The Role of Interfaces and Charge for Chemical Reactivity in Microdroplets
A wide variety of reactions are reported to be dramatically accelerated in aqueous microdroplets, making them a promising platform for environmentally clean chemical synthesis. However to fully utilize the microdroplets for accelerating chemical reactions requires a fundamental understanding of how...
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Main Authors | , , , |
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Format | Journal Article |
Language | English |
Published |
03.11.2024
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Subjects | |
Online Access | Get full text |
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Summary: | A wide variety of reactions are reported to be dramatically accelerated in
aqueous microdroplets, making them a promising platform for environmentally
clean chemical synthesis. However to fully utilize the microdroplets for
accelerating chemical reactions requires a fundamental understanding of how
microdroplet chemistry differs from that of a homogeneous phase. Here we
provide our perspective on recent progress to this end both experimentally and
theoretically. We begin by reviewing the many ways in which microdroplets can
be prepared, creating water/hydrophobic interfaces which have been frequently
implicated in microdroplet reactivity due to preferential surface adsorption of
solutes, persistent electric fields, and their acidity or basicity. These
features of the interface interplay with specific mechanisms proposed for
microdroplet reactivity, including partial solvation and possible gas phase
channels. We especially highlight the role of droplet charge, which appears key
to understanding how certain reactions, like the formation of hydrogen peroxide
and reduced transition metal complexes, are thermodynamically possible in
microdroplets. Lastly, we emphasize opportunities for theoretical advances in
the microdroplet field generally, and to suggest experiments which would
greatly enhance our understanding of this fascinating and emerging subject. |
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DOI: | 10.48550/arxiv.2411.01587 |