Cobalt phthalocyanine modified electrodes utilised in electroanalysis: Nano-structured modified electrodes vs. Bulk modified screen-printed electrodes

68Citations
Citations of this article
84Readers
Mendeley users who have this article in their library.

Abstract

Cobalt phthalocyanine (CoPC) compounds have been reported to provide electrocatalytic performances towards a substantial number of analytes. In these configurations, electrodes are typically constructed via drop casting the CoPC onto a supporting electrode substrate, while in other cases the CoPC complex is incorporated within the ink of a screen-printed sensor, providing a one-shot economical and disposable electrode configuration. In this paper we critically compare CoPC modified electrodes prepared by drop casting CoPC nanoparticles (nano-CoPC) onto a range of carbon based electrode substrates with that of CoPC bulk modified screen-printed electrodes in the sensing of the model analytes L-ascorbic acid, oxygen and hydrazine. It is found that no “electrocatalysis” is observed towards L-ascorbic acid using either of these CoPC modified electrode configurations and that the bare underlying carbon electrode is the origin of the obtained voltammetric signal, which gives rise to useful electroanalytical signatures, providing new insights into literature reports where “electrocatalysis” has been reported with no clear control experiments undertaken. On the other hand true electrocatalysis is observed towards hydrazine, where no such voltammetric features are witnessed on the bare underlying electrode substrate.

Cite

CITATION STYLE

APA

Foster, C. W., Pillay, J., Metters, J. P., & Banks, C. E. (2014). Cobalt phthalocyanine modified electrodes utilised in electroanalysis: Nano-structured modified electrodes vs. Bulk modified screen-printed electrodes. Sensors (Switzerland), 14(11), 21905–21922. https://doi.org/10.3390/s141121905

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free