TY - JOUR
T1 - Automated Measurement of Electrogenerated Redox Species Degradation Using Multiplexed Interdigitated Electrode Arrays
AU - Pence, Michael A.
AU - Rodríguez, Oliver
AU - Lukhanin, Nikita G.
AU - Schroeder, Charles M.
AU - Rodríguez-López, Joaquín
N1 - The research was financially supported by the Joint Center for Energy Storage Research (JCESR), an Energy Innovation Hub funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences. The material presented in this work was carried out in part in the Micro-Nano-Mechanical Systems Cleanroom Laboratory within the Department of Mechanical Science and Engineering at the University of Illinois. We graciously acknowledge Dr. Jingjing Zhang and Dr. Lu Zhang from Argonne National Laboratory, and Dr. Yichao Yan and Dr. Melanie Sanford from University of Michigan at Ann Arbor for synthesizing and supplying us with redox flow battery materials to use. We thank Dr. Inkyu Oh for thoughtful discussions.
PY - 2023/2/15
Y1 - 2023/2/15
N2 - Characterizing the decomposition of electrogenerated species in solution is essential for applications involving electrosynthesis, homogeneous electrocatalysis, and energy storage with redox flow batteries. In this work, we present an automated, multiplexed, and highly robust platform for determining the rate constant of chemical reaction steps following electron transfer, known as the EC mechanism. We developed a generation-collection methodology based on microfabricated interdigitated electrode arrays (IDAs) with variable gap widths on a single device. Using a combination of finite-element simulations and statistical analysis of experimental data, our results show that the natural logarithm of collection efficiency is linear with respect to gap width, and this quantitative analysis is used to determine the decomposition rate constant of the electrogenerated species (kc). The integrated IDA method is used in a series of experiments to measure kcvalues between ∼0.01 and 100 s-1in aqueous and nonaqueous solvents and at concentrations as high as 0.5 M of the redox-active species, conditions that are challenging to address using standard methods based on conventional macroelectrodes. The versatility of our approach allows for characterization of a wide range of reactions including intermolecular cyclization, hydrolysis, and the decomposition of candidate molecules for redox flow batteries at variable concentration and water content. Overall, this new experimental platform presents a straightforward automated method to assess the degradation of redox species in solution with sufficient flexibility to enable high-throughput workflows.
AB - Characterizing the decomposition of electrogenerated species in solution is essential for applications involving electrosynthesis, homogeneous electrocatalysis, and energy storage with redox flow batteries. In this work, we present an automated, multiplexed, and highly robust platform for determining the rate constant of chemical reaction steps following electron transfer, known as the EC mechanism. We developed a generation-collection methodology based on microfabricated interdigitated electrode arrays (IDAs) with variable gap widths on a single device. Using a combination of finite-element simulations and statistical analysis of experimental data, our results show that the natural logarithm of collection efficiency is linear with respect to gap width, and this quantitative analysis is used to determine the decomposition rate constant of the electrogenerated species (kc). The integrated IDA method is used in a series of experiments to measure kcvalues between ∼0.01 and 100 s-1in aqueous and nonaqueous solvents and at concentrations as high as 0.5 M of the redox-active species, conditions that are challenging to address using standard methods based on conventional macroelectrodes. The versatility of our approach allows for characterization of a wide range of reactions including intermolecular cyclization, hydrolysis, and the decomposition of candidate molecules for redox flow batteries at variable concentration and water content. Overall, this new experimental platform presents a straightforward automated method to assess the degradation of redox species in solution with sufficient flexibility to enable high-throughput workflows.
KW - Automation
KW - EC mechanism
KW - electrochemical analysis
KW - interdigitated arrays
KW - microfabrication
KW - redox flow batteries
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U2 - 10.1021/acsmeasuresciau.2c00054
DO - 10.1021/acsmeasuresciau.2c00054
M3 - Article
C2 - 36817007
AN - SCOPUS:85148477018
SN - 2694-250X
VL - 3
SP - 62
EP - 72
JO - ACS Measurement Science Au
JF - ACS Measurement Science Au
IS - 1
ER -