Heavily boron-doped diamond grown on scalable heteroepitaxial quasi-substrates: a promising single crystal material for electrochemical sensing applications

  • In this work, three distinct heteroepitaxial single-crystal boron-doped diamond (SC-BDD) electrodes were fabricated and subjected to detailed surface analysis and electrochemical characterization. Specifically, the heteroepitaxy approach allowed to synthesize large-area (1 cm2) and heavily-doped (100)-oriented SC-BDD electrodes. Their single-crystal nature and crystal orientation were confirmed by X-ray diffraction, while scanning electron and atomic force microscopies revealed marked variations in surface morphology resulting from their growth on respective on-axis and off-axis substrates. Further, absence of sp2 impurities along with heavy boron doping (>1021 cm−3) was demonstrated by Raman spectroscopy and Mott-Schottky analysis, respectively. Cyclic voltammetry (CV) in a 0.1 M KNO3 solution revealed wide potential windows (∼3.3 V) and low double-layer capacitance (<4 μF cm−2) of the SC-BDD electrodes. Their highly conductive, ‘metal-like’ nature was confirmed by CV withIn this work, three distinct heteroepitaxial single-crystal boron-doped diamond (SC-BDD) electrodes were fabricated and subjected to detailed surface analysis and electrochemical characterization. Specifically, the heteroepitaxy approach allowed to synthesize large-area (1 cm2) and heavily-doped (100)-oriented SC-BDD electrodes. Their single-crystal nature and crystal orientation were confirmed by X-ray diffraction, while scanning electron and atomic force microscopies revealed marked variations in surface morphology resulting from their growth on respective on-axis and off-axis substrates. Further, absence of sp2 impurities along with heavy boron doping (>1021 cm−3) was demonstrated by Raman spectroscopy and Mott-Schottky analysis, respectively. Cyclic voltammetry (CV) in a 0.1 M KNO3 solution revealed wide potential windows (∼3.3 V) and low double-layer capacitance (<4 μF cm−2) of the SC-BDD electrodes. Their highly conductive, ‘metal-like’ nature was confirmed by CV with [Ru(NH3)6]3+/2+ probe manifesting near-reversible redox response with ΔEp approaching 0.059 V. The same probe was used to record scanning electrochemical micrographs, which clearly demonstrated homogeneously distributed electrochemical activity of the heteroepitaxial SC-BDD electrodes. Minor differences in their electrochemical performance, presumably resulting from the somewhat different morphological features, were only unveiled during CV with surface sensitive compounds [Fe(CN)6]3−/4− and dopamine. The latter was also used to show the possibility of applying herein developed heteroepitaxial SC-BDD electrodes for electrochemical sensing, whereas experiments with anthraquinone-2,6-disulfonate revealed their enhanced resistance to fouling. All in all, heteroepitaxial SC-BDD represents a highly attractive electrode material which can, owing to the fabrication strategy, easily overcome size limitation, currently preventing broader use of single crystal diamond electrodes in electrochemical applications.show moreshow less

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Metadaten
Author:Zhichao Liu, Simona Baluchová, André F. Sartori, Ziyu Li, Yaiza Gonzalez-Garcia, Matthias SchreckORCiDGND, Josephus G. Buijnsters
URN:urn:nbn:de:bvb:384-opus4-1006406
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/100640
ISSN:0008-6223OPAC
Parent Title (English):Carbon
Publisher:Elsevier BV
Place of publication:Amsterdam
Type:Article
Language:English
Year of first Publication:2023
Publishing Institution:Universität Augsburg
Release Date:2023/01/09
Tag:General Chemistry; General Materials Science
Volume:201
First Page:1229
Last Page:1240
DOI:https://doi.org/10.1016/j.carbon.2022.10.023
Institutes:Mathematisch-Naturwissenschaftlich-Technische Fakultät
Mathematisch-Naturwissenschaftlich-Technische Fakultät / Institut für Physik
Mathematisch-Naturwissenschaftlich-Technische Fakultät / Institut für Physik / Lehrstuhl für Experimentalphysik IV
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 53 Physik / 530 Physik
Licence (German):CC-BY 4.0: Creative Commons: Namensnennung (mit Print on Demand)