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We present a sample of 50 H-alpha detected broad-line active galactic nuclei (BLAGN) at redshifts 3.50), independent of the contributions of emission lines to the broadband photometry. We construct the black hole (BH) mass function at 3.5

In this paper we investigate the ergodicity in total variation of the process $X_t$ related to some integro-differential operator with unbounded coefficients and describe the speed of convergence to the respective invariant measure. Some examples are provided.

We present millimeter observations of the host galaxy of the most distant blazar known, VLASSJ041009.05-013919.88 (hereafter J0410-0139) at z=7, using ALMA and NOEMA observations. The ALMA data reveal a 2e42 erg/s [CII] 158um emission line at z=6.9964 with a [CII]-inferred star-formation rate of 58 Msun/yr. We estimate a dynamical mass of 4.6e9 Msun, implying a black hole mass to host a dynamical mass ratio of 0.15. The 238 GHz continuum (rest-frame IR) decreased by ~33% from the NOEMA to the ALMA observations taken ~10 months apart. The VLA 3-10 GHz radio flux densities showed a ~37% decrease in a similar time frame, suggesting a causal connection. At face value, J0410-0139 would have the lowest [CII]-to-IR luminosity ratio of a z>5.7 quasar reported to date (~1e-4). However, if only <20% of the measured IR luminosity were due to thermal emission from dust, the [CII]-to-IR luminosity ratio would be typical of (U)LIRGS, and the star formation rates derived from [CII] and IR luminosities would be consistent. These results provide further evidence that synchrotron emission significantly contributes to the observed rest-frame IR emission of J0410-0139, similar to what has been reported in some radio-loud AGN at z<1., Comment: Version after addressing referee report. See also companion paper: arXiv:2407.07236

Measurement of lithium abundances in solar-type stars have shown that standard models of stellar evolution are incapable of explaining the observed depletion as a function of stellar age. Beryllium is one of the lightest elements that can be measured in stellar photospheres, and it can be burned in relatively low temperatures. Studying its abundances as a function of stellar age can provide important constraints to stellar mixing models, as the level of depletion as a function of time will indicate how deep the photospheric material must be dredged to explain the observed abundances of both elements. In an effort to provide the most stringent constraints for non-standard stellar mixing models, we observed a sample of solar-twins and concomitantly analyzed their lithium and beryllium abundances. Unlike what is typically observed for lithium, we find that beryllium does not decrease as a function of stellar age, constraining models that predict burning of both materials. Based on our data, models that invoke convective overshoot and convective settling are preferred over typical rotationaly-induced mixing models, as the later burn Be in excess while the former do not. Previous works also proposed mixing due to gravity waves as a possible explanation for observed abundances, which can fit our data as well. We also confirm previous finds of an increase in Be abundance as a function of metallicity, indicative of galactic production via cosmic ray spallation., Comment: Submitted to AJ - Comments are welcome!

Two-dimensional (2D) organic-inorganic hybrid perovskites emerged as a versatile platform for light-emitting and photovol-taic applications due to their unique structural design and chemical flexibility. Their properties depend heavily on both the choice of the inorganic lead halide framework and the surrounding organic layers. Recently, the introduction of chiral cations into 2D perovskites has attracted major interest due to their potential for introducing chirality and tuning the chiro-optical response. Importantly, the optical properties in these materials are dominated by tightly bound excitons that also serve as primary carriers for the energy transport. The mobility of photoinjected excitons is thus important from the perspectives of fundamental material properties and optoelectronic applications, yet remains an open question. Here, we demonstrate exciton propagation in a 2D chiral perovskite methylbenzylammonium lead iodide (MBA2PbI4) using transient photoluminescence microscopy and reveal density-dependent transport over more than 100 nanometers at room temperature with diffusion coeffi-cients as high as 2 cm2/s. We observe two distinct regimes of initially rapid diffusive propagation and subsequent localiza-tion. Moreover, perovskites with enantiomer pure cations are found to exhibit faster exciton diffusion compared to the race-mic mixture, correlated with the impact of the material composition on disorder. Altogether, the observations of efficient exciton diffusion at room temperature highlight the potential of 2D chiral perovskites to merge chiro-optical properties with strong light-matter interaction and efficient energy transport.

Time-resolved photoluminescence is a validated method for tracking the photoexcited carrier dynamics in luminescent materials. This technique probes the photoluminescence decays upon a periodic excitation by short laser pulses. Herein, we demonstrate that this approach cannot directly detect hidden photoexcitations with much slower dynamics than the photoluminescence decay. We demonstrate a new method based on a multi-pulse excitation scheme that enables an unambiguous detection and an easily interpreted tracking of these hidden species. The multi-pulse excitation consists of a single pulse (Read) followed by a burst of many closely separated pulses (Write) and finally another single pulse (Read). To illustrate the efficacy of the Read-Write-Read excitation scheme, we apply it to metal halide perovskites to directly visualize carrier trapping, extract the concentration of trapped charges and determine the rate constant of trap depopulation. The developed approach allows studying performance-limiting processes in energy devices using a versatile, highly applicable all-optical method.

Over the last decade, studies of large samples of binary systems identified chemical anomalies, and showed that they might be attributed to planet formation or planet engulfment. However, both scenarios have primarily been tested in pairs without known exoplanets. In this work, we explore these scenarios in the newly detected planet-hosting wide binary TOI-1173 A/B (projected separation $\sim 11,400$ AU) using high-resolution MAROON-X and ARCES spectra. We determined photospheric stellar parameters both by fitting stellar models and via the spectroscopic equilibrium approach. Both analyses agree and suggest that they are cool main sequence stars located in the thin disc. A line-by-line differential analysis between the components (B$-$A) displays an abundance pattern in the condensation temperature plane where the planet-hosting star TOI-1173 A is enhanced in refractory elements such as iron by more than 0.05 dex. This suggests the engulfment of $\sim$18 M$_{\oplus}$ of rocky material in star A. Our hypothesis is supported by the dynamics of the system detailed in our companion paper Yana Galarza et al. 2024, which suggest that the Super-Neptune TOI-1173 A $b$ might have been delivered to its current short period ($\sim7$ days) through circulatization and von Zeipel-Lidov-Kozai mechanisms, thereby triggering the engulfment of inner rocky exoplanets., Comment: Accepted for publication in the Astronomical Journal on July 29, 2024

The burgeoning short video industry has accelerated the advancement of video-music retrieval technology, assisting content creators in selecting appropriate music for their videos. In self-supervised training for video-to-music retrieval, the video and music samples in the dataset are separated from the same video work, so they are all one-to-one matches. This does not match the real situation. In reality, a video can use different music as background music, and a music can be used as background music for different videos. Many videos and music that are not in a pair may be compatible, leading to false negative noise in the dataset. A novel inter-intra modal (II) loss is proposed as a solution. By reducing the variation of feature distribution within the two modalities before and after the encoder, II loss can reduce the model's overfitting to such noise without removing it in a costly and laborious way. The video-music retrieval framework, II-CLVM (Contrastive Learning for Video-Music Retrieval), incorporating the II Loss, achieves state-of-the-art performance on the YouTube8M dataset. The framework II-CLVTM shows better performance when retrieving music using multi-modal video information (such as text in videos). Experiments are designed to show that II loss can effectively alleviate the problem of false negative noise in retrieval tasks. Experiments also show that II loss improves various self-supervised and supervised uni-modal and cross-modal retrieval tasks, and can obtain good retrieval models with a small amount of training samples., Comment: 10 pages, 7 figures

Atmospheric states derived from reanalysis comprise a substantial portion of weather and climate simulation outputs. Many stakeholders -- such as researchers, policy makers, and insurers -- use this data to better understand the earth system and guide policy decisions. Atmospheric states have also received increased interest as machine learning approaches to weather prediction have shown promising results. A key issue for all audiences is that dense time series of these high-dimensional states comprise an enormous amount of data, precluding all but the most well resourced groups from accessing and using historical data and future projections. To address this problem, we propose a method for compressing atmospheric states using methods from the neural network literature, adapting spherical data to processing by conventional neural architectures through the use of the area-preserving HEALPix projection. We investigate two model classes for building neural compressors: the hyperprior model from the neural image compression literature and recent vector-quantised models. We show that both families of models satisfy the desiderata of small average error, a small number of high-error reconstructed pixels, faithful reproduction of extreme events such as hurricanes and heatwaves, preservation of the spectral power distribution across spatial scales. We demonstrate compression ratios in excess of 1000x, with compression and decompression at a rate of approximately one second per global atmospheric state., Comment: 44 pages, 25 figures

The magnetic resonance of iron garnets is at the heart of rich physics and provides a crucial technology used inside microwave components. A barrier still stands in the way of integrated cryogenic devices with iron garnets, because their epitaxy requires paramagnetic substrates that cause large microwave losses at low temperatures. Finding alternative combinations of substrates and magnetic garnets is thus essential to enabling cryogenic integrated magnonics. With this motivation, we develop a new approach to the synthesis of epitaxial garnet films, based on the co-sputtering of binary oxides, enabling a precise and continuous tuning of the iron garnet composition. By substituting a controlled proportion of the iron with additional yttrium, we obtain Y$_{3}$(Y$_{x}$Fe$_{5-x}$)O$_{12}$ films of high crystalline quality that can be lattice-matched to yttrium scandium gallium garnet (YSGG), a diamagnetic substrate suitable for low-temperature applications. Ferromagnetic resonance performed at low temperatures confirms the elimination of substrate paramagnetism losses on YSGG. We also show that the Y$_{3}$(Y$_{x}$Fe$_{5-x}$)O$_{12}$ system can be matched to other substrates, such as gadolinium yttrium scandium gallium garnet and gadolinium scandium gallium garnet. Additionally, we demonstrate that Bi-substituted films of (Bi$_{0.8}$Y$_{2.2}$)Fe$_{5}$O$_{12}$ also offer ideal lattice matching to YSGG for low-temperature magnetic resonance. The present approach of controlled substitutions in iron garnets to obtain ideal lattice matching with diamagnetic substrates opens a very promising pathway to magnonic devices operating in low-temperature environments., Comment: Main: 18 pages, 6 figures; Supplement: 9 pages, 6 figures

Relativistic jets are thought to play a crucial role in the formation of massive galaxies and supermassive black holes. Here we report multi-wavelength and multi-epoch observations of the quasar VLASSJ0410-0139 at redshift z=7, powered by a 7e8 solar-mass black hole. Its radio variability, X-ray properties, and compact radio emission on parsec scales reveal that J0410-0139 is a blazar with a relativistic jet aligned with our line of sight. This blazar's existence implies that many more similar (unaligned) jetted sources must exist at z=7. One scenario is that we observe an intrinsically low-power radio jet, but we see it at high luminosity due to relativistic beaming effects. In this case, a large fraction (>80%) of the UV bright quasars must have a similar jet to match the number density expected from the UV quasar luminosity function. These jets can enhance the growth of supermassive black holes and substantially affect their host galaxies. However, the implications would be even more severe if the quasar belongs to the top 10% radio luminous quasars, as measured if the beaming enhancement is less than a factor of 10-15. In this scenario, there should be hundreds to thousands of radio-quiet quasars at z=7 with intrinsic properties similar to J0410-0139 -- in strong tension with the number density of bright quasars derived from their UV luminosity function. To reconcile these results, most black hole growth at z=7 must happen in an obscured phase, as some models predict. The existence of supermassive black holes in the epoch of reionization is facilitated by significant jet-enhanced or obscured super-Eddington accretion., Comment: Submitted

Research in the NLP sphere of the Turkic counterparts of Central Asian languages, namely Kazakh, Uzbek, Kyrgyz, and Turkmen, comes with the typical challenges of low-resource languages, like data scarcity and a general lack of linguistic resources. However, in the recent years research has greatly advanced via collection of language-specific datasets and development of downstream task technologies. Aiming to summarize this research up until May 2024, this paper also seeks to identify potential areas of future work. To achieve this, the paper gives a broad, high-level overview of the linguistic properties of the languages, the current coverage and performance of already developed technology, application of transfer learning techniques from higher-resource languages, and availability of labeled and unlabeled data for each language. Providing a summary of the current state of affairs, we hope that further research will be facilitated with the considerations we provide in the current paper.

Aims.We conduct a high-precision differential abundance analysis of the remarkable binary system HD 240429/30 (Krios and Kronos, respectively), whose difference in metallicity is one of the highest detected in systems with similar components to date (approximately 0.20 dex). A condensation temperature TC trend study was performed to search for possible chemical signatures of planet formation. In addition, other potential scenarios have been proposed to explain this disparity. Methods. Fundamental atmospheric parameters (Te f f , log g, [Fe/H], vturb) were calculated using the latest version of the FUNDPAR code employing high resolution MAROON-X spectra. We applied a full line-by-line differential technique to measure the abundances of 26 elements in both stars with equivalent widths and spectral synthesis taking advantage of the non-solar scaled opacities. Results.We found a difference in metallicity of approximately 0.230 dex, being Kronos more metal rich than Krios. The analysis encompassed the examination of the diffusion effect and primordial chemical differences, concluding that the observed chemical discrepancies in the binary system cannot be solely attributed to any of these processes. The results also shown a noticeable excess of Li by approximately 0.56 dex in Kronos, and an enhancement of refractories with respect to Krios. A photometric study with TESS data was carried out, without finding any signal of possible transiting planets around the stars. Several potential planet formation scenarios were also explored to account for the observed excess in both metallicity and lithium in Kronos. Planetary engulfment is a plausible explanation, considering the ingestion of an exceptionally large mass, approximately approximately 27.8M_Earth, but no scenario is definitively ruled out., Comment: 11 pages, 6 figures

Recently, recurrent models based on linear state space models (SSMs) have shown promising performance in language modeling (LM), competititve with transformers. However, there is little understanding of the in-principle abilities of such models, which could provide useful guidance to the search for better LM architectures. We present a comprehensive theoretical study of the capacity of such SSMs as it compares to that of transformers and traditional RNNs. We find that SSMs and transformers have overlapping but distinct strengths. In star-free state tracking, SSMs implement straightforward and exact solutions to problems that transformers struggle to represent exactly. They can also model bounded hierarchical structure with optimal memory even without simulating a stack. On the other hand, we identify a design choice in current SSMs that limits their expressive power. We discuss implications for SSM and LM research, and verify results empirically on a recent SSM, Mamba.

Magic-Angle Twisted Bilayer Graphene shows a wide range of correlated phases which are electrostatically tunable. Despite a growing knowledge of the material, there is yet no consensus on the microscopic mechanisms driving its superconducting phase. In particular, elucidating the symmetry and formation mechanism of the superconducting phase may provide key insights for the understanding of unconventional, strongly coupled and topological superconductivity. A major obstacle to progress in this direction is that key thermodynamic properties, such as specific heat, electron-phonon coupling and superfluid stiffness, are extremely challenging to measure due to the 2D nature of the material and its relatively low energy scales. Here, we use a gate-defined, radio frequency-biased, Josephson junction to probe the electronic dynamics of magic-angle twisted bilayer graphene (MATBG). We reveal both the electronic quasiparticle dynamics, driven by their thermalization through phonon scattering, as well as the condensate dynamics, driven by the inertia of Cooper pairs. From these properties we recover the evolution of thermalization rates, and the superfluid stiffness across the phase diagram. Our findings favor an anisotropic or nodal pairing state and allow to estimate the strength of electron-phonon coupling. These results contribute to understanding the underlying mechanisms of superconductivity in MATBG while establishing an easy-to-implement method for characterizing thermal and superfluid properties of superconducting 2D materials., Comment: 9 pages, 5 figures

The built environment provides an excellent setting for interdisciplinary research on the dynamics of microbial communities. The system is simplified compared to many natural settings, and to some extent the entire environment can be manipulated, from architectural design, to materials use, air flow, human traffic, and capacity to disrupt microbial communities through cleaning. Here we provide an overview of the ecology of the microbiome in the built environment. We address niche space and refugia, population and community (metagenomic) dynamics, spatial ecology within a building, including the major microbial transmission mechanisms, as well as evolution. We also address the landscape ecology connecting microbiomes between physically separated buildings. At each stage we pay particular attention to the actual and potential interface between disciplines, such as ecology, epidemiology, materials science, and human social behavior. We end by identifying some opportunities for future interdisciplinary research on the microbiome of the built environment., Comment: 23 pages

Light-harvesting devices made from PbS quantum dot (QD) absorbers are one of the many promising technologies of third-generation photovoltaics. Their simple, solution-based fabrication together with a highly tunable and broad light absorption makes their application in newly developed solar cells particularly promising. In order to yield devices with reduced voltage and current losses, PbS QDs need to have strategically passivated surfaces, most commonly achieved through lead iodide and bromide passivation. The interdot spacing is then predominantly filled with residual amorphous lead halide species that remain from the ligand exchange, thus hindering efficient charge transport and reducing device stability. Herein, we demonstrate that a post-treatment by iodide based 2-phenylethlyammonium salts (X-PEAI) and intermediate 2D perovskite formation can be used to manage the lead halide excess in the PbS QD active layer. This treatment results in improved device performance and increased shelf-life stability, demonstrating the importance of interdot spacing management in PbS quantum dot photovoltaics.

Conductive metal-organic frameworks (MOFs) are emerging electroactive materials for (opto-)electronics. However, it remains a great challenge to achieve reliable MOF-based devices via the existing synthesis methods that are compatible with the complementary metal-oxide-semiconductor technology, as the surface roughness of thus-far synthetic MOF films or pellets is rather high for efficient electrode contact. Here, we develop an on-liquid-gallium surface synthesis (OLGSS) strategy under chemical vapor deposition (CVD) conditions for the controlled growth of two-dimensional conjugated MOF (2D c-MOF) thin films with ten-fold improvement of surface flatness (surface roughness can reach as low as ~2 {\AA}) compared with MOF films grown by the traditional methods. Supported by theoretical modeling, we unveil a layer-by-layer CVD growth mode for constructing flattening surfaces, that is triggered by the high adhesion energy between gallium (Ga) and planar aromatic ligands. We further demonstrate the generality of the as-proposed OLGSS strategy by reproducing such a flat surface over nine different 2D c-MOF films with variable thicknesses (~2 to 208 nm) and large lateral sizes (over 1 cm2). The resultant ultra-smooth 2D c-MOF films enable the formation of high-quality electrical contacts with gold (Au) electrodes, leading to a reduction of contact resistance by over ten orders of magnitude compared to the traditional uneven MOF films. Furthermore, due to the efficient interfacial interaction benifited from the high-quality contacts, the prepared van der Waals heterostructure (vdWH) of OLGSS c-MOF and MoS2 exhibits intriguing photoluminescence (PL) enhancement, PL peak shift and large work function modulation. The establishment of the reliable OLGSS method provides the chances to push the development of MOF electronics and the construction of multicomponent MOF-based heterostructure materials.

Alkaline water electrolysis is considered a commercially viable option for large-scale hydrogen production. However, this process still faces challenges due to the high voltage (>1.65 V at 10 mA cm$^{-2}$) and its limited stability at higher current densities due to the inefficient electron transport kinetics. Herein, a novel cobalt based metallic heterostructure (Co$_3$Mo3N/Co$_4$N/Co/Co) is designed for application for water electrolysis. Operando Raman experiments reveal that the formation of Co$_3$Mo3N/Co$_4$N/Co heterointerface boosts the free water adsorption and dissociation, resulting in a surplus of protons available for subsequent hydrogen production. Furthermore, the altered electronic structure of Co$_3$Mo3N/Co$_4$N/Co heterointerface optimizes the {\Delta}GH of nitrogen atoms at the interface. This synergistic effect between interfacial nitrogen atoms and metal phase cobalt creates highly efficient hydrogen evolution reaction (HER) active sites, thereby enhancing the overall performance. Additionally, the heterostructure exhibits a rapid OH- adsorption rate, coupled with a strong adsorption strength, leading to improved oxygen evolution reaction (OER) performance. Crucially, the metallic heterojunction facilitates fast electron transport, expediting the aforementioned reaction steps and ultimately improving the overall efficiency of water splitting. The water electrolyzer with Co$_3$Mo3N/Co$_4$N/Co/Co as a catalyst exhibits outstanding performance, requiring an impressively low cell voltage of 1.58 V at 10 mA cm$^{-2}$ and maintaining approximately 100% retention over a remarkable 100 h duration at 200 mA cm$^{-2}$. This performance significantly exceeds that of the commercial Pt/C || RuO2 electrolyzer.

Silver bismuth sulfide (AgBiS$_2$) nanocrystals have emerged as a promising eco-friendly, low-cost solar cell absorber material. Their direct synthesis often relies on the hot-injection method, requiring the application of high temperatures and vacuum for prolonged times. Here, we demonstrate an alternative synthetic approach via a cation exchange reaction. In the first-step, bis(stearoyl)sulfide is used as an air-stable sulfur precursor for the synthesis of small, monodisperse Ag2S nanocrystals at room-temperature. In a second step, bismuth cations are incorporated into the nanocrystal lattice to form ternary AgBiS$_2$ nanocrystals, without altering their size and shape. When implemented into photovoltaic devices, AgBiS$_2$ nanocrystals obtained by cation exchange reach power conversion efficiencies of up to 7.35%, demonstrating the efficacy of the new synthetic approach for the formation of high-quality, ternary semiconducting nanocrystals.

Bismuth oxide iodide (BiOI) has been viewed as a suitable environmentally-friendly alternative to lead-halide perovskites for low-cost (opto-)electronic applications such as photodetectors, phototransistors and sensors. To enable its incorporation in these devices in a convenient, scalable, and economical way, BiOI thin films were investigated as part of heterojunctions with various p-type organic semiconductors (OSCs) and tested in a field-effect transistor (FET) configuration. The hybrid heterojunctions, which combine the respective functionalities of BiOI and the OSCs were processed from solution under ambient atmosphere. The characteristics of each of these hybrid systems were correlated with the physical and chemical properties of the respective materials using a concept based on heteropolar chemical interactions at the interface. Systems suitable for application in lateral transport devices were identified and it was demonstrated how materials in the hybrids interact to provide improved and synergistic properties. These indentified heterojunction FETs are a first instance of successful incorporation of solution-processed BiOI thin films in a three-terminal device. They show a significant threshold voltage shift and retained carrier mobility compared to pristine OSC devices and open up possibilities for future optoelectronic applications.

Vibrational control (VC) of photochemistry through the optical stimulation of structural dynamics is a nascent concept only recently demonstrated for model molecules in solution. Extending VC to state-of-the-art materials may lead to new applications and improved performance for optoelectronic devices. Metal halide perovskites are promising targets for VC due to their mechanical softness and the rich array of vibrational motions of both their inorganic and organic sublattices. Here, we demonstrate the ultrafast VC of FAPbBr3 perovskite solar cells via intramolecular vibrations of the formamidinium cation using spectroscopic techniques based on vibrationally promoted electronic resonance. The observed short (~300 fs) time window of VC highlights the fast dynamics of coupling between the cation and inorganic sublattice. First-principles modelling reveals that this coupling is mediated by hydrogen bonds that modulate both lead halide lattice and electronic states. Cation dynamics modulating this coupling may suppress non-radiative recombination in perovskites, leading to photovoltaics with reduced voltage losses.

Blending of semiconductors for controlling the energy levels (band structure engineering) is an important technique, in particular, for optoelectronic applications. The underlying physics is the delocalized Bloch states, which average over the potential landscape of the blend. For organic semiconductors, it has been shown that two quite different effects, the dielectric constant and electrostatic interaction between molecules, can be used to tune the energy gap and ionization energy of disordered and weakly crystalline organic semiconductor blends. It is so far not known whether the electronic delocalization in organic crystals with large bandwidths can contribute to the energy structure engineering of the blend in a way similar to that in inorganic semiconductors. Here, we investigate the growth of highly ordered organic thin-film blends with a similar chemical structure and show the effect of band structure engineering by spectroscopic methods. We rationalize the experimental results with comprehensive theoretical simulations, showing that the delocalization is a significant effect. Our work paves the way for engineering the band structure of highly ordered organic semiconductor thin films that can be tailored for the desired optoelectronic device application.

The high photoluminescence efficiency, color purity, extended gamut, and solution processability make low-dimensional hybrid perovskites attractive for light-emitting diode (PeLED) applications. However, controlling the microstructure of these materials to improve the device performance remains challenging. Here, the development of highly efficient green PeLEDs based on blends of the quasi-2D (q2D) perovskite, PEA2Cs4Pb5Br16, and the wide bandgap organic semiconductor 2,7 dioctyl[1] benzothieno[3,2-b]benzothiophene (C8-BTBT) is reported. The presence of C8-BTBT enables the formation of single-crystal-like q2D PEA2Cs4Pb5Br16 domains that are uniform and highly luminescent. Combining the PEA2Cs4Pb5Br16:C8-BTBT with self-assembled monolayers (SAMs) as hole-injecting layers (HILs), yields green PeLEDs with greatly enhanced performance characteristics, including external quantum efficiency up to 18.6%, current efficiency up to 46.3 cd/A, the luminance of 45 276 cd m^-2, and improved operational stability compared to neat PeLEDs. The enhanced performance originates from multiple synergistic effects, including enhanced hole-injection enabled by the SAM HILs, the single crystal-like quality of the perovskite phase, and the reduced concentration of electronic defects. This work highlights perovskite:organic blends as promising systems for use in LEDs, while the use of SAM HILs creates new opportunities toward simpler and more stable PeLEDs.

Defects in metal halide perovskites (MHP) are photosensitive, making the observer effect unavoidable when laser spectroscopy methods are applied. Photoluminescence (PL) bleaching and enhancement under light soaking and recovery in dark are examples of the transient phenomena that are consequent to the creation and healing of defects. Depending on the initial sample composition, environment, and other factors, the defect nature and evolution can strongly vary, making spectroscopic data analysis prone to misinterpretations. Herein, the use of an automatically acquired dependence of PL quantum yield (PLQY) on the laser pulse repetition rate and pulse fluence as a unique fingerprint of both charge carrier dynamics and defect evolution is demonstrated. A simple visual comparison of such fingerprints allows for assessment of similarities and differences between MHP samples. The study illustrates this by examining methylammonium lead triiodide (MAPbI3) films with altered stoichiometry that just after preparation showed very pronounced defect dynamics at time scale from milliseconds to seconds, clearly distorting the PLQY fingerprint. Upon weeks of storage, the sample fingerprints evolve toward the standard stoichiometric MAPbI3 in terms of both charge carrier dynamics and defect stability. Automatic PLQY mapping can be used as a universal method for assessment of perovskite sample quality.

Liquid phase exfoliation (LPE) has been used for the successful fabrication of nanosheets from a large number of van der Waals materials. While this allows to study fundamental changes of material properties' associated with reduced dimensions, it also changes the chemistry of many materials due to a significant increase of the effective surface area, often accompanied with enhanced reactivity and accelerated oxidation. To prevent material decomposition, LPE and processing in inert atmosphere have been developed, which enables the preparation of pristine nanomaterials, and to systematically study compositional changes over time for different storage conditions. Here, we demonstrate the inert exfoliation of the oxidation-sensitive van der Waals crystal, CrTe$_3$. The pristine nanomaterial was purified and size-selected by centrifugation, nanosheet dimensions in the fractions quantified by atomic force microscopy and studied by Raman, X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray spectroscopy (EDX) and photo spectroscopic measurements. We find a dependence of the relative intensities of the CrTe$_3$ Raman modes on the propagation direction of the incident light, which prevents a correlation of the Raman spectral profile to the nanosheet dimensions. XPS and EDX reveal that the contribution of surface oxides to the spectra is reduced after exfoliation compared to the bulk material. Further, the decomposition mechanism of the nanosheets was studied by time-dependent extinction measurements after water titration experiments to initially dry solvents, which suggest that water plays a significant role in the material decomposition.

The fabrication of metal halide perovskite films using the solvent-engineering method is increasingly common. In this method, the crystallisation of the perovskite layer is triggered by the application of an antisolvent during the spin-coating of a perovskite precursor solution. Herein, we introduce the current state of understanding of the processes involved in the crystallisation of perovskite layers formed by solvent engineering, focusing in particular on the role of antisolvent properties and solvent-antisolvent interactions. By considering the impact of the Hansen solubility parameters, we propose guidelines for selecting the appropriate antisolvent and outline open questions and future research directions for the fabrication of perovskite films by this method.

Inorganic cesium lead iodide (CsPbI$_3$) perovskite solar cells (PSCs) have attracted enormous attention due to their excellent thermal stability and optical bandgap (~1.73 eV), well-suited for tandem device applications. However, achieving high-performing photovoltaic devices processed at low temperatures is still challenging. Here we reported a new method to fabricate high-efficiency and stable $\gamma$-CsPbI$_3$ PSCs at lower temperatures than was previously possible by introducing the long-chain organic cation salt ethane-1,2-diammonium iodide (EDAI2) and regulating the content of lead acetate (Pb(OAc)2) in the perovskite precursor solution. We find that EDAI2 acts as an intermediate that can promote the formation of $\gamma$-CsPbI$_3$, while excess Pb(OAc)2 can further stabilize the $\gamma$-phase of CsPbI$_3$ perovskite. Consequently, improved crystallinity and morphology and reduced carrier recombination are observed in the CsPbI$_3$ films fabricated by the new method. By optimizing the hole transport layer of CsPbI$_3$ inverted architecture solar cells, we demonstrate up to 16.6% efficiencies, surpassing previous reports examining $\gamma$-CsPbI$_3$ in inverted PSCs. Notably, the encapsulated solar cells maintain 97% of their initial efficiency at room temperature and dim light for 25 days, demonstrating the synergistic effect of EDAI2 and Pb(OAc)2 on stabilizing $\gamma$-CsPbI$_3$ PSCs.

Exposure to environmental factors is generally expected to cause degradation in perovskite films and solar cells. Herein, we show that films with certain defect profiles can display the opposite effect, healing upon exposure to oxygen under illumination. We tune the iodine content of methylammonium lead triiodide perovskite from understoichiometric to overstoichiometric and expose them to oxygen and light prior to the addition of the top layers of the device, thereby examining the defect dependence of their photooxidative response in the absence of storage-related chemical processes. The contrast between the photovoltaic properties of the cells with different defects is stark. Understoichiometric samples indeed degrade, demonstrating performance at 33% of their untreated counterparts, while stoichiometric samples maintain their performance levels. Surprisingly, overstoichiometric samples, which show low current density and strong reverse hysteresis when untreated, heal to maximum performance levels (the same as untreated, stoichiometric samples) upon the photooxidative treatment. A similar, albeit smaller-scale, effect is observed for triple cation and methylammonium-free compositions, demonstrating the general application of this treatment to state-of-the-art compositions. We examine the reasons behind this response by a suite of characterization techniques, finding that the performance changes coincide with microstructural decay at the crystal surface, reorientation of the bulk crystal structure for the understoichiometric cells, and a decrease in the iodine-to-lead ratio of all films. These results indicate that defect engineering is a powerful tool to manipulate the stability of perovskite solar cells.

The synthesis of metal sulfide nanocrystals is a crucial step in the fabrication of quantum dot (QD) photovoltaics. Control over the quantum dot size during synthesis allows for precise tuning of their optical and electronic properties, making them an appealing choice for electronic applications. This flexibility has led to the implementation of quantum dots in both highly-efficient single junction solar cells and other optoelectronic devices including photodetectors and transistors. Most commonly, metal sulfide quantum dots are synthesized using the hot-injection method utilizing toxic, and air- and moisture sensitive sulfur source: bis(trimethylsilyl) sulfide (TMS)2S. Here, we present bis(stearoyl) sulfide (St2S) as a new type of air-stable sulfur precursor for the synthesis of sulfide-based QDs, which yields uniform, pure, and stable nanocrystals. Photovoltaic devices based on these QDs are equally efficient as those fabricated by (TMS)2S but exhibit an enhanced operational stability. These results highlight that St2S can be widely adopted for the synthesis of metal sulfide quantum dots for a range of optoelectronic applications.

Molybdenum sulfide (MoS$_2$) has attracted significant attention due to its great potential as a low-cost and efficient catalyst for the hydrogen evolution reaction. Developing a facile, easily upscalable, and inexpensive approach to produce catalytically active nanostructured MoS$_2$ with a high yield would significantly advance its practical application. Colloidal synthesis offers several advantages over other preparation techniques to overcome the low reaction yield of exfoliation and drawbacks of expensive equipment and processes used in chemical vapor deposition. In this work, we report an efficient synthesis of alloyed Re$_x$Mo$_{1-x}$S$_2$ nanoflakes with an enlarged interlayer distance, among which the composition Re$_{0.55}$Mo$_{0.45}$S$_2$ exhibits excellent catalytic performance with overpotentials as low as 79 mV at 10 mA/cm2 and a small Tafel slope of 42 mV/dec. Density functional theory calculations prove that enlarging the distance between layers in the Re$_x$Mo$_{1-x}$S$_2$alloy can greatly improve its catalytic performance due to a significantly reduced free energy of hydrogen adsorption. The developed approach paves the way to design advanced transition metal dichalcogenide-based catalysts for hydrogen evolution and to promote their large-scale practical application.

Metal halide perovskites are an emerging class of crystalline semiconductors of great interest for application in optoelectronics. Their properties are dictated not only by their composition, but also by their crystalline structure and microstructure. While significant efforts were dedicated to the development of strategies for microstructural control, significantly less is known about the processes that govern the formation of their crystalline structure in thin films, in particular in the context of crystalline orientation. In this work, we investigate the formation of highly oriented triple cation perovskite films fabricated by utilizing a range of alcohols as an antisolvent. Examining the film formation by in-situ grazing-incidence wide-angle X-ray scattering reveals the presence of a short-lived highly oriented crystalline intermediate, which we identify as FAI-PbI2-xDMSO. The intermediate phase templates the crystallisation of the perovskite layer, resulting in highly oriented perovskite layers. The formation of this DMSO containing intermediate is triggered by the selective removal of DMF when alcohols are used as an antisolvent, consequently leading to differing degrees of orientation depending on the antisolvent properties. Finally, we demonstrate that photovoltaic devices fabricated from the highly oriented films, are superior to those with a random polycrystalline structure in terms of both performance and stability.

Metal halide perovskites are of great interest for application in semitransparent solar cells due to their tunable bandgap and high performance. However, fabricating high-efficiency perovskite semitransparent devices with high average visible transmittance (AVT) is challenging because of their high absorption coefficient. Here, we adopt a co-evaporation process to fabricate ultrathin CsPbI3 perovskite films. Due to the smooth surface and orientated crystal growth of the evaporated perovskite films, we are able to achieve 10 nm thin films with compact and continuous morphology without pinholes. When integrated into a p-i-n device structure of glass/ITO/PTAA/perovskite/PCBM/BCP/Al/Ag with an optimized transparent electrode, these ultrathin layers result in an impressive open-circuit voltage (VOC) of 1.08 V and a fill factor (FF) of 80%. Consequently, a power conversion efficiency of 3.6% with an AVT above 50% is demonstrated, achieved in the 10 nm semitransparent perovskite solar cells, which is the first report for a perovskite device of 10 nm active layer with higher VOC, FF and AVT. These findings demonstrate that evaporation process is a possible way for compact ultrathin perovskite film, which has the potential for future smart windows, light emitting diodes, and tandem device applications.

Metal oxide (MO) semiconductors are widely used in electronic devices due to their high optical transmittance and promising electrical performance. This work describes the advancement toward an eco-friendly, streamlined method for preparing thin-film transistors (TFTs) via a pure water-solution blade-coating process with focus on a low thermal budget. Low temperature and rapid annealing of triple-coated indium oxide thin-film transistors (3C-TFTs) and indium oxide/zinc oxide/indium oxide thin-film transistors (IZI-TFTs) on a 300 nm SiO2 gate dielectric at 300 $^{\circ}$C for only 60 s yields devices with an average field effect mobility of 10.7 and 13.8 cm2/Vs, respectively. The devices show an excellent on/off ratio (>10^6), and a threshold voltage close to 0 V when measured in air. Flexible MO-TFTs on polyimide substrates with AlOx dielectrics fabricated by rapid annealing treatment can achieve a remarkable mobility of over 10 cm2/Vs at low operating voltage. When using a longer post-coating annealing period of 20 min, high-performance 3C-TFTs (over 18 cm2/Vs) and IZI-TFTs (over 38 cm2/Vs) using MO semiconductor layers annealed at 300 $^{\circ}$C are achieved.

The Euclidean Steiner problem is the problem of finding a set $St$, with the shortest length, such that $St \cup A$ is connected, where $A$ is a given set in a Euclidean space. The solutions $St$ to the Steiner problem will be called Steiner sets while the set $A$ will be called input. Since every Steiner set is acyclic we call it Steiner tree in the case when it is connected. We say that a Steiner tree is indecomposable if it does not contain any Steiner tree for a subset of the input. We are interested in finding the Steiner set when the input consists of infinitely many points distributed on two lines. In particular we would like to find a configuration which gives an indecomposable Steiner tree. We consider a self-similar input, namely the set $A_{\alpha,\lambda}$ of points with coordinates $(\lambda^{k-1}\cos \alpha,$ $\pm \lambda^{k-1}\sin \alpha)$, where $\lambda>0$ and $\alpha>0$ are small fixed values. These points are distributed on the two sides of an angle of size $2\alpha$ in such a way that the distances from the points to the vertex of the angle are in a geometric progression. To our surprise, we show that in this case the solutions to the Steiner problem for $A_{\alpha,\lambda}$, when $\alpha$ and $\lambda$ are small enough, are always decomposable trees. More precisely, any Steiner tree for $A_{\alpha,\lambda}$ is a countable union of Steiner trees, each one connecting 5 points from the input. By considering only a finite number of components we obtain many solutions to the Steiner problem for finite sets composed of $4k+1$ points distributed on the two lines ($2k+1$ on a line and $2k$ on the other line). These solutions are very similar to the ladders of Chung and Graham.

Molecular-scale diodes made from self-assembled monolayers (SAMs) could complement silicon-based technologies with smaller, cheaper, and more versatile devices. However, advancement of this emerging technology is limited by insufficient electronic performance exhibited by the molecular current rectifiers. We overcome this barrier by exploiting the charge-transfer state that results from co-assembling SAMs of molecules with strong electron donor and acceptor termini. We obtain a substantial enhancement in current rectification, which correlates with the degree of charge transfer, as confirmed by several complementary techniques. These findings provide a previously unexplored method for manipulating the properties of molecular electronic devices by exploiting donor/acceptor interactions. They also serve as a model test platform for the study of doping mechanisms in organic systems. Our devices have the potential for fast widespread adoption due to their low-cost processing and self-assembly onto silicon substrates, which could allow seamless integration with current technologies.

Modern photovoltaic devices are often based on a heterojunction structure where two components with different optoelectronic properties are interfaced. The properties of each side of the junction can be tuned by either utilizing different materials (e.g. donor/acceptor) or doping (e.g. PN Si junction) or even varying their dimensionality (e.g. 3D/2D). In this work we demonstrate the concept of phase heterojunction (PHJ) solar cells by utilizing two polymorphs of the same material. We demonstrate the approach by forming $\gamma$-CsPbI3/$\beta$-CsPbI3 perovskite PHJ solar cells. We find that all of the photovoltaic parameters of the PHJ device significantly surpass those of each of the single-phase devices, resulting in a maximum power conversion efficiency of 20.1%. These improvements originate from the efficient passivation of the $\beta$-CsPbI3 by the larger bandgap $\gamma$-CsPbI3, the increase in the built-in potential of the PHJ devices enabled by the energetic alignment between the two phases and the enhanced absorption of light by the PHJ structure. The approach demonstrated here offers new possibilities for the development of photovoltaic devices based on polymorphic materials.

2D Ruddlesden - Popper perovskites are promising candidates for energy harvesting applications due to their tunable optical properties and excellent ambient stability. Moreover, they are solution-processable and compatible with upscalable manufacturing via various printing techniques. Unfortunately, such methods often induce large degrees of heterogeneity due to poorly controlled crystallization. Here, we address this issue by blending the well-known 2D perovskite (PEA)2PbBr4 with an organic small-molecule, namely C8-BTBT, employed as an additive with different blending ratios. Using terahertz (THz) absorption and temperature-dependent photoluminescence (PL) spectroscopy techniques we observe that with the C8-BTBT additive the photophysical properties are altered while the perovskite structure in the film remains unaffected. More precisely, the inclusion of trace amounts of C8-BTBT in the hybrid films results in defect passivation at perovskite platelet boundaries and at the surfaces, as indicated by increased carrier lifetimes and substantially increased photoluminescence quantum yields (PLQY). This in turn improves the responsivity of photodetectors using the 2D perovskite as active layer. Our study highlights a straightforward strategy for fabricating high-quality 2D perovskites via large-area processing techniques.

Structural colors can be induced on metals not only to fabricate logos or decorative motives but also to embed anti-counterfeit features for product protection. In this study, stainless steel (EN 1.4301) plates are colorized by growing a thin oxide layer using direct laser writing (DLW) and hidden anti-counterfeit measures are included on their surfaces by direct laser interference patterning (DLIP) processing. The periodic microstructures resulting from the DLIP treatment have a spatial period of 1 um and act as relief diffraction gratings, featuring a characteristic diffraction pattern. These microstructures are not visible to the human eye but are easily detectable upon shining a coherent beam on the surface. Furthermore, the reflectance over the visible spectrum of the colorized surfaces with and without the DLIP microtexture is measured, giving low differences in the color perception following the so-called "CIE L*a*b*" color space. Finally, a demonstrator is fabricated, in which colorized fields with and without the security features are shown.

In this paper, we present our novel systems developed for the SemEval-2024 hallucination detection task. Our investigation spans a range of strategies to compare model predictions with reference standards, encompassing diverse baselines, the refinement of pre-trained encoders through supervised learning, and an ensemble approaches utilizing several high-performing models. Through these explorations, we introduce three distinct methods that exhibit strong performance metrics. To amplify our training data, we generate additional training samples from unlabelled training subset. Furthermore, we provide a detailed comparative analysis of our approaches. Notably, our premier method achieved a commendable 9th place in the competition's model-agnostic track and 17th place in model-aware track, highlighting its effectiveness and potential., Comment: 12 pages, 10 tables, 3 figures

Topological boundary states localize at interfaces whenever the interface implies a change of the associated topological invariant encoded in the geometric phase. The generically present dynamic phase, however, which is energy and time dependent, has been known to be non-universal, and hence not to intertwine with any topological geometric phase. Using the example of topological zero modes in composite Su-Schrieffer-Heeger (c-SSH) waveguide arrays with a central defect, we report on the selective excitation and transition of topological boundary mode based on dynamic phase-steered interferences. Our work thus provides a new knob for the control and manipulation of topological states in composite photonic devices, indicating promising applications where topological modes and their bandwidth can be jointly controlled by the dynamic phase, geometric phase, and wavelength in on-chip topological devices.

The growing number of Milky Way satellites detected in recent years has introduced a new focus for stellar abundance analysis. Abundances of stars in satellites have been used to probe the nature of these systems and their chemical evolution. However, for most satellites, only centrally located stars have been examined. This paper presents an analysis of three stars in the Tucana V system, one in the inner region and two at $\sim$10\arcmin\ (7--10 half-light radii) from the center. We find a remarkable chemical diversity between the stars. One star exhibits enhancements in rapid neutron-capture elements (an $r$-I star), and another is highly enhanced in C, N, and O but with low neutron-capture abundances (a CEMP-no star). The metallicities of the stars analyzed span more than 1~dex from $\mathrm{[Fe/H]}=-3.55$ to $-2.46$. This, combined with a large abundance range of other elements like Ca, Sc, and Ni, confirms that Tuc~V is an ultra-faint dwarf (UFD) galaxy. The variation in abundances, highlighted by [Mg/Ca] ratios ranging from $+0.89$ to $-0.75$, among the stars, demonstrates that the chemical enrichment history of Tuc~V was very inhomogeneous. Tuc~V is only the second UFD galaxy in which stars located at large distances from the galactic center have been analyzed, along with Tucana~II. The chemical diversity seen in these two galaxies, driven by the composition of the non-central member stars, suggests that distant member stars are important to include when classifying faint satellites and that these systems may have experienced more complex chemical enrichment histories than previously anticipated., Comment: 19 pages, 11 figures, accepted for publication in ApJ

Among Neptunian mass exoplanets ($20-50$ M$_\oplus$), puffy hot Neptunes are extremely rare, and their unique combination of low mass and extended radii implies very low density ($\rho < 0.3$~g~cm$^{-3}$). Over the last decade, only a few puffy planets have been detected and precisely characterized with both transit and radial velocity observations, most notably including WASP-107~$b$, TOI-1420~$b$, and WASP-193 $b$. In this paper, we report the discovery of TOI-1173 A $b$, a low-density ($\rho = 0.195_{-0.017}^{+0.018}$~g~cm$^{-3}$) super-Neptune with $P = 7.06$ days in a nearly circular orbit around the primary G-dwarf star in the wide binary system TOI-1173 A/B. Using radial velocity observations with the MAROON-X and HIRES spectrographs and transit photometry from TESS, we determined a planet mass of $M_{\rm{p}} = 27.4\pm1.7\ M_{\oplus}$ and radius of $R_{\rm{p}} = 9.19\pm0.18\ R_{\oplus}$. TOI-1173 A $b$ is the first puffy Super-Neptune planet detected in a wide binary system (projected separation $\sim 11,400$~AU). We explored several mechanisms to understand the puffy nature of TOI-1173 A $b$, and showed that tidal heating is the most promising explanation. Furthermore, we demonstrate that TOI-1173 A $b$ likely has maintained its orbital stability over time and may have undergone von-Zeipel-Lidov-Kozai migration followed by tidal circularization given its present-day architecture, with important implications for planet migration theory and induced engulfment into the host star. Further investigation of the atmosphere of TOI-1173 A $b$ will shed light on the origin of close-in low-density Neptunian planets in field and binary systems, while spin-orbit analyses may elucidate the dynamical evolution of the system., Comment: Accepted for publication in the Astronomical Journal on June 2, 2024

Lack of nonreciprocity is one of the major drawbacks of solid-state acoustic devices, which has hindered the development of microwave-frequency acoustic isolators and circulators. Here we report giant nonreciprocal transmission of shear-horizontal surface acoustic waves (SH-SAWs) on a LiTaO3 substrate coated with a negative-positive magnetostrictive bilayer structure of Ni/Ti/FeCoSiB. Although the static magnetic moments of two layers are parallel, SH-SAWs can excite optical-mode spin waves much stronger than acoustic-mode ones at relatively low frequencies via magnetoelastic coupling. The measured magnitude nonreciprocity exceeds 40 dB (or 80 dB/mm) at 2.333 GHz. In addition, maximum nonreciprocal phase accumulation reaches 188{\deg} (376{\deg}/mm), which is desired for an effective SAW circulator. Our theoretical model and calculations provide an insight into the observed phenomena and demonstrate a pathway for further improvement of nonreciprocal acoustic devices.

In this report, we introduce the Gemini 1.5 family of models, representing the next generation of highly compute-efficient multimodal models capable of recalling and reasoning over fine-grained information from millions of tokens of context, including multiple long documents and hours of video and audio. The family includes two new models: (1) an updated Gemini 1.5 Pro, which exceeds the February version on the great majority of capabilities and benchmarks; (2) Gemini 1.5 Flash, a more lightweight variant designed for efficiency with minimal regression in quality. Gemini 1.5 models achieve near-perfect recall on long-context retrieval tasks across modalities, improve the state-of-the-art in long-document QA, long-video QA and long-context ASR, and match or surpass Gemini 1.0 Ultra's state-of-the-art performance across a broad set of benchmarks. Studying the limits of Gemini 1.5's long-context ability, we find continued improvement in next-token prediction and near-perfect retrieval (>99%) up to at least 10M tokens, a generational leap over existing models such as Claude 3.0 (200k) and GPT-4 Turbo (128k). Finally, we highlight real-world use cases, such as Gemini 1.5 collaborating with professionals on completing their tasks achieving 26 to 75% time savings across 10 different job categories, as well as surprising new capabilities of large language models at the frontier; when given a grammar manual for Kalamang, a language with fewer than 200 speakers worldwide, the model learns to translate English to Kalamang at a similar level to a person who learned from the same content.

Amphiphilic polymers in aqueous solutions can self-assemble to form bilayer membranes, and their elastic properties can be captured by the well-known Helfrich model involving several elastic constants. In this paper, we employ the self-consistent field model to simulate sinusoidal bilayers self-assembled from diblock copolymers where a proper constraint term is introduced to stabilize periodic bilayers with prescribed amplitudes. Then, we devise several methods to extract the shape of these bilayers and examine the accuracy of the free energy predicted by the Helfrich model. Numerical results show that when the bilayer curvature is small, the Helfrich model predicts the excess free energy more accurately. However, when the curvature is large, the accuracy heavily depends on the method used to determine the shape of the bilayer. In addition, the dependence of free energy on interaction strength, constraint amplitude, and constraint period are systematically studied. Moreover, we obtain certain periodic cylindrical bilayers that are equilibrium states of the self-consistent field model, which agree with the theoretical predictions made by the shape equations., Comment: 10 pages,10 figures