Showing papers by "Anke Krueger published in 2014"

Tapered fiber coupling of single photons emitted by a deterministically positioned single nitrogen vacancy center

Abstract: A diamond nano-crystal hosting a single nitrogen vacancy (NV) center is optically selected with a confocal scanning microscope and positioned deterministically onto the subwavelength-diameter waist of a tapered optical fiber (TOF) with the help of an atomic force microscope. Based on this nano-manipulation technique, we experimentally demonstrate the evanescent coupling of single fluorescence photons emitted by a single NV-center to the guided mode of the TOF. By comparing photon count rates of the fiber-guided and the free-space modes and with the help of numerical finite-difference time domain simulations, we determine a lower and upper bound for the coupling efficiency of (9.5 ± 0.6)% and (10.4 ± 0.7)%, respectively. Our results are a promising starting point for future integration of single photon sources into photonic quantum networks and applications in quantum information science.

Toward deep blue nano hope diamonds : heavily boron-doped diamond nanoparticles

Abstract: The production of boron-doped diamond nanoparticles enables the application of this material for a broad range of fields, such as electrochemistry, thermal management, and fundamental superconductivity research. Here we present the production of highly boron-doped diamond nanoparticles using boron-doped CVD diamond films as a starting material. In a multistep milling process followed by purification and surface oxidation we obtained diamond nanoparticles of 10–60 nm with a boron content of approximately 2.3 × 1021 cm–3. Aberration-corrected HRTEM reveals the presence of defects within individual diamond grains, as well as a very thin nondiamond carbon layer at the particle surface. The boron K-edge electron energy-loss near-edge fine structure demonstrates that the B atoms are tetrahedrally embedded into the diamond lattice. The boron-doped diamond nanoparticles have been used to nucleate growth of a boron-doped diamond film by CVD that does not contain an insulating seeding layer.

Synthesis of nanodiamond derivatives carrying amino functions and quantification by a modified Kaiser test.

Abstract: Nanodiamonds functionalized with different organic moieties carrying terminal amino groups have been synthesized. These include conjugates generated by Diels–Alder reactions of ortho-quinodimethanes formed in situ from pyrazine and 5,6-dihydrocyclobuta[d]pyrimidine derivatives. For the quantification of primary amino groups a modified photometric assay based on the Kaiser test has been developed and validated for different types of aminated nanodiamond. The results correspond well to values obtained by thermogravimetry. The method represents an alternative wet-chemical quantification method in cases where other techniques like elemental analysis fail due to unfavourable combustion behaviour of the analyte or other impediments.

Room-temperature near-infrared silicon carbide nanocrystalline emitters based on optically aligned spin defects

Abstract: Bulk silicon carbide (SiC) is a very promising material system for bio-applications and quantum sensing. However, its optical activity lies beyond the near infrared spectral window for in-vivo imaging and fiber communications due to a large forbidden energy gap. Here, we report the fabrication of SiC nanocrystals and isolation of different nanocrystal fractions ranged from 600 nm down to 60 nm in size. The structural analysis reveals further fragmentation of the smallest nanocrystals into ca. 10-nm-size clusters of high crystalline quality, separated by amorphization areas. We use neutron irradiation to create silicon vacancies, demonstrating near infrared photoluminescence. Finally, we detect room-temperature spin resonances of these silicon vacancies hosted in SiC nanocrystals. This opens intriguing perspectives to use them not only as in-vivo luminescent markers but also as magnetic field and temperature sensors, allowing for monitoring various physical, chemical, and biological processes.

Electronic spectroscopy of 1-(phenylethynyl)naphthalene.

Abstract: Recently 1-(phenylethynyl)naphthalene (1-PEN) was suggested to be the primary dimerization product of phenylpropargyl radicals and therefore an important polycyclic hydrocarbon in combustion processes. Here we describe a spectroscopic investigation of a genuine 1-PEN sample by several complementary techniques, infrared spectroscopy, multiphoton ionization (MPI), and threshold photoelectron spectroscopy. The infrared spectrum recorded in a gas cell confirms that 1-PEN is indeed the previously observed dimerization product of phenylpropargyl. The origin of the transition into the electronically excited S1 state lies at 30823 cm(-1), as found by MPI. Considerable vibrational activity is observed, and a number of low-wavenumber bands are assigned to a progression in the torsional motion. Values of 6 cm(-1) (S0) and 17 cm(-1) (S1) were derived for the fundamental of the torsion. In the investigated energy range the excited state lifetimes are in the nanosecond range. Spectra of the 1-PEN/Ar cluster exhibit a red shift of the electronic origin of 22 cm(-1), in good agreement with other aromatic molecules. A threshold photoelectron spectrum recorded using synchrotron radiation yields an ionization energy of 7.58 eV for 1-PEN. An excited electronic state of the cation is found at 7.76 eV, and dissociative photoionization does not set in below 15 eV.

Room-temperature near-infrared silicon carbide nanocrystalline emitters based on optically aligned spin defects

Abstract: Bulk silicon carbide (SiC) is a very promising material system for bio-applications and quantum sensing. However, its optical activity lies beyond the near infrared spectral window for in-vivo imaging and fiber communications due to a large forbidden energy gap. Here, we report the fabrication of SiC nanocrystals and isolation of different nanocrystal fractions ranged from 600 nm down to 60 nm in size. The structural analysis reveals further fragmentation of the smallest nanocrystals into ca. 10-nm-size clusters of high crystalline quality, separated by amorphization areas. We use neutron irradiation to create silicon vacancies, demonstrating near infrared photoluminescence. Finally, we detect, for the first time, room-temperature spin resonances of these silicon vacancies hosted in SiC nanocrystals. This opens intriguing perspectives to use them not only as in-vivo luminescent markers, but also as magnetic field and temperature sensors, allowing for monitoring various physical, chemical and biological processes.