ArticleACS electrochemistry2025
Scanning Electrochemical Cell Microscopy for Sub-Micrometer Mass Spectrometric Studies of Electrochemical Reactions.
Article in ACS electrochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed.
- Beyond Imaging: Localized Synthesis, Fabrication, and Surface Modification via Scanning Electrochemical Cell Microscopy.ACS nano · 2026Article
- Overcoming the Limitations of Operando Microscopy and Spectroscopy for Revealing Degradation Mechanisms of Electrocatalysts in Liquid Media: Correlative Approaches.Nano letters · 2026Article
- A Look inside a Flexible Open-Source Scanning Electrochemical Probe Microscope.ACS electrochemistry · 2026Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Nanoscale electrochemistry has been significantly advanced through the utilization of nanopipettes, enabling precise electrode area confinement and localized measurements. In particular, scanning electrochemical cell microscopy (SECCM) has leveraged the use of nanopipettes to facilitate measurement of electrochemical processes with high spatiotemporal resolution. While nano electrochemistry is well-suited to study processes at the sub-micrometer level, there is a need for complementary analytical techniques that can enable the detection of intermediates and help to elucidate reaction pathways that occur in the small volumes. In this work, we demonstrate the coupling of SECCM with MS for the detection of reaction products formed by the oxidation of uric acid. Specifically, species generated at the tip of an SECCM probe could be delivered to a mass spectrometer via nanoelectrospray ionization and exhibit both stable ion signal and high sensitivity. We demonstrate that this workflow enables the detection of analytes generated from SECCM probes of 3 μm and 900 nm tip diameter, despite the low conversion ratio associated with the smaller nanopipette diameters. Results presented herein demonstrate the SECCM-MS workflow as a powerful approach to detect low-abundance species formed from micro- and nanoscale electrochemical reactions.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.