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Highly integrated color center creation with cooled hydrogenated molecules irradiation

MetadataDetails
Publication Date2025-07-09
JournalEPJ Quantum Technology
AuthorsMasatomi Iizawa, Yasuhito Narita
AnalysisFull AI Review Included

Technical Documentation & Analysis: Highly Integrated Color Center Creation

Section titled “Technical Documentation & Analysis: Highly Integrated Color Center Creation”

This documentation analyzes the research on deterministic qubit creation via cooled hydrogenated molecular ion irradiation, highlighting the critical role of high-purity diamond substrates and connecting the technical requirements to 6CCVD’s advanced MPCVD capabilities.

  • Research Focus: Achieving highly integrated, deterministic creation of solid-state qubits (specifically Nitrogen Vacancy, NV, color centers) in diamond via ultra-precise ion irradiation.
  • Technical Breakthrough: Proposal for direct laser cooling of hydrogenated molecular ions (XH$^{+/-}$), such as NH$^{+}$, to replace problematic sympathetic cooling methods.
  • Precision Target: The methodology aims for Ångström-order positional accuracy for single-ion doping, essential for scalable quantum device integration.
  • Performance Improvement: Direct cooling of NH$^{+}$ is theoretically estimated to reach 6.63 ”K, significantly colder than the 0.54 mK achieved by sympathetically cooled Ca$^{+}$. This temperature reduction is key to minimizing ion beam emittance.
  • Integration Advantage: Direct cooling eliminates the need for removing alkaline earth metal ions (contaminants) and drastically shortens the required cooling time, enabling the production of 1 million qubits much faster than the estimated 116+ days required by previous methods.
  • Material Requirement: The success of this technique relies on ultra-high purity, low-defect Single Crystal Diamond (SCD) substrates suitable for NV center formation and high-energy ion implantation.
ParameterValueUnitContext
Target Doping AccuracyÅngström orderN/AEssential for scalable qubit integration
NH$^{+}$ Cooling Temperature (Theoretical)6.63”KAchieved via direct laser cooling
NH$^{-}$ Cooling Temperature (Theoretical)4.47”KAchieved via direct laser cooling
Sympathetic Cooling Temperature (Ca$^{+}$)0.54mKReference for previous methods
NH$^{+}$ Laser Cooling Wavelength438.5nmVisible laser source required for transition
NH$^{+}$ Excited State Lifetime384nsRequired for efficient cooling
Paul Trap 1σ Radial Displacement (NH$^{+}$)50.2nmAfter Paul trap, before conventional focusing optics
Paul Trap 1σ Radial Displacement (Microfabricated)5 x 10-10mAchieved by reducing trap distance (r0) to 3 x 10-4 m
Ion Output Rate (Sympathetic Cooling Limit)0.1cpsRate limiting factor for large-scale integration
Required Qubits for Application1millionTarget for practical quantum devices

The research proposes a novel ion doping technique using a Paul trap to overcome the limitations of sympathetic cooling, focusing on direct laser cooling of hydrogenated molecular ions.

  1. Paul Trap Ion Source: A Paul trap is used to confine ions in a string-like crystal structure, providing an ultra-low emittance source capable of outputting single atoms one-by-one.
  2. Shift from Sympathetic Cooling: Previous methods relied on sympathetic cooling (using laser-coolable ions like Ca$^{+}$ to cool non-coolable dopants like N$^{+}$). This method introduced three major obstacles:
    • Inability to distinguish dopant ions from contamination (“shadow” detection).
    • Excessively long cooling times (116+ days for 1 million qubits).
    • Requirement for a complex mechanism to remove the alkaline earth metal ions (contaminants) at the output.
  3. Direct Cooling of Hydrogenated Ions (XH$^{+/-}$): The solution involves using hydrogenated molecular ions (e.g., NH$^{+}$) which are theoretically laser-coolable using readily available visible light sources (438.5 nm).
  4. Temperature Reduction: Direct cooling of NH$^{+}$ is predicted to achieve temperatures in the low ”K range (6.63 ”K), a factor of ~1000 improvement over sympathetically cooled Ca$^{+}$ (0.54 mK).
  5. Precision via Emittance Control: The reduced ion temperature minimizes the radial displacement (50.2 nm 1σ radius), which, when combined with conventional focusing optics (e.g., einzel lenses), enables Ångström-order positional accuracy.
  6. Microfabrication Potential: Further precision (down to 0.5 nm) can be achieved by implementing MEMS-based surface electrode traps to reduce the electrode distance (r0), leveraging the inverse fourth power dependence of the radial trapping force (kr is proportional to r0-4).

6CCVD provides the essential foundation—high-purity diamond substrates—required to realize integrated solid-state quantum devices based on this advanced ion implantation technique. Our capabilities directly address the material and precision requirements of Ångström-level doping.

To ensure high qubit coherence (T2) and deterministic NV center formation, the substrate must be ultra-low in native defects and contaminants.

  • Optical Grade Single Crystal Diamond (SCD):
    • Requirement: SCD with extremely low native nitrogen concentration (< 1 ppb) is mandatory. This ensures that the only nitrogen atoms present are those intentionally implanted via the Paul trap, guaranteeing deterministic doping.
    • 6CCVD Offering: High-purity SCD plates, optimized for minimal strain and maximum optical transparency, ideal for subsequent laser annealing and optical readout.
  • Boron-Doped Diamond (BDD):
    • Application Extension: While the paper focuses on NV centers, BDD substrates are available for researchers exploring alternative solid-state qubits or integrated quantum sensing applications requiring conductive diamond layers.

The integration of Paul traps and ion beam optics requires highly specific, precision-engineered substrates. 6CCVD offers comprehensive customization services:

Requirement6CCVD CapabilityTechnical Advantage
Substrate Size & ThicknessCustom plates/wafers up to 125mm (PCD). SCD thicknesses from 0.1”m to 500”m. Substrates up to 10mm thick.Provides flexibility for integrating diamond into high-vacuum ion beam systems and for controlling the implantation depth of high-energy ions.
Surface QualityPolishing to achieve Ra < 1nm (SCD) and Ra < 5nm (Inch-size PCD).Essential for minimizing surface scattering and defects, which is critical for shallow NV center creation and subsequent integration with micro-optics or MEMS traps.
Integrated CircuitryInternal metalization capability: Au, Pt, Pd, Ti, W, Cu.Enables the fabrication of surface electrode traps (MEMS-based Paul traps) directly onto the diamond substrate, reducing noise and improving positional accuracy.
Precision ShapingCustom laser cutting and shaping services.Allows for the creation of specific geometries required for quantum photonic integration (e.g., diamond waveguides or resonators).

The realization of integrated solid-state quantum devices requires expertise spanning material science and quantum physics.

  • 6CCVD’s in-house PhD team offers authoritative professional support in material selection, optimizing diamond growth parameters (e.g., nitrogen concentration control) and advising on post-growth processing (e.g., annealing temperatures and atmospheres) necessary for successful NV center activation following Ångström-level ion implantation.

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

View Original Abstract

Abstract Photoluminescent point defects, such as nitrogen vacancy (NV) color centers in diamond, have attracted much attention as solid-state qubits. In recent years, a method has been developed to dope ions one-by-one into a solid substrate with Ångström position accuracy using a Paul trap. However, the dopant atoms must be laser-cooled, and the atoms that are promising dopants for solid-state quantum devices, such as nitrogen, cannot be directly applied. In the previous studies, the cooling of the dopant ions has been achieved using a sympathetic cooling technique, in which the laser-cooled atoms are sandwiched, but this method has several problems such as the need for a mechanism to remove the laser-cooled atoms and the inability to distinguish between the dopant atoms and contaminations. We show that these problems can be overcome by directly cooling the hydrogenated ions instead of sympathetically cooling the ions, and the position accuracy can be improved.