Electrochemical properties of vertically aligned graphenes: tailoring heterogeneous electron transfer through manipulation of the carbon microstructure

Dale A C Brownson; Alejandro Garcia-Miranda Ferrari; Subrata Ghosh; Mohammed Kamruddin; Jesús Iniesta; Craig E Banks

doi:10.1039/d0na00587h

Electrochemical properties of vertically aligned graphenes: tailoring heterogeneous electron transfer through manipulation of the carbon microstructure

Nanoscale Adv. 2020 Oct 6;2(11):5319-5328. doi: 10.1039/d0na00587h. eCollection 2020 Nov 11.

Authors

Dale A C Brownson¹, Alejandro Garcia-Miranda Ferrari¹, Subrata Ghosh^{2

3}, Mohammed Kamruddin², Jesús Iniesta⁴, Craig E Banks¹

Affiliations

¹ Faculty of Science and Engineering, Manchester Metropolitan University Chester Street Manchester M1 5GD UK d.brownson@mmu.ac.uk c.banks@mmu.ac.uk +44 (0)1612476561 +44 (0)1612471196.
² Materials Science Group, Indira Gandhi Centre for Atomic Research Kalpakkam 603102 India.
³ Department of Materials, School of Natural Sciences, The University of Manchester Oxford Road Manchester M13 9PL UK.
⁴ Physical Chemistry Department, Institute of Electrochemistry, University of Alicante 03690 San Vicente del Raspeig Alicante Spain.

Abstract

The electrochemical response of different morphologies (microstructures) of vertically aligned graphene (VG) configurations is reported. Electrochemical properties are analysed using the outer-sphere redox probes Ru(NH₃)₆ ^2+/3+ (RuHex) and N,N,N',N'-tetramethyl-p-phenylenediamine (TMPD), with performances de-convoluted via accompanying physicochemical characterisation (Raman, TEM, SEM, AFM and XPS). The VG electrodes are fabricated using an electron cyclotron resonance chemical vapour deposition (ECR-CVD) methodology, creating vertical graphene with a range of differing heights, spacing and edge plane like-sites/defects (supported upon underlying SiO₂/Si). We correlate the electrochemical reactivity/response of these novel VG configurations with the level of edge plane sites (%-edge) comprising their structure and calculate corresponding heterogeneous electron transfer (HET) rates, k ⁰. Taller VG structures with more condensed layer stacking (hence a larger global coverage of exposed edge plane sites) are shown to exhibit improved HET kinetics, supporting the claims that edge plane sites are the predominant source of electron transfer in carbon materials. A measured k ⁰ _eff of ca. 4.00 × 10^-3 cm s^-1 (corresponding to an exposed surface coverage of active edge plane like-sites/defects (% θ _edge) of 1.00%) was evident for the tallest and most closely stacked VG sample, with the inverse case true, where a VG electrode possessing large inter-aligned-graphene spacing and small flake heights exhibited only 0.08% of % θ _edge and a k ⁰ _eff value one order of magnitude slower at ca. 3.05 × 10^-4 cm s^-1. Control experiments are provided with conventional CVD (horizontal) grown graphene and the edge plane of highly ordered pyrolytic graphite (EPPG of HOPG), demonstrating that the novel VG electrodes exhibit ca. 3× faster k ⁰ than horizontal CVD graphene. EPPG exhibited the fastest HET kinetics, exhibiting ca. 2× larger k ⁰ than the best VG. These results are of significance to those working in the field of 2D-carbon electrochemistry and materials scientists, providing evidence that the macroscale electrochemical response of carbon-based electrodes is dependent on the edge plane content and showing that a range of structural configurations can be employed for tailored properties and applications.