Abstract

Photoluminescent defects in diamond, such as the nitrogen-vacancy (NV) color center, are at the forefront of emerging optical quantum technologies. Most emit in the visible and near-infrared spectral region below 1000 nm (NIR-I), limiting their applications in photonics, fiber communications, and biology. Here, we show that the nitrogen-vacancy-nitrogen (N2V) center, which emits in the visible and near-infrared-II (NIR-II, 1000-1700 nm), is ubiquitous in as-synthesized and processed nitrogen-doped diamond, ranging from bulk samples to nanoparticles. We demonstrate that N2V is also present in commercially available state-of-the-art NV diamond sensing chips made via chemical vapor deposition (CVD). In high-pressure high-temperature (HPHT) diamonds, the photoluminescence (PL) intensity of both N2V charge states, N2V0 in the visible and N2V- in the NIR-II, increases with increasing substitutional nitrogen concentration. We determine the PL lifetime of N2V- to be 0.3 ns and compare a quantum optical and density functional theory model of the N2V- with experimental PL spectra. Finally, we show that detonation nanodiamonds (DND) exhibit stable PL in the NIR-II, which we attribute to the N2V color center, and use this NIR-II PL to image DNDs inside skin cells. Our results contribute to the scientific and technological exploration and development of the N2V color center and help elucidate interactions with other color centers in diamond.

Department(s)

Chemistry

Comments

National Computational Infrastructure, Grant DE200100279

Keywords and Phrases

bioimaging; color centers; detonation nanodiamond; diamond; near-infrared; photoluminescence

International Standard Serial Number (ISSN)

1936-086X; 1936-0851

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 2025 American Chemical Society, All rights reserved.

Publication Date

27 May 2025

PubMed ID

40366900

Included in

Chemistry Commons

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