The smallness of natural molecules and atoms with respect to the wavelength of light imposes severe limits on the nature of their optical response. For example, the well-known argument of Landau and Lifshitz and its recent extensions that include chiral molecules show that the electric dipole response dominates over the magneto-electric (bianisotropic) and an even smaller magnetic dipole optical response for all natural materials. Here, we experimentally demonstrate that both these responses can be greatly enhanced in plasmonic nanoclusters. Using atomic force microscopy nanomanipulation technique, we assemble a plasmonic metamolecule that is designed for strong and simultaneous optical magnetic and magneto-electric excitation. Angle-dependent scattering spectroscopy is used to disentangle the two responses and to demonstrate that their constructive/destructive interplay causes strong directional scattering asymmetry. This asymmetry is used to extract both magneto-electric and magnetic dipole responses and to demonstrate their enhancement in comparison to ordinary atomistic materials.

The optical properties of semiconducting transition metal dichalcogenides are dominated by both neutral excitons (electron–hole pairs) and charged excitons (trions) that are stable even at room temperature. While trions directly influence charge transport properties in optoelectronic devices, excitons may be relevant through exciton–trion coupling and conversion phenomena. In this work, we reveal the coherent and incoherent nature of exciton–trion coupling and the relevant time scales in monolayer MoSe2 using optical two-dimensional coherent spectroscopy. Coherent interaction between excitons and trions is definitively identified as quantum beating of cross peaks in the spectra that persists for a few hundred femtoseconds. For longer times up to 10 ps, surprisingly, the relative intensity of the cross peaks increases, which is attributed to incoherent energy transfer likely due to phonon-assisted up-conversion and down-conversion processes that are efficient even at cryogenic temperature.Keywords: coherent coupling; exciton; Quantum beats; trion; two-dimensional materials;

We investigate photoluminescence from individual “giant” CdSe/CdS core/thick-shell quantum dots (gQDs) placed near an epitaxial Ag film with an atomically smooth surface. The key observation is that the lifetimes of the gQDs are drastically reduced and exhibit a remarkably narrow distribution compared to the gQDs deposited on a thermally deposited Ag film. The larger variations in gQDs’ lifetimes on the thermally deposited Ag film arise from excitonic coupling to localized surface plasmons associated with nanoscale surface corrugations of different heights. A calculation is performed based on a simple model system of a QD coupled to a metallic nanosphere. The calculation shows that the QD lifetime initially shortens and reaches a saturated value with increasing radius of the metal nanoparticle (MNP). Because the epitaxial film can be treated as a sphere with an infinitely large radius, the calculation confirms and explains the different QD dynamics near the two types of Ag films as observed experimentally. Our studies demonstrate that epitaxial Ag films serve as an ideal material platform for reliable control over the QD lifetime and may lead to improved photodetectors and light emitting devices requiring fast response or modulation.

Plasmonic cavities represent a promising platform for controlling light–matter interaction due to their exceptionally small mode volume and high density of photonic states. Using plasmonic cavities for enhancing light’s coupling to individual two-level systems, such as single semiconductor quantum dots (QD), is particularly desirable for exploring cavity quantum electrodynamic (QED) effects and using them in quantum information applications. The lack of experimental progress in this area is in part due to the difficulty of precisely placing a QD within nanometers of the plasmonic cavity. Here, we study the simplest plasmonic cavity in the form of a spherical metallic nanoparticle (MNP). By controllably positioning a semiconductor QD in the close proximity of the MNP cavity via atomic force microscope (AFM) manipulation, the scattering spectrum of the MNP is dramatically modified due to Fano interference between the classical plasmonic resonance of the MNP and the quantized exciton resonance in the QD. Moreover, our experiment demonstrates that a single two-level system can render a spherical MNP strongly anisotropic. These findings represent an important step toward realizing quantum plasmonic devices.

We investigate nonradiative quantum coherence in the presence of coupling between excitons and surface plasmon polaritons (SPPs) in a hybrid metal–semiconductor nanostructure. In particular, we study how quantum coherence between heavy-hole (HH) and light-hole (LH) excitons in a GaAs quantum well (QW) is modified when they are coupled to SPPs of a gold grating. We find that the nonradative coherence is reduced in correlation with the coupling strength between the excitons and SPPs. Under the resonant coupling condition, the nonradiative coherence remains in the range of hundreds of femtoseconds, which is significantly longer than the plasmonic coherence. These experiments directly probe quantum dynamics in a prototypical hybrid system and provide critical information for exploring future quantum plasmonics applications.

Planar quantum dot clusters (QDCs) consisting of six InGaAs quantum dots (QDs) formed around a GaAs nanomound are the most sophisticated self-assembled QDCs grown by molecular beam epitaxy thus far. We present the first photoluminescence measurements on individual hexa-QDCs with high spatial, spectral, and temporal resolution. In the best QDCs, the excitons confined in individual QDs are remarkably close in energy, exhibiting only a 10 meV spread. In addition, a biexponential decay profile and small variation in decay rates for different QDs was observed. The homogeneous energetics and dynamics suggest that the sizes, shapes, and composition of the QDs within these clusters are highly uniform.

Using atomic force microscopy nanomanipulation, we position a single Au nanoparticle near a CdSe/ZnS quantum dot to construct a hybrid nanostructure with variable geometry. The coupling between the two particles is varied in a systematic and reversible manner. The photoluminescence lifetime and blinking of the same quantum dot are measured before and after assembly of the structure. In some hybrid structures, the total lifetime is reduced from about 30 ns to well below 1 ns. This dramatic change in lifetime is accompanied by the disappearance of blinking as the nonradiative energy transfer from the CdSe/ZnS quantum dot to the Au nanoparticle becomes the dominant decay channel. Both total lifetime and photoluminescence intensity changes are well described by simple analytical calculations.

Atomic force microscopy (AFM) has been used to assemble prototype nanostructures consisting of colloidal nanoparticles. In the standard manipulation protocol, the AFM is used either as a manipulation tool or an imaging tool, but not both at the same time. We developed a new nanomanipulation protocol in which simultaneous visual guidance is obtained during manipulation. As an example, Au nanoparticles were manipulated on a substrate in two steps. First, a nanoparticle is kicked with the z feedback off. This kicking event reduces the static friction. Second, the nanoparticle is dribbled to a target position in tapping mode, and visual guidance is provided by a ghost trace of the nanoparticle. The new manipulation protocol greatly improves efficiency of manipulating small nanoparticles (15 nm in diameter or smaller). Our work highlights the importance and challenges of understanding friction at the nanoscale.Keywords: atomic force microscopy; colloidal nanoparticles; friction; nanomanipulation; visual guidance

Localized surface plasmon resonances (LSPRs) associated with metallic nanostructures offer unique possibilities for light concentration beyond the diffraction limit, which can lead to strong field confinement and enhancement in deep subwavelength regions. In recent years, many transformative plasmonic applications have emerged, taking advantage of the spectral and spatial tunability of LSPRs enabled by near-field coupling between constituent metallic nanostructures in a variety of plasmonic metastructures (dimers, metamolecules, metasurfaces, metamaterials, etc.). For example, the “hot spot” formed at the interstitial site (gap) between two coupled metallic nanostructures in a plasmonic dimer can be spectrally tuned via the gap size. Capitalizing on these capabilities, there have been significant advances in plasmon enhanced or enabled applications in light-based science and technology, including ultrahigh-sensitivity spectroscopies, light energy harvesting, photocatalysis, biomedical imaging and theranostics, optical sensing, nonlinear optics, ultrahigh-density data storage, as well as plasmonic metamaterials and metasurfaces exhibiting unusual linear and nonlinear optical properties. In this review, we present two complementary approaches for fabricating plasmonic metastructures. We discuss how meta-atoms can be assembled into unique plasmonic metastructures using a variety of nanomanipulation methods based on single- or multiple-probes in an atomic force microscope (AFM) or a scanning electron microscope (SEM), optical tweezers, and focused electron-beam nanomanipulation. We also provide a few examples of nanoparticle metamolecules with designed properties realized in such well-controlled plasmonic metastructures. For the spatial controllability on the mesoscopic and macroscopic scales, we show that controlled self-assembly is the method of choice to realize scalable two-dimensional, and three-dimensional plasmonic metastructures. In the section of applications, we discuss some key examples of plasmonic applications based on individual hot spots or ensembles of hot spots with high uniformity and improved controllability.