We have investigated the various morphological changes of helical nanofilament (HNF; B4) phases in multiscale nanochannels made of porous anodic aluminum oxide (AAO) film. Single or multihelical structures could be manipulated depending on the AAO pore size and the higher-temperature phase of each molecule. Furthermore, the nanostructures of HNFs affected by the chemical affinity between the molecule and surface were drastically controlled in surface-modified nanochannels. These well-controlled hierarchical helical structures that have multidimensions can be a promising tool for the manipulation of chiral pores or the nonlinear optical applications.
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http://dx.doi.org/10.1021/acs.langmuir.5b01620 | DOI Listing |
Anal Chem
January 2025
Department of Chemistry, The University of Kansas, Lawrence, Kansas 66045, United States.
We are developing a unique protein identification method that consists of generating peptides proteolytically from a single protein molecule (i.e., peptide fingerprints) with peptide detection and identification carried out using nanoscale electrochromatography and label-free resistive pulse sensing (RPS).
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
December 2024
Department of Chemical Engineering, Queen's University, Kingston, Ontario K7L 3N6, Canada.
Hybrid nanoplasmonic structures composed of subwavelength apertures in metallic films and nanoparticles have recently been demonstrated as ultrasensitive plasmonic sensors. This work investigates the electrokinetically driven propagation of the assembly mechanism of the metallic nanoparticles through nanoapertures. The Debye-Hückel approximation for a symmetric electrolyte solution with overlapping electrical double layers (EDLs) is used to obtain an analytical solution to the problem.
View Article and Find Full Text PDFSmall
January 2025
Key Laboratory of Advanced Functional Materials of Ministry of Education, College of Materials Science and Engineering, Beijing University of Technology, Beijing, 100124, P. R. China.
Clay-based 2D nanofluidics present a promising avenue for osmotic energy harvesting due to their low cost and straightforward large-scale preparation. However, a comprehensive understanding of ion transport mechanisms, and horizontal and vertical transmission, remains incomplete. By employing a multiscale approach in combination of first-principles calculations and molecular dynamics simulations, the issue of how transmission directions impact on the clay-based 2D nanofluidics on osmotic energy conversion is addressed.
View Article and Find Full Text PDFJ Mol Model
September 2024
College of Mechanical Engineering, Changzhou University, Changzhou, Jiangsu Province, China.
Context: In a very small surface separation, the fluid flow is actually multiscale consisting of both the molecular scale non-continuum adsorbed layer flow and the intermediate macroscopic continuum fluid flow. Classical simulation of this flow often takes over large computational source and is not affordable owing to using molecular dynamics simulation (MDS) to model the adsorbed layer flow, if the flow field size is on the engineering size scale such as of 0.01-10 mm or even bigger like occurring in micro or macro hydrodynamic bearings.
View Article and Find Full Text PDFJ Chem Phys
July 2024
Laboratory for Multiscale Mechanics and Medical Science, SV LAB, School of Aerospace, Xi'an Jiaotong University, Xi'an 710049, China.
Inspired by biological channels, achieving precise separation of ion/water and ion/ion requires finely tuned pore sizes at molecular dimensions and deliberate exposure of charged groups. Covalent organic frameworks (COFs), a class of porous crystalline materials, offer well-defined nanoscale pores and diverse structures, making them excellent candidates for nanofluidic channels that facilitate ion and water transport. In this study, we perform molecular simulations to investigate the structure and kinetics of water and ions confined within the typical COFs with varied exposure of charged groups.
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