Two-dimensional Phase Behavior Research Articles

Interfacial rheology of polyelectrolyte microgel monolayers: Correlation between mechanical properties and phase behavior at oil-water interfaces

Microgels are confined to fluid interfaces in numerous applications, yet many aspects of the microgel-covered interface remain unclear. In this work, we use interfacial shear and dilatational rheology to study the effects of electrostatics on the mechanical characteristics of polyelectrolyte microgel monolayers at oil-water interfaces as a function of the microgel interfacial concentration. We find a clear correlation between the influence of charges on the mechanical properties of the monolayers and the influence of charges on their two-dimensional phase behavior. At lower microgel interfacial concentrations, the moduli of uncharged monolayers are larger than those of charged monolayers. Consistent with our previous findings on the phase behavior, here, the mechanical response of the interfacial layer is controlled by in-plane interactions of the microgels within the interface. At higher microgel interfacial concentrations, the moduli of charged monolayers are larger than those of uncharged monolayers. The mechanical response becomes dominated by out-of-plane interactions between the fractions of the adsorbed microgels further from the interface. Evidently, electrostatic interactions do not contribute directly to the mechanical response of the interfacial layer, that is, through charge repulsion, but indirectly through the difference in the swelling properties of uncharged and charged microgels. These results advance our understanding of how the charge-dependent microstructure of the interfacial layer affects its mechanical properties, which is not only important from a fundamental point of view but is also relevant to applications where polyelectrolyte microgels are used as responsive emulsion stabilizers.

Influence of the porphyrin structure and linker length on the interfacial behavior of phospholipid-porphyrin conjugates

HypothesisPhospholipid-porphyrin (Pl-Por) conjugates consist of porphyrin derivatives grafted to a lysophosphatidylcholine backbone. Owing to their structural similarities with phospholipids, Pl-Por conjugates can self-assemble into liposome-like assemblies. However, there is a significant lack of information concerning the impact of the porphyrin type and the length of the alkyl chain bearing the porphyrin on the interfacial behavior of the Pl-Por conjugates. We hypothesized that changing the chain length and the porphyrin type could impact their two-dimensional phase behavior and modulate the alignment between the two chains. Experiments6 Pl-Por conjugates with different alkyl chain lengths in the sn2 position of C16 lysophosphatidylcholine and coupled to either pheophorbide-a or pyropheophorbide-a were synthesized. Their interfacial behavior at the air/water interface was assessed using Langmuir balance combined to a variety of other physical techniques including Brewster angle microscopy, atomic force microscopy and X-ray reflectometry. FindingsOur results showed that all 6 Pl-Por form stable monolayers with the porphyrin moiety at the air/water interface. We also showed that changing the porphyrin moiety controlled the packing of the monolayer and thus the formation of organized domains. The chain length dictated the structure of the formed domains with no evidence of the alignment between the two chains.

Supramolecular Architecturing of Quantum Box Arrays from Functionalized Porphyrins and Exploring Their Quantum States

Our research is based on the analysis of structure-function correlations for a broad spectrum of functionalized porphyrins and phthalocyanines in their propensity to create increasingly complex and functional on surface architectures. [1] Thereby we use porphyrin and phthalocyanine functionalization and synthesis, ‘by design’, or ‘on-surface-supramolecular chemistry’ to create structures with specific physical properties towards e.g. future quantum devices.By using a fluoro-bi-phenyl functionalized porphyrin to create a stable, porous organic network, we manufacture arrays of identical quantum boxes. These boxes contain a specific quantum well state arising from the confinement of the electronic (Shockley) surface state within the pores. We show that the electronic quantum box state as well as the interbox coupling can be modified locally by adsorbates, e.g. C60, interacting with the barrier. In view of the wealth of available and differently acting adsorbates, this approach allows for the engineering of quantum states in on-surface network architectures. Thus, by their dance on the nose of the ‘devil’ [3], porphyrins and phthalocyanines justify the emergence of ‘on-surface supramolecular physics’ as reflected by ongoing and future research work.Fig. 1) Adsorbate-induced modification of the confining barriers in a quantum box array formed by a functionalized fluoro-bi-phenyl porphyrin on Ag(111). (Taken from [2])[1] N. Wintjes et al. Two-dimensional phase behavior of a bimolecular porphyrin system at the solid-vacuum interface, J. Am. Chem. Soc. 2010, 132, 21, 7306-7311; N. Wintjes et al., Supramolecular synthons on surfaces: Controlling dimensionality and periodicity of tetraarylporphyrin assemblies by the interplay of cyano and alkoxy substituents Chem. Eur. J. 2008, 14, 5794.[2] S. Nowakowska et al., Adsorbate-induced modification of the confining barriers in a quantum box array, ACS Nano 2018, 12, 768.[3] W. Pauli “God made the bulk; surfaces were invented by the devil.” Quoted, e.g. in the Preface of A. Zangwill, Physics at Surfaces, Cambridge University Press, 1988. ISBN 978-0-521-34752-5 Figure 1

Temperature-sensitive soft microgels at interfaces: air-water versus oil-water.

The formation of smart emulsions or foams whose stability can be controlled on-demand by switching external parameters is of great interest for basic research and applications. An emerging group of smart stabilizers are microgels, which are nano- and micro-sized, three-dimensional polymer networks that are swollen by a good solvent. In the last decades, the influence of various external stimuli on the two-dimensional phase behavior of microgels at air- and oil-water interfaces has been studied. However, the impact of the top-phase itself has been barely considered. Here, we present data that directly address the influence of the top-phase on the microgel properties at interfaces. The dimensions of pNIPAM microgels are measured after deposition from two interfaces, i.e., air- and decane-water. While the total in-plane size of the microgel increases with increasing interfacial tension, the portions or fractions of the microgels situated in the aqueous phase are not affected. We correlate the area microgels occupy to the surface tensions of the interfaces, which allows to estimate an elastic modulus. In comparison to nanoindentation measurements, we observe a larger elastic modulus for the microgels. By combining compression, deposition, and visualization, we show that the two-dimensional phase behavior of the microgel monolayers is not altered, although the microgels have a larger total in-plane size at higher interfacial tension.

On-Surface Supramolecular Chemistry with Porphyrins and Phthalocyanines: An Architectural Concept Leading to Engineered Quantum-Functional Nanostructures

The availability of porphyrin and phthalocyanine functionalization and synthesis, ‘by design’, at the time when sub-molecular resolution imaging at surfaces came into action boosted the emergence of ‘On-Surface-Supramolecular Chemistry’. [1] It is instructive to compare supra-molecular binding motifs in the fluid phase with the corresponding or modified analogues found after assembly on surfaces. In some similarity to chemistry and coordination chemistry translating into the corresponding ‘on-surface’ sciences, there are many factors complicating the on-surface assembly and architecture. Examples are provided by the modified dimensionality and kinetics, the site-specific conformational flexure and chirality and the close to irreversible adsorption in the strong surface potential in absence of a solvent which may complicate the on-surface assembly and architecture. Further, porphyrins and phthalocyanines interact with the substrate by different, competitive interactions, i.e. via (1) the central metal atom and (2) the porphyrin pi-system in addition to (3) the functional side groups. Binary and ternary assemblies of porphyrins and other functional components make it possible to create a wealth of ‘phases’, i.e. different complex supramolecular architectures with interesting physical properties to explore and exploit.We analyze structure-function correlations for a broad spectrum of functionalized porphyrins and phthalocyanines in their propensity to create structures of increasing complexity and functionality, on surfaces, also for future quantum technology. Notably, the large delocalized electronic system of the porphyrins and their easy-to-replace central atom further extend the achievable range of architectures and functions. Thus, by their dance on the nose of the ‘devil’ [3], porphyrins and phthalocyanines justify the emergence of ‘on-surface supramolecular physics’ as reflected by ongoing and future research work.[1] N. Wintjes et al. Two-dimensional phase behavior of a bimolecular porphyrin system at the solid-vacuum interface, J. Am. Chem. Soc. 2010, 132, 21, 7306-7311; N. Wintjes et al., Supramolecular synthons on surfaces: Controlling dimensionality and periodicity of tetraarylporphyrin assemblies by the interplay of cyano and alkoxy substituents Chem. Eur. J. 2008, 14, 5794.[2] S. Nowakowska et al., Adsorbate-induced modification of the confining barriers in a quantum box array, ACS Nano 2018, 12, 768.[3] W. Pauli “God made the bulk; surfaces were invented by the devil.” Quoted, e.g. in the Preface of A. Zangwill, Physics at Surfaces, Cambridge University Press, 1988. ISBN 978-0-521-34752-5Fig. 1) Adsorbate-induced modification of the confining barriers in a quantum box array formed by a functionalized fluoro-bi-phenyl porphyrin on Ag(111). (Taken from [2]) Figure 1

Phase Transitions in Dipalmitoylphosphatidylcholine Monolayers.

A self-assembled phospholipid monolayer at an air-water interface is a well-defined model system for studying surface thermodynamics, membrane biophysics, thin-film materials, and colloidal soft matter. Here we report a study of two-dimensional phase transitions in the dipalmitoylphosphatidylcholine (DPPC) monolayer at the air-water interface using a newly developed methodology called constrained drop surfactometry (CDS). CDS is superior to the classical Langmuir balance in its capacity for rigorous temperature control and leak-proof environments, thus making it an ideal alternative to the Langmuir balance for studying lipid polymorphism. In addition, we have developed a novel Langmuir-Blodgett (LB) transfer technique that allows the direct transfer of lipid monolayers from the droplet surface under well-controlled conditions. This LB transfer technique permits the direct visualization of phase coexistence in the DPPC monolayer. With these technological advances, we found that the two-dimensional phase behavior of the DPPC monolayer is analogous to the three-dimensional phase transition of a pure substance. This study has implications in the fundamental understanding of surface thermodynamics as well as applications such as self-assembled monolayers and pulmonary surfactant biophysics.

Structure, morphology and interfacial behaviour of ethylene/methacrylate copolymers

Two alpha-diimine monometallic Ni catalysts, catalyst 1 and catalyst 2, were studied in the copolymerization reaction of ethylene (E) with methyl methacrylate (MMA). The reaction products of these reactions were characterized using not only the usual techniques such as NMR, GPC and DSC but also the Langmuir balance and AFM. 1H and 13C NMR spectra revealed that both copolymers and mixtures of E and MMA (in a range of 20–70 mol% of MMA) could be obtained with these catalysts. A better insight of the products was possible with 1H DOSY NMR. Since p(E-MMA) copolymers comprising hydrophobic PE blocks and surface active PMMA blocks are amphiphilic, the Langmuir monolayer technique provided further information on the two-dimensional phase behavior of copolymer monolayers at the air-water interface. Additionally, AFM topographic images of the Langmuir-Blodgett (LB) monolayers deposited on mica substrates clearly showed that the morphology of the copolymer LB monolayer is quite different from the corresponding mixture of PE and PMMA homopolymers. These techniques together with molecular modeling calculations allowed us to conclude that with catalyst 2 it was possible to obtain a true block copolymer by a mechanism involving a cationic ester-enolate metal complex as the active species.

Viscoelasticity of semifluorinated alkanes at the air/water interface

As semifluorinated alkanes (SFA) present an unusual class of mesogenic units for supramolecular structure formation, the study of their physical properties and self-assembly at fluid interfaces is of substantial relevance. To this end, the two-dimensional phase behavior and the viscoelastic properties of semifluorinated alkanes with symmetric number of carbon atoms in the fluorinated and hydrogenated side chains (F(CF2)12–(CH2)12H and F(CF2)11CH2–core–(CH2)12H with dibromophenyl core were investigated at the air/water interface and compared to the asymmetric F(CF2)12(CH2)20H system. Surface pressure/area isotherms and compression–expansion cycles were recorded at 20 °C, 40 °C, and 50 °C. Depending on the molecular details, an unexpected phase transition and hysteresis in compression–expansion cycles could be observed. Interfacial rheology revealed for all monolayer systems a solid-like viscoelastic response over the investigated range of surface pressures. The interfacial storage modulus G′i and interfacial loss modulus G′′i increased with increasing surface pressure. More importantly, at constant surface pressure the simple semifluorinated alkanes, forming nearly circular 2D micellar structures at the interface, exhibited rheological properties reminiscent of glass-like colloid systems. On the other hand, the SFA with the dibromophenyl core formed 2D interfacial micelles of highly elongated shape with dendritic domains and exhibited gel-like rheological properties, similar to those of the asymmetric alkane. Moreover, with increasing surface pressure the response of the asymmetric system alters from glassy to gel-like. These findings suggest that fine differences in the molecular structure are reflected in the linear viscoelastic response of the Langmuir films, and hence offer the possibility to molecularly tune the rheology of fluid interfaces.

Two-Dimensional Phase Behavior of a Bimolecular Porphyrin System at the Solid−Vacuum Interface

The "in vacuo" self-assembly of a two-component porphyrin system on a metal surface is studied by means of scanning tunneling microscopy in the sub-monolayer regime. The observed self-assemblies are systematically analyzed by their dependence on the total coverage and on the ratio of the two components resulting in a two-dimensional phase diagram. In a small region within the parameter space, a mixed surface layer is observed. The results are discussed consistently on the basis of molecule-surface and molecule-molecule interactions as well as thermodynamic aspects, leading to a qualitative comprehension of the phase behavior of the two-dimensional bimolecular system.

Nanomechanical Contrasts of Gel and Fluid Phase Supported Lipid Bilayers

Lipid bilayers exhibit structural diversity that contributes to the complex properties of the cell membrane. We use interfacial force microscopy to correlate mechanical properties with the two-dimensional phase behavior of supported lipid bilayers (SLBs). Upon indentation by a 500 nm tungsten tip, a contrast in the mechanical response is observed for gel vs fluid phase SLBs. We measure the yield force and time scale for recovery for these films. Consistent with a gel phase, a DSPC SLB has a relatively high yield force and slow recovery. In the higher mobility fluid phase, a DLPC SLB has a lower yield force and completely recovers within the experimental time scale. Friction measurements offer further contrast between the two SLBs.

Change in the Orientation and Packing upon Adsorption of Pyranine Molecules onto Cationic Langmuir Monolayers and Langmuir–Blodgett Films

Abstract Differrent adsorption behaviors and the orientation of pyranine molecules were investigated for the cationic Langmuir monolayers by using Brewster angle microscopy (BAM), two-dimensional (2D) phase behavior with elasticitic property of the monolayers and in situ visible spectroscopy. The structural change in the cationic Langmuir–Blodgett (LB) films before and after adsorbing pyranine molecules was found by using small angle and in-plane XRD. The excited-state proton-transfer (ESPT) between octadecylamine (ODA) and pyranine adsorbed in the films was investigated using time-resolved fluorescence spectroscopy together with consideration of the film structures.

Interfacial behavior of common food contact polymer additives

Irganox 1076 (IN1076) and Irganox 1010 (IN1010), phenol containing species often used as antioxidant additives in food packaging polymers have both hydrophilic and hydrophobic functional groups. Consequently these additives are likely to absorb to surfaces where their free energy is minimized. Experiments described in this work examine the two-dimensional phase behavior and vibrational structure of IN1076 and IN1010 films adsorbed to the air/water interface. Surface pressure isotherms show that repeated compression of these films leads to continued irreversible loss of molecules and that on a per molecule basis, this loss is more pronounced for IN1076 than for IN1010. Differences in the surface properties of these two antioxidant additives are interpreted based on differences in molecular structure. Surface specific vibrational measurements of these organic films show very little conformational order, implying that even when closely packed, both antioxidant species have little affinity for forming highly organized domains. These findings have important ramifications for mechanisms that reduce antioxidant activity in polymers as well as descriptions of antioxidant blooming on polymer surfaces.

Interaction of the Antimicrobial Peptide Dicynthaurin with Membrane Phospholipids at the Air−Liquid Interface

This paper reports the first study on the interaction of the antimicrobial peptide dicynthaurin with 1,2-dipalmitoyl-glycerophosphatidyl-glycerol investigated in monolayers at the air-liquid interface. The influence of the peptide on the two-dimensional phase behavior of the negatively charged lipid was elucidated by means of pressure-area isotherm measurements, fluorescence microscopy, and grazing incidence X-ray diffraction measurements. The pure peptide forms a stable monolayer at the air-liquid interface up to 30 mN/m as shown for both the monomeric and the dimeric cynthaurins. The peptide lipid interaction was monitored in isotherm measurements showing a strong adsorption of the peptide and stabilization at the interface promoted by the lipid monolayer. The X-ray diffraction measurements in agreement with fluorescence microscopy studies showed that the peptide destabilizes the condensed chain lattice, leading to a complete fluidization of the condensed lipid phase on physiological buffer. The adsorption of the peptide to the negatively charged lipid monolayer and the fluidization of the condensed chain lattice suggest a direct link to the peptides' ability to expand the bacterial membrane that would be relevant for the in vivo mode of action.

Two-Dimensional Self-Assembly and Phase Behavior of an Alkoxylated Sandwich-Type Bisphthalocyanine and Its Phthalocyanine Analogues at the Liquid−Solid Interface

Lanthanide bisphthalocyanine complexes are interesting objects for the construction of two-dimensional (2D) ordered arrays with prospective applications in molecular electronics due to their unique semiconductor and electrochromic properties as well as their double-decker architecture. The 2D self-assembly of dodecyloxy-substituted (bisphthalocyaninato)erbium(III) has been studied at the solid (highly oriented pyrolytic graphite)-liquid interface by scanning tunneling microscopy. The results show that the bisphthalocyanine molecules form an ordered quadratic 2D lattice (a = b = 3.0 +/- 0.1 nm, gamma = 90 +/- 3 degrees), which is nearly identical to that formed by its (phthalocyaninato)cobalt(II) analogue bearing alkoxy chains of the same length. This clearly shows that sandwich molecules adsorb to the graphite surface by one of the phthalocyanine disks and its eight alkoxy groups. Despite the very similar mode of interaction with the surface, mixtures of alkoxylated (bisphthalocyaninato)erbium(III) with its (phthalocyaninato)cobalt(II) analogue show partial phase separation on the nanoscale: areas are enriched in one of the compounds. A much clearer phase separation between (bisphthalocyaninato)erbium(III) and (phthalocyaninato)cobalt(II) molecules was achieved by mixing molecules containing alkoxy groups of different length. The results provide insight for the development of well-ordered nanostructures of bisphthalocyanines in the presence of phthalocyanines, which could be of importance for future nanometer-scale functional materials.

Supramolecular control of two-dimensional phase behavior.

We have used directed two-component self-assembly to "pattern" organic monolayers on the nanometer scale at the liquid/solid interface. The ability of the scanning tunneling microscope to investigate structural details in these adlayers was used to gain insight into the two-component two-dimensional phase behavior. The components are symmetrically alkylated bisurea derivatives (R1-urea-spacer-urea-R2; R1, R2=alkyl, spacer=alkyl or bisthiophene). The bisthiophene unit acts as a marker and its bisurea derivative (T2) is a component in all the mixtures investigated. By varying the position of the hydrogen-bond forming urea groups along the molecule and the length of the alkyl chains of the other components, the effect of 1) hydrogen bonding, 2) molecule length, 3) odd-even effects, and 4) shape complementarity on the two-dimensional phase behavior was investigated. Insight into the effect of these parameters leads to the control of the two-dimensional patterning: from randomly intermixed systems to phase separation.

Nanoparticle assembly and transport at liquid-liquid interfaces.

The self-assembly of particles at fluid interfaces, driven by the reduction in interfacial energy, is well established. However, for nanoscopic particles, thermal fluctuations compete with interfacial energy and give rise to a particle-size-dependent self-assembly. Ligand-stabilized nanoparticles assembled into three-dimensional constructs at fluid-fluid interfaces, where the properties unique to the nanoparticles were preserved. The small size of the nanoparticles led to a weak confinement of the nanoparticles at the fluid interface that opens avenues to size-selective particle assembly, two-dimensional phase behavior, and functionalization. Fluid interfaces afford a rapid approach to equilibrium and easy access to nanoparticles for subsequent modification. A photoinduced transformation is described in which nanoparticles, initially soluble only in toluene, were transported across an interface into water and were dispersed in the water phase. The characteristic fluorescence emission of the nanoparticles provided a direct probe of their spatial distribution.

Step-modified phase diagram of chemisorbed oxygen on nickel

We have studied the effect of an extended array of steps on the two-dimensional phase behavior of chemisorbed oxygen overlayers on a vicinal nickel surface using low energy electron diffraction (LEED), Auger electron spectroscopy, and scanning tunneling microscopy. Phase behavior of oxygen on the vicinal Ni(9 7 7) surface was examined and compared with that for oxygen adsorbed on the flat Ni(1 1 1) surface. There are two significant differences in the phase diagrams for these two surfaces. On Ni(1 1 1) at θ=0.25 ML, oxygen forms a p(2×2) structure that disorders to a lattice gas at 440 K and remains disordered until it is ultimately dissolved into the bulk above 500 K. Surface defects, such as the steps on Ni(9 7 7), substantially modify this phase progression. On Ni(9 7 7), the p(2×2) phase still disorders at 440 K, but a second ordered phase, which can be designated as Ni[ 8(1 1 1)×(1 0 0) ]–2(1d)-O in microfacet notation, exists between room temperature and above 500 K when the oxygen is finally incorporated into the bulk. This adsorbate phase is step-stabilized and can be generated by dosing the surface with a small amount of oxygen or as a result of partial dissolution of oxygen from the higher coverage p(2×2) phase. Moreover, anisotropic disordering effects are evident due to the presence of the steps as indicated by the increasingly oblate shape of diffraction spots as the p(2×2) disorders. The process of oxygen dissolution is also qualitatively altered by the presence of regular steps.

Two-Dimensional Phase Diagram of Decanethiol on Au(111)

On the basis of variable-temperature ultrahigh vacuum scanning tunneling microscopy data, we propose a two-dimensional phase diagram of monolayer decanethiol on Au(111). Four triple-point temperatures were determined: T1 at ≈27 °C, T2 at ≈33 °C, T3 at ≈35 °C, and T4 at ≈56 °C. T1 defines the lowest temperature melting point, and T4 defines the temperature above which striped phases are metastable. These data provide a fundamental framework to understand and control mesoscale monolayer structure; moreover, they provide fundamental insight into the two-dimensional phase behavior of molecules with many degrees-of-freedom.

Influence of steps on the interaction between adsorbed hydrogen atoms and a nickel surface

We have studied the effect of an extended array of defects on the two-dimensional phase behavior of adsorbed hydrogen on a Ni surface using helium atom scattering. Specifically, the interaction of hydrogen with the stepped Ni(977) surface was examined and compared with similar interactions with the flat Ni(111) surface. The phase behavior of hydrogen on Ni(977) is qualitatively the same as that of hydrogen on Ni(111); however, the temperature at which the order–disorder transition occurs is elevated. On the stepped surface, the ordered (2×2)-2H phase exists at a temperature 40 K higher than on the flat surface. This reversible phase transition is second order and is best fit with Tc=310 K and β=0.12, indicative of two-dimensional Ising behavior. Stabilization of the ordered phase is attributed to pinning from the step edges. The cross section for diffuse elastic He scattering by adsorbed hydrogen and the temperature-dependent domain size of ordered hydrogen along the step edges are also discussed.

Time-Dependent Phase Segregation of Dendrimer/n-Alkylthiol Mixed-Monolayers on Au(111): An Atomic Force Microscopy Study

The two-dimensional phase behavior of mixed-monolayers composed of poly(amidoamine) (PAMAM) dendrimers and n-alkylthiols adsorbed to Au(111) surfaces was studied using tapping mode atomic force microscopy (TM-AFM). Mixed-monolayers were prepared by sequential immersion of Au(111) substrates into ethanolic solutions of, first, dendrimers and then n-alkylthiols. Films were prepared by systematically varying the dendrimer generation (G4, G6, and G8) and the n-alkylthiol chain length (CH3(CH2)xSH; x = 4, 11, 15). TM-AFM was used to monitor time-dependent morphological changes in the mixed-monolayers. Dendrimer monolayers immersed in hexane solutions of n-alkylthiols do not phase separate to an appreciable extent, which demonstrates the important role of dendrimer solvation in these processes. In contrast to the amine-terminated dendrimer monolayers, thiol-terminated dendrimers do not phase separate when exposed to ethanolic n-alkylthiol solutions, suggesting that one of the driving forces for this process is ...