Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

We measure the vibrational modes and particle dynamics of quasi-two-dimensional colloidal glasses as a function of interparticle interaction strength. The interparticle attractions are controlled via a temperature-tunable depletion interaction. Specifically, the interparticle attraction energy is increased gradually from a very small value (nearly hard-sphere) to moderate strength (∼4k_{B}T), and the variation of colloidal particle dynamics and vibrations are concurrently probed. The particle dynamics slow monotonically with increasing attraction strength, and the particle motions saturate for strengths greater than ∼2k_{B}T, i.e., as the system evolves from a nearly repulsive glass to an attractive glass. The shape of the phonon density of states is revealed to change with increasing attraction strength, and the number of low-frequency modes exhibits a crossover for glasses with weak compared to strong interparticle attraction at a threshold of ∼2k_{B}T. This variation in the properties of the low-frequency vibrational modes suggests a new means for distinguishing between repulsive and attractive glass states.

Download full-text PDF

Source
http://dx.doi.org/10.1103/PhysRevE.94.042606DOI Listing

Publication Analysis

Top Keywords

interparticle attraction
12
particle dynamics
12
quasi-two-dimensional colloidal
8
colloidal glasses
8
vibrational modes
8
increasing attraction
8
attraction strength
8
attractive glass
8
interparticle
5
attraction
5

Similar Publications

Redox-active organic-inorganic hybrid electrode materials are promising candidates for eco-friendly, high-energy-density supercapacitors. The synergy between organic and inorganic components in energy storage devices has attracted considerable interest due to their complementary attributes, including flexibility, long-term stability, and high conductivity. This study presents an innovative approach for synthesizing an organic-inorganic active electrode material by grafting diazonium salts of 8-aminoquinoline (8-AQ-N ) onto CuFeO nanoparticle (NP) surfaces.

View Article and Find Full Text PDF

Artificial active colloids have been an active area of research in the field of active matter and microrobotic systems. In particular, light driven semi-conductor particles have been shown to display interesting behaviors ranging from phototaxis (movement toward or away from a light source), rising from the substrate, inter-particle attraction, attraction to the substrate, or other phenomenon. However, these observations involve multiple different designs of particles in varying conditions, making it unclear how the experimental parameters, such as pH, peroxide concentration, and light intensity, affect the outcomes.

View Article and Find Full Text PDF

Employing electric fields to induce directional arrangement of one-dimensional nanofillers within specific regions is a powerful strategy for enhancing the performance of composites. However, conventional single-mode electric fields (AC or DC) exhibit inherent "orientation-distribution" contradiction. Specifically, AC fields are effective for orientation but lack spatial control, while DC fields promote filler enrichment but fail to optimize orientation state.

View Article and Find Full Text PDF

It is demonstrated that the effective scattering length can be highly manipulated via time-periodic driving of a short-range interparticle potential. By developing a Floquet-scattering theory we show that sharp Floquet resonances occur at which the effective interaction can be tuned to very large attractive or repulsive values. The resulting s-wave scattering length can be obtained in analytic form and the shape of these resonances is given by a simple formula describing how resonance position and width can be altered by the driving strength.

View Article and Find Full Text PDF

Ligand-protected gold nanoclusters have attracted attention as building blocks for functional materials. In this study, we have demonstrated the programmed assembly of the icosahedral Ir@Au nanoclusters into a dimer, a linear trimer, linear oligomers, or a triangular trimer via the reaction between IrAu with predefined binding sites and bi- or tridentate isocyanide linkers. The formation of the intended structures was confirmed by high-angle annular dark-field scanning transmission electron microscopy using a newly developed sampling protocol.

View Article and Find Full Text PDF