Schnurbus Marco, Kabat Malgorzata, Jarek Ewelina, Krzan Marcel, Warszynski Piotr, Braunschweig Björn
Institute of Physical Chemistry, Westfälische Wilhelms-Universität Münster, Corrensstraße 28/30, 48149 Münster, Germany.
Center for Soft Nanoscience, Westfälische Wilhelms-Universität Münster, Busso-Peus-Straße 10, 48149 Münster, Germany.
Langmuir. 2020 Jun 30;36(25):6871-6879. doi: 10.1021/acs.langmuir.9b03387. Epub 2020 Feb 24.
Responsive foams and interfaces are interesting building blocks for active materials that respond and adapt to external stimuli. We have used the photochromic reaction of a spiropyran sulfonate surfactant to render interfacial, rising bubbles as well as foaming properties active to light stimuli. In order to address the air-water interface on a molecular level, we have applied sum-frequency generation (SFG) spectroscopy which has provided qualitative information on the surface excess and the interfacial charging state as a function of light irradiation and solution pH. Under blue light irradiation, the surfactant forms a closed ring spiro form (SP), whereas under dark conditions the ring opens and the merocyanine (MC) form is generated. Using SFG spectroscopy, we show that at the interface, different pH conditions of the bulk solution lead to changes in the interfacial charging state. We have exploited the fact that the MC surfactant's O-H group can be deprotonated as a function of pH and used that to tune the molecules net charge at the interface. In fact, SFG spectroscopy shows that with increasing pH the intensity of the O-H stretching band from interfacial water molecules increases, which we associate to an increase in surface net charge. At a pH of 5.3, irradiation with blue light leads to a reversible decrease of O-H intensities, whereas the C-H intensities were unchanged compared to the corresponding intensities under dark conditions. These results are indicative of changes in the surface net charge with light irradiation, which are also expected to influence the foam stability via changes in the electrostatic disjoining pressure. In fact, measurements of the foam stabilities are consistent with this hypothesis and show higher foam stability under dark conditions. At pH 2.7 this behavior is reversed as far as the surface tension and surface charging as well as the foam stability are concerned. This is corroborated by rising bubble experiments, which demonstrated an unprecedented reduction of ∼30% in bubble velocity when the bubbles were irradiated with blue light compared to the velocity of bubbles with the surfactants in the dark state. Clearly, the light-triggered changes can be used to control foams, rising bubbles, and fluid interfaces on a molecular level which renders them active to light stimuli.
响应性泡沫和界面是用于活性材料的有趣构建块,这些活性材料能够响应并适应外部刺激。我们利用了磺酸螺吡喃表面活性剂的光致变色反应,使界面处上升的气泡以及发泡特性对光刺激具有活性。为了在分子水平上研究气-水界面,我们应用了和频产生(SFG)光谱,该光谱提供了关于表面过剩和界面电荷状态随光照射和溶液pH值变化的定性信息。在蓝光照射下,表面活性剂形成闭环螺环形式(SP),而在黑暗条件下,环打开并生成部花青(MC)形式。使用SFG光谱,我们表明在界面处,本体溶液的不同pH条件会导致界面电荷状态的变化。我们利用了MC表面活性剂的O-H基团可随pH值去质子化这一事实,并利用它来调节界面处分子的净电荷。实际上,SFG光谱表明,随着pH值的增加,界面水分子的O-H伸缩带强度增加,我们将其与表面净电荷的增加联系起来。在pH为5.3时,蓝光照射导致O-H强度可逆降低,而与黑暗条件下的相应强度相比,C-H强度不变。这些结果表明光照射会导致表面净电荷发生变化,预计这也会通过静电分离压力的变化影响泡沫稳定性。事实上,泡沫稳定性的测量结果与这一假设一致,并表明在黑暗条件下泡沫稳定性更高。就表面张力、表面电荷以及泡沫稳定性而言,在pH 2.7时这种行为会逆转。上升气泡实验证实了这一点,该实验表明,与处于黑暗状态的表面活性剂产生的气泡速度相比,当气泡用蓝光照射时,气泡速度前所未有的降低了约30%。显然,光触发的变化可用于在分子水平上控制泡沫、上升气泡和流体界面,使其对光刺激具有活性。