Electrochemiluminescence using Pencil Graphite Electrodes Interfaced with a Simple Imaging System

Authors' Affiliations

Sandra Ehigiator, Department of Chemistry, College of Arts and Science, East Tennessee State University, Johnson City, TN. Gregory Bishop, Department of Chemistry, College of Arts and Science, East Tennessee State University, Johnson City, TN.

Location

Culp Center Ballroom

Start Date

4-25-2023 9:00 AM

End Date

4-25-2023 11:00 AM

Poster Number

40

Faculty Sponsor’s Department

Chemistry

Name of Project's Faculty Sponsor

Gregory Bishop

Additional Sponsors

Dane Scott, Catherine McCusker

Classification of First Author

Graduate Student-Master’s

Competition Type

Competitive

Type

Poster Presentation

Project's Category

Electrochemical Analysis

Abstract or Artist's Statement

Abstract

Electrochemical sensors are simple, fast, accurate, and low-cost analytical devices. They are especially important to the field of healthcare since they enable measurement of important indicators of patient health such as electrolytes and glucose in blood. Continued development and improvements in electrochemical sensors can result in more accessible, affordable, and effective diagnoses and treatment strategies. Electrochemical sensors employ electrodes, usually modified with a recognition agent specific for the analyte (the biomolecule of interest). The presence of the analyte at the electrode surface is typically measured through an electrochemical reaction that generates a signal in the form of an electric current or difference in electric potential. As an alternative, electrochemiluminescence, a phenomenon whereby an electrochemical reaction generates a product in an electronically excited state that is capable of emitting light, has great benefits due to its high sensitivity, selectivity, and extremely low background signal. Here we employ a camera equipped with a complementary metal-oxide semiconductor (CMOS) detector that is interfaced with a simple zoom lens to measure ECL generated at low-cost pencil graphite electrodes and small electrode arrays using tris(2,2′- bipyridyl) dichlororuthenium(II) hexahydrate ([Ru(bpy)3]2+) with tri-n-propylamine (TPA) as the coreactant. ECL signals produced at pencil graphite working electrodes were linear with respect to [Ru(bpy)3]2+ concentrations for 45–450μM [Ru(bpy)3]2+. The detection limit was found to be 2µM using the CMOS camera with exposure time set at 10s. This proof-of-concept work suggests the pencil graphite electrode with simple imaging system platform can be applied for ECL-based biosensing strategies.

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Apr 25th, 9:00 AM Apr 25th, 11:00 AM

Electrochemiluminescence using Pencil Graphite Electrodes Interfaced with a Simple Imaging System

Culp Center Ballroom

Abstract

Electrochemical sensors are simple, fast, accurate, and low-cost analytical devices. They are especially important to the field of healthcare since they enable measurement of important indicators of patient health such as electrolytes and glucose in blood. Continued development and improvements in electrochemical sensors can result in more accessible, affordable, and effective diagnoses and treatment strategies. Electrochemical sensors employ electrodes, usually modified with a recognition agent specific for the analyte (the biomolecule of interest). The presence of the analyte at the electrode surface is typically measured through an electrochemical reaction that generates a signal in the form of an electric current or difference in electric potential. As an alternative, electrochemiluminescence, a phenomenon whereby an electrochemical reaction generates a product in an electronically excited state that is capable of emitting light, has great benefits due to its high sensitivity, selectivity, and extremely low background signal. Here we employ a camera equipped with a complementary metal-oxide semiconductor (CMOS) detector that is interfaced with a simple zoom lens to measure ECL generated at low-cost pencil graphite electrodes and small electrode arrays using tris(2,2′- bipyridyl) dichlororuthenium(II) hexahydrate ([Ru(bpy)3]2+) with tri-n-propylamine (TPA) as the coreactant. ECL signals produced at pencil graphite working electrodes were linear with respect to [Ru(bpy)3]2+ concentrations for 45–450μM [Ru(bpy)3]2+. The detection limit was found to be 2µM using the CMOS camera with exposure time set at 10s. This proof-of-concept work suggests the pencil graphite electrode with simple imaging system platform can be applied for ECL-based biosensing strategies.