ZnO nanowires were mass produced using a physical vapor deposition approach. The ZnO nanowire monocrystallites have an average diameter around 60 nm and length up to a few micrometers. The unidirectional growth of the ZnO nanowires was controlled by the conventional vapor-liquid-solid mechanism. Intensive UV light emission peaked around 3.27 eV was observed at room temperature, which was assigned to emission from free exciton under low excitation intensity. The observed room temperature UV emission was ascribed to the decrease in structure defects as compared to bulk ZnO materials, and in particularly to the size effect in the ZnO wires.

Graphene is an optical material of unusual characteristics because of its linearly dispersive conduction and valence bands and the strong interband transitions. It allows broadband light-matter interactions with ultrafast responses and can be readily pasted to surfaces of functional structures for photonic and optoelectronic applications. Recently, graphene-based optical modulators have been demonstrated with electrical tuning of the Fermi level of graphene. Their operation bandwidth, however, was limited to about 1 GHz by the response of the driving electrical circuit. Clearly, this can be improved by an all-optical approach. Here, we show that a graphene-clad microfiber all-optical modulator can achieve a modulation depth of 38% and a response time of ∼2.2 ps, limited only by the intrinsic carrier relaxation time of graphene. This modulator is compatible with current high-speed fiber-optic communication networks and may open the door to meet future demand of ultrafast optical signal processing.

We reveal a unique broadband natural quasi-phase-matching (QPM) mechanism underlying an observation of highly efficient second- and third-order harmonic generation at multiple wavelengths in an $x$-cut lithium niobate (LN) microdisk resonator. For light waves in the transverse-electric mode propagating along the circumference of the microdisk, the effective nonlinear optical coefficients naturally oscillate periodically to change both the sign and magnitude, facilitating QPM without the necessity of domain engineering in the micrometer-scale LN disk. The second-harmonic and cascaded third-harmonic waves are simultaneously generated with normalized conversion efficiencies as high as $9.9\%/\mathrm{mW}$ and $1.05\%/{\mathrm{mW}}^2$, respectively, thanks to the utilization of the highest nonlinear coefficient $d_{33}$ of LN. The high efficiency achieved with the microdisk of a diameter of $\sim 30\mu \mathrm{m}$ is beneficial for realizing high-density integration of nonlinear photonic devices such as wavelength convertors and entangled photon sources.

We report on fabrication of high-Q lithium niobate (LN) whispering-gallery-mode (WGM) microresonators suspended on silica pedestals by femtosecond laser direct writing followed by focused ion beam (FIB) milling. The micrometer-scale (diameter ~82 μm) LN resonator possesses a Q factor of ~2.5 × 10⁵ around 1550 nm wavelength. The combination of femtosecond laser direct writing with FIB enables high-efficiency, high-precision nanofabrication of high-Q crystalline microresonators.

In typical epitaxial quantum dots (QDs) the ideally degenerate optical excitons are energy split, preventing the formation of two-photon entanglement in a biexciton decay. We use an external field, here a continuous-wave laser tuned to the QD in the ac Stark limit, to cancel the splitting and create two-photon entanglement. Quantum-state tomography is used to construct the two-photon density matrix. When the splitting is removed it satisfies well-known entanglement tests. Our approach shows that polarization-entangled photons can be routinely produced in semiconductor nanostructures.

Electroluminescence of colloidal nanocrystals promises a new generation of high-performance and solution-processable light-emitting diodes. The operation of nanocrystal-based light-emitting diodes relies on the radiative recombination of electrically generated excitons. However, a fundamental question—how excitons are electrically generated in individual nanocrystals—remains unanswered. Here, we reveal a nanoscopic mechanism of sequential electron-hole injection for exciton generation in nanocrystal-based electroluminescent devices. To decipher the corresponding elementary processes, we develop electrically-pumped single-nanocrystal spectroscopy. While hole injection into neutral quantum dots is generally considered to be inefficient, we find that the intermediate negatively charged state of quantum dots triggers confinement-enhanced Coulomb interactions, which simultaneously accelerate hole injection and hinder excessive electron injection. In-situ/operando spectroscopy on state-of-the-art quantum-dot light-emitting diodes demonstrates that exciton generation at the ensemble level is consistent with the charge-confinement-enhanced sequential electron-hole injection mechanism probed at the single-nanocrystal level. Our findings provide a universal mechanism for enhancing charge balance in nanocrystal-based electroluminescent devices.