of a number of novel nanoscale applications. A rational approach toward engineering a robust system is through chemical recognition. Here, we show the in situ mineralization of crystalline CdTe quantum dots on the surfaces of oxidized multiwalled carbon nanotubes (MWNTs). We coordinate metallic precursors of quantum dots directly onto nanotubes and then proceed with in situ growth. The resulting network of molecular-scale "fused" nanotube-nanocrystal heterojunctions demonstrates a controlled synthetic route to the synthesis of complex nanoscale heterostructures. Extensive characterization of these heterostructures has been performed using scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, UV-visible spectroscopy, and X-ray diffraction (XRD).

Journal Article↗
PubMed2003

Rational chemical strategies for carbon nanotube functionalization.

Whereas the chemistry of fullerenes is well-established, the chemistry of single-walled carbon nanotubes (SWNTs) is a relatively unexplored field of research. Investigations into the bonding of moieties onto SWNTs are important because they provide fundamental structural insight into how nanoscale interactions occur. Hence, understanding SWNT chemistry becomes critical to rational, predictive manipulation of their properties. Among the strategies discussed include molecular metal complexation with SWNTs to control site-selective chemistry in these systems. In particular, work has been performed with Vaska's and Wilkinson's complexes to create functionalized adducts. Functionalization should offer a relatively simple means of tube solubilization and bundle exfoliation, and also allows for tubes to be utilized as recoverable catalyst supports. Solubilization of oxidized SWNTs has also been achieved through derivatization by using a functionalized organic crown ether. The resultant adduct yielded concentrations of dissolved nanotubes on the order of 1 g L(-1) in water and at elevated concentrations in a range of organic solvents, traditionally poor for SWNT manipulation. To further demonstrate chemical processability of SWNTs, we have subjected them to ozonolysis, followed by treatment with various independent reagents, to rationally generate a higher proportion of oxygenated functional groups on the nanotube surface. This protocol has been found to purify nanotubes. More importantly, the reaction sequence has been found to ozonize the sidewalls of these nanotubes. Finally, SWNTs have also been chemically modified with quantum dots and oxide nanocrystals. A composite heterostructure consisting of nanotubes joined to nanocrystals offers a unique opportunity to obtain desired physical, electronic, and chemical properties by adjusting synthetic conditions to tailor the size and structure of the individual sub-components, with implications for self-assembly.

Journal Article↗
PubMed2003

Hydrothermal synthesis of perovskite nanotubes.

A low-temperature hydrothermal reaction has been utilized to generate crystalline barium titanate and strontium titanate nanotubes, which have been characterized by means of X-ray diffraction and transmission electron microscopy, coupled with energy dispersive X-ray analysis.

Journal Article↗
PubMed2002

Structural characterization, optical properties, and improved solubility of carbon nanotubes functionalized with Wilkinson's catalyst.

Oxidized carbon nanotubes have been reacted with Wilkinson's complex. It has been found that the Rh metal coordinates to these nanotubes through the increased number of oxygen atoms, forming a hexacoordinate structure around the Rh atom. The reaction process increases oxidized nanotube solubility in DMSO (>150 mg/L) as well as to a certain extent in DMF and THF. The functionalization process results in exfoliation of larger bundles of SWNTs and may select for the presence of distributions of smaller-diameter tubes. Optical data on the derivatized adducts suggest the possibility of interesting charge-transfer behavior across the metal-nanotube interface. An application has been made of this system as supports for homogeneous catalysis.

Journal Article↗