Study of the hydrogen region at platinum electrodes with linear scan cyclic voltammetry
Applications | 2021 | MetrohmInstrumentation
The electrochemical behavior of platinum electrodes in acidic media underpins fundamental studies and electrocatalytic applications, where surface structure influences processes like hydrogen adsorption and oxygen reduction.
This study compares linear scan and staircase cyclic voltammetry (CV) to characterize the hydrogen region at Pt electrodes, establishing reliable fingerprints of surface reactions using VIONIC powered by INTELLO.
Pt wire (working electrode), Pt sheet (counter), and Ag/AgCl (reference) electrodes were immersed in 0.5 M H₂SO₄. Electrolytes were purified and purged with argon. Linear and staircase CV scans (0.15 V → 1.35 V → –0.21 V → 0.15 V) were performed at 25–500 mV/s with a 10 ms sampling interval. Instrumentation included VIONIC potentiostat/galvanostat with INTELLO software.
Linear CV displayed pronounced peaks in the hydrogen under-potential deposition region, while staircase CV showed flattened peaks due to unsampled charging currents at each potential step. A direct comparison at 500 mV/s highlighted that continuous scanning is required to capture fast surface-limited processes accurately.
Advances in high-speed potentiostat hardware and software will enable deeper insights into rapid interfacial processes. Integrating CV with complementary spectroscopic or impedance techniques may further elucidate reaction mechanisms and support novel catalyst development.
Continuous linear scan CV is essential for reliable characterization of fast surface-limited processes at platinum electrodes. Staircase CV underestimates currents in the hydrogen region and may misrepresent interfacial behavior.
Electrochemistry
IndustriesEnergy & Chemicals
ManufacturerMetrohm
Summary
Significance of the Topic
The electrochemical behavior of platinum electrodes in acidic media underpins fundamental studies and electrocatalytic applications, where surface structure influences processes like hydrogen adsorption and oxygen reduction.
Aims and Study Overview
This study compares linear scan and staircase cyclic voltammetry (CV) to characterize the hydrogen region at Pt electrodes, establishing reliable fingerprints of surface reactions using VIONIC powered by INTELLO.
Methodology and Instrumentation
Pt wire (working electrode), Pt sheet (counter), and Ag/AgCl (reference) electrodes were immersed in 0.5 M H₂SO₄. Electrolytes were purified and purged with argon. Linear and staircase CV scans (0.15 V → 1.35 V → –0.21 V → 0.15 V) were performed at 25–500 mV/s with a 10 ms sampling interval. Instrumentation included VIONIC potentiostat/galvanostat with INTELLO software.
Main Results and Discussion
Linear CV displayed pronounced peaks in the hydrogen under-potential deposition region, while staircase CV showed flattened peaks due to unsampled charging currents at each potential step. A direct comparison at 500 mV/s highlighted that continuous scanning is required to capture fast surface-limited processes accurately.
Benefits and Practical Applications
- Enhanced accuracy in hydrogen adsorption/desorption analysis
- Robust fingerprinting of Pt surface structure for electrocatalysis
- Guidance for catalyst characterization in QA/QC and research settings
Future Trends and Opportunities
Advances in high-speed potentiostat hardware and software will enable deeper insights into rapid interfacial processes. Integrating CV with complementary spectroscopic or impedance techniques may further elucidate reaction mechanisms and support novel catalyst development.
Conclusion
Continuous linear scan CV is essential for reliable characterization of fast surface-limited processes at platinum electrodes. Staircase CV underestimates currents in the hydrogen region and may misrepresent interfacial behavior.
Reference
- Metrohm Application Note AN-EC-007
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