Ultracompact directional optical nanoantennas are rapidly gaining popularity yet still challenging tasks to construct at the nanoscale. Here, we experimentally demonstrate unidirectional emission from a fluorescent nanodiamond coupled with a single gold nanorod. Different configurations of the assembled hybrid nanostructures were realized via step‐by‐step atomic force microscope nanomanipulation. The emission patterns can be controlled by adjusting the configurations, i.e., the gold nanorod orientation and separation with respect to the nanodiamond. Numerical simulation results reveal that the unidirectional emission can be ascribed to the interference between the electromagnetic fields produced by the dipole‐like source and the out‐of‐phase dipole induced in the gold nanorod. The proposed hybrid nanostructures remarkably exhibit highly unidirectional emission even when the emitter is positioned up to 50 nm away from the nanorod antenna and present a broad working spectral bandwidth of ∼200 nm. The distinct features of this hybrid structure suggest potential applications for novel nanoscale light sources, sensing, and quantum information.
Transparent and flexible carbon doped ZnO (C:ZnO) field emission device was successfully fabricated on an arylite substrate. Excellent adhesion of deposited C:ZnO on the flexible substrate was achieved with low sputtering power and Ar flow rate. In the fabricated device, nanostructured C:ZnO and as‐deposited thin films were used as field emitter and phosphor screen, respectively. The C:ZnO thin film showed a transparency of about 80% at 550 nm wavelength and average sheet resistance of 1.96 kΩ/□. The C:ZnO phosphor screen emitted red light during the field emission measurement, correlating the dominant cathodoluminescence peak at 646 nm. Thus, a promising transparent and flexible field emission display can be realized with C:ZnO based material.
Transparent and flexible C:ZnO film phosphor screen (anode) and nanocone emitters (cathode) for field emission device. 相似文献
We propose a ring-groove nanostructure which can achieve toroidal dipolar resonance under normal incidence, and find that this design, due to the strong field confinement for this dipolar resonance, can simultaneously enhance the radiative decay rate and achieve high degree of linear polarization of the fluorescence emission. In addition, both radiation enhancement and degree of linear polarization are higher than those by other structure that cannot obtain toroidal dipolar resonance. It is expected that this design can promote the development of polarized light-emitting devices with enhanced emission intensity and potentially functional toroidal metasurface lasers. 相似文献
Metasurfaces, which consist of resonant metamaterial elements in the form of two‐dimensional thin planar structures, retain great capabilities in manipulating electromagnetic wave and potential applications in modifying interaction with fluorescent molecules. The metasurfaces with magnetic responses are favorable to weakening fluorescence quenching while less investigated in controlling fluorescence. In this paper, we demonstrate control over fluorescence emission by engineering the magnetic and electric modes in plasmonic metasurfaces consisting of 45‐nm‐thick gold split‐ring‐resonators (SRRs). The fluorescence emission exhibits an enhancement factor of ∼18 and is predominantly x‐polarized with assistance of the magnetic mode excited by oblique incidence with an x‐polarized electric field. The magnetic and electric modes excited by oblique incidence with a y‐polarized electric field contribute to the rotation of emission polarization with respect to the incident polarization. The results demonstrate manipulating the interaction of fluorescent emitters with different resonant modes of the SRR‐based metasurface at the nanoscale by the polarization of incident light, providing potential applications of metasurfaces in a wide variety of areas, including optical nanosources, fluorescence spectroscopy and compact biosensors.
下载免费PDF全文