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Ag/Ag2S hybrid structures have recently attracted significant interest due to their high chemical and thermal stability, in addition to their unique optical and electrical properties. However, their standard synthetic protocols have important drawbacks including long term and harsh reaction conditions and the utilization of highly toxic sulfur precursors. Herein, an innovative, simple one-pot green approach for the synthesis of the Ag/Ag2S carbon hybrid structures is reported. The procedure involves a one-step microwave-assisted method using ethylene glycol as a solvent and reducing agent, pig bristles as a sulphur and carbon source and silver nitrate as a metal precursor. Different amounts of silver nitrate were employed in order to investigate the synthetic mechanism for the formation of zerovalent silver over silver sulphide nanoparticles, producing three different samples. The materials were characterized by XRD, SEM, EDX, N2 physisorption and XPS spectroscopy. Aiming to prove the efficiency of the as-synthesized compounds, their electrocatalytic activities were explored in the hydrogen evolution reaction (HER) using linear sweep voltammetry. [ABSTRACT FROM AUTHOR]

A micro- and mesoporous carbon obtained from cherry pit waste and activated with HPO acid has been studied as the sulfur host for Li/S batteries. The carbon has a high specific surface area of 1,662 m·g (SBET) and micropore and mesopore volumes of 0.57 and 0.40 cm·g, respectively. The S/C composite, with a sulfur content of 57% deposited by the disproportionate reaction of a SO solution in an acid medium without an additional heating step above the S melting point, delivers an initial specific capacity of 1,148 mAh·g at a current of C/16. It also has a high capacity retention of 915 mAh·g after 100 cycles and a Coulombic efficiency close to 100%. The good performance of the composite was also observed under higher current rates and long-term cycling tests. The capacities delivered by the cell after 200 cycles were 707 and 410 mAh·g at C/2 and 1C (1C = 1,675 mA·g), respectively, maintaining the high Coulombic efficiency. The overall electrochemical response of this carbon as the sulfur matrix is among the best reported so far among the other biomass-derived carbons, probably because of the micro- and mesopore system formed upon activation. [ABSTRACT FROM AUTHOR]

Abstract: The electrochemical performance of a Li-ion battery made from nanometric, highly crystalline LiNi0.5Mn1.5O4 as positive electrode and mesoporous carbon microbeads (MCMBs) as negative electrode was assessed. The best performance was obtained by using a slight excess of spinel (a cathode/anode mole ratio of 1.3) and lithium bis-oxalate borate (LiBOB) instead of LiPF6 as an electrolyte salt. Higher spinel contents caused the formation of metallic Li in the carbon and the rapid degradation of battery performance as a result. The calculated output energy was 322Whkg−1 which is higher than the value reported for the LiMn2O4/C cell (250Whkg−1). [Copyright &y& Elsevier]

Li-ion batteries (LIBs) employ porous, composite-type electrodes, where few weight percentages of carbonaceous conducting agents and polymeric binders are required to bestow electrodes with electrical conductivity and mechanical robustness. However, the use of such inactive materials has limited enhancements of battery performance in terms of energy density and safety. In this study, we introduced graphene/polyvinylidene fluoride (Gr/PVdF) composites in Ni-rich oxide cathodes for LIBs, replacing conventional conducting agents, carbon black (CB) nanoparticles. By using Gr/PVdF suspensions, we fabricated highly dense LiNi0.85Co0.15Al0.05O2 (NCA) cathodes having a uniform distribution of conductive Gr sheets without CB nanoparticles, which was confirmed by scanning spreading resistance microscopy mode using atomic force microscopy. At a high content of 99 wt.% NCA, good cycling stability was shown with significantly improved areal capacity (Qareal) and volumetric capacity (Qvol), relative to the CB/PVdF-containing NCA electrode with a commercial-level of electrode parameters. The NCA electrodes using 1 wt.% Gr/PVdF (0.9:0.1) delivered a high Qareal of ~3.7 mAh cm−2 (~19% increment) and a high Qvol of ~774 mAh cm−3 (~18% increment) at a current rate of 0.2 C, as compared to the conventional NCA electrode. Our results suggest a viable strategy for superseding conventional conducting agents (CB) and improving the electrochemical performance of Ni-rich cathodes for advanced LIBs. [ABSTRACT FROM AUTHOR]

The global demand for electricity is rising due to the increased electrification of multiple sectors of economic activity and an increased focus on sustainable consumption. Simultaneously, the share of cleaner electricity generated by transient, renewable sources such as wind and solar energy is increasing. This has made additional buffer capacities for electrical grids necessary. Battery energy storage systems have been investigated as storage solutions due to their responsiveness, efficiency, and scalability. Storage systems based on the second use of discarded electric vehicle batteries have been identified as cost-efficient and sustainable alternatives to first use battery storage systems. Large quantities of such batteries with a variety of capacities and chemistries are expected to be available in the future, as electric vehicles are more widely adopted. These batteries usually still possess about 80% of their initial capacity and can be used in storage solutions for high-energy as well as high-power applications, and even hybrid solutions encompassing both. There is, however, no holistic review of current research on this topic. This paper first identifies the potential applications for second use battery energy storage systems making use of decommissioned electric vehicle batteries and the resulting sustainability gains. Subsequently, it reviews ongoing research on second use battery energy storage systems within Europe and compares it to similar activities outside Europe. This review indicates that research in Europe focuses mostly on "behind-the-meter" applications such as minimising the export of self-generated electricity. Asian countries, especially China, use spent batteries for stationary as well as for mobile applications. In developing countries, off-grid applications dominate. Furthermore, the paper identifies economic, environmental, technological, and regulatory obstacles to the incorporation of repurposed batteries in second use battery energy storage systems and lists the developments needed to allow their future uptake. This review thus outlines the technological state-of-the-art and identifies areas of future research on second use battery energy storage systems. [ABSTRACT FROM AUTHOR]

In the manufacturing process of lithium-ion batteries, the current organic solvent-based processes will inevitably be replaced with eco-friendly water-based processes. For this purpose, the current organic-soluble binder should be replaced with a water-soluble or water-dispersed binder. In this study, a new polyacrylate latex dispersed in water was successfully applied as a binder of lithium-ion battery cathodes for the first time. One of the biggest advantages of the polyacrylate binder is that it is electrochemically stable at the working voltage of typical cathodes, unlike a conventional water-dispersed styrene-butadiene binder. This implies that the water-dispersed polyacrylate has no limitations for the usage of a cathodic binder. The performance of the polyacrylate binder for lithium iron phosphate cathodes was compared with those of a conventional organic-based polyvinylidene fluoride binder as well as a water-dispersed styrene-butadiene binder. The polyacrylate binder exhibited an electrochemical performance that was comparable to that of an existing styrene-butadiene binder and much better than that of the polyvinylidene fluoride binder. This superior performance of the polyacrylate binder is attributed to the point-to-point bonding mechanism of an emulsified binder, which leads to a strong adhesion strength as well as the low electrical and charge transfer resistances of the cathodes. [ABSTRACT FROM AUTHOR]

This paper presents results of the analysis of the impact of activation temperature and mass ratio of activator to carbonized precursor R on the porous structure of nitrogen-doped activated carbons derived from lotus leaves by carbonization and chemical activation with sodium amide NaNH2. The analyses were carried out via the new numerical clustering-based adsorption analysis (LBET) method applied to nitrogen adsorption isotherms at −195.8 °C. On the basis of the results obtained it was shown that the amount of activator, as compared to activation temperatures, has a significantly greater influence on the formation of the porous structure of activated carbons. As shown in the study, the optimum values of the porous structure parameters are obtained for a mass ratio of R = 2. At a mass ratio of R = 3, a significant decrease in the values of the porous structure parameters was observed, indicating uncontrolled wall firing between adjacent micropores. The conducted analyses confirmed the validity of the new numerical clustering-based adsorption analysis (LBET) method, as it turned out that nitrogen-doped activated carbons prepared from lotus leaves are characterized by a high share of micropores and a significant degree of surface heterogeneity in most of the samples studied, which may, to some extent, undermine the reliability of the results obtained using classical methods of structure analysis that assume only a homogeneous pore structure. [ABSTRACT FROM AUTHOR]

This paper aims to design thermal dummy cells (TDCs) that can be used in the development of lithium-ion battery thermal management systems. Based on physical property and geometry of real 18,650 cylindrical cells, a three-dimensional model of TDCs was designed, and it is used to numerically simulate the thermal performance of TDCs. Simulations show that the TDC can mimic the temperature change on the surface of a real cell both at static and dynamic current load. Experimental results show that the rate of heating resistance of TDC is less than 0.43% for temperatures between 27.5 °C and 90.5 °C. Powered by a two-step voltage source of 12 V, the temperature difference of TDCs is 1 °C and 1.6 °C along the circumference and the axial directions, respectively. Powered by a constant voltage source of 6 V, the temperature rising rates on the surface and in the core are higher than 1.9 °C/min. Afterwards, the proposed TDC was used to simulate a real cell for investigating its thermal performance under the New European Driving Cycle (NEDC), and the same tests were conducted using real cells. The test indicates that the TDC surface temperature matches well with that of the real battery during the NEDC test, while the temperature rise of TDC exceeds that of the real battery during the suburban cycle. This paper demonstrates the feasibility of using TDCs to replace real cells, which can greatly improve safety and efficiency for the development of lithium-ion battery thermal management systems. [ABSTRACT FROM AUTHOR]

Lithium-ion (Li-I) batteries have recently become pervasive and are used in many physical assets. For the effective management of the batteries, reliable predictions of the end-of-discharge (EOD) and end-of-life (EOL) are essential. Many detailed electrochemical models have been developed for the batteries. Their parameters are calibrated before they are taken into operation and are typically not re-calibrated during operation. However, the degradation of batteries increases the reality gap between the computational models and the physical systems and leads to inaccurate predictions of EOD/EOL. The current calibration approaches are either computationally expensive (model-based calibration) or require large amounts of ground truth data for degradation parameters (supervised data-driven calibration). This is often infeasible for many practical applications. In this paper, we introduce a reinforcement learning-based framework for reliably inferring calibration parameters of battery models in real time. Most importantly, the proposed methodology does not need any labeled data samples of observations and the ground truth parameters. The experimental results demonstrate that our framework is capable of inferring the model parameters in real time with better accuracy compared to approaches based on unscented Kalman filters. Furthermore, our results show better generalizability than supervised learning approaches even though our methodology does not rely on ground truth information during training. [ABSTRACT FROM AUTHOR]

A mesoporous MnOx network (MMN) structure and MMN/C composites were prepared and evaluated as anodes for high-energy and high-rate lithium-ion batteries (LIB) in comparison to typical manganese oxide nanoparticle (MnNP) and graphite anodes, not only in a half-cell but also in a full-cell configuration (assembled with an NCM523, LiNi0.5Co0.2Mn0.3O2, cathode). With the mesoporous features of the MMN, the MMN/C exhibited a high capacity (approximately 720 mAh g−1 at 100 mA g−1) and an excellent cycling stability at low electrode resistance compared to the MnNP/C composite. The MMN/C composite also showed much greater rate responses than the graphite anode. Owing to the inherent high discharge (de-lithiation) voltage of the MMN/C than graphite as anodes, however, the MMN‖NCM523 full cell showed approximately 87.4% of the specific energy density of the Gr‖NCM523 at 0.2 C. At high current density above 0.2 C, the MMN‖NCM523 cell delivered much higher energy than the Gr‖NCM523 mainly due to the excellent rate capability of the MMN/C anode. Therefore, we have demonstrated that the stabilized and high-capacity MMN/C composite can be successfully employed as anodes in LIB cells for high-rate applications. [ABSTRACT FROM AUTHOR]

Biomass residues are often considered as a resource if conveniently converted in fuel and alternative feedstock for chemical processes, and their conversion into valuable products may occur by different pathways. This work is focused on the thermochemical conversion at moderate temperature and in steam atmosphere, a mild process in comparison to hydrothermal liquefaction, followed by extraction of soluble products in a solvent. Such process has been already applied to various residues and here extended to the case of marc, the residual pomace from wine making, largely produced worldwide. A pressurized batch reactor was used for the quantitative determination of produced solid and liquid fractions, and their qualitative characterization was performed by instrumental analyses. The pressurized steam conversion of marc was effective, providing a yield in liquid fraction, upon extraction in solvent, up to 30% of the raw dried biomass. The use of polar and nonpolar solvent for the extraction of the liquid fraction was inspected. Applied operating conditions, namely residence time in the batch reactor and extraction modality, showed a significant influence on the process performance. In particular, long residence and extraction times and use of nonpolar solvent substantially improved the yield in liquid fraction. [ABSTRACT FROM AUTHOR]

TiO2 aggregates of controlled size have been successfully prepared by hydrothermal synthesis using TiO2 nanoparticles of different sizes as a building unit. In this work, different techniques were used to characterize the as-prepared TiO2 aggregates, e.g., X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Brunauer, Emmett and Teller technique (BET), field emission gun scanning electron microscopy (FEGSEM), electrochemical measurements etc. The size of prepared TiO2 aggregates varied from 10–100 nm, and their pore size from around 5–12 nm; this size has been shown to depend on synthesis temperature. The mechanism of the aggregate formations was discussed in terms of efficiency of collision and coalescence processes. These newly synthetized TiO2 aggregates have been investigated as potential negative insertion electrode materials for lithium-ion batteries. The influence of specific surface areas and pore sizes on the improved capacity was discussed—and conflicting effects pointed out. [ABSTRACT FROM AUTHOR]

Fms-like tyrosine kinase 3 (FLT3) expression and mutation have been considered a poor prognostic factor in acute myeloid leukemia (AML). FLT3-ITD mutation is present in 30% of adult patients with AML and 2–5% in childhood acute lymphoblastic leukemia (ALL). The impact of these mutations on the prognosis of ALL patients, has not yet been established. Moreover, a limited number of publications regarding the level of expression of the FLT3 receptor (CD135) in both leukemias exist. This study aimed to analyze the clinical outcomes associated to the presence of FLT3-ITD mutation and the expression of CD135. 82 adult patients with newly diagnosed acute leukemia (39 with AML and 43 with ALL) were included. Flow cytometry and RT-PCR were done to analyze the expression of CD135 and the presence of FLT3 ITD mutation, respectively. FLT3-ITD was present in 14 (36%) of AML and 15 (35%) of ALL patients. Disease free survival (DFS) and overall survival (OS) were lower in ALL patients having a CD135 expression >3000 cells/μL. There was a trend for poor OS in AML patients expressing FLT3 ITD. OS was worse in AML patients with high expression of CD135. A higher (35%) frequency of FLT3-ITD was found in adult ALL patients. The presence of FLT3-ITD was associated with a trend of poor OS in AML cases, and overexpression of CD135 was correlated with poor DFS in ALL cases and poor OS in both acute leukemias. [ABSTRACT FROM AUTHOR]

VE-cadherin plays a central role in controlling endothelial barrier function, which is transiently disrupted by proinflammatory cytokines such as tumor necrosis factor (TNFα). Here we show that human endothelial cells compensate VE-cadherin degradation in response to TNFα by inducing VE-cadherin de novo synthesis. This compensation increases adherens junction turnover but maintains surface VE-cadherin levels constant. NF-κB inhibition strongly reduced VE-cadherin expression and provoked endothelial barrier collapse. Bacterial lipopolysaccharide and TNFα upregulated the transcription factor ETS1, in vivo and in vitro, in an NF-κB dependent manner. ETS1 gene silencing specifically reduced VE-cadherin protein expression in response to TNFα and exacerbated TNFα-induced barrier disruption. We propose that TNFα induces not only the expression of genes involved in increasing permeability to small molecules and immune cells, but also a homeostatic transcriptional program in which NF-κB- and ETS1-regulated VE-cadherin expression prevents the irreversible damage of endothelial barriers. [ABSTRACT FROM AUTHOR]

Surface sensing initiates bacterial colonization of substrates. The protein PilY1 plays key roles during this process-surface detection, host adhesion, and motility-while experiencing mechanical perturbations of varying magnitudes. In Pseudomonas aeruginosa , the adhesion and motility functions of PilY1 are associated with integrin and calcium ligand-binding sites; however, how mechanical forces influence PilY1's dynamics and its interactions with these ligands remain unknown. Here, using single-molecule magnetic tweezers, we reveal that PilY1 is a mechanosensor protein that exhibits different behaviors depending on the force load. At high forces (>20 pN), PilY1 unfolds through a hierarchical sequence of intermediates, whose mechanical stability increases with calcium binding. This enhanced stability may help counteract type IV pilus retraction forces during motility. At low forces (<7 pN), we identify the dynamics of the integrin-binding domain, which is reminiscent of the behavior of mechanosensor proteins. Integrin binding induces a force-dependent conformational change in this domain, shortening its unfolded extension. Our findings suggest that PilY1 roles are force- and ligand-modulated, which could entail a mechanical-based compartmentalization of its functions., (© 2025 Cao-Garcia et al.)

The classical "one sequence, one structure, one function" paradigm has shaped much of our intuition of how proteins work inside the cell. Partially due to the insight provided by bulk biochemical assays, individual biomolecules are often assumed to behave as identical entities, and their characterization relies on ensemble averages that flatten any conformational diversity into a unique phenotype. While the emergence of single-molecule techniques opened the gates to interrogating individual molecules, technical shortcomings typically limit the duration of these measurements, which precludes a complete characterization of an individual protein and, hence, capturing the heterogeneity among molecular populations. Here, we introduce an ultrastable magnetic tweezers design, which enables us to measure the folding dynamics of a single protein during several uninterrupted days with high temporal and spatial resolution. Thanks to this instrumental development, we fully characterize the nanomechanics of two proteins with a very distinct force response, the talin R3 IVVI domain and protein L. Days-long recordings on the same protein individual accumulate thousands of folding transitions with submicrosecond resolution, allowing us to reconstruct their free energy landscapes and describe how they evolve with force. By mapping the nanomechanical identity of many different protein individuals, we directly capture their molecular diversity as a quantifiable dispersion on their force response and folding kinetics. By significantly expanding the measurable timescales, our instrumental development offers a tool for profiling individual molecules, opening the gates to directly characterizing biomolecular heterogeneity., Competing Interests: Declaration of interests The authors declare no competing interests., (Copyright © 2024 Biophysical Society. Published by Elsevier Inc. All rights reserved.)

Purpose of Review: Chronic lymphocytic leukemia (CLL) is the most frequent lymphoproliferative disease in the elderly of the western world. Immune defective responses and treatment can worsen the immune system's competence of CLL patients. Consequently, they may present a higher incidence of recurrent severe infections, second malignancies, and reduced efficacy of vaccines. The outbreak of COVID-19 is an ongoing pandemic, and patients with comorbidities experience more severe forms of the disease. Hematological malignancies are associated with higher case fatality rates (CFRs) than other cancers. Knowledge about COVID-19 incidence, clinical course, and immune response to the infection and vaccination in CLL may contribute to design strategies that improve the outcomes of patients in the future., Recent Findings: The prevalence of SARS-CoV-2 positivity in CLL is not significantly higher than seen in the general population. CFRs for CLL patients are 16.5-fold more elevated than the median reported worldwide and even higher in older patients, those who require hospitalization have significant comorbidities or need oxygen therapy. CLL status decreases the anti-SARS-CoV-2 positivity after infection or vaccination by around 40%, and the spike-specific antibody titers are 74-fold lower than healthy age-matched controls. The response rate to COVID-19 vaccines is even worse in patients with active CLL-directed therapies like BTKi, BCL-2 antagonists, or anti-CD20 monoclonal antibodies. CLL patients are at a greater risk of death from COVID-19. Inherent immunosuppression of CLL and immune deficiencies caused by treatment significantly decrease the ability to produce natural or vaccine-induced anti-SARS-CoV-2 immune responses., (© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

Disulfide bonds play a pivotal role in the mechanical stability of proteins. Numerous proteins that are known to be exposed to mechanical forces in vivo contain disulfide bonds. The presence of cryptic disulfide bonds in a protein structure may be related to its resistance to an applied mechanical force. Disulfide bonds in proteins tend to be highly conserved but their evolution might be directly related to the evolution of the protein mechanical stability. Hence, tracking the evolution of disulfide bonds in a protein can help to derive crucial stability/function correlations in proteins that are exposed to mechanical forces. Phylogenic analysis and ancestral sequence reconstruction (ASR) allow tracking the evolution of proteins from the past ancestors to our modern days and also establish correlations between proteins from different species. In addition, ASR can be combined with single-molecule force spectroscopy (smFS) to investigate the mechanical properties of proteins including the occurrence and function of disulfide bonds. Here we present a detailed protocol to study the mechanochemical evolution of proteins using a fragment of the giant muscle protein titin as example. The protocol can be easily adapted to AFS studies of any resurrected mechanical force bearing protein of interest., (© 2022. Springer Science+Business Media, LLC, part of Springer Nature.)

To obtain a wide variety of green materials, numerous investigations have been undertaken on industrial waste that can act as sustainable resources. The use of hazardous wastes derived from wastewater treatment plants (WWTPs), especially the activated carbon used in odor control systems, is a highly abundant, scalable, and cost-effective strategy. The reuse of waste materials is a key aspect, especially for the sustainable development of emerging energy storage systems, such as lithium-sulfur (Li-S) batteries. Herein, granular active carbons from two WWTP treatment lines were regenerated in air at low temperature and utilized as the sulfur host with micro-/mesoporous framework. The resulting regenerated carbon and sulfur composites were employed as cathodes for Li-S cells. The SL-ACt3@S composite electrode with 60 wt% loaded sulfur exhibited a remarkable initial capacity of 1100 mAh g -1 at C/10 rate and higher than 800 mAh g -1 at C/2. Even at a rate of 1C, it maintained a high capacity of almost 700 mAh g -1 with a capacity retention of 85.4 % after 350 cycles, demonstrating a very low capacity fading of only 0.042 % per cycle. It is essential to note that the coulombic efficiency was always higher than 96 % during all the cycles. In this proposal, the only used source material was expired carbon from WWTP that was obtained with a simple and effective regeneration process. This "trash into treasure" strategy leads to a new way for using hazardous waste material as high-performance and environmentally safe electrodes for advanced Li-S batteries., (© 2021 The Authors. ChemSusChem published by Wiley-VCH GmbH.)

The mTORC1 node plays a major role in autophagy modulation. We report a role of the ubiquitous Gαq subunit, a known transducer of plasma membrane G protein-coupled receptors signaling, as a core modulator of mTORC1 and autophagy. Cells lacking Gαq/11 display higher basal autophagy, enhanced autophagy induction upon different types of nutrient stress along with a decreased mTORC1 activation status. They are also unable to reactivate mTORC1 and thus inactivate ongoing autophagy upon nutrient recovery. Conversely, stimulation of Gαq/11 promotes sustained mTORC1 pathway activation and reversion of autophagy promoted by serum or amino acids removal. Gαq is present in autophagic compartments and lysosomes and is part of the mTORC1 multi-molecular complex, contributing to its assembly and activation via its nutrient status-sensitive interaction with p62, which displays features of a Gαq effector. Gαq emerges as a central regulator of the autophagy machinery required to maintain cellular homeostasis upon nutrient fluctuations., (© 2021. The Author(s).)

Gram-positive bacteria colonize mucosal tissues, withstanding large mechanical perturbations such as coughing, which generate shear forces that exceed the ability of non-covalent bonds to remain attached. To overcome these challenges, the pathogen Streptococcus pyogenes utilizes the protein Cpa, a pilus tip-end adhesin equipped with a Cys-Gln thioester bond. The reactivity of this bond towards host surface ligands enables covalent anchoring; however, colonization also requires cell migration and spreading over surfaces. The molecular mechanisms underlying these seemingly incompatible requirements remain unknown. Here we demonstrate a magnetic tweezers force spectroscopy assay that resolves the dynamics of the Cpa thioester bond under force. When folded at forces <6 pN, the Cpa thioester bond reacts reversibly with amine ligands, which are common in inflammation sites; however, mechanical unfolding and exposure to forces >6 pN block thioester reformation. We hypothesize that this folding-coupled reactivity switch (termed a smart covalent bond) could allow the adhesin to undergo binding and unbinding to surface ligands under low force and remain covalently attached under mechanical stress.