Abstract:Water drops sliding down inclined planes are an everyday phenomenon and are important in many technical applications. Previous understanding is that the motion is mainly dictated by viscous and capillary forces. Here we demonstrate that, in addition to these forces, drops on hydrophobic surfaces are affected by self-generated electrostatic forces. In a novel approach to determine forces on moving drops we imaged their trajectory when sliding down a tilted surface and apply the equation of motion. We found that… Show more
“…The high permittivity of silicon substrates reduces electrostatic forces, thus eliminating the influence of charging. 26 The surface preparation was identical to that on glass. One thousand drops (33 μL) were then deposited (Δ t = 2 s) on the functionalized silicon substrates at a tilt angle of 50° (i.e., charge measurement conditions).…”
Section: Resultsmentioning
confidence: 99%
“…To this end, a silicon substrate was employed (Figures d and S3). The high permittivity of silicon substrates reduces electrostatic forces, thus eliminating the influence of charging . The surface preparation was identical to that on glass.…”
When a water drop
slides over a hydrophobic surface, it usually
acquires a positive charge and deposits the negative countercharge
on the surface. Although the electrification of solid surfaces induced
after contact with a liquid is intensively studied, the actual mechanisms
of charge separation, so-termed slide electrification, are still unclear.
Here, slide electrification is studied by measuring the charge of
a series of water drops sliding down inclined glass plates. The glass
was coated with hydrophobic (hydrocarbon/fluorocarbon) and amine-terminated
silanes. On hydrophobic surfaces, drops charge positively while the
surfaces charge negatively. Hydrophobic surfaces coated with a mono-amine
(3-aminopropyltriethyoxysilane) lead to negatively charged drops and
positively charged surfaces. When coated with a multiamine (
N
-(3-trimethoxysilylpropyl)diethylenetriamine), a gradual
transition from positively to negatively charged drops is observed.
We attribute this tunable drop charging to surface-directed ion transfer.
Some of the protons accepted by the amine-functionalized surfaces
(−NH
2
with H
+
acceptor) remain on the
surface even after drop departure. These findings demonstrate the
facile tunability of surface-controlled slide electrification.
“…The high permittivity of silicon substrates reduces electrostatic forces, thus eliminating the influence of charging. 26 The surface preparation was identical to that on glass. One thousand drops (33 μL) were then deposited (Δ t = 2 s) on the functionalized silicon substrates at a tilt angle of 50° (i.e., charge measurement conditions).…”
Section: Resultsmentioning
confidence: 99%
“…To this end, a silicon substrate was employed (Figures d and S3). The high permittivity of silicon substrates reduces electrostatic forces, thus eliminating the influence of charging . The surface preparation was identical to that on glass.…”
When a water drop
slides over a hydrophobic surface, it usually
acquires a positive charge and deposits the negative countercharge
on the surface. Although the electrification of solid surfaces induced
after contact with a liquid is intensively studied, the actual mechanisms
of charge separation, so-termed slide electrification, are still unclear.
Here, slide electrification is studied by measuring the charge of
a series of water drops sliding down inclined glass plates. The glass
was coated with hydrophobic (hydrocarbon/fluorocarbon) and amine-terminated
silanes. On hydrophobic surfaces, drops charge positively while the
surfaces charge negatively. Hydrophobic surfaces coated with a mono-amine
(3-aminopropyltriethyoxysilane) lead to negatively charged drops and
positively charged surfaces. When coated with a multiamine (
N
-(3-trimethoxysilylpropyl)diethylenetriamine), a gradual
transition from positively to negatively charged drops is observed.
We attribute this tunable drop charging to surface-directed ion transfer.
Some of the protons accepted by the amine-functionalized surfaces
(−NH
2
with H
+
acceptor) remain on the
surface even after drop departure. These findings demonstrate the
facile tunability of surface-controlled slide electrification.
“…Using this contact time, we fit eq (9) to the saturated drop voltage as a function of ∆t, and obtained the A2C model parameters as follows: U d = 6.6 ± 0.3 V and U w ≈ 0.9 ± 0.2 V; t w = 0.11 ± 0.01 s and t d = 152 ± 13 s. Using these parameters and equation above 9, we calculated U cl (n) and simulated the drop charge versus drop number and slide length. Deviations from the model could be explained by variations in the drop contact time coming from slight changes in drop path or variations in velocity, either caused because the drop not yet reaching terminal velocity, or by electrostatic forces between the drop and surface charges [40]. Furthermore, the observed behavior might be caused by more complex adaptation processes involving several time scales or an additional adaptation in one of the other parameters.…”
Slide electrification is a spontaneous charge separation between a surface and a sliding drop. Here, we describe this effect in terms of a voltage generated at the three-phase contact line. This voltage moves charges between capacitors, one formed by the drop and one on the surface. By introducing an adaptation of the voltage upon water contact, we can model drop charge experiments on many surfaces, including more exotic ones with drop-rate dependent charge polarity. Thus, the adaptive two capacitor model enables new insights into the molecular details of the charge separation mechanism.
“…However, careful observation into the initial dynamics of drop contact provides further information. On macroscopically flat nonpolar hydrophobic bilayer surfaces (Figure a,c, purple data, PFOTS–PDMS), we see a rapid alignment between the initial and final contact angle, measured at t contact = 0.02 or 60 s at 115°, respectively, well within the hysteresis range , of typical PFOTS-functionalized surfaces (Figure S9). Fluctuations in measured contact angles (Figure c, purple data, PFOTS–PDMS) exist due to the drop vibration after detachment.…”
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