2019
DOI: 10.1021/acsami.9b08697
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Dual Droplet Functionality: Phototaxis and Photopolymerization

Abstract: The use of phototaxis to move droplets in liquids offers the opportunity to emulate natural processes such as the controlled transport of materials in fluidic environments and to undertake chemistry at specific locations. We have developed a photoactive organic droplet whose movement in aqueous solution is driven by a photoinitiator, as a result of a light induced reaction within the droplet generating a Marangoni flow. The photoinitiator not only drives the droplet motion but can also be used to initiate poly… Show more

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Cited by 8 publications
(11 citation statements)
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“…To date, the commonly used families of photochromic molecules for mediating dynamic processes, e.g., droplet motion are azobenzenes that undergo trans-cis photoisomerization, [24,25] and spiropyran and its derivatives that overgo photocleavage primary to the proton release, resulting in minute-length reaction timescales. [26][27][28][29][30][31][32] Therefore, a yet-to-beresolved challenge in the use of such photochromic molecules is the associated timescales and especially the reversibility of the dynamic process.Herein, we propose a new approach to chemophototaxis for gaining fast subsecond responses not only to turning on the light, but also for the reversible process of turning the light off, which is based on the use of Brønsted-Lowry photoacids and photobases. This class of organic molecules undergoes a dramatic change in their dissociation equilibrium constant (pKa) upon light excitation.…”
mentioning
confidence: 99%
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“…To date, the commonly used families of photochromic molecules for mediating dynamic processes, e.g., droplet motion are azobenzenes that undergo trans-cis photoisomerization, [24,25] and spiropyran and its derivatives that overgo photocleavage primary to the proton release, resulting in minute-length reaction timescales. [26][27][28][29][30][31][32] Therefore, a yet-to-beresolved challenge in the use of such photochromic molecules is the associated timescales and especially the reversibility of the dynamic process.Herein, we propose a new approach to chemophototaxis for gaining fast subsecond responses not only to turning on the light, but also for the reversible process of turning the light off, which is based on the use of Brønsted-Lowry photoacids and photobases. This class of organic molecules undergoes a dramatic change in their dissociation equilibrium constant (pKa) upon light excitation.…”
mentioning
confidence: 99%
“…To date, the commonly used families of photochromic molecules for mediating dynamic processes, e.g., droplet motion are azobenzenes that undergo trans-cis photoisomerization, [24,25] and spiropyran and its derivatives that overgo photocleavage primary to the proton release, resulting in minute-length reaction timescales. [26][27][28][29][30][31][32] Therefore, a yet-to-beresolved challenge in the use of such photochromic molecules is the associated timescales and especially the reversibility of the dynamic process.…”
mentioning
confidence: 99%
“…[ 30 ] Light‐induced Marangoni flow can serve as the mediation for phototaxis motion, for example, within photoactive microdroplets under 365 nm laser irradiation. [ 286 ] Electric field is programmable with respect to its voltage, frequency, and conductive surfaces. In a nonuniform electric field, 2D patterning of heterogeneous particles can be performed on ITO glass substrates because of electrowetting and dielectrophoresis (DEP) between two parallel plates (Figure 10F).…”
Section: Synthetic Collective Taxesmentioning
confidence: 99%
“…Previously, we have used oil droplets as a convenient model for an artificial system capable of stimuli-responsiveness and motion. While there are many examples where chemical or physical signals, such as a change in pH or light, were used as a stimulus for a droplet’s self-propulsion, we were the first to use Brønsted photoacids to control their motion. Brønsted photoacids are organic molecules that undergo a dramatic drop of p K a in their electronically excited state. Accordingly, such photoacids can be considered as a transient source of proton donors only upon their light excitation.…”
Section: Introductionmentioning
confidence: 99%