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arXiv:2605.14697

Telecom-Wavelength-Compatible Quantum Information Transcription Using Nitrogen-Vacancy Centers

B. Göblyös, S. Kollarics, R. Kucsera, D. Plitt, K. Koltai, B. G. Márkus, L. Forró, F. Simon

cond-mat.mtrl-sciquant-phSubmitted May 14, 2026• Announced May 15, 2026• 0 citations
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Abstract

Nitrogen-vacancy (NV) centers in diamond are a leading platform for solid-state quantum sensing and quantum information processing. While most optical studies rely on the visible fluorescence associated with the triplet transitions, the infrared singlet transition near $1042$ nm, which is typically considered dark within the singlet manifold of the NV optical cycle, provides an alternative optical channel. Here, we report wavelength-resolved optically detected magnetic resonance (ODMR) measurements of this infrared emission. We directly observe ODMR contrast in the $1042$ nm emission and analyze its dependence on the magnetic field. The field-dependent spectral dispersion of the ODMR signal demonstrates that the spin-state information encoded in the NV center is transcribed to the infrared singlet emission through the spin-selective intersystem crossing, in close analogy to the visible fluorescence readout. These results establish infrared ODMR as a high-fidelity optical readout pathway. Crucially, by extending spin-state transcription directly into the $1300-1600$ nm range, this work demonstrates a direct, conversion-free interface between diamond spin-qubits and standard telecommunication infrastructure, bypassing the efficiency bottlenecks of active frequency conversion and benefiting from the already well-developed technologies in this range of the electromagnetic spectrum.

Comments
6 pages, 4 figures, plus Supplementary Information

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Nitrogen-vacancy (NV) centers in diamond are a leading platform for solid-state quantum sensing and quantum information processing. While most optical studies rely on the visible fluorescence associated with the triplet transitions, the infrared singlet transition near 104210421042 nm, which is typically considered dark within the singlet manifold of the NV optical cycle, provides an alternative optical channel. Here, we report wavelength-resolved optically detected magnetic resonance (ODMR) measurements of this infrared emission. We directly observe ODMR contrast in the 104210421042 nm emission and analyze its dependence on the magnetic field. The field-dependent spectral dispersion of the ODMR signal demonstrates that the spin-state information encoded in the NV center is transcribed to the infrared singlet emission through the spin-selective intersystem crossing, in close analogy to the visible fluorescence readout. These results establish infrared ODMR as a high-fidelity optical readout pathway. Crucially, by extending spin-state transcription directly into the 1300−16001300-16001300−1600 nm range, this work demonstrates a direct, conversion-free interface between diamond spin-qubits and standard telecommunication infrastructure, bypassing the efficiency bottlenecks of active frequency conversion and benefiting from the already well-developed technologies in this range of the electromagnetic spectrum.
Magnetometry with nitrogen-vacancy (NV) centers in diamond has so far been measured via emission of light from NV centers or via absorption at the singlet transition at 1042 nm. Here, we demonstrate a phenomenon of broadband optical absorption by the NV centers starting in the emission wavelength and reaching up to 1000 nm. The measurements are enabled by a high-finesse cavity, which is used for room-temperature continuous wave pump-probe experiments. The red to infrared probe beam shows the typical optically detected magnetic resonance (ODMR) signal of the NV spin with contrasts up to 42 %. This broadband optical absorption has not yet been reported in terms of NV magnetometry. We argue that the lower level of the absorbing transition could be the energetically lower NV singlet state, based on the increased optical absorption for a resonant microwave field and the spectral behavior. Investigations of the photon-shot-noise-limited sensitivity show improvements with increasing probe wavelength, reaching an optimum of 7.5pT/Hz. The results show significantly improved ODMR contrast compared to emission-based magnetometry. This opens a new detection wavelength regime with coherent laser signal detection for high-sensitivity NV magnetometry.
Nitrogen-vacancy (NV) centers in diamond have been used in recent years for a wide range of applications, from nanoscale NMR to quantum computation. These applications depend strongly on the efficient readout of the NV center's spin state, which is currently limited. Here we suggest a method of reading the NV center's spin state, using the weak optical transition in the singlet manifold. We numerically calculate the number of photons collected from each spin state using this technique, and show that an order of magnitude enhancement in spin-readout signal-to-noise ratio is expected, making single-shot spin readout within reach. Thus, this method could lead to an order of magnitude enhancement in sensitivity for ubiquitous NV-based sensing applications, and remove a major obstacle from using NVs for quantum information processing.
The color centers in diamonds are promising candidates in the context of quantum information science, quantum computation, and spin-based quantum sensors due to their exceptional spin-dependent emission properties. The manipulation and the optical readout of the spin state is measured using a spectroscopic technique known as the Optically Detected Magnetic Resonance (ODMR). Here, we discuss the indigenous development of an ODMR setup to manipulate and measure the spin state of nitrogen-vacancy centers in diamond. The study involves the confocal mapping of NV centers to measure the spin state by applying a micro-wave field. The spin state control appears as a dip in the measured emission intensity as a function of micro-wave frequency.
Magnetometry with nitrogen-vacancy (NV) centers in diamond has shown great promise in recent years. In particular, absorption-based magnetometry techniques, employing a cavity to enhance the absorption length, can improve the contrast and sensitivity compared to conventional techniques based on reading out the NV−^-− triplet fluorescence. The absorption techniques rely on magnetic-field-dependent absorption at the NV−^-− singlet zero phonon line at 1042 \,nm and its phonon sideband. In a cavity-enhanced spectroscopy approach, we study pump-laser- and microwave-induced cavity signal changes at room temperature over a spectral range of 680-1050 \,nm. Through normalization, we eliminate the cavity-enhancement effect and provide quasi-single-pass values for the absorption and optically detected magnetic resonance (ODMR) contrast. The highest contrast is found at 1042 \,nm, but multiple points of high contrast are found at the peaks of the phonon sideband. Additionally, cavity-enhanced ODMR contrasts in the range of 50-80 %\,\%% are presented. We further measure the broadband singlet absorption cross section at room temperature with a novel method through microwave-induced signal changes. This method is insensitive to pump-laser-induced signal changes by other defects and quantifies the room-temperature absorption strength of the singlet transition and its entire phonon sideband. We determine the absorption cross section at 1042 \,nm to be σ1042 ★=(0.89±0.14)⋅10−21 m2σ^{\,\bigstar}_{1042}=(0.89\pm0.14)\cdot 10^{-21}\,\text{m}^2σ1042★​=(0.89±0.14)⋅10−21m2 or σ1042 ▲=(2.9±0.5)⋅10−21 m2σ^{\,\blacktriangle}_{1042}=(2.9\pm0.5)\cdot 10^{-21}\,\text{m}^2σ1042▲​=(2.9±0.5)⋅10−21m2. depending on the employed 532 \,nm NV−^-− absorption cross section.
Nitrogen vacancy (NV-) color centers in diamond are a prime candidate for use in quantum information devices, owing to their spin-1 ground state, straightforward optical initialization and readout, and long intrinsic coherence times in a room-temperature solid. While the 13C nuclear spin is often a dominant source of magnetic noise, we observe transitions between electron-nuclear hyperfine states of NV- centers in 99% 13C diamond that are robust to decoherence. At magnetic field strengths ranging from 550 - 900 G, these transitions are observable by optically detected magnetic resonance (ODMR), and exhibit linewidths narrowed by factors as high as ~130 at room temperature over typical electron-type transitions observed from this spin system. We anticipate the use of these decoherence-protected transitions, in combination with dynamical decoupling methods, for storage of quantum information.
Abstract Transverse-magnetic-field-induced spin mixing in nitrogen-vacancy (NV) centers hybridizes the |0⟩ and | ± 1⟩ manifolds, degrading optical spin polarization and spin-dependent fluorescence and thereby limiting optically detected magnetic resonance (ODMR) contrast and quantum-sensor fidelity. While recent work has clarified key elements of NV photophysics, how spin mixing evolves with temperature under device-relevant operating conditions─and how it intertwines with charge-state dynamics─remains insufficiently quantified. Here we perform systematic magnetic-field-temperature (B-T) mapping of transverse-field-induced photoluminescence (PL) quenching in an ensemble of NV centers. By spectrally resolving the NV– and NV0 zero-phonon-line emission, we disentangle spin-mixing-driven contrast loss within NV– from correlated changes in charge-state-resolved fluorescence. We introduce an operational critical field Bc extracted from the PL-contrast line shape, which provides a compact, reproducible figure-of-merit for transverse-field robustness and enables straightforward comparison across temperatures and field geometries. The measured temperature dependence of Bc is captured by a concise model incorporating phonon-mediated excited-state orbital dynamics, establishing a predictive framework for optimizing operating conditions and benchmarking ensemble NV sensing platforms.