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Liquid–Liquid Interfacial Imaging Using Atomic Force Microscopy
Author(s) -
Costa Luca,
LiDestri Giovanni,
Pontoni Diego,
Konovalov Oleg,
Thomson Neil H.
Publication year - 2017
Publication title -
advanced materials interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.671
H-Index - 65
ISSN - 2196-7350
DOI - 10.1002/admi.201700203
Subject(s) - materials science , nanoscopic scale , monolayer , nanomaterials , polystyrene , nanotechnology , nanoparticle , soft matter , mica , layer (electronics) , microscopy , polymer , chemical engineering , composite material , optics , colloid , physics , engineering
Nanoscale imaging of a liquid/liquid interface by atomic force microscopy (AFM) is achieved through the self‐assembly of interfacial layers of either polymers, lipids, or nanoparticles. Stabilization of the interface through spreading of a thin film of polystyrene‐b‐poly(methyl‐methacrylate) block copolymer or 1,2‐dioleoyl‐sn‐glycero‐3‐phosphoethanolamine lipids or adsorption of monolayers of silica nanoparticles allows reproducible imaging of these soft materials at an oil/water interface with nanoscale resolution on a timescale of 10 s. Amplitude modulation AFM is employed and requires that the subphase of water is below a critical depth of 100 µm to prevent excitation of gravity waves at the interface. The amplitude of these vertical oscillations is of the order of 1 nm but increases with the water layer depth. Below this critical water layer depth, force measurements show a linear compliance of the water/heptane and water/octane interfaces to be close to 10 −2 N m −1 . This study discusses in detail the experimental setup, sample preparation procedures, and AFM parameters necessary to achieve nanoscale resolution at the extremely soft and dynamic liquid interface. This expands the application of AFM to structural and dynamic nanoscale measurements for soft matter, biological, and nanomaterials away from solid supports.