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X-ray quantification of oxygen groups on diamond surfaces for quantum applications

MetadataDetails
Publication Date2023-10-04
JournalMaterials for Quantum Technology
AuthorsNikolai Dontschuk, LVH Rodgers, Jyh‐Pin Chou, DA Evans, Kane M. O’Donnell
InstitutionsPrinceton Plasma Physics Laboratory, Institute for Solid State Physics and Optics
Citations9

Abstract Identifying the surface chemistry of diamond materials is increasingly important for device applications, especially quantum sensors. Oxygen-related termination species are widely used because they are naturally abundant, chemically stable, and compatible with stable nitrogen vacancy centres near the diamond surface. Diamond surfaces host a mixture of oxygen-related species, and the precise chemistry and relative coverage of different species can lead to dramatically different electronic properties, with direct consequences for near-surface quantum sensors. However, it is challenging to unambiguously identify the different groups or quantify the relative surface coverage. Here we show that a combination of x-ray absorption and photoelectron spectroscopies can be used to quantitatively identify the coverage of carbonyl functional groups on the <mml:math xmlns:mml=“http://www.w3.org/1998/Math/MathML” overflow=“scroll”> <mml:mo fence=“false” stretchy=“false”>{</mml:mo> <mml:mn>100</mml:mn> <mml:mo fence=“false” stretchy=“false”>}</mml:mo> </mml:math> diamond surface. Using this method we reveal an unexpectedly high fraction of carbonyl groups ( <mml:math xmlns:mml=“http://www.w3.org/1998/Math/MathML” overflow=“scroll”> <mml:mrow> <mml:mo>&gt;</mml:mo> </mml:mrow> </mml:math> 9%) on a wide range of sample surfaces. Furthermore, through a combination of ab initio calculations and spectroscopic studies of engineered surfaces, we reveal unexpected complexities in the x-ray spectroscopy of oxygen terminated diamond surfaces. Of particular note, we find the binding energies of carbonyl-related groups on diamond differs significantly from other organic systems, likely resulting in previous misestimation of carbonyl fractions on diamond surfaces.

  1. 2014 - Subnanometre resolution in three-dimensional magnetic resonance imaging of individual dark spins [Crossref]
  2. 2014 - Magnetic resonance detection of individual proton spins using quantum reporters [Crossref]
  3. 2019 - Origins of diamond surface noise probed by correlating single-spin measurements with surface spectroscopy [Crossref]
  4. 2022 - Probing spin dynamics on diamond surfaces using a single quantum sensor [Crossref]
  5. 2017 - Charge state stabilization of shallow nitrogen vacancy centers in diamond by oxygen surface modification [Crossref]
  6. 2022 - Nanoscale solid-state nuclear quadrupole resonance spectroscopy using depth-optimized nitrogen-vacancy ensembles in diamond [Crossref]
  7. 2014 - A near edge x-ray absorption fine structure study of oxidized single crystal and polycrystalline diamond surfaces [Crossref]
  8. 2001 - Surface electronic states of the partially hydrogenated diamond C(100)−( 2×1 ) : H surface [Crossref]
  9. 2019 - Evidence for primal sp 2 defects at the diamond surface: candidates for electron trapping and noise sources [Crossref]
  10. 2008 - Water-induced negative electron affinity on diamond (100) [Crossref]