Directed Two-Photon Absorption in CdSe Nanoplatelets Revealed by k-Space Spectroscopy.

We show that two-photon absorption (TPA) is highly anisotropic in CdSe nanoplatelets, thus promoting them as a new class of directional two-photon absorbers with large cross sections. Comparing two-dimensional k-space spectroscopic measurements of the one-photon and two-photon excitation of an oriented monolayer of platelets, it is revealed that TPA into the continuum is a directional phenomenon. This is in contrast to one-photon absorption. The observed directional TPA is shown to be related to fundamental band anisotropies of zincblende CdSe and the ultrastrong anisotropic confinement. We recover the internal transition dipole distribution and find that this directionality arises from the intrinsic directionality of the underlying Bloch and envelope functions of the states involved. We note that the photoemission from the CdSe platelets is highly anisotropic following either one- or two-photon excitation. Given the directionality and high TPA cross-section of these platelets, they may, for example, find employment as efficient logic AND elements in integrated photonic devices, or directional photon converters.

Directed emission of CdSe nanoplatelets originating from strongly anisotropic 2D electronic structure.

Intrinsically directional light emitters are potentially important for applications in photonics including lasing and energy-efficient display technology. Here, we propose a new route to overcome intrinsic efficiency limitations in light-emitting devices by studying a CdSe nanoplatelets monolayer that exhibits strongly anisotropic, directed photoluminescence. Analysis of the two-dimensional k-space distribution reveals the underlying internal transition dipole distribution. The observed directed emission is related to the anisotropy of the electronic Bloch states governing the exciton transition dipole moment and forming a bright plane. The strongly directed emission perpendicular to the platelet is further enhanced by the optical local density of states and local fields. In contrast to the emission directionality, the off-resonant absorption into the energetically higher 2D-continuum of states is isotropic. These contrasting optical properties make the oriented CdSe nanoplatelets, or superstructures of parallel-oriented platelets, an interesting and potentially useful class of semiconductor-based emitters.

The dual annihilation of a surface plasmon and a photon by virtue of a three-wave mixing interaction.

The enhanced nonlinear interactions that are driven by surface-plasmon resonances have readily been exploited for the purpose of optical frequency conversion in metallic structures. As of yet, however, little attention has been payed to the exact particulate nature of the conversion process. We show evidence that a surface plasmon and photon can annihilate simultaneously to generate a photon having the sum frequency. The signature for this nonlinear interaction is revealed by probing the condition for momentum conservation using a two-beam k-space spectroscopic method that is applied to a gold film in the Kretschmann geometry. The inverse of the observed nonlinear interaction-an exotic form of parametric down-conversion-would act as a source of surface plasmons in the near-field that are quantum correlated with photons in the far-field.

Nonlinear plasmon-photon interaction resolved by k-space spectroscopy.

Metallic nanostructures support extreme localization and enhancement of optical fields via surface-plasmon (SP) resonances. Although SP are associated with giant enhancements of nonlinear phenomena such as second-harmonic generation (SHG), the role of SP in the process, whether as a field-enhancing catalyst or as a quasiparticle converted in the interaction, has remained experimentally elusive. We demonstrate how k-space spectroscopy can distinguish between the plasmonic and photonic SHG processes that occur in a metal nanofilm when it is optically driven via the Kretschmann geometry. The results revealed a nonlinear interaction where two SP annihilate to create a second-harmonic photon. This knowledge has implications for realizing the inverse process, plasmonic parametric down-conversion, which could act as a coherent source of entangled SP pairs.

Observation of entanglement between two light beams spanning an octave in optical frequency.

We have experimentally demonstrated how two beams of light separated by an octave in frequency can become entangled after their interaction in a chi;{(2)} nonlinear medium. The entangler was a nonlinear optical resonator that was strongly driven by coherent light at the fundamental and second-harmonic wavelengths. An interconversion between the fields created quantum correlations in the amplitude and phase quadratures, which were measured by two independent homodyne detectors. Analysis of the resulting correlation matrix revealed a wave function inseparability of 0.74(1)<1, thereby satisfying the criterion of entanglement.

Measuring photon antibunching from continuous variable sideband squeezing.

We present a technique for measuring the second-order coherence function g(2)(tau) of light using a Hanbury Brown-Twiss intensity interferometer modified for homodyne detection. The experiment was performed entirely in the continuous-variable regime at the sideband frequency of a bright carrier field. We used the setup to characterize g(2)(tau) for thermal and coherent states and investigated its immunity to optical loss. We measured g(2)(tau) of a displaced-squeezed state and found a best antibunching statistic of g(2)(0)=0.11+/-0.18.

Harmonic entanglement with second-order nonlinearity.

We investigate the second-order nonlinear interaction as a means to generate entanglement between fields of differing wavelengths and show that perfect entanglement can, in principle, be produced between the fundamental and second-harmonic fields in these processes. Neither pure second-harmonic generation nor parametric oscillation optimally produce entanglement; such optimal entanglement is rather produced by an intermediate process.