Riccardo Scott

p-State luminescence in CdSe nanoplatelets : role of lateral confinement and a longitudinal optical phonon bottleneck

We evidence excited state emission from p states well below ground state saturation in CdSe nanoplatelets. Size-dependent exciton ground and excited state energies and population dynamics are determined by four independent methods: time-resolved PL, time-integrated PL, rate equation modeling, and Hartree renormalized k·p calculations-all in very good agreement. The ground state-excited state energy spacing strongly increases with the lateral platelet quantization. Depending on its detuning to the LO phonon energy, the PL decay of CdSe platelets is governed by a size tunable LO phonon bottleneck, related to the low exciton-phonon coupling, very large oscillator strength, and energy spacing of both states. This is, for instance, ideal to tune lasing properties. CdSe platelets are perfectly suited to control the exciton-phonon interaction by changing their lateral size while the optical transition energy is determined by their thickness.

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.

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.

Tuning intraband and interband transition rates via excitonic correlation in low-dimensional semiconductors

We show that electron–hole correlation can be used to tune interband and intraband optical transition rates in semiconductor nanostructures with at least one weakly confined direction. The valence-to-conduction band transition rate can be enhanced by a factor (L/aB)N, with L being the length of the weakly confined direction, aB is the exciton Bohr radius, and N is the dimensionality of the nanostructure, while the rate of intraband and intervalence-band transitions can be slowed down by the inverse factor, (aB/L)N. Adding a hitherto underexplored degree of freedom to engineer excitonic transition rates, this size dependence is of interest for various optoelectronic applications. It also offers an interpretation of the superlinear volume scaling of two-photon absorption (TPA) cross-section recently reported for CdSe nanoplatelets, thus, laying foundations to obtain unprecedented TPA cross sections, well above those of conventional two-photon absorbers. Further, our concept explains the background of the va...

Impact of Shell Growth on Recombination Dynamics and Exciton–Phonon Interaction in CdSe–CdS Core–Shell Nanoplatelets

We investigate the impact of shell growth on the carrier dynamics and exciton-phonon coupling in CdSe-CdS core-shell nanoplatelets with varying shell thickness. We observe that the recombination dynamics can be prolonged by more than one order of magnitude, and analyze the results in a global rate model as well as with simulations including strain and excitonic effects. We reveal that type I band alignment in the hetero platelets is maintained at least up to three monolayers of CdS, resulting in approximately constant radiative rates. Hence, observed changes of decay dynamics are not the result of an increasingly different electron and hole exciton wave function delocalization as often assumed, but an increasingly better passivation of nonradiative surface defects by the shell. Based on a global analysis of time-resolved and time-integrated data, we recover and model the temperature dependent quantum yield of these nanostructures and show that CdS shell growth leads to a strong enhancement of the photoluminescence quantum yield. Our results explain, for example, the very high lasing gain observed in CdSe-CdS nanoplatelets due to the type I band alignment that also makes them interesting as solar energy concentrators. Further, we reveal that the exciton-LO-phonon coupling is strongly tunable by the CdS shell thickness, enabling emission line width and coherence length control.

Time-resolved stark spectroscopy in CdSe nanoplatelets: A route to field controlled emitters

We study [1] the application potential of CdSe nanoplatelets (NPLs) [2], a model system for colloidal 2D materials, as field-controlled emitters and their properties. We show that their luminescence emission can be modulated by 28% upon application of electrical fields up to 175 kV/cm. This is a very high modulation depth for field-controlled nanoemitters. Based on our experimental results we estimate the exciton binding energy in 5.5 monolayer CdSe nanoplatelets to be Eb = 170 meV. Therefore CdSe NPLs exhibit highly robust excitons being stable even at room temperature. This allows to tune the emission and recombination dynamics efficiently by external electric fields.

Surface-wave phenomena and anisotropic photoluminescence in nano-film structures

The investigation of surfaces and thin films is of particular interest in current research as it provides a basis for a multiplicity of applications such as waveguides, sensors, solar cells and optoelectronics. The losses of light emitting structures, here CdSe nano-platelets, can be reduced by harmonizing the orientation of the transition dipoles with the optical mode that the light is coupled to. The electronic structure of the emitting nanoparticle can be optimized via its shape and the density of states strongly depends on the dielectric function of the environment which can be tuned to modify the emission characteristics.