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Kunal Mukherjee

Publications and source records attributed to Kunal Mukherjee.

At least 37 records · Page 2Linked to original sources

Epitaxial PbGeSe thin films and their photoluminescence in the mid-wave infrared

PbSe is a narrow bandgap IV-VI compound semiconductor with application in mid-wave infrared optoelectronics, thermoelectrics, and quantum devices. Alkaline earth or rare earth elements such as Sr and Eu can substitute Pb to widen the bandgap of PbSe in heterostructure devices, but they come with challenges such as deteriorating optical and electronic properties, even in dilute concentrations due to their dissimilar atomic nature. We substitute Pb instead with column-IV Ge and assess the potential of rocksalt phase PbGeSe as a wider bandgap semiconductor in thin films grown by molecular beam epitaxy on GaAs substrates. Low sticking of GeSe adatoms requires synthesis temperatures below 260 °C to incorporate Ge, but this yields poor structural and compositional uniformity as determined by X-ray diffraction. Consequently, as-grown films in the range Pb0.94Ge0.06Se to Pb0.83Ge0.17Se (6-17% Ge) show much less bandgap widening in photoluminescence than prior work on bulk crystals using absorption. We observe that post-growth rapid thermal annealing at temperatures of 375-450 °C improves the crystal quality and recovers bandgap widening. Rapid interdiffusion of Ge during annealing, however, remains a challenge in harnessing such PbGeSe materials for compositionally sharp heterostructures. Annealed 17%-Ge films emit light at 3-3.1 um with minimal shift in wavelength versus temperature. These samples are wider in bandgap than PbSe films by 55 meV at room temperature and the widening increases to 160 meV at 80 K, thanks to sharply different dependence of bandgap on temperature in PbSe and PbGeSe.

cond-mat.mtrl-sci↗

Heteroepitaxial growth of highly anisotropic $Sb_{2}Se_{3}$ films on GaAs

The epitaxial integration of anisotropic materials with mainstream cubic semiconductors opens new routes to advanced electronic and photonic devices with directional properties. In this work, we synthesize heteroepitaxial thin films of orthorhombic "quasi-1D" $Sb_{2}Se_{3}$ on cubic GaAs(001) using molecular beam epitaxy. Traditionally, the synthesis of anisotropic films with low symmetry materials is challenging due to multiple grain orientations that form. On a macroscopic scale, such a film tends towards isotropic properties, even if individual grains possess anisotropic responses. We achieve epitaxial $Sb_{2}Se_{3}$ grains on pristine homoepitaxial GaAs templates at low temperatures of 180-200 °C. With the $Sb_{2}Se_{3}$ 1D axis aligned in-plane to GaAs [110] and the primary van der Waals direction lying out-of-plane, we find a birefringence of 0.2 between in-plane orthogonal directions and a giant out-of-plane birefringence greater than 1 at telecom wavelengths. Growth at higher temperatures up to 265 °C yields $Sb_{2}Se_{3}$ of an unusual in-plane rotated texture that further enhances the in-plane optical index anisotropy to 0.3.

cond-mat.mtrl-sci↗

Scalable, nanoscale positioning of highly coherent color centers in prefabricated diamond nanostructures

Nanophotonic devices in color center-containing hosts provide efficient readout, control, and entanglement of the embedded emitters. Yet control over color center formation - in number, position, and coherence - in nanophotonic devices remains a challenge to scalability. Here, we report a controlled creation of highly coherent diamond nitrogen-vacancy (NV) centers with nanoscale three-dimensional localization in prefabricated nanostructures with high yield. Combining nitrogen $δ$-doping during chemical vapor deposition diamond growth and localized electron irradiation, we form shallow NVs registered to the center of diamond nanopillars with wide tunability over NV number. We report positioning precision of ~ 4 nm in depth and 46(1) nm laterally in pillars (102(2) nm in bulk diamond). We reliably form single NV centers with long spin coherence times (average $T_2^{Hahn}$ = 98 $μs$) and 1.8x higher average photoluminescence compared to NV centers randomly positioned in pillars. We achieve a 3x improved yield of NV centers with single electron-spin sensitivity over conventional implantation-based methods. Our high-yield defect creation method will enable scalable production of solid-state defect sensors and processors.

quant-ph↗

Michael's selection theorem and applications to the Maréchal topology

The Maréchal topology, also called the Effros-Maréchal topology, is a natural topology one can put on the space of all von Neumann subalgebras of a given von Neumann algebra. It is a result of Maréchal from 1973 that this topology is Polish as soon as the ambient algebra has separable predual, but the sketch of proof in her research announcement appears to have a small gap. Our main goal in this paper is to fill this gap by a careful look at the topologies one can put on the space of weak-$*$ closed subspaces of a dual space. We also indicate how Michael's selection theorem can be used as a step towards Maréchal's theorem, and how it simplifies the proof of an important selection result of Haagerup and Winsløw for the Maréchal topology. As an application, we show that the space of finite von Neumann algebras is $\mathbfΠ^0_3$-complete.

math.OA↗

A strongly interacting, two-dimensional, dipolar spin ensemble in (111)-oriented diamond

Systems of spins with strong dipolar interactions and controlled dimensionality enable new explorations in quantum sensing and simulation. In this work, we investigate the creation of strong dipolar interactions in a two-dimensional ensemble of nitrogen-vacancy (NV) centers generated via plasma-enhanced chemical vapor deposition (PECVD) on (111)-oriented diamond substrates. We find that diamond growth on the (111) plane yields high incorporation of spins, both nitrogen and NV centers, where the density of the latter is tunable via the miscut of the diamond substrate. Our process allows us to form dense, preferentially aligned, 2D NV ensembles with volume-normalized AC sensitivity down to $η_{AC}$ = 810 pT um$^{3/2}$ Hz$^{-1/2}$. Furthermore, we show that (111) affords maximally positive dipolar interactions amongst a 2D NV ensemble, which is crucial for leveraging dipolar-driven entanglement schemes and exploring new interacting spin physics.

quant-ph↗

Expanded stability of layered SnSe-PbSe alloys and evidence of displacive phase transformation from rocksalt in heteroepitaxial thin films

Bulk PbSnSe has a two-phase region or miscibility gap as the crystal changes from a Van der Waals-bonded orthorhombic 2D layered structure in SnSe-rich compositions to the related 3D-bonded rocksalt structure in PbSe-rich compositions with large contrast in the electrical, optical, and thermal properties across this transition. With an aim to understand and harness this transition in thin films devices, we epitaxially integrate PbSnSe on GaAs by molecular beam epitaxy using an in-situ PbSe surface treatment and show a significantly reduced two-phase region by stabilizing the Pnma layered structure out to Pb$_{0.45}$Sn$_{0.55}$Se, beyond the bulk-limit of Pb$_{0.25}$Sn$_{0.75}$Se. Pushing further, we directly access metastable two-phase epitaxial films of layered and rocksalt grains that are nearly identical in composition around Pb$_{0.5}$Sn$_{0.5}$Se and entirely circumvent the miscibility gap. We present microstructural evidence for an incomplete displacive transformation from rocksalt to layered structure in these films that we speculate occurs during the sample cool down to room temperature after synthesis. In situ temperature-cycling experiments on a Pb$_{0.58}$Sn$_{0.42}$Se rocksalt film reproduce characteristic attributes of a displacive transition and show a modulation in electronic properties. We find well-defined orientation relationships between the phases formed and reveal unconventional strain relief mechanisms involved in the crystal structure transformation, using transmission electron microscopy. Overall, our work adds a scalable thin film integration route to harnessing the dramatic contrast in material properties in PbSnSe across a potentially ultrafast structural transition.

cond-mat.mtrl-sci↗

Quasinormalizers in crossed products of von Neumann algebras

We study the relationship between the dynamics of the action $α$ of a discrete group $G$ on a von Neumann algebra $M$, and structural properties of the associated crossed product inclusion $L(G) \subseteq M \rtimes_αG$, and its intermediate subalgebras. This continues a thread of research originating in classical structural results for ergodic actions of discrete, abelian groups on probability spaces. A key tool in the setting of a noncommutative dynamical system is the set of quasinormalizers for an inclusion of von Neumann algebras. We show that the von Neumann algebra generated by the quasinormalizers captures analytical properties of the inclusion $L(G) \subseteq M \rtimes_αG$ such as the Haagerup Approximation Property, and is essential to capturing "almost periodic" behavior in the underlying dynamical system. Our von Neumann algebraic point of view yields a new description of the Furstenberg-Zimmer distal tower for an ergodic action on a probability space, and we establish new versions of the Furstenberg-Zimmer structure theorems for general, tracial $W^*$-dynamical systems. We present a number of examples contrasting the noncommutative and classical settings which also build on previous work concerning singular inclusions of finite von Neumann algebras.

math.OA↗

Role of Oxygen in Laser Induced Contamination at Diamond-Vacuum Interfaces

Many modern-day quantum science experiments rely on high-fidelity measurement of fluorescent signals emitted by the quantum system under study. A pernicious issue encountered when such experiments are conducted near a material interface in vacuum is "laser-induced contamination" (LIC): the gradual accretion of fluorescent contaminants on the surface where a laser is focused. Fluorescence from these contaminants can entirely drown out any signal from e.g. optically-probed color centers in the solid-state. Crucially, while LIC appears often in this context, it has not been systematically studied. In this work, we probe the onset and growth rate of LIC for a diamond nitrogen-vacancy center experiment in vacuum, and we correlate the contamination-induced fluorescence intensities to micron-scale physical build-up of contaminant on the diamond surface. Drawing upon similar phenomena previously studied in the space optics community, we use photo-catalyzed oxidation of contaminants as a mitigation strategy. We vary the residual oxygen pressure over 9 orders of magnitude and find that LIC growth is inhibited at near-atmospheric oxygen partial pressures, but the growth rate at lower oxygen pressure is non-monotonic. Finally, we discuss a model for the observed dependence of LIC growth rate on oxygen content and propose methods to extend in situ mitigation of LIC to a wider range of operating pressures.

quant-ph↗

Two-dimensional spin systems in PECVD-grown diamond with tunable density and long coherence for enhanced quantum sensing and simulation

Systems of spins engineered with tunable density and reduced dimensionality enable a number of advancements in quantum sensing and simulation. Defects in diamond, such as nitrogen-vacancy (NV) centers and substitutional nitrogen (P1 centers), are particularly promising solid-state platforms to explore. However, the ability to controllably create coherent, two-dimensional spin systems and characterize their properties, such as density, depth confinement, and coherence is an outstanding materials challenge. We present a refined approach to engineer dense ($\gtrsim$1 ppm$\cdot$nm), 2D nitrogen and NV layers in diamond using delta-doping during plasma-enhanced chemical vapor deposition (PECVD) epitaxial growth. We employ both traditional materials techniques, e.g. secondary ion mass spectrometry (SIMS), alongside NV spin decoherence-based measurements to characterize the density and dimensionality of the P1 and NV layers. We find P1 densities of 5-10 ppm$\cdot$nm, NV densities between 1 and 3.5 ppm$\cdot$nm tuned via electron irradiation dosage, and depth confinement of the spin layer down to 1.6 nm. We also observe high (up to 0.74) ratios of P1 to NV centers and reproducibly long NV coherence times, dominated by dipolar interactions with the engineered P1 and NV spin baths.

cond-mat.mtrl-sci↗

Dislocation-induced structural and luminescence degradation in InAs quantum dot emitters on silicon

We probe the extent to which dislocations reduce carrier lifetimes and alter luminescence and growth morphology in InAs quantum dots (QD) grown on silicon. These heterostructures are key ingredients to achieving a highly reliable monolithically integrated light source on silicon necessary for photonic integrated circuits. We find up to 20-30% shorter carrier lifetimes at spatially resolved individual dislocations from both the QD ground and excited states at room temperature using time-resolved cathodoluminescence spectroscopy. These lifetimes are consistent with differences in the intensity measured under steady-state excitation suggesting that trap-assisted recombination limits the minority carrier lifetime, even away from dislocations. Our techniques also reveal the dramatic growth of misfit dislocations in these structures under carrier injection fueled by recombination-enhanced dislocation glide and III-V/Si residual strain. Beyond these direct effects of increased nonradiative recombination, we find the long-range strain field of misfit dislocations deeper in the defect filter layers employed during III-V/Si growth alter the QD growth environment and introduce a crosshatch-like variation in the QD emission color and intensity when the filter layer is positioned close to the QD emitter layer. Sessile threading dislocations generate even more egregious hillock defects that also reduce emission intensities by altering layer thicknesses, as measured by transmission electron microscopy and atom probe tomography. Our work presents a more complete picture of the impacts of dislocations relevant for the development of light sources for scalable silicon photonic integrated circuits.

cond-mat.mes-hall↗

Versatile strain relief pathways in epitaxial films of (001)-oriented PbSe on III-V substrates

PbSe and related IV-VI rocksalt-structure semiconductors have important electronic properties that may be controlled by epitaxial strain and interfaces, thus harnessed in an emerging class of IV-VI/III-V heterostructures. The synthesis of such heterostructures and understanding mechanisms for strain-relief is central to achieving this goal. We show that a range of interfacial defects mediate lattice mismatch in (001)-oriented epitaxial thin films of PbSe with III-V templates of GaAs, InAs, and GaSb. While the primary slip system {100}<110> for dislocation glide in PbSe is well-studied for its facile glide properties, it is inactive in (001)-oriented films used in our work. Yet, we obtain nearly relaxed PbSe films in the three heteroepitaxial systems studied with interfaces ranging from incoherent without localized misfit dislocations on 8.3% mismatched GaAs, a mixture of semi-coherent and incoherent patches on 1.5% mismatched InAs, to nearly coherent on 0.8% mismatched GaSb. The semi-coherent portions of the interfaces to InAs form by 60° misfit dislocations gliding on higher order {111}<110> slip systems. On the more closely lattice-matched GaSb, arrays of 90° (edge) misfit dislocations form via a climb process. The diversity of strain-relaxation mechanisms accessible to PbSe makes it a rich system for heteroepitaxial integration with III-V substrates.

cond-mat.mtrl-sci↗

On the factoriality of q-deformed Araki-Woods von Neumann algebras

The $q$-deformed Araki-Woods von Neumann algebras $Γ_q(\mathcal{H}_\mathbb{R}, U_t)^{\prime \prime}$ are factors for all $q\in (-1,1)$ whenever $dim(\mathcal{H}_\mathbb{R})\geq 3$. When $dim(\mathcal{H}_\mathbb{R})=2$ they are factors as well for all $q$ so long as the parameter defining $(U_t)$ is `small' or $1$ $($trivial$)$ as the case may be.

math.OA↗

Bright mid-infrared photoluminescence from high dislocation density epitaxial PbSe films on GaAs

We report on photoluminescence in the 3-7 $μ$m mid-wave infrared (MWIR) range from sub-100 nm strained thin films of rocksalt PbSe(001) grown on GaAs(001) substrates by molecular beam epitaxy. These bare films, grown epitaxially at temperatures below 400 °C, luminesce brightly at room temperature and have minority carrier lifetimes as long as 172 ns. The relatively long lifetimes in PbSe thin films are achievable despite threading dislocation densities exceeding $10^9$ $cm^{-2}$ arising from island growth on the nearly 8% lattice- and crystal-structure-mismatched GaAs substrate. Using quasi-continuous-wave and time-resolved photoluminescence, we show Shockley-Read-Hall recombination is slow in our high dislocation density PbSe films at room temperature, a hallmark of defect tolerance. Power-dependent photoluminescence and high injection excess carrier lifetimes at room temperature suggest that degenerate Auger recombination limits the efficiency of our films, though the Auger recombination rates are significantly lower than equivalent, III-V bulk materials and even a bit slower than expectations for bulk PbSe. Consequently, the combined effects of defect tolerance and low Auger recombination rates yield an estimated peak internal quantum efficiency of roughly 30% at room temperature, unparalleled in the MWIR for a severely lattice-mismatched thin film. We anticipate substantial opportunities for improving performance by optimizing crystal growth as well as understanding Auger processes in thin films. These results highlight the unique opportunity to harness the unusual chemical bonding in PbSe and related IV-VI semiconductors for heterogeneously integrated mid-infrared light sources constrained by tight thermal budgets in new device designs.

cond-mat.mtrl-sci↗

Ferroelastic Hysteresis in Thin Films of Methylammonium Lead Iodide

Mechanical strain can modify the structural and electronic properties of methylammonium lead iodide MAPbI3. The consequences of ferroelastic hysteresis, which involves the retention of structural memory upon cycles of deformation, in polycrystalline thin films of MAPbI3 are reported. Repeatedly bent films of MAPbI3 on flexible polyimide substrates were examined using Grazing Incidence Wide-Angle X-ray Scattering (GIWAXS) to quantitatively characterize the strain state, populations, and minimum sizes of twin domains. Approximate locations for the coercive stress and saturation on the ferroelastic stress-strain curve are identified, and domains from differently-strained twin sets in the films are found to interact with each other. The presence of specific twin domains is found to correlate to reports of the heterogeneity of strain states with defect content. Long-term stability testing reveals that domain walls are highly immobile over extended periods. Nucleation of new domain walls occurs for specific mechanical strains and correlates closely with degradation of the films. These results help to explain the behavior of ion migration, degradation rate, and photoluminescence in thin films under compressive and tensile strain.

cond-mat.mtrl-sci↗

Defect filtering for thermal expansion induced dislocations in III-V lasers on silicon

Epitaxially integrated III-V semiconductor lasers for silicon photonics have the potential to dramatically transform information networks, but currently, dislocations limit performance and reliability even in defect tolerant InAs quantum dot (QD) based lasers. Despite being below critical thickness, QD layers in these devices contain previously unexplained misfit dislocations, which facilitate non-radiative recombination. We demonstrate here that these misfit dislocations form during post-growth cooldown due to the combined effects of (1) thermal-expansion mismatch between the III-V layers and silicon and (2) precipitate and alloy hardening in the active region. By incorporating an additional sub-critical thickness, indium-alloyed misfit dislocation trapping layer, we leverage these mechanical hardening effects to our advantage, successfully displacing 95% of misfit dislocations from the QD layer in model structures. Unlike conventional dislocation mitigation strategies, the trapping layer reduces neither the number of threading dislocations nor the number of misfit dislocations. It simply shifts the position of misfit dislocations away from the QD layer, reducing the defects' impact on luminescence. In full lasers, adding a misfit dislocation trapping layer both above and below the QD active region displaces misfit dislocations and substantially improves performance: we measure a twofold reduction in lasing threshold currents and a greater than threefold increase in output power. Our results suggest that devices employing both traditional threading dislocation reduction techniques and optimized misfit dislocation trapping layers may finally lead to fully integrated, commercially viable silicon-based photonic integrated circuits.

physics.app-ph↗

Engineering quantum-coherent defects: the role of substrate miscut in chemical vapor deposition diamond growth

The engineering of defects in diamond, particularly nitrogen-vacancy (NV) centers, is important for many applications in quantum science. A materials science approach based on chemical vapor deposition (CVD) growth of diamond and in-situ nitrogen doping is a promising path toward tuning and optimizing the desired properties of the embedded defects. Herein, with the coherence of the embedded defects in mind, we explore the effects of substrate miscut on the diamond growth rate, nitrogen density, and hillock defect density, and we report an optimal angle range between 0.66° < θ < 1.16° for the purposes of engineering coherent ensembles of NV centers in diamond. We provide a model that quantitatively describes hillock nucleation in the step-flow regime of CVD growth, shedding insight on the physics of hillock formation. We also report significantly enhanced incorporation of nitrogen at hillock defects, opening the possibility for templating hillock-defect-localized NV center ensembles for quantum applications.

physics.app-ph↗

Defects in Cd3As2 Epilayers Via Molecular Beam Epitaxy and Strategies for Reducing Them

Molecular beam epitaxy offers an exciting avenue for investigating the behavior of topological semimetal Cd3As2, by providing routes for doping, alloying, strain engineering, and heterostructure formation. To date, however, minimal exploration has been devoted to the impact of defects that are incorporated into epilayers due to contraints imposed by the substrate and narrow growth window. Here, we use a combination of lattice-matched ZnxCd1-xTe buffer layers, miscut substrates and broadband illumination to study how dislocations, twins and point defects influence the electron mobility of Cd3As2. A combination of defect suppression approaches produces Cd3As2 epilayers with electron mobilities upwards of 15,000 cm2/V-s at room temperature.

cond-mat.mtrl-sci↗