4.8 Article

Redox Mediated Control of Electrochemical Potential in Liquid Cell Electron Microscopy

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 143, Issue 31, Pages 12082-12089

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c03906

Keywords

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Funding

  1. Photonics at Thermodynamic Limits Energy Frontier Research Center - U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences [DE-SC0019140]
  2. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  3. National Science Foundation's Graduate Research Fellowship Program (NSF GRFP)
  4. Kavli Philomathia Graduate Student Fellowship

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Researchers developed a new method that utilizes redox species to scavenge radicals and control electrochemical potential in situ, enabling precise control over liquid environment for near-atomic resolution observation of electrochemical structural dynamics. This approach shows promise for generalization across various chemical systems and provides unprecedented detail for the study of complex nanoscale dynamics.
Liquid cell electron microscopy enables the study of nanoscale transformations in solvents with high spatial and temporal resolution, but for the technique to achieve its potential requires a new level of control over the reactivity caused by radical generation under electron beam irradiation. An understanding of how to control electron-solvent interactions is needed to further advance the study of structural dynamics for complex materials at the nanoscale. We developed an approach that scavenges radicals with redox species that form well-defined redox couples and control the electrochemical potential in situ. This approach enables the observation of electrochemical structural dynamics at near-atomic resolution with precise control of the liquid environment. Analysis of nanocrystal etching trajectories indicates that this approach can be generalized to several chemical systems. The ability to simultaneously observe heterogeneous reactions at near-atomic resolution and precisely control the electrochemical potential enables the fundamental study of complex nanoscale dynamics with unprecedented detail.

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