Molecular strategies to read and write at the nanoscale with far-field optics.

Nanoscale

Department of Chemistry, University of Miami, 1301 Memorial Drive, Coral Gables, Florida 33146-0431, USA.

Published: January 2011

Diffraction prevents the focusing of ultraviolet and visible radiations within nanoscaled volumes and, as a result, the imaging and patterning of nanostructures with conventional far-field illumination. Specifically, the irradiation of a fluorescent or photosensitive material with focused light results in the simultaneous excitation of multiple chromophores distributed over a large area, relative to the dimensions of single molecules. It follows that the spatial control of fluorescence and photochemical reactions with molecular precision is impossible with conventional illumination configurations. However, the photochemical and photophysical properties of organic chromophores can be engineered to overcome diffraction in combination with patterned or reiterative illumination. These ingenious strategies offer the opportunity to confine excited chromophores within nanoscaled volumes and, therefore, restrict fluorescence or photochemical reactions within subdiffraction areas. Indeed, information can be "read" in the form of fluorescence and "written" in the form of photochemical products with resolution down to the nanometre level on the basis of these innovative approaches. In fact, these promising far-field optical methods permit the convenient imaging of biological samples and fabrication of miniaturized objects with unprecedented resolution and can have long-term and profound implications in biomedical research and information technology.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c0nr00546kDOI Listing

Publication Analysis

Top Keywords

nanoscaled volumes
8
fluorescence photochemical
8
photochemical reactions
8
molecular strategies
4
strategies read
4
read write
4
write nanoscale
4
nanoscale far-field
4
far-field optics
4
optics diffraction
4

Similar Publications

Synergistic strengthening of nano-scaled MC and β-NiAl has become a new route to develop ultra-high secondary-hardening steel. At present, the effect of Co on the synergistic precipitation behavior of duplex phases of MC and β-NiAl has been rarely reported. This paper revealed the effects of Co on the mechanical properties and duplex precipitates of MC and β-NiAl in a novel 2.

View Article and Find Full Text PDF

Structural Reversibility of Nanoscaled Sn Anodes.

Nano Lett

May 2024

State Key Laboratory of Low-Dimensional Quantum Physics and Department of Physics, Tsinghua University, Beijing 100084, China.

Alloying-type anode materials provide high capacity for lithium-ion batteries; however, they suffer pulverization problems resulting from the volume change during cycling. Realizing the cycling reversibility of these anodes is therefore critical for sustaining their electrochemical performance. Here, we investigate the structural reversibility of Sn NPs during cycling at atomic-level resolution utilizing high-resolution TEM.

View Article and Find Full Text PDF

Room temperature bio-engineered multifunctional carbonates for CO sequestration and valorization.

Sci Rep

October 2023

UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria, South Africa.

This contribution reports, for the first time, on an entirely green bio-engineering approach for the biosynthesis of single phase crystalline 1-D nano-scaled calcite CaCO. This was validated using HO as the universal solvent and natural extract of Hyphaene thebaica fruit as an effective chelating agent. In this room temperature green process, CaCl and CO are used as the unique source of Ca and CO respectively in view of forming nano-scaled CaCO with a significant shape anisotropy and an elevated surface to volume ratio.

View Article and Find Full Text PDF

Facile and Scalable Development of High-Performance Carbon-Free Tin-Based Anodes for Sodium-Ion Batteries.

ACS Appl Mater Interfaces

August 2023

Advanced Batteries and Ceramics Laboratory, Department of Metallurgical Engineering and Materials Science, Indian Institute of Technology (IIT) Bombay, Powai, Mumbai 400076, India.

Tin (Sn)-based anodes for sodium (Na)-ion batteries possess higher Na-storage capacity and better safety aspects compared to hard carbon -based anodes but suffer from poor cyclic stability due to volume expansion/contraction and concomitant loss in mechanical integrity during sodiation/desodiation. To address this, the usage of nanoscaled electrode-active particles and nanoscaled-carbon-based buffers has been explored, but with compromises with the tap density, accrued irreversible surface reactions, overall capacity (for "inactive" carbon), and adoption of non-scalable/complex preparation routes. Against this backdrop, anode-active "layered" bismuth (Bi) has been incorporated with Sn via a facile-cum-scalable mechanical-milling approach, leading to individual electrode-active particles being composed of well-dispersed Sn and Bi phases.

View Article and Find Full Text PDF

Ultra-fine SnOnanocrystals anchored on reduced graphene oxide as a high-performance anode material for sodium-ion batteries.

Nanotechnology

May 2023

Yazhou Bay Innovation Research Institute, College of Marine Science & Technology, Hainan Tropical Ocean University, Sanya, 572022, People's Republic of China.

SnOhas attracted extensive research attentions as a promising anode material for sodium-ion batteries (SIBs) due to its high theoretical capacity. However, its application is largely hindered by sluggish sodium ion diffusion and drastic volume change during the conversion reaction and alloying process. Herein, ultra-fine SnOnanocrystals (3-5 nm) anchored on reduced graphene oxide (rGO) is demonstrated as a promising anode material for SIBs.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!