Abstract
Highrate deformation of soft matter is an emerging area central to our understanding of farfromequilibrium phenomena during shock, fracture, and phase change. Monolayers of colloidal particles are a convenient twodimensional model system to visualise emergent behaviours in soft matter, but previous studies have been limited to slow deformations. Here we probe and visualise the evolution of a monolayer of colloids confined at a bubble surface during highrate deformation driven by ultrasound. We observe the emergence of a transient network of strings, and use discrete particle simulations to show that it is caused by a delicate interplay of dynamic capillarity and hydrodynamic interactions between particles oscillating at high frequency. Remarkably for a colloidal system, we find evidence of inertial effects, caused by accelerations approaching 10,000g. These results also suggest that extreme deformation of soft matter offers new opportunities for pattern formation and dynamic selfassembly.
Introduction
Particles floating at liquid interfaces are a useful twodimensional model to visualise the structure and deformation of condensed matter. A fascinating example dates back to L. Bragg, who used rafts of floating bubbles to illustrate grain boundaries and plastic flow in metals^{1}. Colloidal particles confined at liquid interfaces have been used widely for this purpose, as the interparticle interactions can be finely tuned through electrostatics^{2,3} and capillarity^{4,5,6}, giving access to a range of twodimensional condensed phases^{7,8,9,10,11}. Recently, colloids adsorbed on a curved interface were used to probe growth^{12}, freezing^{13}, healing^{10} and mechanical resistance of colloidal crystals^{14}. Beyond their use as twodimensional model, colloid monolayers at interfaces, and interfacial soft matter in general, play an important role in natural and industrial processes^{15}. For instance, the mechanical strength imparted to the interface by the colloids enables the formation of bicontinuous emulsions by arrested spinodal decomposition^{16}, suppression of the coffeering effect^{17}, and arrested dissolution of bubbles^{18,19}.
Previous studies of dynamic deformation of colloid monolayers have been limited to relatively low deformation rates^{8,11,20,21,22,23} in the range 10^{−2}–1 s^{−1}. However, in realistic conditions, such as in the flow of emulsions and foams, and the evaporation of suspensions, interface deformations can occur on much shorter timescales, driving the system far from equilibrium. In bulk suspensions under flow, colloids form outofequilibrium structures stemming from the interplay of interparticle and hydrodynamic interactions^{24}. Similarly, hydrodynamic interactions between colloids at interfaces can be expected to affect their assembly upon dynamic interface deformation. In more extreme conditions, phenomena that are usually not observed in a colloidal system can become important, for instance elastic collisions during shock propagation^{25}. Furthermore, some of the phenomena observed for interface deformations of large amplitude, or at high rate, have no counterpart in threedimensions: when compressed beyond hexagonal close packing, a monolayer of colloids at an interface can buckle out of plane^{26,27} or expel colloids in the surrounding fluid^{28,29}. Yet, the behaviour of interfacial soft matter under extreme deformation remains poorly understood due to the experimental challenge of simultaneously imparting highrate deformation and visualising rearrangements of the microstructure.
Here we use acoustic excitation of particlecoated bubbles to explore the farfromequilibrium phenomena of colloid monolayers at fluid interfaces. The particles, initially forming a cohesive disordered structure at rest, rearrange into a transient network of strings upon dynamic deformation. To explain this unexpected microstructure, we propose an interaction model including hydrodynamic interactions between particles oscillating at high frequency, and dynamic capillary interactions. In particular, we propose that the acceleration of the particles, approaching 10,000g, causes inertial effects leading to dynamic deformations of the interface, which result in capillary attraction. Discrete particle simulations based on this interaction model predict the observed microstructure in great detail.
Results
Evolution of the microstructure during highrate deformation
Bubbles (equilibrium radius R_{0} ≈ 20–100 μm) were coated with a monolayer of polystyrene spheres (radius a ≈ 1–5 μm). Electrostatic repulsion between the particles was completely screened by addition of electrolyte (Methods). We found no evidence of additional electrostatic interactions arising from an asymmetric charge distribution on the particles at the interface^{7}. The initial microstructure of the monolayer at moderate surface coverage was determined by capillary attraction, due to nanoscale undulations of the contact line with an estimated amplitude Q_{2} ≈ 50 nm^{30,31}. This interaction is directional, as can be seen from a decomposition of the interface deformation in twodimensional multipoles, which shows that contact line undulations result in capillary quadrupoles^{30}. Isolated bubbles were driven into periodic compression–expansion by ultrasound at frequency f = ω/2π = 30–50 kHz, where ω is the angular frequency, in an acousticaloptical setup (Methods), and imaged at 300,000 frames per second. From the highspeed videos, we extracted the evolution of the bubble radius R(t), the maximum oscillation amplitude ΔR, and the trajectories of the particles on the surface of the bubble (Supplementary Note 1). The surface coverage \({{\Phi }} = {\textstyle{{N\pi a^2} \over A}}\), where N is the number of particles in the region of interest, and A is the surface area of the region of interest (Supplementary Fig. 1), and the equilibrium bubble radius, R_{0}, were measured from highresolution still images. Figure 1a shows a sequence of frames during one cycle of oscillations of a 65μm bubble coated with 5μm particles at Φ = 0.54 ± 0.04. Particles initially at contact are driven apart during bubble expansion, and pushed back into contact during compression, as is clearly seen for the two particles marked in red and blue. The separation of the particles typically occurs in less than 10 μs.
A striking change in the microstucture of the monolayer is observed over a few hundreds of cycles of oscillations, as shown in Fig. 1b. Initially the particles, 2.5 μm in radius and with surface coverage Φ = 0.48 ± 0.05, form a disordered, cohesive structure on the interface of a bubble with equilibrium radius R_{0} ≈ 53 μm. The arrangement of the particles evolves towards a network of strings in a few hundreds of cycles (Supplementary Movies 1 and 2). The breakup of the initially aggregated structure is made possible by the mechanical energy input provided to the system during highrate oscillations. The quadrupolar capillary attraction energy is \(E_{{\mathrm{quad}}} \propto \gamma Q_2^2\) ~ 10^{4}–10^{5} k_{B}T at contact^{32}, where γ is the surface tension, resulting in kinetically trapped structures. For comparison, the kinetic energy of a particle in our experimental conditions, based on the maximum velocity of the interface ωΔR, is E_{k} ~ a^{3}ρ_{p}ω^{2}ΔR^{2} ~ 10^{3}–10^{7} k_{B}T, where ρ_{p} is the particle density.
The network of strings is a transient microstructure that relaxes after the forcing stops. Figure 1c shows frames of the initial, disordered microstructure before oscillations (t = 0 s), of the string network formed after 1000 cycles of oscillations (t = 0.03 s), and of the subsequent relaxation after the forcing has stopped (t = 0.5–1.5 s). It can be seen that some of the strings break upon relaxation over 1.5 s. The two highresolution still images in Fig. 1d show strings formed at low surface coverage, Φ ≈ 0.37 and Φ ≈ 0.20. The two fluorescence images (Methods) in Fig. 1d highlight additional characteristic features of the observed microstructures, such as loops (Φ ≈ 0.30) and lone particles (Φ ≈ 0.43). Loops and lone particles, neither of which are observed at rest, also disappear upon relaxation.
Quantitative characterisation of the microstructure
A quantitative characterisation of the microstructure shows that the formation of strings is accompanied by a decrease in the number of nearest neighbours, n, as can be seen by comparing the initial (Fig. 2a) and final (Fig. 2b) states of the experiment of Fig. 1b. In Fig. 2a, b, the particles are colourcoded according to the value of n. Initially, particles mainly have 3–5 neighbours. After 1000 cycles of oscillations, particles predominantly have 2 or 3 neighbours. The probability p(n) of a particle having a number n of neighbours is shown in Fig. 2c for the initial state, and in Fig. 2d for the final state. The time evolution of p(n) over 1,000 cycles is shown in Supplementary Fig. 2. The statistics show clearly that particles can have up to 5 or 6 neighbours in the initial state, whereas in the final state p(n = 5) and p(n = 6) become zero, and there is a sharp increase in p(n = 2). Correspondingly, the mean number of neighbours per particle decreases from \(\bar n = 3.4\) to \(\bar n = 2.4\). Not only the number of neighbours is reduced, but the neighbours are aligned, as indicated by the increase of the bond order parameter \(\left {{\mathrm{\Psi }}_2} \right\) over time, as shown in Fig. 2e (see Supplementary Note 1 and Supplementary Fig. 3). Similarly to the \(\left {{\mathrm{\Psi }}_6} \right\) twodimensional bondorientational order parameter that measures the orientation and degree of hexagonal order around a particle (6fold symmetry), the \(\left {{\mathrm{\Psi }}_2} \right\) function is a metric for the alignment of particles (2fold symmetry). We also observe an increase of the \(\left {{\mathrm{\Psi }}_3} \right\) order parameter, representing particles having three neighbours organised with a sp^{2} (3fold) symmetry. The final structure is therefore formed by particles aligned in strings that are connected respecting a sp^{2} symmetry. The evolution of the peaks in the paircorrelation function, g(r), shows that the nearest neighbours remain at contact (r = 2a) while the second neighbours move from \(r = 2\sqrt 3 a\), corresponding to hexagonal close packing, to r = 4a, corresponding to a chain (Fig. 2f). All the order parameters considered relax to their initial values after the forcing stops, confirming quantitatively the transient nature of the microstructure (Fig. 3 and Supplementary Fig. 4).
Dynamic capillary interactions
We propose that the directional interparticle force leading to the transient formation of strings is due to dynamic capillarity. Hydrodynamic interactions alone, responsible for string formation in the bulk^{24}, are not sufficient, because they are repulsive for oscillating particles at a fluid interface^{33}. Capillary interactions with dipolar symmetry would be sufficient to drive the formation of strings at fluid interfaces^{34}, but they can be ruled out in our system. Indeed, although dynamic capillary dipoles can be induced by the motion of particles along an interface between two fluids with a large viscosity mismatch^{35,36}, in our experiments the viscous stresses due to the lateral motion of the particles are negligible compared to surface tension forces. Another possibility for a directional interaction with dipolelike symmetry is that between a monopole and a quadrupole^{37} (Supplementary Fig. 5). The possibility of a monopolar deformation of the interface in our system is not immediately apparent, because it would only be expected if a body force acts on the particles^{38}. In our experiments, the only body force acting on the particles is gravity, but the Bond number is in the range \({\mathrm{Bo}} = {\textstyle{{{\mathrm{\Delta }}\rho ga^2} \over \gamma }}\) ≈ 10^{−7}–10^{−5}, hence surface tension forces dominate, and the interface deformation is negligible. We hypothesise that a dynamic monopolar deformation is generated by the motion of the particle relative to the interface during bubble oscillations (Fig. 4a). The maximum acceleration of the interface is on the order of \(\ddot R\) ~ ω^{2}ΔR ≈ 6000g, an extremely large value for a colloidal system, leading to unexpected inertial effects. The Weber number based on the maximum acceleration, comparing the inertia of the particle to capillary forces, is \({\mathrm{We}} = {\textstyle{{{\mathrm{\Delta }}\rho \omega ^2{\mathrm{\Delta }}Ra^2} \over \gamma }}\) ≈ 10^{−3}–10^{−1} sufficiently large for the resulting interface deformation to drive capillary interactions.
Discrete particle simulations confirm that dynamic capillary interactions between monopole and quadrupole can cause the transient microstructure observed in the experiments. The dynamics of spherical particles confined to the surface of a sphere with timedependent radius are computed from a force balance on each particle including a simplified model for the capillary and hydrodynamic interactions. The particles are assigned a permanent quadrupolar deformation of amplitude Q_{2}, with an associated orientation vector. The inertia of a particle is assumed to cause a timedependent monopolar deformation of the interface, Q(t) = Q_{0} sin(ωt), in phase with the motion of the interface (Supplementary Note 2 and Supplementary Fig. 6). Furthermore, a particle undergoing highfrequency oscillations in a fluid generates a steady recirculating flow, with velocity proportional to \(Q_0^2\)^{39}. We model the resulting hydrodynamic repulsion between particles at an interface^{33} as the viscous drag experienced by a point particle in the streaming flow generated by a neighbouring particle (Fig. 4c). The pairwise force is therefore assumed to scale as \(F_{{\mathrm{hyd}}} \approx \beta {\kern 1pt} Q_0^2{\kern 1pt} f_{{\mathrm{hyd}}}(d)\), where d is the interparticle distance, and it is further assumed that f_{hyd} = ηωa^{2}/d^{2} is the spatial dependence of the radial streaming velocity field generated by a neighbouring particle (Supplementary Fig. 7). For a particle at an interface, the numerical prefactor β is an unknown function of the Reynolds number, \({\mathrm{Re}} = {\textstyle{{\rho {\kern 1pt} a^2\omega } \over \eta }}\), of the capillary number \({\mathrm{Ca}} = {\textstyle{{\eta a\omega } \over \gamma }}\), with η the viscosity of water, and of the contact angle of the particles. The case of a sphere in a bulk fluid corresponds to β = 6π, and β could be larger or smaller for particles at an interface. The magnitude of the total interaction force along the line of centres of two particles i and j therefore has the form
The first term is the interaction between dynamic monopoles, with f_{00} = γ/(2πd), the second term is the interaction between a dynamic monopole and a permanent quadrupole, and the third term is the interaction between permanent quadrupoles, with f_{22} = (γa^{4})(48π/d^{5})cos(2φ_{i} + 2φ_{j}). The angles φ_{i} and φ_{j} define the orientation of the quadrupoles of particle i and particle j relative to the line of centres. The function f_{02} = (γa^{2})(4π/d^{3})[cos(2φ_{i}) + cos(2φ_{j})] accounts both for the effect of monopole i on quadrupole j, and of monopole j on quadrupole i.
We first equilibrate the system with only interactions between permanent quadrupoles (Q_{2}/a = 1/100). The resulting aggregated structure (Fig. 2g) presents rafts of particles with hexagonal packing and herringbone alignment of the orientation vectors^{40}. The dynamics are simulated by allowing the radius of the sphere to vary as R(t) = R_{0} + ΔR sin(ωt), and by including the effect of the dynamic monopole. The amplitude of the oscillatory monopolar deformation is set to Q_{0}/a = 7 × 10^{−2} and the other parameters are in the range of those used in the experiments (Supplementary Note 3).
The microstructure after 1000 cycles of oscillations, shown in Fig. 2h, is a network of strings with a striking similarity to the experimental results (see Supplementary Movie 5). The evolution of the pair correlation function g(r) confirms quantitatively the formation of strings (Fig. 2i). In keeping with the experimental results, the first peak (at r = 2a) decreases in amplitude and the second peak shifts from \(r = 2\sqrt 3 a\) to r = 4a, the signature of evolution from hexagonal closepacking to a string of particles. The orientation vectors of particles inside a string are aligned endtoend. The evolution of p(n), \(\overline n\), \(\left {{\mathrm{\Psi }}_2} \right\) and \(\left {{\mathrm{\Psi }}_3} \right\) (Supplementary Fig. 8) are all in good agreement with the experimental measurements. The spherical shape of the interface allows to detect the effect of the dynamic monopole, which would otherwise be timereversible on a planar interface undergoing oscillations, because the interparticle distance is not constant during one cycle of oscillations. The distance between two particles positioned on a sphere having timedependent radius R(t) = R_{0} + ΔR sin(ωt) varies as d(t) = d_{0} + Δd sin(ωt). If the particles are initially in contact, the maximum separation distance is given by Δd = aΔR/R_{0}. The time average of the monopole–quadrupole force over one period of oscillations, T = 2π/ω, is given by \(\left\langle {F_{02}} \right\rangle _T \propto  {\textstyle{3 \over 2}}\gamma a^2Q_0Q_2{\textstyle{1 \over {d_0^3}}}{\textstyle{{{\mathrm{\Delta }}d} \over {d_0}}}\) and is therefore nonzero only for a curved interface (Δd ≠ 0). Simulations of the relaxation of the microstructure after the forcing stops also reproduce the behaviour observed in experiments: the order parameters recover their initial values before forcing (Supplementary Fig. 9).
Estimate of the dynamic monopole amplitude
To verify that the amplitude of the dynamic monopolar deformation that gives agreement with the experiments is physically justified, we use a harmonic oscillator model of a particle attached to an interface by capillary force^{41} (Supplementary Note 2). The dimensionless displacement x of the particle relative to its equilibrium position provides an estimate of the amplitude of the monopolar deformation, Q_{0}/a. The normalised relative displacement Q_{0}/a as a function of the oscillation frequency f = ω/2π is shown in Fig. 4b for four cases, using limiting values of the mass m and spring constant γ corresponding to the experimental parameters (grey lines: a = 1 μm; black lines: a = 5 μm; solid lines: γ = 73 mN/m; dashed lines: γ = 25 mN/m). In the range of frequencies used in the experiments, highlighted by the shaded area, the monopole amplitude varies from Q_{0}/a ~ 10^{−3}, up to Q_{0}/a ~ 1. In the range Q_{0}/a ~ 10^{−2}–10^{−1} (red shaded area in Fig. 4b), the monopole amplitude is sufficiently large to drive capillary interactions between particles, as has been observed in experiments with heavy particles^{42}. The value Q_{0}/a = 7 × 10^{−2} used in the simulations of Fig. 2 is therefore justified. For amplitudes smaller than Q_{0}/a ~ 10^{−2} (blue shaded area in Fig. 4b), the interface deformation is expected to be insufficient to drive significant interactions. For Q_{0}/a ~ 1 and larger, detachment of particles from the interface can be expected^{27,41}.
Conditions for string formation in simulations
Discrete particle simulations predict string formation for physically realistic values of the monopole amplitude, Q_{0}, and of the prefactor of the hydrodynamic interaction, β, which are the two unknown parameters in Eq. (1). We performed a parametric study for values of β varying over more than one order of magnitude, and values of Q_{0} varying in the range predicted by the harmonic oscillator model. The results are presented in the regime map in Fig. 4d. The microstructure obtained after 1000 cycles is classified according to the values of p(n) and g(r) as either an aggregated network (blue diamonds), a network of strings (red squares), or an ordered lattice (black circles). The final microstructure is found not to depend very strongly on the parameter β. However if β = 0 the structure does not evolve from an aggregated network, suggesting that repulsive hydrodynamic interactions are responsible for the breakup of the initially aggregated structure. The emergence of strings depends strongly on Q_{0}/a, which determines the magnitude of the monopole–monopole attractive force, of the directional monopole–quadrupole interaction, and of the repulsive hydrodynamic force (see Eq. (1)). An aggregated network is obtained when dynamic effects are not important (Q_{0}/a ≲ 10^{−2}), and capillary interactions between permanent quadrupoles dominate, giving a final structure that remains similar to the initial structure. Formation of strings is predicted for Q_{0}/a ~ 10^{−2}–10^{−1}, which is indeed the range in which monopolar deformations are sufficiently large to cause capillary interactions^{42}. When the monopole amplitude exceeds a critical value, Q_{0}/a ≳ 10^{−1}, the repulsive hydrodynamic interactions are found to dominate, leading to the formation of an ordered lattice. This ordered structure is never observed in the experiments, likely because it is in the range of deformations where particle expulsion occurs. Additional simulations are shown in Fig. 5 for limiting cases where only one type of interaction is included in the model. These results highlight the effect of each type of interaction on the final microstructure.
Experimental conditions for string formation
String formation is robust over a broad range of experimental conditions. The two control parameters for the emergence of strings are the surface coverage and the Weber number. The surface coverage determines the extent to which rearrangements of the microstructure are possible. Random close packing of spheres in two dimensions occurs at Φ_{rcp} ≈ 0.82, and hexagonal close packing at Φ_{hcp} ≈ 0.91^{43}. In the experiments, the surface coverage was varied in the range Φ ≈ 0.33–0.90 (Supplementary Fig. 10). The Weber number, which determines the magnitude of the dynamic monopolar deformation, was varied in the range We ≈ 1 × 10^{−3}–5.5 × 10^{−2} by varying the particle size (2a = 1.8, 3, 5, 10 μm), the oscillation frequency (f = 30, 40, 50 kHz), and the amplitude of oscillations (ΔR ≈ 0.2–3.5 μm, with ΔR/R_{0} ≈ 0.003–0.13 and a/R_{0} ~ 10^{−2}–10^{−1}). We performed over 40 experiments, with three possible outcomes: no evolution of the microstructure, emergence of strings, or expulsion of particles from the interface (see Supplementary Movies 2–4 respectively). The results are presented in the (Φ, We) plane in Fig. 6. The area highlighted in blue, at high Φ and low We, corresponds to experiments where the structure did not evolve during 1000 cycles of oscillations. In these conditions, rearrangements are limited due to jamming of the monolayer, and the magnitude of the dynamic interactions is insufficient to drive an evolution of the microstructure. The area highlighted in green corresponds to experiments where the amplitude of oscillations is so large that particles are expelled from the interface^{28}. In this regime it is no longer possible to observe structures at constant Φ. Finally, the area highlighted in red corresponds to string formation. Even though this microstructure results from a delicate interplay between hydrodynamics and dynamic capillary interactions, it is consistently observed for a broad range of accessible experimental conditions.
Discussion
In summary, we have observed and explained the emergence of a transient microstructure formed by colloids undergoing extreme accelerations at a fluid interface. We have shown that dynamic interface deformation can be used to break kinetically trapped structures, and to impart dynamic capillary interactions. Despite being transient, the microstructure has a sufficiently long relaxation time that it could be exploited for subsequent processing by highthroughput methods, for instance photopolymerisation^{44}. Our results therefore present new opportunities for programmable selfassembly and pattern formation in soft matter at interfaces. Beyond these potential applications, our experimental approach opens the way to future studies of interfacial soft matter far from equilibrium, at deformation rates that are otherwise inaccessible to existing techniques, but relevant to realistic flow and deformation conditions.
Methods
Particlecoated bubbles
Particlecoated bubbles were made by mechanical agitation of an aqueous suspension containing 0.4% w/v of colloids, using a vortex mixer. We used hydrophilic, spherical microparticles of nominal diameter 1.8, 3, 5 and 10 μm with sulfate surface groups (IDC surfactantfree latex particles, Life Technologies). For fluorescence imaging we used red fluorescent microparticles, 4 μm in diameter, sulfate coated (FluoSpheres, Invitrogen). All particles were used as received. Addition of NaCl (VWR Chemicals, AnalaR NORMAPUR, 99.5%) with 500 mM concentration was necessary to promote particle adsorption to the water–air interface. The resulting Debye length is 0.5 nm. Ultrapure water with resistivity 18.2 MΩ cm was produced by a MilliQ filtration system (Millipore).
Acousticaloptical setup
We injected particlecoated bubbles in an observation cell made of a microscope slide and a glass coverslip separated by a 1mm spacer. Prior to every experiment, the cell was rinsed with ethanol and ultrapure water, and dried with compressed air. Small numbers of bubbles were injected in the chamber, and we only observed isolated bubbles (at least 10 diameters away from other bubbles). The observation chamber was placed on an inverted microscope (IX71, Olympus) equipped with 10× and 20× objectives. A singleelement piezoelectric transducer (SMD50T21F45R, Steminc) with resonance frequency (45 ± 3) kHz was glued to the glass slide. The driving signal was generated by a waveform generator (33220A, Agilent) and amplified by a linear, radiofrequency power amplifier (AG1021, T& C Power Conversion Inc.). The frequencies used were 30, 40 and 50 kHz, resulting in different bubble oscillation amplitudes. Since the wavelength of ultrasound at these frequencies in water is λ > 3 cm, the pressure can be considered to be uniform over distances of the order of the bubble size. The bubbles were driven for 1000 cycles and the dynamics recorded at 300,000 frames per second using a high speed camera (FASTCAM SA5, Photron). The waveform generator and the highspeed camera are triggered simultaneously using a pulsedelay generator (9200 Sapphire, Quantum Composer). The image resolution at 10× and 20× magnification is 2 and 1 μm, respectively. Highresolution still images in different focal planes were taken before and after excitation at 32× magnification using a CCD camera (QImaging), resulting in an image resolution of 0.1 μm. For fluorescence imaging, illumination was provided by a Lumen 200 (Prior Scientific) UV lamp combined with a ET mCHTR (Chroma) fluorescence cube.
Interaction model and discrete particle simulations
We consider N spherical particles confined to a spherical surface with a timedependent radius. The particles are assumed to interact through capillary forces and torques induced by static and dynamic deformations of the spherical surface, and through hydrodynamic forces. Brownian motion is neglected as the total duration of the experiments is much smaller than the diffusion timescale of the colloids. The irregular contact line of each particle generates a static quadrupolar deformation of the spherical surface^{30}, which is characterised by an orientation vector p_{i} (Supplementary Fig. 11). The overlap of the deformations induced by two quadrupoles drives an interaction force \({\bf{F}}_{22}^{ \ast ^{ij}}\) and a torque \({\bf{T}}_{22}^{ \ast ^{ij}}\) between particle i and particle j, which depends on the relative orientation of the quadrupoles p_{i} and p_{j}^{38}. In addition, we assume that each colloidal particle imparts a periodic monopolar deformation of the interface, which is responsible for additional dynamic capillary interactions. The overlap of two dynamic monopolar deformations generated by particle i and j drives an attractive capillary force \({\bf{F}}_{00}^{ \ast ^{ij}}\)^{38}. The superposition of a monopolar and a quadrupolar deformation drives two capillary interaction forces \({\bf{F}}_{02}^{ \ast ^{ij}}\) and \({\bf{F}}_{20}^{ \ast ^{ij}}\) and a capillary torque \({\bf{T}}_{20}^{ \ast ^{ij}}\), which depend on the orientation of the quadrupole. Finally, the relative motion between a particle and the interface generates a net recirculating flow^{39} (see Fig. 4c) that is responsible for an hydrodynamic repulsive force \({\bf{F}}_{{\mathrm{hyd}}}^{ \ast ^{ij}}\). The detailed expression of the interaction forces and torques is reported in Supplementary Note 3. The evolution of the position of each particle \({\bf{r}}_i^ \ast\) and of the orientation of the quadrupole p_{i} are obtained solving the dimensionless balances of linear and angular momentum:
where St = ρ_{p}a^{2}ω/η is the Stokes number comparing the relative importance of the inertia of a particle and the viscous force acting on it. In typical experimental conditions St ≈ 1. Since the particles are only partially immersed in water, we assumed that the drag coefficient in Eqs. (2)–(4) is equal to half of the Stokes drag. To confine the particles to the surface of the sphere, we included a stiff restoring force \({\bf{F}}_{\mathrm{S}}^{ \ast ^i}\) in the balance of linear momentum. The overlap between particle i and particle j is prevented by enforcing a stiff excluded volume force \({\bf{F}}_{{\mathrm{EV}}}^{ \ast ^{ij}}\). Eqs. (2)–(5) are solved using a secondorder explicit linear multistep method. We used a dimensionless time step Δt* = 3 × 10^{−3}, which has been checked to give convergent results. To avoid expensive computations we enforce a cutoff length of 7a for all the interaction forces and torques between the particles. Simulations with larger and smaller cutoff lengths were found to give similar results. The computational time of evaluating the interactions between the particles scales as N^{2}. The computation of the interactions was therefore parallelised over ten or more cores.
Data availability
The experimental data that support the findings of this study and the computer code used to generate the numerical results are available from the corresponding author upon reasonable request.
References
Bragg, L. A model illustrating intercrystalline boundaries and plastic flow in metals. J. Sci. Instrum. 19, 148 (1942).
Nikolaides, M. G. et al. Electricfieldinduced capillary attraction between likecharged particles at liquid interfaces. Nature 420, 299–301 (2002).
Masschaele, K., Park, B. J., Furst, E. M., Fransaer, J. & Vermant, J. Finite ionsize effects dominate the interaction between charged colloidal particles at an oilwater interface. Phys. Rev. Lett. 105, 048303 (2010).
Loudet, J. C., Alsayed, A. M., Zhang, J. & Yodh, A. G. Capillary interactions between anisotropic colloidal particles. Phys. Rev. Lett. 94, 018301 (2005).
Cavallaro, M., Botto, L., Lewandowski, E. P., Wang, M. & Stebe, K. J. Curvaturedriven capillary migration and assembly of rodlike particles. Proc. Natl Acad. Sci. USA 108, 20923–20928 (2011).
Ershov, D., Sprakel, J., Appel, J., Cohen Stuart, M. A. & van der Gucht, J. Capillarityinduced ordering of spherical colloids on an interface with anisotropic curvature. Proc. Natl Acad. Sci. USA 110, 9220–9224 (2013).
Pieranski, P. Twodimensional interfacial colloidal crystals. Phys. Rev. Lett. 45, 569–572 (1980).
Cicuta, P., Stancik, E. J. & Fuller, G. G. Shearing or compressing a soft glass in 2d: Timeconcentration superposition. Phys. Rev. Lett. 90, 236101 (2003).
Madivala, B., Fransaer, J. & Vermant, J. Selfassembly and rheology of ellipsoidal particles at interfaces. Langmuir 25, 2718–2728 (2009).
Irvine, W. T. M., Bowick, M. J. & Chaikin, P. M. Fractionalization of interstitials in curved colloidal crystals. Nat. Mater. 11, 948–951 (2012).
Keim, N. C. & Arratia, P. E. Mechanical and microscopic properties of the reversible plastic regime in a 2d jammed material. Phys. Rev. Lett. 112, 028302 (2014).
Meng, G., Paulose, J., Nelson, D. R. & Manoharan, V. N. Elastic instability of a crystal growing on a curved surface. Science 343, 634–637 (2014).
Guerra, R. E., Kelleher, C. P., Hollingsworth, A. D. & Chaikin, P. M. Freezing on a sphere. Nature 554, 346 (2018).
Taccoen, N., Lequeux, F., Gunes, D. Z. & Baroud, C. N. Probing the mechanical strength of an armored bubble and its implication to particlestabilized foams. Phys. Rev. X 6, 011010 (2016).
Sagis, L. M. C. Dynamic properties of interfaces in soft matter: experiments and theory. Rev. Mod. Phys. 83, 1367–1403 (2011).
Herzig, E. M., White, K. A., Schofield, A. B., Poon, W. C. K. & Clegg, P. S. Bicontinuous emulsions stabilized solely by colloidal particles. Nat. Mater. 6, 966–971 (2007).
Yunker, P. J., Still, T., Lohr, M. A. & Yodh, A. G. Suppression of the coffeering effect by shapedependent capillary interactions. Nature 476, 308–311 (2011).
Abkarian, M. et al. Dissolution arrest and stability of particlecovered bubbles. Phys. Rev. Lett. 99, 188301 (2007).
Beltramo, P. J. et al. Arresting dissolution by interfacial rheology design. Proc. Natl Acad. Sci. USA 114, 10373–10378 (2017).
Stancik, E. J. et al. Structure and dynamics of particle monolayers at a liquid–liquid interface subjected to extensional flow. Langmuir 18, 4372–4375 (2002).
Masschaele, K., Fransaer, J. & Vermant, J. Flowinduced structure in colloidal gels: direct visualization of model 2d suspensions. Soft Matter 7, 7717–7726 (2011).
Barman, S. & Christopher, G. F. Role of capillarity and microstructure on interfacial viscoelasticity of particle laden interfaces. J. Rheol. 60, 35–45 (2015).
Buttinoni, I. et al. Colloidal polycrystalline monolayers under oscillatory shear. Phys. Rev. E 95, 012610 (2017).
Cheng, X., Xu, X., Rice, S. A., Dinner, A. R. & Cohen, I. Assembly of vorticityaligned hardsphere colloidal strings in a simple shear flow. Proc. Natl Acad. Sci. U. S. A. 109, 63–67 (2012).
Buttinoni, I. et al. Direct observation of impact propagation and absorption in dense colloidal monolayers. Proc. Natl Acad. Sci. USA 114, 12150–12155 (2017).
Pitois, O., Buisson, M. & Chateau, X. On the collapse pressure of armored bubbles and drops. Eur. Phys. J. E 38, 48 (2015).
Gu, C. & Botto, L. Buckling vs. particle desorption in a particlecovered drop subject to compressive surface stresses: a simulation study. Soft Matter 14, 711–724 (2018).
Poulichet, V. & Garbin, V. Ultrafast desorption of colloidal particles from fluid interfaces. Proc. Natl Acad. Sci. USA 112, 5932–5937 (2015).
Gao, Y. et al. Controlled nanoparticle release from stable magnetic microbubble oscillations. NPG Asia Mater. 8, e260 (2016).
Stamou, D., Duschl, C. & Johannsmann, D. Longrange attraction between colloidal spheres at the airwater interface: The consequence of an irregular meniscus. Phys. Rev. E 62, 5263–5272 (2000).
Zanini, M. et al. Universal emulsion stabilization from the arrested adsorption of rough particles at liquid–liquid interfaces. Nat. Commun. 8, 15701 (2017).
Fournier, J.B. & Galatola, P. Anisotropic capillary interactions and jamming of colloidal particles trapped at a liquid–fluid interface. Phys. Rev. E 65, 031601 (2002).
Singh, P., Joseph, D. D., Gurupatham, S. K., Dalal, B. & Nudurupati, S. Spontaneous dispersion of particles on liquid surfaces. Proc. Natl Acad. Sci. USA 106, 19761–19764 (2009).
Davies, G. B., Krüger, T., Coveney, P. V., Harting, J. & Bresme, F. Assembling ellipsoidal particles at fluid interfaces using switchable dipolar capillary interactions. Adv. Mater. 26, 6715–6719 (2014).
Dörr, A. & Hardt, S. Driven particles at fluid interfaces acting as capillary dipoles. J. Fluid. Mech. 770, 5–26 (2015).
Dörr, A., Hardt, S., Masoud, H. & Stone, H. A. Drag and diffusion coefficients of a spherical particle attached to a fluidfluid interface. J. Fluid. Mech. 790, 607–618 (2016).
Danov, K. D., Kralchevsky, P. A., Naydenov, B. N. & Brenn, G. Interactions between particles with an undulated contact line at a fluid interface: capillary multipoles of arbitrary order. J. Colloid Interface Sci. 287, 121–134 (2005).
Kralchevsky, P. & Nagayama, K. Particles at Fluid Interfaces and Membranes. (Elsevier Science New York, NY, 2001).
Riley, N. On a sphere oscillating in a viscous fluid. Quart. J. Mech. Appl. Math. 19, 461–472 (1966).
van Nierop, E. A., Stijnman, M. A. & Hilgenfeldt, S. Shapeinduced capillary interactions of colloidal particles. EPL 72, 671–677 (2005).
Pitois, O. & Chateau, X. Small particle at a fluid interface: effect of contact angle hysteresis on force and work of detachment. Langmuir 18, 9751–9756 (2002).
Vassileva, N. D., van den Ende, D., Mugele, F. & Mellema, J. Capillary forces between spherical particles floating at a liquid–liquid interface. Langmuir 21, 11190–11200 (2005).
Berryman, J. G. Random close packing of hard spheres and disks. Phys. Rev. A. 27, 1053–1061 (1983).
Dendukuri, D., Pregibon, D. C., Collins, J., Hatton, T. A. & Doyle, P. S. Continuousflow lithography for highthroughput microparticle synthesis. Nat. Mater. 5, 365–369 (2006).
Acknowledgements
We thank L. Botto and A. Striolo for useful discussions. This work is supported by the European Research Council, Starting Grant No. 639221 (ExtreFlow).
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A.H. and V.G. designed the experiments. A.H. performed the experiments and analysed the data. M.D.C. designed and implemented the simulations. A.H., M.D.C. and V.G. interpreted the results and wrote the manuscript. V.G. designed the research.
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Huerre, A., De Corato, M. & Garbin, V. Dynamic capillary assembly of colloids at interfaces with 10,000g accelerations. Nat Commun 9, 3620 (2018). https://doi.org/10.1038/s41467018060499
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DOI: https://doi.org/10.1038/s41467018060499
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