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Creation of NV centers by Phthalocyanine implantation into diamond

Shinobu Onoda, Kosuke Kimura, K. Yamada, Wataru Kada, Junichi Isoya, Tokuyuki Teraji, Hideyuki Watanabe, Kyotaro Kanehisa, Hiroshi Kawarada, Osamu Hanaizumi, Takeshi Ohshima, Onoda Shinobu, Kimura Kosuke, Yamada Keisuke, Ohshima Takeshi

Published Nov 4, 2020• 0 citations
OpenAlex

Abstract

A nitrogen vacancy (NV) center in diamond is known as a qubit with excellent magneto-optical properties at room temperature. Not only is NV center used for Quantum Information Processing (QIP), it is utilized for quantum sensing. The integrated NV centers in nanometer range have the potential of further improvement of sensitivity, etc. Ion implantation into diamond is known as one of the most popular methods for creating multiple qubits. In 2019, we have reported that the creation of three qubits was realized by implantation of the organic molecular (C5N4Hn) ion containing four nitrogen atoms1). In this study, we successfully developed Phthalocyanine (C32N8H18) ion beam for further integration of NV centers. After implantation and annealing, we succeeded to observe the fluorescence spots from NV centers. Fig. 1. shows schematic diagram of 284 keV-C32N8H18 ion implantation into diamond. Red, black, blue, and gray circles indicate nitrogen, carbon, hydrogen, and vacancy, respectively. Dashed circles indicate the NV centers. The average distance between nitrogen atoms is calculated to be 9±4 nm by SRIM (Stopping and Range In Matter) code. After annealing at 1000 oC for 2 hours in vacuum, the fluorescent image is observed by using home-build confocal laser scanning fluorescent microcopy.

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Creation of multiple NV centers by phthalocyanine ion implantation

Kosuke Kimura, Shinobu Onoda, K. Yamada +5 more

Abstract A nitrogen vacancy (NV) center in diamond is known as a solid-state spin qubit at room temperature. NV centers coherently coupled by dipole–dipole interactions have a potential to accomplish quantum registers at room temperature. This study reports to develop a phthalocyanine ion implantation technique to fabricate multiple dipole-coupled NV centers. Photon counts and optically detected magnetic resonance spectra show that up to four NV centers were successfully created in a confocal spot. The histogram of photon counts is fitted by a Poisson distribution, and the ratio of multiple NV spots suggests the potential for a five NV centers creation.

Applied Physics Express•May 16, 2022•6 citations

Generation and Characterization of NV Quantum Registers Using Isotopically Enriched Molecular Ions

Onoda Shinobu, Kimura Kosuke, Oguro Tsubasa +5 more

A nitrogen vacancy (NV) center in diamond is known as a solid-state spin quantum bit (qubit) at room temperature. The fabrication of scalable quantum registers based on NV centers is a long-standing issue. In 2005, spin-spin interaction between NV-N pairs, which were fabricated by N2 ion implantation, was reported. An entanglement between two electron-spin qubits becomes an excellent quantum information processing component, as accomplished by an NV-NV pair with a nanometer-scale distance in 2010 and 2013. More recently,strongly dipolar coupled NV-NV pairs were realized by 14N 30 keV implantationvia nanoholes in PMMA resist mask. The creation yields of NV-NV pairs dramatically improved, and the nanohole implantation had been thought to be the most promising technique to integrate NV centers. However, the problem of the technique is the finite size of nanoholes. The distribution of nitrogen atoms is determined by both ion straggling and nanohole diameter. The scaling of NV centers is stagnant up to two for several years. To overcome the barrier of triple NV centers, our previous research gave a ground-breaking idea of a highly populated NV center complex by introducing a molecular ion implantation technique in 2019. Since the molecular ion is regarded as an idea point source, the distribution of nitrogen atoms is determined by only ion straggling. Therefore, our proposed method is more effective than other implantation techniques including nanohole implantation. Instead of a pure nitrogen cluster which is commonly unstable, the stable organic molecular ions (adenine; C5N5H5) were utilized as the ion source. We successfully implanted C5N4Hn ions into single crystalline diamonds. Three NV centers were integrated, and the dipolar interactions among them were successfully observed. In 2022, we succeeded in creating more than 5 NV centers by phthalocyanine (C32H18N8) ion implantation. The next challenge is the implantation of isotopically enriched molecular ions. The isotopically enriched ion contains 13C and 15N. The implantation of isotopically enriched molecular ions is able to create 15NV-13C hybrid quantum registers. In this presentation, we will show the development of the isotopically enriched molecular ion beam and the characterization of created NV centers by laboratory-built confocal microscopy (CFM) and optically detected magnetic resonance (ODMR).

•Jul 7, 2025•0 citations

Hot ion implantation to create dense NV center ensembles in diamond

Midrel Wilfried Ngandeu Ngambou, Pauline Perrin, Ionuț Gabriel Balașa +9 more

Creating dense and shallow nitrogen-vacancy (NV) ensembles with good spin properties is a prerequisite for developing diamond-based quantum sensors exhibiting better performance. Ion implantation is a key enabling tool for precisely controlling spatial localization and density of NV color centers in diamond. However, it suffers from a low creation yield, while higher ion fluences significantly damage the crystal lattice. In this work, we realize N2+ ion implantation in the 30–40 keV range at high temperatures. At 800 °C, NV's ensemble photoluminescence emission is three to four times higher than room temperature implanted films, while narrow electron spin resonance linewidths of 1.5 MHz, comparable to well-established implantation techniques, are obtained. In addition, we found that ion fluences above 2 × 1014 ions/cm2 can be used without graphitization of the diamond film, in contrast to room temperature implantation. This study opens promising perspectives in optimizing diamond films with implanted NV ensembles that could be integrated into quantum sensing devices.

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Engineering of nitrogen-vacancy color centers in high purity diamond by ion implantation and annealing

Julius O. Orwa, Charles Santori, Kai‐Mei C. Fu +11 more

The negatively-charged nitrogen-vacancy (NV) center is the most studied optical center in diamond and is very important for applications in quantum information science. Many proposals for integrating NV centers in quantum and sensing applications rely on their tailored fabrication in ultra pure host material. In this study, we use ion implantation to controllably introduce nitrogen into high purity, low nitrogen chemical vapor deposition diamond samples. The properties of the resulting NV centers are studied as a function of implantation temperature, annealing temperature, and implantation fluence. We compare the implanted NV centers with native NV centers present deep in the bulk of the as-grown samples. The results for implanted NV centers are promising but indicate, at this stage, that the deep native NV centers possess overall superior optical properties. In particular, the implanted NV centers obtained after annealing at 2000 °C under a stabilizing pressure of 8 GPa showed an ensemble linewidth of 0.17 nm compared to 0.61 nm after annealing at 1000 °C. Over the same temperature range, the ensemble NV−/NV0 ratio increased by a factor of ∼5, although this was accompanied by an overall decrease in the NV count.

Journal of Applied Physics•Apr 15, 2011•122 citations

ダイヤモンドNV–¹³Cハイブリッド量子ビット生成に向けた L-アルギニン分子イオン注入エネルギーの最適化

Biswas Biswajit, P. Balasubramanian, Takenaka Kouta +3 more

The nitrogen-vacancy (NV) centers in diamond, also known as quantum bit operating at room temperature, have been recognized as a leading platform for quantum information and sensing. The electron spin of the NV center, along with the nuclear spins of the incorporated nitrogen atom and the neighboring isotope of carbon-13, act as a hybrid quantum register. By utilizing such quantum resister, quantum error correction, magnetic sensing and quantum teleportation have been demonstrated. Previously, we have developed ion beams of 65 keV adenine (C5N4Hn) containing four nitrogen atoms, 284 keV phthalocyanine (C32N8H18) containing eight nitrogen atoms, and 90 or 100 keV L-arginine (13C6H14 15N4O2) with isotopically enriched 13C and 15N. The implanted molecular ions are designed to dissociate into individual atoms at the surface, then progress through the diamond forming vacancies, halting with a spatial spread (~9±4 nm) for all molecular ions. The implanted nitrogen atoms combined with the vacancies via thermal treatment, forming the NV centers. In this study, we optimized the implantation energy of L-arginine ions to make a strong hyperfine coupling where the distance between NV and 13C is closer. A comparative analysis of the molecular ion energy for creating 15N-13C has been conducted where the resulting hybrid multi-qubits are characterized by pulsed optically detected magnetic resonance (ODMR), Ramsey spectroscopy, XY8 spectroscopy, etc. In the presentation we will explain the NV created by L-arginine implantation.

•Sep 8, 2026•0 citations

Hot ion implantation to create dense NV centre ensembles in diamond

Midrel Wilfried Ngandeu Ngambou, Perrin, Pauline, Ionuț Gabriel Balașa +9 more

Creating dense and shallow nitrogen vacancy (NV) ensembles with good spin properties, is a prerequisite for developing diamond-based quantum sensors exhibiting better performance. Ion implantation is a key enabling tool for precisely controlling spatial localisation and density of NV colour centres in diamond. However, it suffers from a low creation yield, while higher ion fluences significantly damage the crystal lattice. In this work, we realize N2 ion implantation in the 30 to 40 keV range at high temperatures. At 800 C, NV ensemble photoluminescence emission is three to four times higher than room temperature implanted films, while narrow electron spin resonance linewidths of 1.5 MHz, comparable to well established implantation techniques are obtained. In addition, we found that ion fluences above 2E14 ions per cm2 can be used without graphitization of the diamond film, in contrast to room temperature implantation. This study opens promising perspectives in optimizing diamond films with implanted NV ensembles that could be integrated into quantum sensing devices.

arXiv:2311.05328•Nov 9, 2023•0 citations
A nitrogen vacancy (NV) center in diamond is known as a qubit with excellent magneto-optical properties at room temperature. Not only is NV center used for Quantum Information Processing (QIP), it is utilized for quantum sensing. The integrated NV centers in nanometer range have the potential of further improvement of sensitivity, etc. Ion implantation into diamond is known as one of the most popular methods for creating multiple qubits. In 2019, we have reported that the creation of three qubits was realized by implantation of the organic molecular (C5N4Hn) ion containing four nitrogen atoms1). In this study, we successfully developed Phthalocyanine (C32N8H18) ion beam for further integration of NV centers. After implantation and annealing, we succeeded to observe the fluorescence spots from NV centers. Fig. 1. shows schematic diagram of 284 keV-C32N8H18 ion implantation into diamond. Red, black, blue, and gray circles indicate nitrogen, carbon, hydrogen, and vacancy, respectively. Dashed circles indicate the NV centers. The average distance between nitrogen atoms is calculated to be 9±4 nm by SRIM (Stopping and Range In Matter) code. After annealing at 1000 oC for 2 hours in vacuum, the fluorescent image is observed by using home-build confocal laser scanning fluorescent microcopy.
Abstract A nitrogen vacancy (NV) center in diamond is known as a solid-state spin qubit at room temperature. NV centers coherently coupled by dipole–dipole interactions have a potential to accomplish quantum registers at room temperature. This study reports to develop a phthalocyanine ion implantation technique to fabricate multiple dipole-coupled NV centers. Photon counts and optically detected magnetic resonance spectra show that up to four NV centers were successfully created in a confocal spot. The histogram of photon counts is fitted by a Poisson distribution, and the ratio of multiple NV spots suggests the potential for a five NV centers creation.
A nitrogen vacancy (NV) center in diamond is known as a solid-state spin quantum bit (qubit) at room temperature. The fabrication of scalable quantum registers based on NV centers is a long-standing issue. In 2005, spin-spin interaction between NV-N pairs, which were fabricated by N2 ion implantation, was reported. An entanglement between two electron-spin qubits becomes an excellent quantum information processing component, as accomplished by an NV-NV pair with a nanometer-scale distance in 2010 and 2013. More recently,strongly dipolar coupled NV-NV pairs were realized by 14N 30 keV implantationvia nanoholes in PMMA resist mask. The creation yields of NV-NV pairs dramatically improved, and the nanohole implantation had been thought to be the most promising technique to integrate NV centers. However, the problem of the technique is the finite size of nanoholes. The distribution of nitrogen atoms is determined by both ion straggling and nanohole diameter. The scaling of NV centers is stagnant up to two for several years. To overcome the barrier of triple NV centers, our previous research gave a ground-breaking idea of a highly populated NV center complex by introducing a molecular ion implantation technique in 2019. Since the molecular ion is regarded as an idea point source, the distribution of nitrogen atoms is determined by only ion straggling. Therefore, our proposed method is more effective than other implantation techniques including nanohole implantation. Instead of a pure nitrogen cluster which is commonly unstable, the stable organic molecular ions (adenine; C5N5H5) were utilized as the ion source. We successfully implanted C5N4Hn ions into single crystalline diamonds. Three NV centers were integrated, and the dipolar interactions among them were successfully observed. In 2022, we succeeded in creating more than 5 NV centers by phthalocyanine (C32H18N8) ion implantation. The next challenge is the implantation of isotopically enriched molecular ions. The isotopically enriched ion contains 13C and 15N. The implantation of isotopically enriched molecular ions is able to create 15NV-13C hybrid quantum registers. In this presentation, we will show the development of the isotopically enriched molecular ion beam and the characterization of created NV centers by laboratory-built confocal microscopy (CFM) and optically detected magnetic resonance (ODMR).
Creating dense and shallow nitrogen-vacancy (NV) ensembles with good spin properties is a prerequisite for developing diamond-based quantum sensors exhibiting better performance. Ion implantation is a key enabling tool for precisely controlling spatial localization and density of NV color centers in diamond. However, it suffers from a low creation yield, while higher ion fluences significantly damage the crystal lattice. In this work, we realize N2+ ion implantation in the 30–40 keV range at high temperatures. At 800 °C, NV's ensemble photoluminescence emission is three to four times higher than room temperature implanted films, while narrow electron spin resonance linewidths of 1.5 MHz, comparable to well-established implantation techniques, are obtained. In addition, we found that ion fluences above 2 × 1014 ions/cm2 can be used without graphitization of the diamond film, in contrast to room temperature implantation. This study opens promising perspectives in optimizing diamond films with implanted NV ensembles that could be integrated into quantum sensing devices.
The negatively-charged nitrogen-vacancy (NV) center is the most studied optical center in diamond and is very important for applications in quantum information science. Many proposals for integrating NV centers in quantum and sensing applications rely on their tailored fabrication in ultra pure host material. In this study, we use ion implantation to controllably introduce nitrogen into high purity, low nitrogen chemical vapor deposition diamond samples. The properties of the resulting NV centers are studied as a function of implantation temperature, annealing temperature, and implantation fluence. We compare the implanted NV centers with native NV centers present deep in the bulk of the as-grown samples. The results for implanted NV centers are promising but indicate, at this stage, that the deep native NV centers possess overall superior optical properties. In particular, the implanted NV centers obtained after annealing at 2000 °C under a stabilizing pressure of 8 GPa showed an ensemble linewidth of 0.17 nm compared to 0.61 nm after annealing at 1000 °C. Over the same temperature range, the ensemble NV−/NV0 ratio increased by a factor of ∼5, although this was accompanied by an overall decrease in the NV count.
The nitrogen-vacancy (NV) centers in diamond, also known as quantum bit operating at room temperature, have been recognized as a leading platform for quantum information and sensing. The electron spin of the NV center, along with the nuclear spins of the incorporated nitrogen atom and the neighboring isotope of carbon-13, act as a hybrid quantum register. By utilizing such quantum resister, quantum error correction, magnetic sensing and quantum teleportation have been demonstrated. Previously, we have developed ion beams of 65 keV adenine (C5N4Hn) containing four nitrogen atoms, 284 keV phthalocyanine (C32N8H18) containing eight nitrogen atoms, and 90 or 100 keV L-arginine (13C6H14 15N4O2) with isotopically enriched 13C and 15N. The implanted molecular ions are designed to dissociate into individual atoms at the surface, then progress through the diamond forming vacancies, halting with a spatial spread (~9±4 nm) for all molecular ions. The implanted nitrogen atoms combined with the vacancies via thermal treatment, forming the NV centers. In this study, we optimized the implantation energy of L-arginine ions to make a strong hyperfine coupling where the distance between NV and 13C is closer. A comparative analysis of the molecular ion energy for creating 15N-13C has been conducted where the resulting hybrid multi-qubits are characterized by pulsed optically detected magnetic resonance (ODMR), Ramsey spectroscopy, XY8 spectroscopy, etc. In the presentation we will explain the NV created by L-arginine implantation.
Creating dense and shallow nitrogen vacancy (NV) ensembles with good spin properties, is a prerequisite for developing diamond-based quantum sensors exhibiting better performance. Ion implantation is a key enabling tool for precisely controlling spatial localisation and density of NV colour centres in diamond. However, it suffers from a low creation yield, while higher ion fluences significantly damage the crystal lattice. In this work, we realize N2 ion implantation in the 30 to 40 keV range at high temperatures. At 800 C, NV ensemble photoluminescence emission is three to four times higher than room temperature implanted films, while narrow electron spin resonance linewidths of 1.5 MHz, comparable to well established implantation techniques are obtained. In addition, we found that ion fluences above 2E14 ions per cm2 can be used without graphitization of the diamond film, in contrast to room temperature implantation. This study opens promising perspectives in optimizing diamond films with implanted NV ensembles that could be integrated into quantum sensing devices.