Transition in Dynamics as Nanoparticles Jam at the Liquid/Liquid Interface
Author(s) -
Mengmeng Cui,
Caroline Miesch,
Irem Kosif,
Huarong Nie,
Paul Y. Kim,
Hyunki Kim,
Todd Emrick,
Thomas P. Russell
Publication year - 2017
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/acs.nanolett.7b03159
Subject(s) - chemical physics , nanoparticle , liquid liquid , absorption (acoustics) , materials science , molecular dynamics , absorption spectroscopy , nanotechnology , chemistry , optics , computational chemistry , chromatography , physics , composite material
Nanoparticles (NPs) segregated to the liquid/liquid interface form disordered or liquid-like assemblies that show diffusive motions in the plane of the interface. As the areal density of NPs at the interface increases, the available interfacial area decreases, and the interfacial dynamics of the NP assemblies change when the NPs jam. Dynamics associated with jamming was investigated by X-ray photon correlation spectroscopy. Water-in-toluene emulsions, formed by a self-emulsification at the liquid/liquid interface and stabilized by ligand-capped CdSe-ZnS NPs, provided a simple, yet powerful platform, to investigate NP dynamics. In contrast to a single planar interface, these emulsions increased the number of NPs in the incident beam and decreased the absorption of X-rays in comparison to the same path length in pure water. A transition from diffusive to confined dynamics was manifested by intermittent dynamics, indicating a transition from a liquid-like to a jammed state.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom