Exploring the Role of the Connection Length of Screen-Printed Electrodes towards the Hydrogen and Oxygen Evolution Reactions

Author:

Wuamprakhon Phatsawit12ORCID,Ferrari Alejandro Garcia-Miranda1ORCID,Crapnell Robert D.1ORCID,Pimlott Jessica L.1ORCID,Rowley-Neale Samuel J.1ORCID,Davies Trevor J.3,Sawangphruk Montree2ORCID,Banks Craig E.1ORCID

Affiliation:

1. Faculty of Science and Engineering, Manchester Metropolitan University, Chester Street, Manchester M1 5GD, UK

2. Centre of Excellence for Energy Storage Technology (CEST), Department of Chemical and Biomolecular Engineering, Vidyasirimedhi Institute of Science and Technology, School of Energy Science and Engineering, Rayong 21210, Thailand

3. INEOS Electrochemical Solutions, Bankes Lane Office, Bankes Lane, Runcorn, Cheshire WA7 4JE, UK

Abstract

Zero-emission hydrogen and oxygen production are critical for the UK to reach net-zero greenhouse gasses by 2050. Electrochemical techniques such as water splitting (electrolysis) coupled with renewables energy can provide a unique approach to achieving zero emissions. Many studies exploring electrocatalysts need to “electrically wire” to their material to measure their performance, which usually involves immobilization upon a solid electrode. We demonstrate that significant differences in the calculated onset potential for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) can be observed when using screen-printed electrodes (SPEs) of differing connection lengths which are immobilized with a range of electrocatalysts. This can lead to false improvements in the reported performance of different electrocatalysts and poor comparisons between the literature. Through the use of electrochemical impedance spectroscopy, uncompensated ohmic resistance can be overcome providing more accurate Tafel analysis.

Funder

EPSRC

Publisher

MDPI AG

Subject

Electrical and Electronic Engineering,Biochemistry,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

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