Investigating the effects of pyridine and poly(4-vinylpyridine) on CO2 reduction electrocatalysis at gold electrodes using in situ surface-enhanced Raman spectroelectrochemistry

Literature Information

Publication Date 2020-05-21
DOI 10.1039/D0CP00632G
Impact Factor 3.676
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Abstract

The CO2 reduction reaction (CO2RR) at metal electrodes is altered in the presence of pyridine and related species. Thick films of poly(4-vinylpyridine) on Au electrodes result in large current enhancements at low applied potentials but do not enhance CO2RR at these potentials. Surface-enhanced Raman spectroelectrochemistry can probe CO2-surface interactions and reveals that desorption of CO2 as bicarbonate is retarded in the presence of 4-PVP, with implications for ion-transport limitations in thick film CO2RR.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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