School of Physics - Research Publications

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    Photon extraction enhancement of praseodymium ions in gallium nitride nanopillars
    Sato, S-I ; Li, S ; Greentree, ADD ; Deki, M ; Nishimura, T ; Watanabe, H ; Nitta, S ; Honda, Y ; Amano, H ; Gibson, BCC ; Ohshima, T (NATURE PORTFOLIO, 2022-12-08)
    Lanthanoid-doped Gallium Nitride (GaN) integrated into nanophotonic technologies is a promising candidate for room-temperature quantum photon sources for quantum technology applications. We manufactured praseodymium (Pr)-doped GaN nanopillars of varying size, and showed significantly enhanced room-temperature photon extraction efficiency compared to unstructured Pr-doped GaN. Implanted Pr ions in GaN show two main emission peaks at 650.3 nm and 651.8 nm which are attributed to 3P0-3F2 transition in the 4f-shell. The maximum observed enhancement ratio was 23.5 for 200 nm diameter circular pillars, which can be divided into the emitted photon extraction enhancement by a factor of 4.5 and the photon collection enhancement by a factor of 5.2. The enhancement mechanism is explained by the eigenmode resonance inside the nanopillar. Our study provides a pathway for Lanthanoid-doped GaN nano/micro-scale photon emitters and quantum technology applications.
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    Vitrification within a nanoliter volume: oocyte and embryo cryopreservation within a 3D photopolymerized device (August, 10.1007/s10815-022-02589-8, 2022)
    Yagoub, SH ; Lim, M ; Tan, TCY ; Chow, DJX ; Dholakia, K ; Gibson, BC ; Thompson, JG ; Dunning, KR (SPRINGER/PLENUM PUBLISHERS, 2022-10)
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    Vitrification within a nanoliter volume: oocyte and embryo cryopreservation within a 3D photopolymerized device
    Yagoub, SH ; Lim, M ; Tan, TCY ; Chow, DJX ; Dholakia, K ; Gibson, BC ; Thompson, JG ; Dunning, KR (SPRINGER/PLENUM PUBLISHERS, 2022-09)
    PURPOSE: Vitrification permits long-term banking of oocytes and embryos. It is a technically challenging procedure requiring direct handling and movement of cells between potentially cytotoxic cryoprotectant solutions. Variation in adherence to timing, and ability to trace cells during the procedure, affects survival post-warming. We hypothesized that minimizing direct handling will simplify the procedure and improve traceability. To address this, we present a novel photopolymerized device that houses the sample during vitrification. METHODS: The fabricated device consisted of two components: the Pod and Garage. Single mouse oocytes or embryos were housed in a Pod, with multiple Pods docked into a Garage. The suitability of the device for cryogenic application was assessed by repeated vitrification and warming cycles. Oocytes or early blastocyst-stage embryos were vitrified either using standard practice or within Pods and a Garage and compared to non-vitrified control groups. Post-warming, we assessed survival rate, oocyte developmental potential (fertilization and subsequent development) and metabolism (autofluorescence). RESULTS: Vitrification within the device occurred within ~ 3 nL of cryoprotectant: this volume being ~ 1000-fold lower than standard vitrification. Compared to standard practice, vitrification and warming within our device showed no differences in viability, developmental competency, or metabolism for oocytes and embryos. The device housed the sample during processing, which improved traceability and minimized handling. Interestingly, vitrification-warming itself, altered oocyte and embryo metabolism. CONCLUSION: The Pod and Garage system minimized the volume of cryoprotectant at vitrification-by ~ 1000-fold-improved traceability and reduced direct handling of the sample. This is a major step in simplifying the procedure.
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    Magnetic-field-dependent stimulated emission from nitrogen-vacancy centers in diamond
    Hahl, FA ; Lindner, L ; Vidal, X ; Luo, T ; Ohshima, T ; Onoda, S ; Ishii, S ; Zaitsev, AM ; Capelli, M ; Gibson, BC ; Greentree, AD ; Jeske, J (AMER ASSOC ADVANCEMENT SCIENCE, 2022-06-03)
    Negatively charged nitrogen-vacancy (NV) centers in diamond are promising magnetic field quantum sensors. Laser threshold magnetometry theory predicts improved NV center ensemble sensitivity via increased signal strength and magnetic field contrast. Here, we experimentally demonstrate laser threshold magnetometry. We use a macroscopic high-finesse laser cavity containing a highly NV-doped and low absorbing diamond gain medium that is pumped at 532 nm and resonantly seeded at 710 nm. This enables a 64% signal power amplification by stimulated emission. We test the magnetic field dependency of the amplification and thus demonstrate magnetic field-dependent stimulated emission from an NV center ensemble. This emission shows an ultrahigh contrast of 33% and a maximum output power in the milliwatt regime. The coherent readout of NV centers pave the way for novel cavity and laser applications of quantum defects and diamond NV magnetic field sensors with substantially improved sensitivity for the health, research, and mining sectors.
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    Proximal nitrogen reduces the fluorescence quantum yield of nitrogen-vacancy centres in diamond
    Capelli, M ; Lindner, L ; Luo, T ; Jeske, J ; Abe, H ; Onoda, S ; Ohshima, T ; Johnson, B ; Simpson, DA ; Stacey, A ; Reineck, P ; Gibson, BC ; Greentree, AD (IOP Publishing Ltd, 2022-03-01)
    Abstract The nitrogen-vacancy colour centre in diamond is emerging as one of the most important solid-state quantum systems. It has applications to fields including high-precision sensing, quantum computing, single photon communication, metrology, nanoscale magnetic imaging and biosensing. For all of these applications, a high quantum yield of emitted photons is desirable. However, diamond samples engineered to have high densities of nitrogen-vacancy centres show levels of brightness varying significantly within single batches, or even within the same sample. Here we show that nearby nitrogen impurities quench emission of nitrogen-vacancy centres via non-radiative transitions, resulting in a reduced fluorescence quantum yield. We monitored the emission properties of nitrogen-vacancy centre ensembles from synthetic diamond samples with different concentrations of nitrogen impurities. All samples were irradiated with high energy electrons to create high densities of nitrogen-vacancy centres relative to the concentration of nitrogen impurities. While at low nitrogen densities of 1.81 ppm we measured a lifetime of 13.9 ns, we observed a strong reduction in lifetime with increasing nitrogen density. We measure a lifetime as low as 4.4 ns at a nitrogen density of 380 ppm. The change in lifetime matches a reduction in relative fluorescence quantum yield from 77.4% to 32% with an increase in nitrogen density from 88 ppm to 380 ppm, respectively. These results will inform the conditions required to optimise the properties of diamond crystals devices based on the fluorescence of nitrogen-vacancy centres. Furthermore, this work provides insights into the origin of inhomogeneities observed in high-density nitrogen-vacancy ensembles within diamonds and nanodiamonds.
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    Optical properties of neodymium ions in nanoscale regions of gallium nitride: erratum
    Sato, S-I ; Deki, M ; Watanabe, H ; Nitta, S ; Honda, Y ; Nishimura, T ; Gibson, BC ; Greentree, AD ; Amano, H ; Ohshima, T (The Optical Society, 2021-02-01)
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    Optical properties of neodymium ions in nanoscale regions of gallium nitride (vol 10, pg 2614, 2020)
    Sato, S-I ; Deki, M ; Watanabe, H ; Nitta, S ; Honda, Y ; Nishimura, T ; Gibson, BC ; Greentree, AD ; Amano, H ; Ohshima, T (OPTICAL SOC AMER, 2021-02-01)
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    Fabrication on the microscale: a two-photon polymerized device for oocyte microinjection
    Yagoub, SH ; Thompson, JG ; Orth, A ; Dholakia, K ; Gibson, BC ; Dunning, KR (SPRINGER/PLENUM PUBLISHERS, 2022-07)
    PURPOSE: Intracytoplasmic sperm injection (ICSI) addresses male sub-fertility by injecting a spermatozoon into the oocyte. This challenging procedure requires the use of dual micromanipulators, with success influenced by inter-operator expertise. We hypothesized that minimizing oocyte handling during ICSI will simplify the procedure. To address this, we designed and fabricated a micrometer scale device that houses the oocyte and requires only one micromanipulator for microinjection. METHODS: The device consisted of 2 components, each of sub-cubic millimeter volume: a Pod and a Garage. These were fabricated using 2-photon polymerization. Toxicity was evaluated by culturing single-mouse presumptive zygotes (PZs) to the blastocyst stage within a Pod, with several Pods (and embryos) docked in a Garage. The development was compared to standard culture. The level of DNA damage/repair in resultant blastocysts was quantified (γH2A.X immunohistochemistry). To demonstrate the capability to carry out ICSI within the device, PZs were microinjected with 4-μm fluorescent microspheres and cultured to the blastocyst stage. Finally, the device was assessed for oocyte traceability and high-throughput microinjection capabilities and compared to standard microinjection practice using key parameters (pipette setup, holding then injecting oocytes). RESULTS: Compared to standard culture, embryo culture within Pods and a Garage showed no differences in development to the blastocyst stage or levels of DNA damage in resultant blastocysts. Furthermore, microinjection within our device removes the need for a holding pipette, improves traceability, and facilitates high-throughput microinjection. CONCLUSION: This novel device could improve embryo production following ICSI by simplifying the procedure and thus decreasing inter-operator variability.
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    Targeting cell surface glycans with lectin-coated fluorescent nanodiamonds
    Fard, MG ; Khabir, Z ; Reineck, P ; Cordina, NM ; Abe, H ; Ohshima, T ; Dalal, S ; Gibson, BC ; Packer, NH ; Parker, LM (ROYAL SOC CHEMISTRY, 2022-03-15)
    Glycosylation is arguably the most important functional post-translational modification in brain cells and abnormal cell surface glycan expression has been associated with neurological diseases and brain cancers. In this study we developed a novel method for uptake of fluorescent nanodiamonds (FND), carbon-based nanoparticles with low toxicity and easily modifiable surfaces, into brain cell subtypes by targeting their glycan receptors with carbohydrate-binding lectins. Lectins facilitated uptake of 120 nm FND with nitrogen-vacancy centers in three types of brain cells - U87-MG astrocytes, PC12 neurons and BV-2 microglia cells. The nanodiamond/lectin complexes used in this study target glycans that have been described to be altered in brain diseases including sialic acid glycans via wheat (Triticum aestivum) germ agglutinin (WGA), high mannose glycans via tomato (Lycopersicon esculentum) lectin (TL) and core fucosylated glycans via Aleuria aurantia lectin (AAL). The lectin conjugated nanodiamonds were taken up differently by the various brain cell types with fucose binding AAL/FNDs taken up preferentially by glioblastoma phenotype astrocyte cells (U87-MG), sialic acid binding WGA/FNDs by neuronal phenotype cells (PC12) and high mannose binding TL/FNDs by microglial cells (BV-2). With increasing recognition of glycans having a role in many diseases, the lectin bioconjugated nanodiamonds developed here are well suited for further investigation into theranostic applications.
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    Near-Infrared Fluorescence from Silicon- and Nickel-Based Color Centers in High-Pressure High-Temperature Diamond Micro- and Nanoparticles
    Shames, AI ; Dalis, A ; Greentree, AD ; Gibson, BC ; Abe, H ; Ohshima, T ; Shenderova, O ; Zaitsev, A ; Reineck, P (WILEY-V C H VERLAG GMBH, 2020-12)
    Abstract Fluorescent color centers in diamond are invaluable room temperature quantum systems in fundamental scientific studies and vital for many emerging applications from inertial navigation to quantum sensing in biology. Yet, controlled production of specific color centers in synthetic diamond at scale remains challenging. Characteristics of silicon‐ and nickel‐based defects with strong fluorescence in the 700–950 nm spectral region formed in Si‐ and Ni‐doped diamond, created via high‐pressure high‐temperature synthesis in commercial quantities without irradiation, are reported. Using electron paramagnetic resonance spectroscopy and fluorescence spectroscopy, the presence of defects including the negatively charged silicon‐vacancy (SiV−), silicon‐boron (SiB) and positively charged substitutional nickel center (Nis+) in micrometer‐sized particles is identified and quantified. The color centers’ optical properties are investigated via time‐resolved and steady‐state fluorescence spectroscopy below 10 K and at room temperature. In ensemble measurements, the particles show no detectable signals from nitrogen‐vacancy (NV−) defects. The particles’ relative fluorescence brightness is quantified and compared to particles containing ≈1 ppm NV− centers. It is demonstrated that the Nis+ center fluorescence characteristics are preserved in 50 nm nanoparticles. The work paves the way for the use of fluorescent nanodiamonds in the first near‐infrared biological window between 700 nm and 950 nm in biomedical applications.