Electron Spectrum, Localization and Tunneling in Double Nanoscale Structures

2014 ◽  
Vol 2 (2) ◽  
Author(s):  
Igor Filikhin ◽  
Sergei Matinyan ◽  
Branislav Vlahovic
Keyword(s):  
Electron Spectrum ◽  
Nanoscale Structures ◽  
Spectrum Localization

scholarly journals Asymmetry of the electron spectrum in hole-doped and electron-doped cuprates

2006 ◽  
Vol 355 (6) ◽  
pp. 473-480 ◽  
Author(s):  
Huaiming Guo ◽  
Shiping Feng
Keyword(s):  
Electron Spectrum

Finite element modeling of nanoscale structures

2011 ◽  
Vol 6 (9-10) ◽  
pp. 597-606 ◽  
Author(s):  
M. A. Zhuravkov ◽  
Yu. E. Nagornyi ◽  
V. I. Repchenkov
Keyword(s):  
Finite Element ◽  
Finite Element Modeling ◽  
Nanoscale Structures ◽  
Element Modeling

scholarly journals Synthesis and spectral characterizations of vanadyl(ii) and chromium(iii) mixed ligand complexes containing metformin drug and glycine amino acid

2021 ◽  
Vol 19 (1) ◽  
pp. 735-744
Author(s):  
Samar O. Aljazzar
Keyword(s):  
Amino Acid ◽  
Type Ii Diabetes ◽  
Mixed Ligand ◽  
Mixed Ligand Complexes ◽  
Spectroscopic Techniques ◽  
Nanoscale Structures ◽  
Pyramidal Geometry ◽  
Effective Drugs ◽  
Square Pyramidal Geometry ◽  
Spectral Characterizations

Abstract Metformin is one of the most effective drugs for the treatment of type II diabetes. Two new mixed ligand complexes of vanadyl(ii) and chromium(iii) ions with the general formula [VOL1L2]SO4 and [CrL1L2(Cl)2]Cl, respectively, where L1 is the metformin and L2 is the glycine amino acid, have been synthesized in MeOH solvent with 1:1:1 stoichiometry and characterized by several spectroscopic techniques. The spectroscopic data suggested that the [VOL1L2]SO4 complex possesses a square pyramidal geometry, where the [CrL1L2(Cl)2]Cl complex possesses an octahedral geometry. The L1 ligand coordinated to the VO(ii) and Cr(iii) ions via the N atoms of the imino (‒C═NH) groups, where the L2 ligand coordinated via the O atom of the carboxylate group (COO) and the N atom of the amino group (NH2). The interaction of ligands L1 and L2 with the metal ions leads to complexes that have organized nanoscale structures with a main diameter of ∼14 nm for the [CrL1L2(Cl)2]Cl complex and ∼40 nm for the [VOL1L2]SO4 complex.

scholarly journals Erratum: Signature of Energy Losses on the Cosmic Ray Electron Spectrum [Phys. Rev. Lett. 125 , 051101 (2020)]

2021 ◽  
Vol 126 (24) ◽  
Author(s):  
Carmelo Evoli ◽  
Pasquale Blasi ◽  
Elena Amato ◽  
Roberto Aloisio
Keyword(s):  
Electron Spectrum ◽  
Cosmic Ray ◽  
Energy Losses

scholarly journals Kerogen nanoscale structure and CO2 adsorption in shale micropores

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Aleksandra Gonciaruk ◽  
Matthew R. Hall ◽  
Michael W. Fay ◽  
Christopher D. J. Parmenter ◽  
Christopher H. Vane ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Chemical Composition ◽  
Focused Ion Beam ◽  
Gas Adsorption ◽  
Ion Beam ◽  
Molecular Size ◽  
Gas Sorption ◽  
Nanoscale Structures ◽  
Adsorption Sites ◽  
Nanoscale Structure

AbstractGas storage and recovery processes in shales critically depend on nano-scale porosity and chemical composition, but information about the nanoscale pore geometry and connectivity of kerogen, insoluble organic shale matter, is largely unavailable. Using adsorption microcalorimetry, we show that once strong adsorption sites within nanoscale network are taken, gas adsorption even at very low pressure is governed by pore width rather than chemical composition. A combination of focused ion beam with scanning electron microscopy and transmission electron microscopy reveal the nanoscale structure of kerogen includes not only the ubiquitous amorphous phase but also highly graphitized sheets, fiber- and onion-like structures creating nanoscale voids accessible for gas sorption. Nanoscale structures bridge the current gap between molecular size and macropore scale in existing models for kerogen, thus allowing accurate prediction of gas sorption, storage and diffusion properties in shales.

scholarly journals Hybrid Nanoassemblies from Viruses and DNA Nanostructures

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1413
Author(s):  
Sofia Ojasalo ◽  
Petteri Piskunen ◽  
Boxuan Shen ◽  
Mauri A. Kostiainen ◽  
Veikko Linko
Keyword(s):  
Cell Activation ◽  
Immune Cell ◽  
Dna Nanotechnology ◽  
Biological Properties ◽  
Dna Nanostructures ◽  
Dna Structures ◽  
Nanoscale Structures ◽  
Immune Cell Activation ◽  
Wide Range ◽  
Structural Dna Nanotechnology

Viruses are among the most intriguing nanostructures found in nature. Their atomically precise shapes and unique biological properties, especially in protecting and transferring genetic information, have enabled a plethora of biomedical applications. On the other hand, structural DNA nanotechnology has recently emerged as a highly useful tool to create programmable nanoscale structures. They can be extended to user defined devices to exhibit a wide range of static, as well as dynamic functions. In this review, we feature the recent development of virus-DNA hybrid materials. Such structures exhibit the best features of both worlds by combining the biological properties of viruses with the highly controlled assembly properties of DNA. We present how the DNA shapes can act as “structured” genomic material and direct the formation of virus capsid proteins or be encapsulated inside symmetrical capsids. Tobacco mosaic virus-DNA hybrids are discussed as the examples of dynamic systems and directed formation of conjugates. Finally, we highlight virus-mimicking approaches based on lipid- and protein-coated DNA structures that may elicit enhanced stability, immunocompatibility and delivery properties. This development also paves the way for DNA-based vaccines as the programmable nano-objects can be used for controlling immune cell activation.

scholarly journals Fabrication of elastic, conductive, wear-resistant superhydrophobic composite material

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Seyed Mehran Mirmohammadi ◽  
Sasha Hoshian ◽  
Ville P. Jokinen ◽  
Sami Franssila
Keyword(s):  
Contact Angle ◽  
Composite Material ◽  
Contact Angles ◽  
Wet Etching ◽  
Sliding Angle ◽  
Electrically Conductive ◽  
Wear Resistant ◽  
Nanoscale Structures ◽  
Mechanical Abrasion ◽  
Mechanical Durability

AbstractA polydimethylsiloxane (PDMS)/Cu superhydrophobic composite material is fabricated by wet etching, electroless plating, and polymer casting. The surface topography of the material emerges from hierarchical micro/nanoscale structures of etched aluminum, which are rigorously copied by plated copper. The resulting material is superhydrophobic (contact angle > 170°, sliding angle < 7° with 7 µL droplets), electrically conductive, elastic and wear resistant. The mechanical durability of both the superhydrophobicity and the metallic conductivity are the key advantages of this material. The material is robust against mechanical abrasion (1000 cycles): the contact angles were only marginally lowered, the sliding angles remained below 10°, and the material retained its superhydrophobicity. The resistivity varied from 0.7 × 10–5 Ωm (virgin) to 5 × 10–5 Ωm (1000 abrasion cycles) and 30 × 10–5 Ωm (3000 abrasion cycles). The material also underwent 10,000 cycles of stretching and bending, which led to only minor changes in superhydrophobicity and the resistivity remained below 90 × 10–5 Ωm.

Nanoscale control of internal inhomogeneity enhances water transport in desalination membranes

Science ◽  
2020 ◽  
Vol 371 (6524) ◽  
pp. 72-75 ◽  
Author(s):  
Tyler E. Culp ◽  
Biswajit Khara ◽  
Kaitlyn P. Brickey ◽  
Michael Geitner ◽  
Tawanda J. Zimudzi ◽  
...  
Keyword(s):  
Water Transport ◽  
Water Permeability ◽  
Three Dimensional ◽  
Density Fluctuations ◽  
Active Layer Thickness ◽  
Chemical Compositions ◽  
Design Strategies ◽  
Nanoscale Structures ◽  
Density Maps ◽  
Similar Chemical

Biological membranes can achieve remarkably high permeabilities, while maintaining ideal selectivities, by relying on well-defined internal nanoscale structures in the form of membrane proteins. Here, we apply such design strategies to desalination membranes. A series of polyamide desalination membranes—which were synthesized in an industrial-scale manufacturing line and varied in processing conditions but retained similar chemical compositions—show increasing water permeability and active layer thickness with constant sodium chloride selectivity. Transmission electron microscopy measurements enabled us to determine nanoscale three-dimensional polyamide density maps and predict water permeability with zero adjustable parameters. Density fluctuations are detrimental to water transport, which makes systematic control over nanoscale polyamide inhomogeneity a key route to maximizing water permeability without sacrificing salt selectivity in desalination membranes.

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