Issue 18, 2023

The role of analyte concentration in accelerated reaction rates in evaporating droplets

Abstract

Accelerated reactions in microdroplets have been reported for a wide range of reactions with some microdroplet reactions occurring over a million times faster than the same reaction in bulk solution. Unique chemistry at the air–water interface has been implicated as a primary factor for accelerated reaction rates, but the role of analyte concentration in evaporating droplets has not been as well studied. Here, theta-glass electrospray emitters and mass spectrometry are used to rapidly mix two solutions on the low to sub-microsecond time scale and produce aqueous nanodrops with different sizes and lifetimes. We demonstrate that for a simple bimolecular reaction where surface chemistry does not appear to play a role, reaction rate acceleration factors are between 102 and 107 for different initial solution concentrations, and these values do not depend on nanodrop size. A rate acceleration factor of 107 is among the highest reported and can be attributed to concentration of analyte molecules, initially far apart in dilute solution, but brought into close proximity in the nanodrop through evaporation of solvent from the nanodrops prior to ion formation. These data indicate that analyte concentration phenomenon is a significant factor in reaction acceleration where droplet volume throughout the experiment is not carefully controlled.

Graphical abstract: The role of analyte concentration in accelerated reaction rates in evaporating droplets

Supplementary files

Article information

Article type
Edge Article
Submitted
13 Jan 2023
Accepted
04 Apr 2023
First published
12 Apr 2023
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2023,14, 4704-4713

The role of analyte concentration in accelerated reaction rates in evaporating droplets

C. J. Chen and E. R. Williams, Chem. Sci., 2023, 14, 4704 DOI: 10.1039/D3SC00259D

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