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Zeger Hens

Publications and source records attributed to Zeger Hens.

13 recordsLinked to original sources

Interfacial Reconstructions and Engineering in III-V@II-VI Core-Shell Quantum Dots

In core/shell quantum dots (QDs), the interface between semiconductors of different chemical character largely determines their optoelectronic properties. In III-V/II-VI systems, this boundary involves pronounced chemical and electronic discontinuities that can generate trap states even under complete surface passivation. Using density functional theory on atomistic models of InAs/CdSe QDs, we systematically reconstruct atomic arrangements at the surface and interface to evaluate how local coordination and interfacial dipoles influence the electronic structure. Abrupt interfaces induce charge imbalance and band-gap collapse, whereas introducing an alloyed interlayer that mixes core and shell atoms and vacancies restores energetic alignment and yields delocalized band-edge states, consistent with experimental findings. We also introduce a charge-flow analysis that quantifies charge redistribution across the QD, providing a framework for realistic modeling of interlayer formation and predictive design of defect-free interfaces in core@shell architectures.

cond-mat.mtrl-sci

Fuzzy band structure of quantum dots by Bloch Orbital Expansion, unconventional insights into geometry-electronic structure relations

The extension of ab-initio methods like density functional theory (DFT) to quantum dot (QD) geometries has enabled researchers to explore relationships between QD surface termination and electronic structure. However, fully utilizing the data from DFT requires novel classification methods for QD orbitals. Here, we identify relationships between QD geometry and electronic structure by transforming real-space QD orbitals into momentum-space using Bloch orbital expansion (BOE), yielding a fuzzy QD band structure. Comparing with bulk band structures, we show that truncated, unpassivated facets in III-V and II-VI QDs produce mid-gap orbitals derived from bulk surface orbitals; an identification challenging in real space. QDs with reconstructed facets, however, feature delocalized orbitals formed by superposition of bulk Bloch orbitals. Moreover, we prepare for the first time atomistic core/shell QD models and by the BOE expansion we can clearly identify the core/shell band alignment not possible in real space. These findings emphasize BOE as a vital tool for connecting computational and experimental insights in nanocrystal research.

cond-mat.mtrl-sci

Vanishing quantum confinement enables bright and thermally excited multi-carrier emission from semiconductor nanocrystals

Recently, nanocrystals in the regime of vanishing quantum confinement-termed bulk nanocrystals (BNCs)-have demonstrated remarkable optical gain characteristics. While their high-power lasing performance was demonstrated convincingly, the photophysics at low and intermediate powers-where charge-carrier populations are discrete-remain unexplored. Using single-photon avalanche diode (SPAD) array technology, we resolve the dynamics and energetics of six multi-carrier excited states in individual CdSe/CdS core/shell BNCs, containing up to four electrons and two holes. Each state exhibits bimodal emission, indicative of thermal equilibrium between closely spaced electron and hole levels, confirmed via temperature-dependent single-particle measurements. Quantification of radiative and nonradiative decay channels reveals strongly suppressed Auger recombination through both the negative- and positive-trion pathways. We present a model that combines statistical scaling of rate constants with Fermi-Dirac thermal occupations of electron and hole levels, bridging the transitional regime between quantum-confined and bulk nanocrystals, and providing a comprehensive framework for understanding this emerging class of materials.

cond-mat.mtrl-sci

Direct observation of the exciton polaron by serial femtosecond crystallography on single CsPbBr$_3$ quantum dots

The outstanding opto-electronic properties of lead halide perovskites have been related to the formation of polarons. Nevertheless, the observation of the atomistic deformation brought about by one electron-hole pair in these materials has remained elusive. Here, we measure the diffraction patterns of single CsPbBr$_3$ quantum dots (QDs) with and without resonant excitation in the single exciton limit using serial femtosecond crystallography (SFX). By reconstructing the 3D differential diffraction pattern, we observe small shifts of the Bragg peaks indicative of a crystal-wide deformation field. Building on DFT calculations, we show that these shifts are consistent with the lattice distortion induced by a delocalized electron and a localized hole, forming a mixed large/small exciton polaron. This result creates a clear picture of the polaronic deformation in CsPbBr$_3$ QDs, highlights the exceptional sensitivity of SFX to lattice distortions in few-nanometer crystallites, and establishes an experimental platform for future studies of electron-lattice interactions.

cond-mat.mtrl-sci

Hot-carrier trapping preserves high quantum yields but limits optical gain in InP-based quantum dots

Indium phosphide is the leading material for commercial applications of colloidal quantum dots. To date, however, the community has failed to achieve successful operation under strong excitation conditions, contrasting sharply with other materials. Here, we report how the unusual photophysics of state-of-the-art InP-based quantum dots make them unattractive as a gain material. A combination of ensemble-based time-resolved spectroscopy over timescales from femtoseconds to microseconds and single-quantum-dot spectroscopy reveals ultrafast trapping of hot charge carriers. This process leads to charge-carrier losses, thereby reducing the achievable population inversion which limits amplification of light in a gain material. Interestingly, fluorescence is only delayed, not quenched, by hot charge-carrier trapping, explaining why InP-based quantum dots are successful as bright luminescent colour convertors for low-intensity applications. Comparison with other popular quantum-dot materials, such as CdSe, Pb-halide perovskites, and CuInS2, indicate that the hot-carrier dynamics observed are unique to InP.

cond-mat.mtrl-sci

A silicon photonics waveguide-coupled colloidal quantum dot photodiode sensitive beyond 1.6 um

Silicon photonics faces a persistent challenge in extending photodetection capabilities beyond the 1.6 um wavelength range, primarily due to the lack of appropriate epitaxial materials. Colloidal quantum dots (QDs) present a promising solution here, offering distinct advantages such as infrared wavelength tunability, cost-effectiveness, and facile deposition. Their unique properties position them as a potential candidate for enabling photodetection in silicon photonics beyond the conventional telecom wavelength, thereby expanding the potential applications and capabilities within this domain. In this study, we have successfully integrated lead sulfide (PbS) colloidal quantum dot photodiodes (QDPDs) onto silicon waveguides using standard process techniques. The integrated photodiodes exhibit a remarkable responsivity of 1.3 A/W (with an external quantum efficiency of 74.8%) at a wavelength of 2.1 um, a low dark current of only 106 nA and a bandwidth of 1.1 MHz under a -3 V bias. To demonstrate the scalability of our integration approach, we have developed a compact 8-channel spectrometer incorporating an array of QDPDs. This achievement marks a significant step toward realizing a cost-effective photodetector solution for silicon photonics, particularly tailored for a wide range of sensing applications around the 2 um wavelength range.

physics.optics

A Roadmap to Decipher Ultrafast Photophysics in Two-Dimensional Nanomaterials

Atomically thin two-dimensional (2D) semiconductors are extensively investigated for opto-electronic applications that require strong light-matter interactions. In view of such applications, it is essential to understand how (photo)excitation alters the non-linear optical response of these materials under high carrier density conditions. Broadband transient absorption (TA) spectroscopy is by now a widely used tool to study semiconductor physics in such highly excited systems. However, the complex interplay between different many-body interactions in 2D materials produces highly congested spectral information and an ensuing non-trivial nonlinear photo-response, thereby masking the desired intrinsic photophysics. Herein, we outline a concise roadmap for analyzing such congested datasets based on examples of TA analysis of various 2D materials. In particular, we emphasize the synergy between an initial qualitative understanding of the transient photo-response based on line shapes and their derivatives, and a consequent quantitative spectral deconvolution backed by such insights.

cond-mat.mtrl-sci

Zero-threshold optical gain in electrochemically doped nanoplatelets and the physics behind it

Colloidal nanoplatelets (NPLs) are promising materials for lasing applications. The properties are usually discussed in the framework of 2D materials, where strong excitonic effects dominate the optical properties near the band edge. At the same time, NPLs have finite lateral dimensions such that NPLs are not true extended 2D structures. Here we study the photophysics and gain properties of CdSe/CdS/ZnS core-shell-shell NPLs upon electrochemical n doping and optical excitation. Steady-state absorption and PL spectroscopy show that excitonic effects are weaker in core-shell-shell nanoplatelets due to the reduced exciton binding energy. Transient absorption studies reveal a gain threshold of only one excitation per nanoplatelet. Using electrochemical n doping we observe the complete bleaching of the band edge exciton transitions. Combining electrochemical doping with transient absorption spectroscopy we demonstrate that the gain threshold is fully removed over a broad spectral range and gain coefficients of several thousand cm-1 are obtained. These doped NPLs are the best performing colloidal nanomaterial gain medium reported to date. The low exciton binding energy due to the CdS and ZnS shells, in combination with the relatively small lateral size of the NPLs, result in excited states that are effectively delocalised over the entire platelet. Core-shell NPLs are thus on the border between strong confinement in QDs and dominant Coulombic effects in 2D materials. We demonstrate that this limit is in effect ideal for optical gain, and that it results in an optimal lateral size of the platelets where the gain threshold per nm2 is minimal.

physics.app-ph

Generating Triplets in Organic Semiconductor Tetracene upon Photoexcitation of Transition Metal Dichalcogenide ReS$_2$

We studied the dynamics of transfer of photoexcited electronic states in a bilayer of the two-dimensional transition metal dichalcogenide ReS$_2$ and tetracene, with the aim to produce triplets in the latter. This material combination was used as the band gap of ReS$_2$ (1.5 eV) is slightly larger than the triplet energy of tetracene (1.25 eV). Using time-resolved optical absorption spectroscopy, transfer of photoexcited states from ReS$_2$ to triplet states in tetracene was found to occur within 5 ps with an efficiency near 38%. This result opens up new possibilities for heterostructure design of two-dimensional materials with suitable organics to produce long-lived triplets. Triplets are of interest as sensitizers in a wide variety of applications including optoelectronics, photovoltaics, photocatalysis, and photon upconversion.

physics.chem-ph

Unraveling the Photophysics of Liquid-Phase Exfoliated Two-Dimensional ReS2 Nanoflakes

Few-layered transition metal dichalcogenides (TMDs) are increasingly popular materials for optoelectronics and catalysis. Amongst the various types of TMDs available today, rhenium-chalcogenides (ReX2) stand out due to their remarkable electronic structure, such as the occurrence of anisotropic excitons and potential direct bandgap behavior throughout multi-layered stacks. In this letter, we have analyzed the nature and dynamics of charge carriers in highly crystalline liquid-phase exfoliated ReS2, using a unique combination of optical pump-THz probe and broadband transient absorption spectroscopy. Two distinct time regimes are identified, both of which are dominated by unbound charge carriers despite the high exciton binding energy. In the first time regime, the unbound charge carriers cause an increase and a broadening of the exciton absorption band. In the second time regime, a peculiar narrowing of the excitonic absorption profile is observed, which we assign to the presence of built-in fields and/or charged defects. Our results pave the way to analyze spectrally complex transient absorption measurements on layered TMD materials and indicate the potential for ReS2 to produce mobile free charge carriers, a feat relevant for photovoltaic applications.

cond-mat.mtrl-sci

On-Chip Integrated Quantum-Dot Silicon-Nitride Microdisk Lasers

Hybrid SiN-QD microlasers coupled to a passive SiN output waveguide with 7μm diameter and record low threshold density of 27 μJ cm-2 are demonstrated. A new design and unique processing scheme starting from SiN/QD/SiN stacks offer long term stability and facilitate in depth laser characterization. This approach opens up new paths for optical communication, lab-on-a-chip, gas sensing and, potentially, on-chip cavity quantum electrodynamics and quantum optics.

physics.optics

Nearly Blinking-Free, High-Purity Single-Photon Emission by Colloidal InP/ZnSe Quantum Dots

Colloidal core/shell InP/ZnSe quantum dots (QDs), recently produced using an improved synthesis method, have a great potential in life-science applications as well as in integrated quantum photonics and quantum information processing as single-photon emitters. Single-particle spectroscopy of 10-nm QDs with 3.2-nm cores reveals strong photon antibunching attributed to fast (70-ps) Auger recombination of multiple excitons. The QDs exhibit very good photostability under strong optical excitation. We demonstrate that the antibunching is preserved when the QDs are excited above the saturation intensity of the fundamental-exciton transition. This result paves the way towards their usage as high-purity on-demand single-photon emitters at room temperature. Unconventionally, despite the strong Auger blockade mechanism, InP/ZnSe QDs also display very little luminescence intermittency ("blinking"), with a simple on/off blinking pattern. The analysis of single-particle luminescence statistics places these InP/ZnSe QDs in the class of nearly blinking-free QDs, with emission stability comparable to state-of-the-art thick-shell and alloyed-interface CdSe/CdS, but with improved single-photon purity.

cond-mat.mes-hall

Coherent absorption and enhanced photoluminescence in thin layers of nanorods

We demonstrate a large light absorptance (80%) in a nanometric layer of quantum dots in rods (QRs) with a thickness of 23 nm. This behavior is explained in terms of the coherent absorption by interference of the light incident at a certain angle onto the very thin QR layer. We exploit this coherent light absorption to enhance the photoluminescent emission from the QRs. Up to a seven- and fivefold enhancement of the photoluminescence is observed for p- and s-polarized incident light, respectively.

physics.optics