Affiliations 

  • 1 Institute for Research in Molecular Medicine, (INFORMM), Universiti Sains Malaysia (USM), 11800, Gelugor, Penang, Malaysia
  • 2 Department of Pharmacy, Raparin Technical and Vocational Institute, Rania, Sulaymaniyah, Kurdistan Region 46012, Iraq
  • 3 School of Health and Life Sciences, Teesside University, Middlesbrough, TS1 3BX, Tees Valley, England, UK. [email protected]
  • 4 Department of Chemistry, Karabuk University, 78050 Karabuk, Turkey
  • 5 School of Chemical Sciences, Universiti Sains Malaysia (USM), 11800, Gelugor, Penang, Malaysia
  • 6 School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia (USM), 14300, Nibong Tebal, Penang, Malaysia
Analyst, 2024 Nov 04;149(22):5401-5410.
PMID: 39373774 DOI: 10.1039/d4an00990h

Abstract

Sulfuric acid is commonly used to electrochemically activate gold electrodes in a variety of electrochemical applications. This work provides the first evaluations of the electrochemical behaviors and a 3D image of an activated screen-printed gold electrode (SPGE, purchased commercially) through electrochemical and imaging analyses. The activated SPGE surface appears rougher than the unactivated SPGE surface when viewed through microtopography images using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Nevertheless, the roughened microscopy structure does not exhibit any substantial changes in roughness factor for the activated SPGE, as indicated by capacitive current analyses. The significant improvement in electrochemical responsiveness of the activated SPGE is mainly attributed to the presence of surface pores created in the microscopic structure as a result of gold oxide layer formation. The presence of surface pores on the activated surface has significantly improved its conductivity by 10-fold. As a result, electron transfer kinetics and mass transports of the activated SPGE are greatly improved. The results presented in this work indicate that the surface of the activated SPGE greatly increased its intrinsic surface pores, and conductivity of the electrode surface and uncovered the electrocatalytic active sites. This significantly improves the activated SPGE's performance in electrochemical applications such as oxygen reduction reaction (ORR). An activated SPGE considerably enhanced limiting current density as well as ∼172 mV versus Ag shifted onset potential to more positive potentials compared to unactivated SPGE.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.