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Time-space-encoded readout for noise suppression and scalable scanning in optically active solid-state spin systems

MetadataDetails
Publication Date2025-06-06
JournalPhysical Review Applied
AuthorsJoachim P. Leibold, Nick R. von Grafenstein, Xiaoxun Chen, Linda MĂŒller, Karl D. Briegel
InstitutionsTechnical University of Munich, Munich Center for Quantum Science and Technology
AnalysisFull AI Review Included

Technical Documentation: Time-Space-Encoded Readout (T2S) for Scalable Quantum Sensing

Section titled “Technical Documentation: Time-Space-Encoded Readout (T2S) for Scalable Quantum Sensing”

6CCVD Analysis of Physical Review Applied 23, 064018 (2025)


This research introduces the Time-to-Space (T2S) encoding readout scheme, leveraging high-quality MPCVD diamond and Acousto-Optic Modulators (AOMs) to revolutionize data acquisition in solid-state spin systems.

  • Core Innovation: T2S decouples microwave (MW) spin manipulation from rapid optical readout, enabling multiple spatially resolved measurements within the spin system’s T1 lifetime.
  • Material Focus: Demonstrated using Nitrogen-Vacancy (N-V) center ensembles in high-purity Single Crystal Diamond (SCD).
  • Noise Reduction: Achieved efficient common-mode noise cancellation, resulting in a 60% reduction in the noise floor and a 3x increase in Signal-to-Noise Ratio (SNR) in N-V-NMR experiments.
  • Scalability & Speed: Enables scalable multipixel scanning/imaging, potentially accelerating data acquisition by several hundred times compared to conventional scanning methods.
  • Readout Speed: Achieved rapid readout cycles of 2.5 ”s per spot (2 ”s laser pulse + 0.5 ”s spot movement), significantly faster than typical T1 relaxation times (ms range).
  • Future Potential: The scheme is readily applicable to other quantum defects (SiC, h-BN) and single spin-defect experiments, requiring only standard ODMR components.

The following hard data points were extracted from the experimental results, focusing on material performance and system throughput:

ParameterValueUnitContext
N-V Layer Thickness (Shallow)~5nmUsed for T1 and XY8 measurements.
N-V Layer Thickness (Thick)~10”mUsed for high-sensitivity CASR/NMR.
T1 Relaxation Time (Plain Diamond)1.1 ± 0.05msReference spot performance.
T1 Relaxation Time (Mn2+ Coated)0.5 ± 0.03msSample spot performance (reduced T1).
SNR Improvement (NMR)3xAchieved via common-mode noise subtraction.
Noise Reduction (Noise Floor)60%Reduction attributed to MW phase noise cancellation.
Readout Time per Spot2.5”sIncludes 2 ”s laser pulse and 0.5 ”s spot movement.
Maximum Readouts (T1 limited, 1 ms)400spotsTheoretical maximum for long pulse sequences.
Maximum Readouts (T2 limited, 100 ”s)40spotsAchievable for shorter pulse sequences.
AOM Active Aperture0.25mmLimits maximum beam diameter.
AOM Acoustic Velocity (Quartz)5.7mm/”sUsed for fast scanning implementation.
Laser Wavelength532nmGreen excitation source.

The T2S scheme relies on precise material engineering and high-speed optical control, implemented as follows:

  1. Material Preparation: High-purity diamond was used, featuring N-V ensembles created via nitrogen implantation (2.5 keV, 2 x 1012/cm2) to achieve near-surface (shallow, ~5 nm) or thick (~10 ”m) N-V layers, depending on the sensing application (T1/XY8 vs. NMR).
  2. Homogeneous MW Control: A simple loop antenna or resonator was used to ensure uniform MW fields across the entire region of interest, allowing simultaneous spin manipulation of all target spots.
  3. Fast Optical Scanning (T2S Encoding): The conventional single-tone RF input of the Acousto-Optic Modulator (AOM) driver was replaced with a train of pulses of different RF frequencies.
  4. Position-Time Linkage: Each distinct RF frequency drives the AOM to a specific deflection angle, linking the time of the optical readout pulse to a specific spatial position (spot S1, S2, etc.) on the diamond surface.
  5. High-Speed Readout: The AOM’s fast response time (nanosecond scale) allows the laser spot to be moved and fluorescence read out in 2.5 ”s cycles, ensuring multiple readouts occur faster than the N-V T1 relaxation time (milliseconds).
  6. Noise Cancellation: By simultaneously manipulating and subsequently reading out two or more spatially separated spots (one sample, one reference), common-mode noise sources (e.g., magnetic field drifts, MW phase noise) are correlated and efficiently canceled via time-domain data subtraction.

The T2S encoding scheme demands ultra-high-quality diamond substrates with precise defect engineering and surface preparation. 6CCVD is uniquely positioned to supply the foundational materials required to replicate, scale, and advance this research.

To achieve the high SNR and long coherence times necessary for advanced quantum sensing, the following 6CCVD materials are recommended:

Research Requirement6CCVD Material SolutionTechnical Specification Match
High Purity SubstratesOptical Grade SCDSCD ensures minimal native defects and low strain, critical for maximizing T1 and T2 times.
Shallow N-V EnsemblesCustom Implanted SCDWe supply SCD wafers ready for low-energy implantation (e.g., 2.5 keV) to create near-surface N-V layers (down to 5 nm depth) for surface-sensitive NMR/relaxometry.
Thick N-V LayersHigh-Growth Rate SCDWe provide SCD plates with controlled nitrogen incorporation during growth, achieving homogeneous N-V layers up to 500 ”m thick, ideal for high-sensitivity ensemble sensing (as used in the CASR experiments).
Scalable Imaging AreaLarge Area PCDFor future large-scale imaging, we offer Polycrystalline Diamond (PCD) plates up to 125 mm diameter with high uniformity and low surface roughness (Ra < 5 nm).
Microfluidic IntegrationUltra-Smooth SCDWe guarantee SCD polishing to Ra < 1 nm, ensuring optimal optical coupling and compatibility with microfluidic bonding and surface functionalization layers.

The T2S scheme, especially when scaled to 2D scanning using AODs (as discussed in Appendix G), requires highly customized components. 6CCVD offers comprehensive engineering services to meet these demands:

  • Custom Dimensions: We provide plates and wafers in custom sizes and shapes, essential for integrating diamond chips into complex optical setups (e.g., F-Ξ lens systems, 4f configurations) and microfluidic platforms.
  • Advanced Metalization: While the paper did not detail on-chip metalization for MW delivery, 6CCVD offers in-house deposition of standard contacts (Au, Pt, Ti, Pd, Cu, W). This is crucial for fabricating high-performance on-chip microwave antennas or resonators (as referenced in the paper) directly onto the SCD surface.
  • Thickness Control: We offer precise control over substrate thickness, from 0.1 ”m SCD membranes (for ultimate proximity sensing) up to 10 mm thick substrates (for robust thermal management and handling).

The successful implementation of T2S relies on optimizing the diamond material properties (T1, T2) relative to the optical scanning speed (AOM/AOD performance).

6CCVD’s in-house PhD team specializes in the physics of N-V centers and can assist researchers with material selection and specification for similar Quantum Sensing and High-Speed Imaging projects. We ensure that the chosen diamond grade and defect density are optimized for the required pulse sequence duration and target SNR.

For custom specifications or material consultation, visit 6ccvd.com or contact our engineering team directly.

View Original Abstract

Optically active solid-state spin systems have been extensively studied in quantum technologies. We introduce a new readout scheme, termed “time-to-space” (T2S) encoding, which decouples spin manipulation from optical readout both temporally and spatially. This is achieved by simultaneously controlling the spin state within a region of interest, followed by rapid scanning of the optical readout position using an acousto-optic modulator. Time tracking allows the optical readout position to be encoded as a function of time. Using nitrogen-vacancy center ensembles in diamond, we demonstrate that the T2S scheme enables correlated experiments for efficient common-mode noise cancellation in various nano- and microscale sensing scenarios. Additionally, we show scalable multipixel imaging that does not require a camera and has the potential to accelerate data acquisition by several hundred times compared to conventional scanning methods. We anticipate widespread adoption of this technique, as it requires no additional components beyond those commonly used in experiments with optically adressable spin systems.