ABSTRACT
Whispering-gallery-mode (WGM) microresonators are a promising platform for highly sensitive, label-free detection and probing of individual nano-objects. Our work expands these capabilities by providing the analysis tools required for three-dimensional (3D) characterization of arbitrarily shaped nanoparticles. Specifically, we introduce a theoretical model that describes interactions between nanoparticles and WGM resonators, taking into account effects that were often not considered, such as the elliptical polarization of the transverse-magnetic (TM) mode, the possible non-spherical shape of the nanoparticle, its finite size, and the open-system nature of the modes. We also introduce a self referencing measurement method that allows the extraction of information from measurements done at arbitrary positions of the nanoparticles within the WGM. We verify our model by experimentally probing a single Tungsten-disulfide (WS2) nanotube with a silica microtoroid resonator inside a scanning electron-microscope (SEM) and perform 3D characterization of the nanotube.
ABSTRACT
Spectroscopy of whispering-gallery mode microresonators has become a powerful scientific tool, enabling the detection of single viruses, nanoparticles and even single molecules. Yet the demonstrated timescale of these schemes has been limited so far to milliseconds or more. Here we introduce a scheme that is orders of magnitude faster, capable of capturing complete spectral snapshots at nanosecond timescales-cavity ring-up spectroscopy. Based on sharply rising detuned probe pulses, cavity ring-up spectroscopy combines the sensitivity of heterodyne measurements with the highest-possible, transform-limited acquisition rate. As a demonstration, we capture spectra of microtoroid resonators at time intervals as short as 16 ns, directly monitoring submicrosecond dynamics of their optomechanical vibrations, thermorefractive response and Kerr nonlinearity. Cavity ring-up spectroscopy holds promise for the study of fast biological processes such as enzyme kinetics, protein folding and light harvesting, with applications in other fields such as cavity quantum electrodynamics and pulsed optomechanics.
ABSTRACT
The prospect of quantum networks, in which quantum information is carried by single photons in photonic circuits, has long been the driving force behind the effort to achieve all-optical routing of single photons. We realized a single-photon-activated switch capable of routing a photon from any of its two inputs to any of its two outputs. Our device is based on a single atom coupled to a fiber-coupled, chip-based microresonator. A single reflected control photon toggles the switch from high reflection (R ~ 65%) to high transmission (T ~ 90%), with an average of ~1.5 control photons per switching event (~3, including linear losses). No additional control fields are required. The control and target photons are both in-fiber and practically identical, making this scheme compatible with scalable architectures for quantum information processing.
ABSTRACT
The general nanoprinting and nanoinjection of proteins on non-conducting or conducting substrates with a high degree of control both in terms of positional and timing accuracy is an important goal that could impact diverse fields from biotechnology (protein chips) to molecular electronics and from fundamental studies in cell biology to nanophotonics. In this paper, we combine capillary electrophoresis (CE), a separation method with considerable control of protein movement, with the unparalleled positional accuracy of an atomic force microscope (AFM). This combination provides the ability to electrophoretically or electroosmotically correlate the timing of protein migration with AFM control of the protein deposition at a high concentration in defined locations and highly confined volumes estimated to be 2 al. Electrical control of bovine serum albumin printing on standard protein-spotting glass substrates is demonstrated. For this advance, fountain pen nanolithography (FPN) that uses cantilevered glass-tapered capillaries is amended with the placement of electrodes on the nanopipette itself. This results in imposed voltages that are three orders of magnitude less than what is normally used in capillary electrophoresis. The development of atomic-force-controlled capillary electrophoretic printing (ACCEP) has the potential for electrophoretic separation, with high resolution, both in time and in space. The large voltage drop at the tip of the tapered nanopipettes allows for significant increases in concentration of protein in the small printed volumes. All of these attributes combine to suggest that this methodology should have a significant impact in science and technology.
