Methods for Color Center Preserving Hydrogen‐Termination of Diamond

Author:

McCloskey Daniel J.1ORCID,Roberts Daniel2,Rodgers Lila V. H.3ORCID,Barsukov Yuri4ORCID,Kaganovich Igor D.4ORCID,Simpson David A.1ORCID,de Leon Nathalie P.3ORCID,Stacey Alastair25ORCID,Dontschuk Nikolai1ORCID

Affiliation:

1. School of Physics University of Melbourne Parkville VIC 3010 Australia

2. School of Science RMIT University Melbourne VIC 3001 Australia

3. Department of Electrical and Computer Engineering Princeton University Princeton NJ 08544 USA

4. Princeton Plasma Physics Laboratory Princeton University Princeton NJ 08540 USA

5. Princeton Plasma Physics Laboratory 100 Stellarator Road Princeton NJ 08540 USA

Abstract

AbstractChemical functionalization of diamond surfaces by hydrogen is an important method for controlling the charge state of near‐surface fluorescent color centers, an essential process in fabricating devices such as diamond field‐effect transistors and chemical sensors, and a required first step for realizing families of more complex terminations through subsequent chemical processing. In all these cases, termination is typically achieved using hydrogen plasma sources that can etch or damage the diamond, as well as deposited materials or embedded color centers. This work explores alternative methods for lower‐damage hydrogenation of diamond surfaces, specifically the annealing of diamond samples in high‐purity, non‐explosive mixtures of nitrogen and hydrogen gas, and the exposure of samples to microwave hydrogen plasmas in the absence of intentional stage heating. The effectiveness of these methods are characterized by x‐ray photoelectron spectroscopy (XPS), and comparison of the results to density‐functional modelling of the surface hydrogenation energetics implicates surface oxygen ligands as the primary factor limiting the termination quality of annealed samples. Finally, photoluminescence (PL) spectroscopy is used to verify that both the annealing and reduced sample temperature plasma methods are non‐destructive to near‐surface ensembles of nitrogen‐vacancy (NV) centers, in stark contrast to plasma treatments that use heated sample stages.

Funder

Australian Research Council

University of Melbourne

U.S. Department of Energy

National Science Foundation

Fusion Energy Sciences

Publisher

Wiley

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