Intrinsic Research Articles

Uncovering low-frequency vibrations in surface-enhanced Raman of organic molecules

Accessing the terahertz (THz) spectral domain through surface-enhanced Raman spectroscopy (SERS) is challenging and opens up the study of low-frequency molecular and electronic excitations. Compared to direct THz probing of heterogenous ensembles, the extreme plasmonic confinement of visible light to deep sub-wavelength scales allows the study of hundreds or even single molecules. We show that self-assembled molecular monolayers of a set of simple aromatic thiols confined inside single-particle plasmonic nanocavities can be distinguished by their low-wavenumber spectral peaks below 200 cm−1, after removal of a bosonic inelastic contribution and an exponential background from the spectrum. Developing environment-dependent density-functional-theory simulations of the metal-molecule configuration enables the assignment and classification of their THz vibrations as well as the identification of intermolecular coupling effects and of the influence of the gold surface configuration. Furthermore, we show dramatically narrower THz SERS spectra from individual molecules at picocavities, which indicates the possibility to study intrinsic vibrational properties beyond inhomogeneous broadening, further supporting the key role of local environment.

Optimizing compressive strength prediction using adversarial learning and hybrid regularization

The infrastructure industry consumes natural resources and produces construction waste, which has a detrimental impact on the environment. To mitigate these adverse effects and reduce raw material consumption, waste materials can be repurposed to achieve sustainability. However, recycled materials deteriorate the intrinsic properties of concrete. A suitable ratio of natural resources and recycled aggregates can produce the desired compressive strength. Compiling sufficient data in civil engineering laboratories to make reliable conclusions is time-consuming and costly. Therefore, this research proposes a novel approach for predicting compressive strengths using limited data. The generative adversarial network was employed to generate synthetic data. Hybrid training, utilizing either conventional loss or heuristic loss, prevents the model from overfitting by adaptively adjusting the regularization term. Random noise from a multivariate normal distribution is embedded heuristically into the training samples to capture intricate data variations. Sensitivity analysis indicated that the size of recycled coarse aggregate and water are the most significant features, aligning with their correlations. Interestingly, superplasticizer, density of recycled coarse aggregate, and water absorption ratio of recycled coarse aggregate contributed significantly to predictions despite their low correlations. The propounded method outperforms random forest, support vector regression, artificial neural network, and adaptive boosting by scoring a mean squared error of 7.97, a root mean squared error of 2.82, a mean absolute error of 2.13, and a coefficient of determination of 0.96. These results suggest that the proposed technique can effectively contribute to sustainable construction practices by accurately predicting compressive strengths.

Sympathetic Motor Neuron Dysfunction is a Missing Link in Age-Associated Sympathetic Overactivity.

Overactivity of the sympathetic nervous system is a hallmark of aging. The cellular mechanisms behind this overactivity remain poorly understood, with most attention paid to likely central nervous system components. In this work, we hypothesized that aging also affects the function of motor neurons in the peripheral sympathetic ganglia. To test this hypothesis, we compared the electrophysiological responses and ion-channel activity of neurons isolated from the superior cervical ganglia of young (12 weeks), middle-aged (64 weeks), and old (115 weeks) mice. These approaches showed that aging does impact the intrinsic properties of sympathetic motor neurons, increasing spontaneous and evoked firing responses. A reduction of M current emerged as a major contributor to age-related hyperexcitability. Thus, it is essential to consider the effect of aging on motor components of the sympathetic reflex as a crucial part of the mechanism involved in sympathetic overactivity.

The importance of spatial scale and vegetation complexity in woody species diversity and its relationship with remotely sensed variables

Plant species diversity is key to ecosystem functioning, but in recent decades anthropogenic activities have prompted an alarming decline in this community trait. Thus, developing strategies to understand diversity dynamics based on affordable and efficient remote sensing monitoring is essential, as well as examining the relevance of spatial scale and vegetation structural complexity to these dynamics. Here, we used two mathematical approaches to assess the relationship between tropical woody species diversity and spectral diversity in a human-modified landscape in two vegetation types differing in their degree of complexity. Vegetation complexity was measured through the fraction of species that concentrate different proportions of the cumulative importance value index. Species diversity was assessed using Hill numbers at three spatial scales, and metrics of spectral heterogeneity, vegetation indices, as well as raw data from Landsat 9 and Sentinel-2 sensors were calculated and analysed through general linear models (GLM) and Random Forest. Vegetation complexity emerged as an important variable in modelling species from remote sensing metrics, indicating the need to model species diversity by vegetation type rather than region. Hill numbers showed different relationships with remotely sensed metrics, in consistency with the scale-dependency of ecological processes on species diversity. Contrary to multiple previous reports, in our study, GLMs produced the best fits between Hill numbers of all orders and remotely sensed metrics. If we are to meet the need of conducting efficient and speedy woody species diversity monitoring globally, we propose modelling this diversity from remotely-sensed variables as an attractive strategy, so long as the intrinsic properties of each vegetation type are acknowledged to avoid under- or overestimation biases.

Evolution of Surface Chemistry in Two-Dimensional MXenes: From Mixed to Tunable Uniform Terminations.

Surface chemistry of MXenes is of great interest as the terminations can define the intrinsic properties of this family of materials. The diverse and tunable terminations also distinguish MXenes from many other 2D materials. Conventional fluoride-containing reagents etching approaches resulted in MXenes with mixed fluoro-, oxo-, and hydroxyl surface groups. The relatively strong chemical bonding of MXenes' surface metal atoms with oxygen and fluorine makes post-synthetic covalent surface modifications of such MXenes unfavorable. In this minireview, we focus on the recent advances in MXenes with uniform surface terminations. Unconventional methods, including Lewis acidic molten salt etching (LAMS) and bottom-up direct synthesis, have been proven successful in producing halide-terminated MXenes. These synthetic strategies have opened new possibilities for MXenes because weaker surface chemical bonds in halide-terminated MXenes facilitate post-synthetic covalent surface modifications. Both computational and experimental results on surface termination-dependent properties are summarized and discussed. Finally, we offer our perspective on the opportunities and challenges in this exciting research field.

Sedimentation dynamics of triply twisted Möbius bands: Geometry versus topology

We explore the sedimentation dynamics of triply twisted Möbius bands, each characterized by threefold rotational symmetry but distinguished by its construction and intrinsic geometrical properties. Three types of bands are considered: one with vanishing Gaussian curvature, constructed by isometrically deforming flat rectangular strips through bending without stretching; and two with negative Gaussian curvature, one being constructed by isometrically deforming helicoids. Experiment on these three types of bands, with a focus on varying aspect ratios, reveals a singular phenomenon: while the spin directions of bands not derived from helicoids spin in directions consistent with their inherent chirality, bands derived from helicoids exhibit an aspect-ratio-dependent spin, pointing to the existence of a critical aspect ratio at which geometric factors dominate over chiral influences. Supported by numerical simulations and a detailed analysis of the resistance tensors, we propose the unique response of bands derived from helicoids originates from a complex interaction among geometry, topology, and hydrodynamics. Two explanations are offered for the chiral transition observed in bands derived from helicoid. First, this transition may parallel the dynamics of superhelices, for which competing chiralities influence rotational behavior. Second, the unique geometrical properties of bands derived from helicoids, coupled with deviations between the rotation axis and the local symmetry axis, may underlie the observed aspect-ratio-dependent chiral transition. Our study underscores the significant role of geometrical and topological nuances in determining the behavior of chiral objects suspended in fluids. In addition to offering transformative potential across diverse fields, it promises advancements in mixing, separation processes, and innovative passive swimmers. Published by the American Physical Society 2024

A lamellar-morphology-based computational modeling for predicting the thermal conductivity of semicrystalline polymers

Molecular-scale design of crystal structures is an emerging approach for significantly improving the intrinsic properties of polymers. In this study, we performed computational modeling to quantitatively predict the thermal conductivity of polymers based on their crystal morphology. Polyethylene lamellae with alternating crystalline and amorphous phases were prepared using isothermal crystallization within a coarse-grained molecular dynamics framework. The crystalline bulk, transient, and amorphous regions were clearly distinguished based on the distribution of the Steinhardt-bond order parameter. The thermal conductivity of the local regions was estimated discretely by applying a steady heat flow, facilitating a bottom-up prediction of the thermal response depending on the morphology of the lamellae. In particular, the integration with homogenization theory can evaluate the effective thermal conductivity of the system in terms of crystallinity, temperature, lamella thickness and orientation. The modeling successfully provided quantitative predictions for two representative hierarchical structures: spherulites and oriented crystals. Therefore, this study serves as a theoretical guide for molecular-level rational design of semicrystalline materials with high thermal conductivity.

Polymorph‐Dependent Multi‐Level Supramolecular Self‐Assembly and Local Charge Transport of a Conjugated Polymer in Solution and Solid States

AbstractThe polymorphic behavior of conjugated polymers enables tunable optoelectronic properties, but their transport mechanism remains elusive due to the inherent complexity and uncontrollability of polymorphic self‐assembly behaviors and electronic processes at various length scales, alongside the ambiguous relationship between solution and solid states. Herein, precise control of multi‐level supramolecular self‐assembly of a polymorphic conjugated polymer, N‐PDPP4T‐HD with two distinct semi‐crystalline aggregated phases (β1 and β2) via solvent engineering is demonstrated. β1 forms 1D worm‐like nanostructures in solution, whereas β2 generates 2D nanoscale lamellar configuration, confirmed by experimental observation and molecular dynamic simulation. Such solution‐state features are inherited in the solid state (1D nanofibers for β1 and 2D granular‐like structures for β2). X‐ray characterizations reveal larger crystalline domains on the nanometer scale, reduced π‐stacking distance on the Ångstrom scale, and diminished paracrystallinity disorder for solid‐state β2. Going beyond conventional DC transistor characterizations, contact‐free ultrafast terahertz spectroscopy to unveil AC short‐range, intrinsic transport properties is employed. Longer charge carrier scattering time and thus intrinsic mobility of β2 result in threefold higher short‐range photoconductivity than β1. This work establishes the “solution structure – solid structure – local transport” relation in polymorphic conjugated polymers and provides new opportunities for high‐performance plastic electronic devices.

Five‐ or six‐membered aluminum metallocyclic complexes containing N, N bidentate oxazolinyl‐indolate chelate ring: Synthesis, structural, and catalytic studies

Treatment of two classes of oxazolinyl‐indolate ligand precursors with an equivalent trimethylaluminum reagent afforded four corresponding aluminum dimethyl complexes. Intramolecular functional groups were employed to switch coordination behaviors, resulting in the formation of two classes of five‐ or six‐membered aluminum metallocyclic complexes. The screening of the prepared aluminum complexes, mediated by 9‐anthracenemethanol as the initiating reagent in the ring‐opening polymerization of ε‐caprolactone, showed significant activities at room temperature. The aluminum compound ligated by 2‐(1H‐indol‐2‐yl)‐4,4‐dimethyl‐4,5‐dihydrooxazole possessed a suitable chelated ring size, and its intrinsic electronic properties maintained higher activity.

Enhancing charge storage capacity of cellulose-sweat-based electrolyte flexible supercapacitors with electrochemically exfoliated free-standing carbon yarn electrodes

The Internet of Things (IoT) provides an interface between different electronic devices such as flexible electronics, and e-textiles to capture and receive real-time data and help humans to devise systems that will adequately respond to these environmental stimuli. The main limitations of these devices to work 24/7 are the lack of continuous power supply and easy integration into textiles to perform their functions. The other issues are poor adhesion of active materials with substrates and peeling-off of active material from the electrode substrates and consequently, degradation of electrochemical performance. A potential and evolving strategy is fabricating a current collector-less and integrable carbon yarn-based energy storage device. Herein, we are presenting a facile and novel technique to exfoliate carbon yarn fibers to enhance their electrochemical performance by 3 orders of magnitude. Activated carbon yarn wires acting as current collector-less electrodes along with cellulose acetate-based composite separators offer a large surface area to simulated sweat electrolyte ions and show a gravimetric capacitance of 11.28 Fg−1 at the scan rate of 5 mVs−1. Activated carbon yarn-based symmetric supercapacitor device in a simulated sweat solution electrolyte offers excellent cyclic and bending stability with over 95 % capacitance retention in both tests. Theoretical insightSupercapacitors (SCs) comprise many active and passive elements. The most passive and vital elements are current collectors, separators, binders, electrolytes, and packaging. Two key elements, current collector and binders can be eliminated by developing current collector-free or free-standing electrodes. Carbonaceous materials such as graphene [1,2], carbon nanotubes (CNT) [3], porous carbon [2], and carbon onions[4,5] are common alternatives of active materials for SCs electrodes owing to their low cost, chemical stability, large surface area, and high electrical conductivity. These active materials show exceptional attributes such as long cyclic life, and high-rate capability owing to their intrinsic operation mechanism e.g., surface charge storage due to large surface area. However, they also suffer from low specific capacitance ascribed to low surface area exposed to electrolyte ions and low charge storage due to poor wettability. The most efficient technique to address this problem is to incorporate doped heteroatoms or surface functional groups such as surface oxygen groups present on the surface of carbon yarn. The inclusion of these doped heteroatoms and functional groups boosts the intrinsic properties, such as electrical conductivity, and wettability. The increased electro-active surface area offers more active sites for electrolyte ions, resulting in more charge storage and higher pseudocapacitance [6–8].Carbon yarn comprised of long-chain carbon filaments of 2.5–5 µm in radius, excellent conductivity, high chemical and mechanical stability, and light weightiness make it a potential candidate as an active material or a free-standing electrode for SCs. However, due to its low specific capacitance, limited surface area, and low porosity, carbon yarn failed to be directly exploited as a free-standing or current collector-less electrode for flexible supercapacitor applications.

Binding between Cu2+/Zn2+ and aged polyethylene and polyethylene terephthalate microplastics in swine wastewaters: Adsorption behavior, and mechanism insights

Microplastics (MPs) have aroused growing environmental concerns due to their biotoxicity and vital roles in accelerating the spread of toxic elements. Illuminating the interactions between MPs and heavy metals (HMs) is crucial for understanding the transport and fate of HM-loaded MPs in specific environmentally relevant scenarios. Herein, the adsorption of copper (Cu2+) and zinc (Zn2+) ions over polyethylene (PE) and polyethylene terephthalate (PET) particulates before and after heat persulfate oxidation (HPO) treatment was comprehensively evaluated in simulated and real swine wastewaters. The effects of intrinsic properties (i.e., degree of weathering, size, type) of MPs and environmental factors (i.e., pH, ionic strength, and co-occurring species) on adsorption were investigated thoroughly. It was observed that HPO treatment expedites the fragmentation of pristine MPs, and renders MPs with a variety of oxygen-rich functional groups, which are likely to act as new active sites for binding both HMs. The adsorption of both HMs is pH- and ionic strength-dependent at a pH of 4–6. Co-occurring species such as humic acid (HA) and tetracycline (TC) appear to enhance the affinity of both aged MPs for Cu2+ and Zn2+ ions via bridging complexation. However, co-occurring nutrient species (e.g., phosphate and ammonia) demonstrate different impacts on the adsorption, improving uptake of Cu2+ by precipitation while lowering affinity for Zn2+ owing to the formation of soluble zinc-ammonia complex. Spectroscopic analysis indicates that the dominant adsorption mechanism mainly involves electrostatic interactions and surface complexation. These findings provided fundamental insights into the interactions between aged MPs and HMs in swine wastewaters and might be extended to other nutrient-rich wastewaters.

Soil organic matter persistence in hyperhumic colluvial soils caused by palaeofires, root inputs and mineral binding

Understanding the formation of long-term persistent soil organic matter (SOM) is key to optimizing soil management and predicting the response of the terrestrial organic carbon (OC) pool to climate change, yet our knowledge of the soil-type dependent weight of different stabilization pathways (e.g., recalcitrance and mineral binding) is fragmentary. Owing to their stratigraphy, the exceptionally SOM-rich (up to 2 m of mineral soil with >5% OC) colluvial slope deposits of Atlantic Europe (Haplic Umbrisol [colluvic/hyperhumic]) are archives of palaeo-environmental conditions including SOM formation pathways. The objective of this study was to determine how the different drivers of persistent SOM formation influenced the formation of these organic-rich soils. For this purpose, we use Holocene (∼9000 yrs) molecular composition records obtained from pyrolysis-GC–MS (Py-GC–MS) and thermally assisted hydrolysis and methylation (THM-GC–MS). The results emphasize three pathways to stability (i.e., persistence on millennial timescales): 1) palaeofires that generated recalcitrant pyrogenic SOM, 2) release of root-derived aliphatic macromolecules (suberin-like SOM), and 3) formation of microbial necromass. Pathways 1 and 2 are controlled by land use: Pathway 1 was relatively important under intense anthropogenic fire regimes and pyrophytic shrubland expansion; Pathway 2 was stimulated during early forest phases and under pasture conditions, when past societies focused vegetation management on grazing instead of fire; Pathway 3 was controlled by binding with aluminium-dominated mineral phases. However, we found indications that Pathway 2 (suberin input and preservation) relied partially on sorptive preservation as well. Aided by structured equation modeling (SEM), we show that the formation of persistent SOM pools was driven by balanced weights of i) microbial vs. plant-derived SOM and ii) intrinsic chemical properties of SOM (recalcitrance continuum) vs. mineral binding/occlusion, which varied in keeping with interactions between past land use, topography and vegetation. These findings are inconsistent with the prevalent paradigm of persistent SOM formation by sorptive/occlusive preservation of microbial necromass alone.

Screening diluents to optimize cesium contaminant separation using t-BAMBP extractant

The widespread use of nuclear energy has raised concerns about nuclear safety and radioactive waste management, particularly due to the release of radioactive cesium. This study investigates the use of t-BAMBP (4-tert-butyl-2-(α-methylbenzyl) phenol) for the extraction and separation of cesium from simulate high concentration cesium containing wastewater, focusing on the selection of suitable diluents to enhance the efficiency of the process. We performed a systematic study using density functional theory (DFT) calculations to evaluate the intrinsic properties and interactions of various common diluents with t-BAMBP. The diluents studied include aromatic hydrocarbons (benzene, toluene, xylene), alkanes (cyclohexane, hexane, heptane), and alcohols (hexanol, octanol). Our computational results revealed that cyclohexane is the most suitable diluent due to its moderate solvation-free energy, high nonpolarity, and optimal balance between solubility and reactivity. Experimental validation confirmed the computational findings. The cyclohexane-diluted t-BAMBP system achieved the highest cesium extraction efficiency of over 94 %, with a separation factor (βCs/K) of 767.67. Cyclohexane demonstrated the lowest toxicity and cost among the diluents evaluated, making it a safer and more economical choice for practical applications. The results of this study provide a comprehensive theoretical and experimental basis for the selection of diluents in the t-BAMBP extraction system, offering insights for the sustainable utilization of cesium resources and effective management of radioactive waste.

Unveiling Negative Differential Resistance and Superionic Conductivity: Water Anchored on Layered Materials.

Unravelling the perplexing nature of negative differential resistance (NDR) in 2D transition metal dichalcogenide (2D TMD) devices, especially regarding intrinsic properties, is hindered by experiments conducted in ambient environments. A thorough investigation is essential for unveiling the actual mechanism. In this study, we provide compelling evidence of the NDR effect with a remarkably high peak-to-valley current ratio and proton-diffused superionic conductivity in quantum-confined water molecules anchored to a thin film of 2D TMDs. Our investigation underscores the crucial role of ambient moisture for this robust NDR effect independent of underlying materials used. The bonding of water molecules to the existing sulfur defect sites on 2D TMD nanoflakes facilitates the formation of bridges between two planar metal electrodes, thus enabling superionic in-plane protonic conduction. During electrolysis of chemisorbed water, protons are liberated at the anode and migrate toward the cathode during bias voltage sweeping. Nevertheless, proton diffusion encounters increasing impedance beyond a certain applied bias, thereby restricting current flow even with higher biasing voltages, which is attributed to the interfacial Schottky energy barrier influenced by the Fermi level pinning effect. Our DFT simulations corroborate this mechanism, revealing minimal intermolecular interaction of H+ ions compared to OH- ions at distinct atomic sites on 2D TMD nanoflakes.

Orexin increases the neuronal excitability of several brain areas associated with maintaining of arousal.

Orexin is exclusively produced in neurons localized within the lateral hypothalamic area (LHA) and perifornical area (PFA). Orexin has been identified as a key promotor of arousal. The selective loss of orexinergic neurons results in narcolepsy. It is known that the intrinsic electrophysiological properties are critical for neurons to perform their functions in corresponding brain regions. In addition to hypothalamic orexin, other brain nuclei are involved in the regulation of sleep and wakefulness. Quite a lot of studies focus on elucidating orexin-induced regulation of sleep-wake states and modulation of neuronal electrophysiological properties in several brain regions. Here, we summarize that the orexinergic neurons exhibit spontaneous firing activity which is associated with the states of sleep-wake cycle. Orexin mainly exerts postsynaptic excitatory effects on multiple brain nuclei associated with the process of sleep and wakefulness. This review may provide a background to guide future research about the cellular mechanisms of orexin-induced maintaining of arousal.

Development of novel superconductivity with higher Tc via the suppression of magnetism in quasi-two-dimensional electride Y2C under high pressures

Discovery of superconductivity in electride materials has been a topic of interest as their intrinsic electron-rich properties might suggest a considerable electron-phonon interaction. LayeredY2Cis a ferromagnetic quasi-two-dimensional electride with polarized anionic electrons confined in the interlayer space. In this theoretical study, we reportY2Cundergoes a series of structural phase transitions into two superconducting phases with estimatedTcof 9.2 and 21.0 K at 19 and 80 GPa, respectively, via the suppression of magnetism. Our extensive first-principles swarm structure searches identify that these two high-pressure superconducting phases possess an orthorhombicPnmaand a tetragonalI4/mstructures, respectively, where thePnmaphase is found to be a one-dimensional electride characterized by electron confinements in channel spaces of the crystal lattice, while the electride property inI4/mphase has been completely destroyed. We attribute the development of an unprecedentedly highTcsuperconductivity in Y-C system to the destructions of magnetism and the delocalization of interlayered anionic electrons under pressures. This work provides a unique example of pressure-induced collapse of magnetism at the onset of superconductivity in electride materials, along with the dramatic changes of electron-confinement topology in crystal lattices.

Mechanisms of sensory adaptation and inhibition of the cold and menthol receptor TRPM8.

Our sensory adaptation to cold and chemically induced coolness is mediated by the intrinsic property of TRPM8 channels to desensitize. TRPM8 is also implicated in cold-evoked pain disorders and migraine, highlighting its inhibitors as an avenue for pain relief. Despite the importance, the mechanisms of TRPM8 desensitization and inhibition remained unclear. We found, using cryo-electron microscopy, electrophysiology, and molecular dynamics simulations, that TRPM8 inhibitors bind selectively to the desensitized state of the channel. These inhibitors were used to reveal the overlapping mechanisms of desensitization and inhibition and that cold and cooling agonists share a common desensitization pathway. Furthermore, we identified the structural determinants crucial for the conformational change in TRPM8 desensitization. Our study illustrates how receptor-level conformational changes alter cold sensation, providing insights into therapeutic development.

Fluorescence of BODIPY dyes in gas phase at near-ambient conditions

Molecular fluorescence is a phenomenon that is usually observed in condensed phase. It is strongly affected by molecular interactions. The study of fluorescence spectra in gas-phase can provide a nearly ideal model for the evaluation of the intrinsic properties of fluorophores. Unfortunately, most conventional fluorophores are not volatile enough to allow for the study of their fluorescence in gas phase. Here we report very bright gas phase fluorescence of simple BODIPY dyes that can be readily observed at atmospheric pressure using conventional fluorescence instrumentation. To our knowledge, this is the first example of visible-range gas-phase fluorescence at near-ambient conditions. Evaporation of the dye in vacuum allowed us to demonstrate organic molecular electroluminescence in gas discharge excited by the electric field produced by a Tesla coil.

Programmed electrochemical reconstruction of NiCoxMo4-xN5 for making Core-Shell shaped Schottky junction electrocatalyst

Electrochemical reconstruction (ECR) sets natural limit to exploring reactivity of pristine catalysts in the electrocatalytic reactions. The ECR phenomena need to be regulated to unveil intrinsic property of pristine catalysts. Herein, we introduced ‘sacrificial cation optimization’ method to control element-leaching phenomenon at NiMo4N5 surface during the ECR. Partial substitution of sacrificial Mo with Co enabled timely cessation of the ECR of NiCoxMo4-xN5 with forming stable oxyhydroxide outer shell. This controlled ECR generated classic Schottky junction (SJ) at the core–shell interface of NiCoxMo4-xN5 | Ni1-yCoyOOH. The in situ formed SJ remarkably enhanced electron transfer with nullifying the poor conductance of front-line oxyhydroxides. As a result, the core–shell SJ yielded the current density of 10 mA/cm2 at a low overpotential of 126 mV (without iR compensation). The in situ formation of core–shell SJ proposed a breakthrough in the research to regulate ECR process as well as produced a new type of electrode beyond the oxyhydroxides.

In situ encapsulation of capsaicinoids into MIL-88A as a food-grade nanopreservative for precooked chicken

The biocompatible MIL-88A metal-organic framework (MOF), synthesized from food-grade fumaric acid and ferric chloride, was introduced for the efficient one-step in situ encapsulation of capsaicinoids as a nanopreservative. The resulting MIL-88A@Caps nanoparticles can load 61.43 mg/g of capsaicinoids, surpassing conventional MOF-based encapsulation. The potent MIL-88A@Caps nanoformulations synergize the intrinsic antimicrobial properties of MIL-88A and capsaicinoids. At the same concentration (0.5 mg/mL), MIL-88A@Caps was highly effective against S. aureus and Salmonella, with inhibition rates of 94.90 ± 0.58% and 94.30 ± 1.24%, respectively, compared to MIL-88A (62.28 ± 5.04% and 70.46 ± 1.96%) and capsaicinoids (63.68 ± 1.25% and 49.53 ± 1.22%), respectively. Model precooked-chicken preservation experiments revealed that MIL-88A@Caps significantly delayed spoilage parameters compared to untreated samples, with more favorable viable counts (8.08 lgCFU/g), pH value (6.60 ± 0.02), TVB-N value (8.59 ± 0.21 mg/100 g), and color changes on day 9. Our findings yield a green nanopreservative for meat safety.