Kebin Shi

Single nanoparticle detection using split-mode microcavity Raman lasers

Significance Optical sensing with ultrahigh sensitivity of single nanoscale objects is strongly desirable for applications in various fields, such as in early-stage diagnosis of human diseases and in environmental monitoring, as well as in homeland security. In this article, we report an optical technique for single nanoparticle detection in both air and an aqueous environment, with an ultralow detection limit. Ultrasensitive nanoparticle detection holds great potential for early-stage diagnosis of human diseases and for environmental monitoring. In this work, we report for the first time, to our knowledge, single nanoparticle detection by monitoring the beat frequency of split-mode Raman lasers in high-Q optical microcavities. We first demonstrate this method by controllably transferring single 50-nm–radius nanoparticles to and from the cavity surface using a fiber taper. We then realize real-time detection of single nanoparticles in an aqueous environment, with a record low detection limit of 20 nm in radius, without using additional techniques for laser noise suppression. Because Raman scattering occurs in most materials under practically any pump wavelength, this Raman laser-based sensing method not only removes the need for doping the microcavity with a gain medium but also loosens the requirement of specific wavelength bands for the pump lasers, thus representing a significant step toward practical microlaser sensors.

Photoluminescence of a single complex plasmonic nanoparticle

We report detailed investigations of the photoluminescence (PL) generated from an individual gold nanoflower, a highly branched plasmonic nanoparticle. Compared to nanostructures with simple shapes, such as spheres, nanorods, and bipyramids, nanoflowers exhibit more distinct features, i.e., the PL spectra and far-field emission patterns are strongly dependent on the wavelength and polarization of the excitation light. The experimental results are qualitatively explained using theoretical calculations. In addition, the intrinsic PL signal is highly dominated by localized surface plasmon resonances. The crucial role of plasmonic coupling in complex nanostructures during the plasmon-enhanced PL process is highlighted. The findings contribute to a deeper understanding of the PL properties of metallic nanoparticles. This study will be beneficial for several potential applications, including optical imaging and sensing in the fields of materials science and biology.

Simultaneously precise frequency transfer and time synchronization using feed-forward compensation technique via 120 km fiber link

Precision time synchronization between two remote sites is desired in many applications such as global positioning satellite systems, long-baseline interferometry, coherent radar detection and fundamental physics constant measurements. The recently developed frequency dissemination technologies based on optical fiber link have improved the transfer instability to the level of 10−19/day at remote location. Therefore it is possible to keep clock oscillation at remote locations continuously corrected, or to reproduce a “virtual” clock on the remote location. However the initial alignment and the correction of 1 pps timing signal from time to time are still required, besides the highly stabilized clock frequency transfer between distant locations. Here we demonstrate a time synchronization based on an ultra-stable frequency transfer system via 120-km commercial fiber link by transferring an optical frequency comb. Both the phase noise compensation in frequency dissemination and temporal basis alignment in time synchronization were implemented by a feed-forward digital compensation (FFDC) technique. The fractional frequency instability was measured to be 6.18 × 10−20 at 2000 s. The timing deviation of time synchronization was measured to be 0.6 ps in 1500 s. This technique also can be applied in multi-node fiber network topology.

Tuning the photo-response in monolayer MoS2 by plasmonic nano-antenna.

Monolayer molybdenum disulfide (MoS2) has recently attracted intense interests due to its remarkable optical properties of valley-selected optical response, strong nonlinear wave mixing and photocurrent/photovoltaic generation and many corresponding potential applications. However, the nature of atomic-thin thickness of monolayer MoS2 leads to inefficient light-matter interactions and thereby hinders its optoelectronic applications. Here we report on the enhanced and controllable photo-response in MoS2 by utilizing surface plasmonic resonance based on metallic nano-antenna with characteristic lateral size of 40 × 80 nm. Our nano-antenna is designed to have one plasmonic resonance in the visible range and can enhance the MoS2 photoluminescence intensity up to 10 folds. The intensity enhancement can be effectively tuned simply by the manipulation of incident light polarization. In addition, we can also control the oscillator strength ratio between exciton and trion states by controlling polarization dependent hot carrier doping in MoS2. Our results demonstrate the possibility in controlling the photo-response in broad two-dimensional materials by well-designed nano-antenna and facilitate its coming optoelectronic applications.

Robust Stacking-Independent Ultrafast Charge Transfer in MoS2/WS2 Bilayers

Van der Waals-coupled two-dimensional (2D) heterostructures have attracted great attention recently due to their high potential in the next-generation photodetectors and solar cells. The understanding of charge-transfer process between adjacent atomic layers is the key to design optimal devices as it directly determines the fundamental response speed and photon-electron conversion efficiency. However, general belief and theoretical studies have shown that the charge transfer behavior depends sensitively on interlayer configurations, which is difficult to control accurately, bringing great uncertainties in device designing. Here we investigate the ultrafast dynamics of interlayer charge transfer in a prototype heterostructure, the MoS2/WS2 bilayer with various stacking configurations, by optical two-color ultrafast pump-probe spectroscopy. Surprisingly, we found that the charge transfer is robust against varying interlayer twist angles and interlayer coupling strength, in time scale of ∼90 fs. Our observation, together with atomic-resolved transmission electron characterization and time-dependent density functional theory simulations, reveals that the robust ultrafast charge transfer is attributed to the heterogeneous interlayer stretching/sliding, which provides additional channels for efficient charge transfer previously unknown. Our results elucidate the origin of transfer rate robustness against interlayer stacking configurations in optical devices based on 2D heterostructures, facilitating their applications in ultrafast and high-efficient optoelectronic and photovoltaic devices in the near future.

Tunneling-induced transparency in a chaotic microcavity

We demonstrate experimentally a new form of induced transparency, i.e., chaos-induced transparency, in a slightly deformed microcavity which support both continuous chaotic modes and discrete regular modes with Q factors exceeding 3×10. When excited by a focused laser beam, the induced transparency in the transmission spectrum originates from the destructive interference of two parallel optical pathways: (i) directly refractive excitation of the chaotic modes, and (ii) excitation of the ultra-high-Q regular mode via chaos-assisted dynamical tunneling mechanism coupling back to the chaotic modes. By controlling the focal position of the laser beam, the induced transparency experiences a highly tunable Fano-like asymmetric lineshape. The experimental results are modeled by a quantum scattering theory and show excellent agreement. This chaos-induced transparency is accompanied by extremely steep normal dispersion, and may open up new possibilities a dramatic slow light behavior and a significant enhancement of nonlinear interactions.

Spectrally tunable femtosecond erbium fiber laser based on large-normal-dispersion cavity

We report on a wavelength-tunable large-normal-dispersion erbium-doped mode-locking fiber oscillator. By using a grating as spectral filter, the intra-cavity mode-locking spectrum can be tuned continuously. The laser produces 250fs pulses with average power of 130mW and a tunable center wavelength range from 1528nm to 1570nm.

Generation of femtosecond pulses based on efficient frequency doubling of erbium fiber oscillator-amplifier laser

We report on frequency doubling of 1.55-μm fiber oscillator-amplifier laser with conversion efficiency of 27% by using off-the-shelf nonlinear crystal. The system generates 135-femto-second (fs) pulses with average power of 110 mW at 80 MHz repetition rate. Frequency doubling efficiency as a function of pulse pre-chirp in front of a single mode erbium fiber amplifier was investigated.

Chaos-induced transparency in an ultrahigh-Q optical microcavity

We demonstrate experimentally a new form of induced transparency, i.e., chaos-induced transparency, in a slightly deformed microcavity which support both continuous chaotic modes and discrete regular modes with Q factors exceeding 3×10. When excited by a focused laser beam, the induced transparency in the transmission spectrum originates from the destructive interference of two parallel optical pathways: (i) directly refractive excitation of the chaotic modes, and (ii) excitation of the ultra-high-Q regular mode via chaos-assisted dynamical tunneling mechanism coupling back to the chaotic modes. By controlling the focal position of the laser beam, the induced transparency experiences a highly tunable Fano-like asymmetric lineshape. The experimental results are modeled by a quantum scattering theory and show excellent agreement. This chaos-induced transparency is accompanied by extremely steep normal dispersion, and may open up new possibilities a dramatic slow light behavior and a significant enhancement of nonlinear interactions.

A Tunable Optofluidic Microlaser in a Photostable Conjugated Polymer

The optofluidic laser has become an important platform for biological sensing and medical diagnosis. To date, fluorescent dyes and proteins have been widely utilized as gain materials for biological analysis due to their good biocompatibility, but the limited photostability restricts their reliability and sensitivity. Here, an optofluidic microlaser with an ultralow threshold down to 7.8 µJ cm-2 in the ultrahigh-Q whispering-gallery microcavity, which is filled with a biocompatible conjugated polymer, is demonstrated. This conjugated polymer exhibits a significant enhancement in the lasing stability compared with a typical laser dye (Nile red). In the experiment, after 20 min of illumination with the excitation intensity of 23.2 MW cm-2 , the lasing intensity of the conjugated polymer experiences a decrease of less than 10%, while the lasing feature of Nile red completely disappears. Additionally, by mechanically stretching the resonator, the lasing frequency can be fine-tuned with the range of about 2 nm, exceeding the free spectral range of the resonator.