self-cleaning and antifouling ability for repelling the deposition of other materials and liquid confining properties for enhancing printing resolution and avoiding coffee-ring effects. [13] However, inertial water drops impacting superhydrophobic surfaces can bounce off quickly or splash violently. [14][15][16][17][18][19][20][21][22][23] Undesired rebound and splash cause material waste [24] and weaken the related performance and efficiency. Many attempts have been conducted to promote water drop spreading on hydrophobic surfaces by using polymers [1,23,[25][26][27][28] or surfactants. [22,[29][30][31][32] However, these two methods still have drawbacks for achieving drop deposition, not to mention uniform spreading: 1) Polymer additives can delay drop retraction but leave drops with hemispherical shape and nonuniform material distribution on the hydrophobic substrate.2) The poor wettability and large mole cular weight of polymer additives restrict the ejecting process during inkjet printing. 3) Surfactant additives can promote drop spreading in a static state owing to the reduced surface tension (γ); [33] however, the low surface tension increases the instability of the impacting drop and leads to drop splashing with satellite droplets, according to the Kelvin-Helmholtz instability, [34] k max ∼ 2ρ a U r 2 /3γ (ρ a is the air density). It is therefore a great challenge for uniform shape spreading on superhydrophobic surfaces without any loss of the drops. Here, we show a new and simple strategy for uniform round-shape drop spreading on superhydrophobic surfaces after high-speed impact, up to 5.0 m s −1 , by utilizing live-oligomeric surfactant jamming, diethylenetriamine/sodium dodecyl sulfate (triamine/SDS). The live-oligomeric surfactant, which noncovalently constructed by SDS and triamine through electrostatic interaction, has a dynamic equilibrium between monomer surfactant and oligomeric surfactant. Figure 1 shows the contrast spread dynamics of a liveoligomeric surfactant drop and other drops impacting superhydrophobic surfaces at an impacting velocity (U ) of 2.42 m s −1 from side and bottom views (Movie S1, Supporting Information). The diameter (D 0 ) of pure water and the surfactant drops is ≈2.25 and 1.90-2.00 mm, respectively (Figure S1, Supporting Information for experimental setup). The Weber number (We), We = ρDV 2 /γ, of water, SDS, N2C3/SDS, triamine/SDS, and 12-3-12-3-12 is 182. 68, 295.29, 358.29, 383.00, and 292.29, respectively. The superhydrophobic surface [35] composed of random micro-nanostructures of typical size and spacing of Inkjet printing of water-based inks on superhydrophobic surfaces is important in high-resolution bioarray detection, chemical analysis, and highperformance electronic circuits and devices. Obtaining uniform spreading of a drop on a superhydrophobic surface is still a challenge. Uniform round drop spreading and high-resolution inkjet printing patterns are demonstrated on superhydrophobic surfaces without splash or rebound after high-speed impacting by introducing...

This work studied gemini-like surfactants formed from anionic surfactant sodium dodecyl sulfate (SDS) and cationic charged bola-type diamines with hydrophilic or hydrophobic spacers of different lengths using surface tension, small angle neutron scattering, isothermal titration microcalorimetry and cryogenic transmission electron microscopy. The critical micelle concentrations (CMC) and the surface tension at CMC (γ) for all the diamine/SDS mixtures are markedly lower than that of SDS. The shorter diamines reduce γ to a greater extent regardless of the hydrophilicity/hydrophobicity of the diamines. Meanwhile, either the hydrophobic diamine with a longer spacer or the hydrophilic diamine with a shorter spacer is more beneficial to decrease CMC and leads to the transition from spherical micelles into rodlike or wormlike micelles. This is principally because of the formation of gemini-like surfactants by the electrostatic binding between SDS and the diamines, where the electrostatic repulsion between the adjacent headgroups of SDS becomes much weaker due to the electrostatic binding of oppositely charged diamine with SDS, and the longer hydrophobic spacer may also bend into the hydrophobic domain of micelles to promote micellar growth. However, the hydrophilic spacers are more compatible with the headgroup region, leading to micelles with a larger curvature. This work contributes to the understanding of the relationship between the properties of constructed gemini-like surfactants and the natures of connecting molecules, and provides guidance to efficiently improve the performance of surfactants.

This work has investigated the interaction of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) vesicles with oligomeric surfactants noncovalently formed by sodium dodecyl sulfate (SDS) and a series of polyamines, 1,3-diaminopropane (PDA), triamine, spermidine, and spermine. The partition coefficients (P) of these surfactants between lipid bilayers and the aqueous phase are measured by isothermal titration microcalorimetry (ITC), showing that the P value increases and the Gibbs free energy of the partition becomes more negative with increasing oligomerization degree of the surfactants. This changing trend is similar to that of synthetic oligomeric surfactants regardless of the charge properties, suggesting that the polyamine and SDS molecules interact with the DOPC bilayer simultaneously. Meanwhile, the DOPC solubilization by these surfactants is evaluated by the effective surfactant-to-lipid molar ratios for the onset (R e sat ) and end (R e sol ) of the solubilization process, which are determined from the phase boundaries obtained by ITC, turbidity, and dynamic light scattering measurements. With the increment of oligomerization degree, the R e sat and R e sol values increase anomalously and are much larger than those of the synthetic surfactants with the same oligomerization degree, suggesting that noncovalently constructed oligomeric surfactants exhibit lower solubilization ability to phospholipid vesicles than the corresponding covalent oligomeric surfactants. Therefore, the noncovalently constructed oligomeric-like surfactants facilitate strong partition but weak solubilization to phospholipid vesicles, which may provide a useful strategy to mildly adjust the permeation and fluidity of phospholipid vesicles with solubilization delay.

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