video: From the wind-whipped surface of the open ocean, to the mist rising from a forest, environments where air and water meet are the site of many key natural chemical processes, such as cleaning the air of pollutants. Some scientists have suggested the air-water interface forms a special surface for catalyzing chemical reactions, but their results have been hotly debated. Researchers at KAUST have used several complementary analytical techniques to help settle the debate. To learn more, visit KAUST Discovery at: discovery.kaust.edu.sa/en/article/795/probing-water's-skin view more
Credit: KAUST 2019
From the wind-whipped surface of the open ocean, to trillions of tiny water drops in clouds, the air-water interface--water's skin-- is the site for crucial natural processes, including ocean-atmosphere exchange and cloud acidification. The air-water interface has even been postulated as the cradle of life. However, factors such as its subnanometer size and dynamic nature, render the investigation of interfacial wanter a daunting task.
In recent years, researchers have investigated the air-water interface using electrosprays of water: fine sprays produced by applying greater than 5000 V to water solutions passing through a metallic capillary. Traditionally, electrosprays have been used to study ions in the gas phase. Using electrosprays, researchers have suggested that the surface of mildly acidic water behaves as a highly reactive superacid. But the debate remains whether the air-water interface at mild pH can really behave as a superacid.
Now, KAUST researchers led by Himanshu Mishra have employed complementary techniques to disentangle purely interfacial effects from electrospray-specific effects.
The researchers investigated the reactivity of isoprene--a volatile molecule released by plants experiencing heat stress--at the water interface. "We compared two scenarios: electrosprays of water interacting with isoprene gas and vigorously stirred mixtures of water and isoprene in closed vials," explains Adair Gallo Jr., a Ph.D. student in Mishra's team and lead author of the study.
The team looked for the formation of short isoprene chains called oligomers. "Intriguingly, isoprene spontaneously formed oligomers in electrosprays, under acidic and basic conditions, and even in the absence of water," Gallo says. No oligomerization products were detected when acidified water was vigorously stirred with isoprene for hours. But when the same organic phase was electrosprayed, oligomers formed. The findings unequivocally establish that the oligomerization took place exclusively in electrosprays.
Computer simulations carried out by Adriano Sanchez, a postdoctoral scholar in Mishra's team, gave molecular-scale insights into the results. "We found that oligomer formation was only possible on gas-phase clusters comprising not more than three water molecules and an excess proton," Sanchez says.
Collectively, the team's results demonstrated that electrosprays present highly energetic gas-phase pathways for chemical reactions to occur that are impossible at natural air-water interfaces. "Electrosprays should therefore be complemented with surface-specific techniques and computer simulations to avoid incorrect conclusions when studying interfacial processes," Mishra says. "I have been thinking about this problem for over six years, and now, thanks to my team, we have managed to disentangle purely interfacial effects from artifacts" says Mishra. This contribution will feature on the cover of the journal Chemical Science.
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Journal
Chemical Science