Spectroscopy Methods Research Articles

A novel turbidity compensation method for fluorescence spectroscopy and application in the detection of two algae species

Turbidity interference in measurements can reduce the accuracy of fluorescence detection. Conventional turbidity compensation methods directly establish the relationship between turbidity value and fluorescence but cannot accurately characterize the complex interference of turbidity on fluorescence detection. This paper introduces a novel turbidity compensation technique that separates the interference caused by turbidity particles into scattering intensifying and scattering-absorption attenuating components and corrects them separately. First, the scattering spectrum overlapping with fluorescence is estimated and subtracted from the actual sample spectrum to mitigate the fluorescence intensification caused by scattering. Then, attenuation coefficients at different turbidity intervals are calculated to compensate for fluorescence attenuation. Finally, the two components are combined to obtain the final corrected result. Based on the proposed method, the fluorescence spectra data of Platymonas helgolandica var. tsingtaoensis and Synechococcus elongatus under different turbidity interferences were analyzed. Intensifying and attenuating coefficients based on turbidity values and scattering spectra were determined, ensuring adaptability to known and unknown turbidity conditions. The study results show that the fluorescence variation at different concentrations and turbidity levels are influenced by sample concentration and turbidity, exhibiting nonlinear behavior. The compensation model developed was applied to experimental data, achieving a mean relative error of less than 4% and a satisfactory root-mean-square error, significantly enhancing prediction accuracy. This method offers a straightforward and rapid application to detect a wide range of fluorescent substances.

A comprehensive method to analyze single-cell vibrations

All living cells vibrate depending on metabolism. It has been hypothesized that vibrations are unique for a given phenotype and thereby suitable to diagnose cancer type and stage and to pre-assess the effectiveness of pharmaceutical treatments in real time. However, cells exhibit highly variable vibrational signals, can be subject to environmental noise, and may be challenging to differentiate, having so far limited the phenomenon’s applicability. Here, we combined the sensitive method of force spectroscopy using optical tweezers with comprehensive statistical analysis. After data acquisition, the signal was decomposed into its spectral components via fast Fourier transform. Peaks were parameterized and subjected to principal-component analysis to perform an unbiased multivariate statistical evaluation. This method, which we term cell vibrational profiling (CVP), systematically assesses cellular vibrations. To validate the CVP technique, we conducted experiments on five U251 glioblastoma cells, using 8- to 10-μm polystyrene beads as a control for comparison. We collected raw data using optical tweezers, segmenting into 150+ 5-s intervals. Each segment was converted into power spectra representing a frequency resolution of 10,000 Hz for both cells and controls. U251 glioblastoma cells exhibited significant vibrations at 402.6, 1254.6, 1909.0, 2169.4, and 3462.8 Hz (p < 0.0001). This method was further verified with principal-component analysis modeling, which revealed that, in cell-cell comparisons using the selected frequencies, overlap frequently occurred, and clustering was difficult to discern. In contrast, comparison between cell-bead models showed that clustering was easily distinguishable. Our paper establishes CVP as an unbiased, comprehensive technique to analyze cell vibrations. This technique effectively differentiates between cell types and evaluates cellular responses to therapeutic interventions. Notably, CVP is a versatile, cell-agnostic technique requiring minimal sample preparation and no labeling or external interference. By enabling definitive phenotypic assessments, CVP holds promise as a diagnostic tool and could significantly enhance the evaluation of pharmaceutical treatments.

Hydrogen evolution reaction activity of 3D-printed TiB2 and MgB2 matrix reinforced with graphene and carbon nanofiber in alkaline media

In the present study, the TiB2, MgB2/ Graphene (GRP)/PLA and TiB2, MgB2/Carbon Nanofiber (CNF)/PLA 3D-printed electrodes were fabricated via the Fused Deposition Modeling (FDM) technique. The hydrogen Evolution Reaction (HER) performance of 3D electrodes was studied using electrochemical impedance spectroscopy (EIS) and cathodic polarization analysis methods in 1 M KOH media. The EIS measurement results showed that the total resistance values were significantly reduced due to the addition of GRP and CNF to TiB2/PLA and MgB2/PLA 3D electrodes. In addition, the increase in current density with the addition of GRP and CNF to the 3D electrodes from the cathodic polarization curves supported the EIS measurement results. Moreover, a new activation method without using solvent was applied as different from the literature, to enhance the conductivity of 3D electrodes. The activation process was performed by implementing 50 cycles in 1 M KOH solution with the cyclic voltammetry method. As a result, with this study, both the synergistic effect of multiple composites and the application of the activation method have increased the HER efficiency of the 3D electrocatalyst. Thus, 3D electrocatalysts have been introduced to the energy application field.

Reports of tropane alkaloid poisonings and analytical techniques for their determination in food crops and products from 2013 to 2023.

Food safety is crucial to attaining food security and sustainability. Unsafe foods for human and animal consumption lead to product recalls and rejection, negatively impacting the global economy and trade. Similarly, climate change can adversely affect the availability of safe and nutritious food at the table. The changing climatic conditions and global food trade and transport can make the movement of toxic plants possible, resulting in food crops being increasingly invaded by some species of plants that produce toxic secondary metabolites, such as tropane alkaloids (TAs).Datura stramoniumfrom the Solanaceae plant family is an invasive and virulent plant that produces high amounts of two TAs, atropine and scopolamine. Various food poisoning events following accidental or deliberate ingestion of foods contaminated by atropine and scopolamine from seeds ofD. stramoniumhave been recorded in different locations globally. Due to these incidents, regulatory agencies require the development of plant toxin detection methods that can be used in the food chain as early as possible. This systematic review thus focuses on the TA determination techniques in food and feeds published between 2013 and 2023. A particular focus was given to the sample preparation methods, the improvements of each technique claimed, and data to support the performance of each method, especially the ability to measure at or below the maximum level. The review concludes with other technological advancements, including rapid spectroscopy, electrophoresis, and colorimetric methods, as well as the possibility of coupling with smartphones for use in on-farm detection and the challenges in applying them.

Optimization of the Raman spectroscopic method for crystal orientation and residual stress of aluminum oxide

A half-wavelength plate was set in the common light path to simultaneously alter the polarization directions of both incident laser and scattered Raman signals, and the distribution functions of the polarized Raman scattering intensity about the polarization rotation angle and the crystal orientation angle were deduced. The measurement accuracies of crystal orientations when using different correction methods of light intensity were compared, and on that basis, a measurement system and a measurement method for the crystal orientation of 95% aluminum oxide (Al2O3) were established, which improved the accuracy and handleability of crystal orientation detection. Then, the number of Raman peak shifts needed for solving equations was reduced to three by studying the simplification method of stress fields, exploring the Raman selection method, and introducing the differential evolution algorithm. In this way, the method that can calculate the residual stress in the absence of peaks in Raman spectroscopic tests was proposed. The established test system and method were also adopted to test single-crystal and polycrystal Al2O3 samples with known stress. Results show that the established stress measurement method is highly reliable and accurate. Finally, the residual stress distribution in the ceramic side of 95%Al2O3/4J33 brazed joints was also tested.

A reflection-spectroscopy measured skin carotenoid score strongly correlates with plasma concentrations of all major dietary carotenoid species except for lycopene

Skin carotenoids can be measured non-invasively using spectroscopy methods to provide a biomarker of total dietary carotenoid and carotenoid-rich fruit and vegetable intake. However, the degree to which skin carotenoid biomarkers reflect intakes of specific carotenoids must be determined for specific devices. Previously, findings were mixed regarding the correlation between reflection spectroscopy (RS)-assessed skin carotenoids and individual plasma carotenoid concentrations. The current study expands on prior analyses to examine the cross-sectional associations between adult RS-assessed skin carotenoids and individual carotenoid species intakes and plasma concentrations, controlling for potential covariates. We hypothesized that RS-assessed skin carotenoid scores would strongly correlate with all major plasma carotenoid species other than lycopene. Cross-sectional data from two prior studies (n = 213 and n = 162) examining the validity and sensitivity of RS-assessed skin carotenoids as a biomarker of fruit and vegetable intake were used. Skin carotenoids were assessed using the Veggie Meter ®, which quantifies combined skin carotenoid concentrations. Plasma concentrations of α-carotene, β-carotene, β-cryptoxanthin, lycopene, and lutein and zeaxanthin were determined using high-performance liquid chromatography. Self-reported carotenoid intake was estimated from validated food frequency questionnaires. Skin carotenoid scores correlated moderately to strongly with individual plasma carotenoid species (Pearson's r=0.52 – r=0.78) except for lycopene (r=0.04 to r=0.07). Low correlations between skin carotenoid score and lycopene plasma concentrations and intake could be due to differential deposition, preferential oxidation/degradation, and/or device measurement bias. Validating skin carotenoid measurement techniques relative to other concentration biomarkers informs the interpretation of skin carotenoid biomarkers.

Thermal Expansion of Römerite under Low-Temperature Conditions Revision 2

Abstract Römerite, a triclinic hydrous sulfate in the P1 space group with the chemical formula Fe2+Fe3+2 (SO4)4 × 14(H2O), is of potential interest in studies of planetary environments, with particular relevance to Mars and the icy Jovian satellites. Past work has indicated the presence of hydrous sulfates on said bodies and the mixed-valence iron in the structure of römerite makes the mineral a worthwhile end-member composition in thermodynamic models. Such models should be constrained with measurements at the low temperatures relevant to the planetary environments in question. We characterized single crystals of römerite with time-domain Mössbauer spectroscopy, Raman spectroscopy, and X-ray diffraction methods. Through our X-ray diffraction experiment, we refined the unit–cell parameters of the crystal between 100 and 300 K. The resulting temperature-variant lattice parameters and volumes are reported and are fit by physical and empirical models of the thermal expansion coefficient. The physical model considered, a Debye model of thermal expansion, provides estimates of additional thermodynamic parameters: the ratio of the bulk modulus at 0 K and 1 bar to the thermodynamic Grüneisen parameter (K0,0K/γth), the volume at 0 K and 1 bar (V0,0K), and the Debye temperature (θD).

Effects of robot-assisted hand function therapy on brain functional mechanisms: a synchronized study using fNIRS and sEMG.

Robot-assisted hand function therapy is pivotal in the rehabilitation of patients with stroke; however, its therapeutic mechanism remains elusive. Currently, research examining the impact of robot-assisted hand function therapy on brain function in patients with stroke is scarce, and there is a lack of studies investigating the correlation between muscle activity and alterations in brain function. This study aimed to investigate the correlation between forearm muscle movement and brain functional activation by employing the synchronized use of functional near-infrared spectroscopy and surface electromyography methods. Moreover, it sought to compare neural activity patterns during different rehabilitation tasks and refine the mechanism of robot-assisted hand function therapy for post-stroke hand function impairments. Stroke patients with hand dysfunction underwent three sessions of robot-assisted hand function therapy within 2 weeks to 3 months of onset. The fNIRS-sEMG synchronous technique was used to observe brain function and forearm muscle activation. Ten participants were randomly assigned to receive mirror, resistance, or passive rehabilitation training. During the intervention, cortical and muscle activation information was obtained using fNIRS and electromyographic signals. The primary outcomes included changes in oxyhemoglobin concentration and root mean square of surface electromyography. Compared to the resting state, the Oxy-Hb concentration in the brain regions involved in three rehabilitation tasks with robot-assisted hand function therapy significantly increased (p < 0.05). Mirror therapy significantly enhanced the prefrontal cortex and the superior frontal cortex activation levels. In contrast, resistance therapy significantly promoted the activation of the supplementary motor area and the premotor cortex. Passive rehabilitation tasks showed some activation in the target brain area premotor cortex region. Robot-assisted hand function therapy has shown that forearm muscle movement is closely related to oxygenated hemoglobin concentration activity in specific brain regions during different rehabilitation tasks. The simultaneous sEMG-fNIRS study found a significant correlation between muscle movement and brain activity after stroke, which provides an important basis for understanding the treatment mechanism of hand function impairment.

The effects of six sprint interval training sessions on muscle oxygenation and swimming performance in untrained swimmers.

The current study examined the changes in muscle oxygenation values and swimming performance after six sessions of sprint interval training during a three-week period in untrained swimmers. Twelve swimmers of both genders (age: 23.5 ± 5.6yrs) executed the twice-weekly experimental training protocol (EXP, n = 12), consisting of a 4 × 50 m front-crawl swimming (repeated sprint training-RST) with maximal intensity, and 2 min of passive recovery in between, after a short in-water warm-up. The control group (CON, n = 9) performed a continuous swimming set (200 m) at 120 b pm-1, with the same weekly frequency. Performance times in two maximum swim trials (400 m: T400 and 50 m: T50), muscle oxygenation of the deltoid muscle (SmO2) immediately after T400 and T50, 1-min heart rate recovery (HRR1) after T400, T50, and swim strokes during both swim trials (S/T400, S/T50) were assessed. For the EXP group, T400 improved by 2.4 (p = 0.011). In contrast, T50 presented no significant improvement (1%, p > 0.05). SmO2 decreased at T400 (5.5%, p = 0.017) and increased at T50 (3.7%, p = 0.030). HRR1 improved after T400 (7.9%, p = 0.002), T50 (4.6%, p = 0.005) and RST (9.6%, p = 0.002). S/T400 and S/T50 remained relatively unchanged (p > 0.05). The CON group presented no significant changes in any of the variables examined. In conclusion, six sprint interval training sessions can improve aerobic capacity over a 3-week training period, as indicated by the enhanced T400 performance and the reduced HRR1 values, in previously trained swimmers. Finally, the sensitivity of the near-infrared spectroscopy method to detect short-term training-induced changes is highlighted.

Exploring and Controlling Chemistry Using Quantum Logic.

Over the past years, the development of experimental techniques for the coherent manipulation and control of isolated quantum systems has made impressive progress. Such 'quantum-logic' methods are also highly attractive in a chemical context in view of unravelling and controlling the quantum dynamics of molecular collisions and chemical reactions. Quantum technologies have the potential to transform the way chemical dynamics are investigated - by providing highly sensitive methods for state readout and spectroscopy, by opening up new pathways for the quantum-state preparation of molecules and by enabling an improved control of their microscopic behavior on the single-particle level. However, for complex quantum systems like molecules, these techniques are still in their infancy and their considerable potential remains to be unlocked. The aim of the present research program supported by an Advanced Grant of the Swiss National Science Foundation is to merge the fields of quantum science and chemical dynamics by advancing quantum technologies to polyatomic molecular ions and by applying them to the study of ion-molecule collisions and chemical reactions. In this article, we review the salient experimental methods as well as prospects and challenges in the development of molecular quantum technologies and their applications to chemistry.

Quantitative estimation and validation of Alectinib hydrochloride drug substance using quantitative nuclear magnetic resonance spectroscopy

Nuclear magnetic resonance spectroscopy has been recently used for quantitative estimation of drug substance which has numerous merits in pharmaceutical applications when compared to traditional methods of chromatography. Present study focuses on method development and validation of quantitative proton nuclear magnetic spectroscopy method for estimation of alectinib hydrochloride drug substance. This method involves use of internal standard in presence of alectinib hydrochloride. For quantitation, 1H NMR signals at 8.4 ppm and 6.7 ppm corresponding to analyte proton of alectinib and ethyl 4-(dimethyl amino) benzoate internal standard respectively were used. Moreover, this method was validated as per ICH guidelines for accuracy, precision, linearity, limit of detection, limit of quantitation, range and robustness. Assay estimation by Q-NMR is facile and time-efficient which does not require reference standard of analyte and yet accurate and precise alternative as compared to estimation by other chromatographic techniques.

Synthesis, Crystal Structure, Intermolecular Interactions, HOMO-LUMO, MEP, NLO Properties, and DFT/TD-DFT Investigation of (Z)-5-(4-Nitrobenzylidene)-3-N(3-Chlorophenyl)-2-Thioxothiazolidin-4-One

A novel heterocyclic compound named (Z)-5-(4-nitrobenzylidene)-3-N(3-chlorophenyl)-2-thioxothiazolidin-4-one (NCTh) was synthesized and analyzed using various techniques, including single crystal X-ray diffraction, FT-IR, UV-Vis, NMR spectroscopy, and mass spectral data methods. NCTh was observed to crystallize in the triclinic crystal system P-1 space group. To validate the experimental findings, density functional theory (DFT) calculations were performed using the B3LYP functional with the 6-311 G(d,p) basis set. The results indicated good agreement in geometrical parameters between the experimental and theoretical outcomes. The study also calculated HOMO-LUMO energies, molecular electrostatic potential (MEP), and global chemical reactivity descriptors to evaluate the compound’s reactivity. Additionally, the study conducted reduced density gradient and Hirshfeld surface analyses to reveal attractive, repulsive, and van der Waals strong and weak interactions. The calculation of thermodynamic parameters was also included. The study focused on investigating the nonlinear optical (NLO) properties of NCTh, which were characterized through key parameters such as the electric dipole moment (µ), polarizability (α), first-order hyperpolarizability (β), and second-order hyperpolarizability (γ). These properties provide insights into the material’s potential applications in optical and photonic technologies. Additionally, a molecular docking study was performed to further explore the structure-activity relationship, particularly in a biological context. The docking results revealed a strong ligand-protein interaction, with a binding energy of −10.3 kcal/mol, indicating significant affinity. Moreover, the inhibition constant (Ki) was calculated to be 0.0281 μM, suggesting a highly potent interaction, which could be relevant for drug design or biochemical applications.

Rapid Prediction of Moisture and Ash Content in Sungkai Leaves Herbal Tea (Peronema canescens Jack.) using NIR Spectroscopy

It is imperative to measure the chemical composition of Sungkai leaf herbal tea in order to produce high-quality goods that promote human health. The moisture and ash content of Sungkai leaf herbal tea are critical parameters for assessing the quality of herbal tea. This study aimed to evaluate an NIR spectroscopy method for quickly determining the moisture and ash content of Sungkai leaf herbal tea. Sungkai leaf herbal tea has a moisture content between 3.93% and 7.59%, and an ash content between 3.94% and 5.51%. We developed a calibration model using partial least squares (PLS) with several pretreatment methods. We split the data into calibration and prediction sets and performed an internal random cross-validation. A PLS calibration model with Rp2 = 0.86, a root means square error of prediction (RMSEP) of 0.30 (%), and a residual predictive deviation (RPD) of 2.76, performed exceptionally well at predicting the moisture content when the standard normal variate (SNV) pre-treatment was applied to the NIR spectra. The Savitzky-Golay derivative (a 9-point smoothing window, second-order polynomial, dg2) pre-treatment method also generated the best PLS calibration model for ash content determination, with Rp2 = 0.70, RMSEP = 0.16 (%), and RPD = 1.86. NIR spectroscopy can quickly determine the moisture and ash content of Sungkai leaf herbal tea, as suggested by these findings.

Conjugated Polymers Based on Carbazole and Tridentate Ligands as the "On-Off-On" Fluorescent Probes for Detection of Ni (II) Ion and Lysine.

Two novel conjugated polymers (polymer 1 and polymer 2) containing trisheterocyclic systemsand carbazole as the copolymerization unit were synthesized by the Suzuki coupling reaction and characterized using NMR spectroscopy and other methods. 4'-(3,5-Dibromophenyl)-2,2':6',2''-terpyridine and 2,2'-(4-(3,5-dibromophenyl)pyridine-2,6-diyl)dithiazole were used as the recognizing units of the two polymers respectively. The polymers show blue-violet fluorescence when dissolved in THF. The ability of the polymers to identify anions and metal ions was investigated by fluorescence sensing tests. It was found that I- not only quenched the fluorescence but also undergone some redshift. Ni (II) efficiently quenched the fluorescence of the polymers, and polymer 2 recognized Ni2+ with higher specificity. UV-visible absorption titration experiments showed that Ni2+ formed complexes with the polymers. In addition, the formation of complexes between Ni2+ and polymers were used for the detection of amino acids, and it was found that lysine could regenerate the fluorescence of [polymer 1-Ni2+] and [polymer 2-Ni2+] with 99% fluorescence recovery.

Direct One-Stage Plasma Chemical Synthesis of Nanostructured Thin Films of the System β-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;-GaN of Different Composition

For the first time, nanostructured thin films of the β-Ga2O3−GaN system were obtained by plasma chemical deposition from the gas phase (PECVD) on c-sapphire substrates. High-purity metallic gallium, as well as high-purity gaseous nitrogen and oxygen were used as sources of macro components. The low-temperature nonequilibrium plasma of an inductively coupled HF (40.68 MHz) discharge at a reduced pressure (0.01 Torr) was the initiator of chemical transformations between the starting substances. A mixture of oxygen and nitrogen was used as a plasma-forming gas. The plasma chemical process was studied using the optical emission spectroscopy (OES) method. The obtained thin films of the β-Ga2O3−GaN system with a GaN phase content of 2 to 7% were characterized by various analytical methods.

Sinulariapeptide F, a new peptide from culture broth of marine-derived fungus Simplicillium sp. SCSIO 41222.

One new compound named sinulariapeptide F (1) together with one known butyrolactone (2) and seven known peptides (3-9) were isolated from the fungus Simplicillium sp. SCSIO 41222. Their structures and absolute configurations were established using HRESIMS, NMR spectroscopy (1H, 13C, HSQC, HMBC) and marfey's method. All of these compounds were assessed their inhibitory activity of acetylcholinesterase (AChE) and pancreatic lipase (PL). Compounds 4 and 6 were selected to test for the inhibitory activity against programmed cell death-1 (PD-1)/ programmed cell death-ligand 1 (PD-L1). The results indicated that compound 4 displayed potent inhibition activity against PD-1/ PD-L1 with an IC50 value of 0.656 μM. Furthermore, the docking analysis demonstrated the interactions between 4 and proteins, suggesting PD-L1 to be a probable target for compound 4.

Ca(Mo,W)O4 Solid Solutions Formation in CaMoO4‐CaWO4 System

AbstractThe formation of solid solutions in the CaMoO4‐CaWO4 binary system is investigated by X‐ray diffraction, Raman spectroscopy, and scanning electron microscopy methods. The intermixtures of CaMoO4 and CaWO4 components are sintered in 600—1200 °C temperature range (in 100 °C increments). The solidus of the CaMoxW(1‐x)O4 system is studied by the differential scanning calorimetry method in the x = 0.3 … 1.0 range. CaMoO4‐CaWO4 phase diagram is constructed up to 1550 °C. The minimal sintering temperature in order to get CaMoxW(1‐x)O4 solid solution is shown to be 800 °C. Cathodoluminescence study of CaMoxW(1‐x)O4 compounds showed higher intensity of molybdate luminescence type.

The comparison of eight different common in vitro and ex vivo environments with in vivo conditions applying model collagen samples: Correlation possibilities and their limits

New biomaterials are routinely evaluated for their degradation behaviour in the real body environment. Following the 3R strategy, in vitro simulated body conditions are often preferred. No studies that simultaneously compare such conditions with the real body environment have been conducted to date. Model porous collagen scaffolds were exposed for 21 days to eight different environments: simple salt-based and enzymatic media, human blood plasma, cell culture media with and without human fibroblasts and ex vivo model cortical bone, and subsequently compared with an in vivo environment represented by a pig peritoneum. The mechanical properties of the scaffolds were then determined via uniaxial compression testing, and the structural properties via the micro-CT, weight loss, infrared spectroscopy, X-ray diffraction and histological methods. Interestingly, the various analysed simulated body conditions caused differing alterations in the collagen scaffold characteristics when compared with the real body environment. The mechanical properties were similar during the first 7 days of incubation but diverged after 14 and 21 days. The structural properties varied significantly after just 7 days of incubation. The histological evaluation of the scaffolds exposed to the cellular, ex vivo and in vivo conditions revealed the poor ability of cells to completely populate the scaffolds, accompanied by the massive ingrowth of connective tissue into the in vivo exposed scaffolds, which resulted in their variable global behaviour. In conclusion, the value of in vitro simulated body environments lies in their screening capacity and feasibility; however, direct extrapolation to real body conditions needs to be verified going forward.

Development of a 31P magnetic resonance spectroscopy technique to quantify NADH and NAD+ at 3 T

NADH and NAD+ act as electron donors and acceptors and NAD+ was shown to stimulate mitochondrial biogenesis and metabolic health. We here develop a non-invasive Phosphorous Magnetic Resonance Spectroscopy (31P-MRS) method to quantify these metabolites in human skeletal muscle on a clinical 3 T MRI scanner. This new MR-sequence enables NADH and NAD+ quantification by suppressing α-ATP signal, normally overlapping with NADH and NAD+. The sequence is based on a double spin echo in combination with a modified z-Filter achieving strong α-ATP suppression with little effect on NAD+ and NADH. Here we test and validate it in phantoms and in humans by measuring reproducibility and detecting a physiological decrease in NAD+ and increase in NADH induced by ischemia. Furthermore, the 31P-MRS outcomes are compared to analysis in biopsies. Additionally, we show higher NAD+ and lower NADH content in physically active older adults compared to sedentary individuals, reflecting increased metabolic health.

Charge-Compensation-Driven Failure Mechanism of Ni Redox in Fe-Rich Ni/Fe/Mn-Based O3-Type Layered Oxide Sodium-Ion Cathodes.

For cathode materials of sodium-ion batteries, O3-type Ni/Fe/Mn-based (Na-NFM) layered oxides have garnered extensive attention because of high economic viability, environmental friendliness, and the potential for high energy density. Among them, Fe-rich compositions exhibit higher initial charge capacity and lower bill-of-material costs, while they fade rapidly and exhibit low initial coulombic efficiency, hindering their commercialization prospects. In this work, we investigate the failure of Fe-rich Na-NFM materials through X-ray absorption spectroscopy methods. The results reveal a combined failure mechanism that encompasses not only the conventional theory of Fe migration but also an abnormal Ni-redox deterioration, which has not yet been reported. More factors related to the failure of Fe-rich Na-NFM layered oxides are discussed in detail. These findings are expected to inspire targeted research efforts toward Fe-rich Na-NFM materials, thereby accelerating the practical application of sodium-ion batteries.