Evidence map›Paper›PMID 40635876›Full record

ArticleACS electrochemistry2025

Scanning Electrochemical Cell Microscopy for Sub-Micrometer Mass Spectrometric Studies of Electrochemical Reactions.

Lingjie Zhang, Madison E Edwards, Oluwasegun J Wahab, Hugo Y Samayoa-Oviedo, Dallas P Freitas, Xin Yan, Lane A Baker

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Lingjie ZhangDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0002-5183-465X
Madison E EdwardsDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0002-0041-5017
Oluwasegun J WahabDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0003-4280-9089
Hugo Y Samayoa-OviedoDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0001-9024-7071
Dallas P FreitasDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0003-2957-4158
Xin YanDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0002-8292-130X
Lane A BakerDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0001-5127-507X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

mass spectrometrynanoelectrospray ionizationscanning electrochemical cell microscopyscanning probesingle entity electrochemistry

Identifiers

PMID40635876
PMCPMC12235642

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Registered trials

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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.