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We present a rigorous quantum scattering study of the effects of hyperfine and Zeeman interactions on cold Li–H2 collisions in the presence of an external magnetic field using a recent ab initio potential energy surface. We find that the low-field-seeking states of H2 predominantly undergo elastic collisions: the ratio of elastic-to-inelastic cross sections exceeds 100 for collision energies below 100 mK. Furthermore, we demonstrate that most inelastic collisions conserve the space-fixed projection of the nuclear spin. We show that the anisotropic hyperfine interaction between the nuclear spin of H2 and the electron spin of Li can have a significant effect on inelastic scattering in the ultracold regime, as it mediates two processes: the electron spin relaxation in lithium and the nuclear spin–electron spin exchange. Given the predominance of elastic collisions and the propensity of inelastic collisions to retain H2 in its low-field-seeking states, our results open up the possibility of sympathetic cooling of molecular hydrogen by atomic lithium, paving the way for future exploration of ultracold collisions and high-precision spectroscopy of H2 molecules. [ABSTRACT FROM AUTHOR]

Purpose: To assess the impact of fatigue loading on the internal and marginal fit of CAD/CAM-fabricated endocrowns for restoring endodontically treated molars using different machinable blocks. Materials and Methods: A total of 72 mandibular first molars were prepared using a standardized method and were divided into four groups (n = 18), each restored with a different CAD/CAM material: group V = polymerinfiltrated ceramic (Vita Enamic); group K = partially stabilized tetragonal zirconia (Katana); group E = lithium disilicate ceramic (IPS e.max CAD; and group B = polyetheretherketone (BioHPP). Endocrowns were subjected to thermomechanical fatigue loading. Internal and marginal adaptation of the endocrowns were examined at 66 points using the sectioning technique and a stereomicroscope. Data were analyzed using one-way ANOVA and Tukey post hoc test (a = .05). Results: Statistical tests showed that adhesive cementation resulted in significantly increased marginal and internal gap values in all regions in all four tested groups (P < .001). After thermomechanical fatigue loading, all regions in groups B and K showed a statistically significant difference, while no significant differences were found in the regions in group V (P > .05). In group E, the marginal (F = 71.00) and pulpal (F = 28.065) regions showed statistically significant differences (P < .001). Conclusion: Polymer-infiltrated ceramics showed the lowest gap even after thermomechanical fatigue loading and may therefore provide enhanced clinical survival of the restored tooth, favoring the use of this material for fabricating endocrown restorations. [ABSTRACT FROM AUTHOR]

Purpose: To compare the fracture resistance of five different groups of chairside CAD/CAM molar crowns fabricated from various lithium disilicate ceramic materials (LDC): one conventional precrystallized CAD/CAM LDC, two novel precrystallized LDCs, and one fully crystallized LDC tested both with and without optional sintering. Materials and Methods: A total of 60 chairside CAD/CAM lithium disilicate molar crowns (n = 12 per group) with 1.5-mm occlusal thickness and a 1.0-mm chamfer finish were designed and fabricated with a chairside CAD/CAM system (CEREC, Dentsply Sirona). The restorations were divided into five groups: (1) IPS e.max CAD; (2) Amber Mill; (3) Straumann n!ce; (4) Straumann n!ce with optional sintering; and (5) Supreme CAD. Restorations were cemented using conventional resin luting cement and primer system to 3D-printed resin dies. Bonded restorations were loaded for 100,000 cycles with 275-N force, and the load at break (LB) and peak load (PL) until fracture were measured. SEM images of fracture surfaces on the printed dies were obtained. Results: Fracture resistance was significantly different depending on the material. Supreme CAD showed the highest fracture resistance (LB: 1,557.2 N; PL: 1,785.8 N), followed by Amber Mill (LB: 1,393.0 N; PL: 1,604.2 N) and IPS e.max CAD (LB: 1,315.7 N; PL: 1,461.9 N). Straumann n!ce without (LB: 862.4 N; PL: 942.9 N) and with the optional sintering (LB: 490.4 N; PL: 541.0 N) showed significantly lower fracture resistance than the others. Conclusion: The fracture resistance of chairside CAD/CAM lithium disilicate molar crowns varied depending on the material, and the novel materials did not perform as well as the conventional equivalents. Fully crystallized lithium disilicate ceramic block materials showed lower fracture resistance than precrystallized counterparts and should be used with caution in the clinic, especially with optional sintering. [ABSTRACT FROM AUTHOR]

All‐solid‐state Li batteries are desired for better safety and energy density than Li‐ion batteries. However, the lack of a penetrating liquid electrolyte requires a much different approach to the design of cathodes. The solid catholyte must enable good Li+ conduction, form good interfaces with active material particles, and have the strength to bind the cathode together during repeated volume changes. Catholyte formulation is often simply adapted from Li‐ion design principles, adding a Li salt to the PVDF binder. Here we show that such a PVDF binder at 10 wt % loading is a starved catholyte condition that compromises cell performance. By substituting a 70 : 30 blend of PVDF:PEO, performance is improved while maintaining nearly the same areal loading of LFP active material. Increasing the catholyte fraction to 16 % can also improve performance, but in this case the benefit of including PEO is lessened, with PVDF alone being an adequate catholyte. EIS analysis shows that PEO helps to form charge transfer interfaces at 10 % catholyte, but that its inclusion can degrade interfaces when there is ample catholyte at 16 %. It is also shown that catholyte agglomeration can impede bulk Li conduction, indicating that microstructural factors are of critical importance. [ABSTRACT FROM AUTHOR]

Mg-Li alloys can be promising candidates as bioresorbable Li-releasing implants for bipolar disorder and other neurodegenerative disorders. In order to compare the therapeutic efficacy of conventional Li salts and Li delivered through Mg-Li alloy extracts, we tested an in vitro model based on the neuroinflammation hypothesis of mood disorders (peripheral inflammation inducing neuroinflammation) wherein, a coculture of microglia and astrocytes was treated with conditioned medium from pro-inflammatory macrophages. Two alloys, Mg-1.6Li and Mg-9.5Li, were tested in the form of material extracts and well-known outcomes of Li treatment such as GSK3β phosphorylation (indirect flow cytometry) and influence on inflammation-related gene expression (qPCR) were compared against Li salts. This is the first study demonstrating that Li can increase the phosphorylation of GSK3β in glial cells in the presence of excess Mg. Furthermore, Mg-Li alloys were more effective than Li salts in downregulating IL6 and upregulating the neurotrophin GDNF. Mg had no antagonistic effects toward Li-driven downregulation of astrogliosis markers. Overall, the results provide evidence to support further studies employing Mg-Li alloys for neurological applications. [ABSTRACT FROM AUTHOR]

The synthetic potential of substituted 1,4‐dioxenes is well recognised, although the chemistry of 2‐aryl‐1,4‐dioxenes is relatively unexplored. Their transition metal‐catalysed synthesis has been limited to Stille‐type cross‐coupling chemistry, typically showing long reaction times, or proceeding at high reaction temperatures. Here we present a facile and general methodology for the cross‐coupling of aryl bromides with lithium 1,4‐dioxene, affording a range of 2‐aryl‐1,4‐dioxenes in generally good yields. We highlight the synthetic applicability of this transformation at multigram scale, and demonstrate the versatility of the products by conversion of the dioxene units to various carbonyl‐based functionalities. Additionally, we present a concise two‐step synthesis of an arylated analogue to a known 1,4‐dioxene‐based antifungal agent. [ABSTRACT FROM AUTHOR]

Introduction: The rising prevalence of battery powered devices is driving a steady increase in lithium‐ion battery‐related burns. We present a case series of patients with lithium‐ion battery‐related burns and describe the clinical characteristics of this cohort. To further understand emerging trends, we compare our specialty inpatient case series with emergency department (ED) data collated by the Queensland Injury Surveillance Unit (QISU). Methods: This is a retrospective case series of all patients admitted to the Professor Stuart Pegg Adult Burns Centre for burns relating to lithium‐ion batteries between January 2014 and October 2023. In addition, we provide a retrospective data analysis of ED presentations for lithium‐ion battery‐related burns or blast injuries collated by the QISU. Results: Within the case series data, the most common injuries caused by lithium‐ion batteries leading to burn unit admissions were due to e‐scooters (57.1%). Burns relating to e‐scooter batteries were more likely to involve a larger total body surface area and to be deeper in nature, than burns due to other products. The most common ED presentations were from energy storage devices such as powerpacks (43%). Conclusion: Lithium‐ion battery‐related burns are becoming more frequent. The majority of inpatient managed cases involved burns due to larger lithium‐ion batteries used in e‐scooters. This is the first Australian case series describing severe burns caused by this mechanism. Primary prevention through design, technological and behavioural strategies is required. [ABSTRACT FROM AUTHOR]

This article aims to contribute to aligning the legal regimes for energy transition minerals with sustainability and justice. The focus of the article is on effectively embedding the human right to a healthy environment into the design of these regimes. The article distinguishes between two models of legal design for mineral extraction and argues that the present predominant model must evolve towards one that bridges the normative and enforcement gaps for exercising public authority. Legal regimes need therefore to be reorganised to protect the integrity and resilience of ecosystems while upholding the right to a healthy environment and interdependent human rights. The task of redesigning regimes in ways that are embedded in a thicker environmental rule of law is emerging through litigation and policy reform. The complexity of this task must be recognised and upscaled for transformative change. This article is based on a case study focusing on lithium found in brines (highly saline waters), and in the legal regime and judicial decisions in Argentina and policy initiatives in Chile. [ABSTRACT FROM AUTHOR]

Suicide, as an avoidable cause of death in public health systems, currently lacks effective global strategies to prevent it. However, several epidemiological studies found a correlation between the concentration of lithium (Li) in drinking water and lower suicide rates in the general population. Our ecological study investigated this hypothesis in the Rafsanjan district of Iran. Samples from the public water supply in 16 areas in the district were analyzed using the graphite furnace atomic absorption. The resulting data were examined in relation to the suicide attempt from March 2019 to March 2020 obtained from Iran's Ministry of Health's registration system. During that period, 239 suicide attempts were recorded, resulting in an average of 69 individuals (85 women and 54 men) per 100,000 residents of the area. The average Li concentration in the drinking water was 47.30 µg/L (ranging from 9.4 to 141 µg/L). A negative significant correlation (r = -0.551, p = 0.027) between Li concentration in water and the rate of suicide attempt were observed in the studied population. Notably, these findings indicate an inverse significant relationship between Li levels and suicide attempt rate in women (r = -0.725, p = 0.001). This is the first study in Iran that examines the relationship between Li levels in drinking water and suicide attempt rate. The findings of this study support an inverse relationship between the level of Li in public drinking water and the rate of women suicide attempt. [ABSTRACT FROM AUTHOR]

Introduction Pharmacoepidemiological data suggest that lithium prescriptions for bipolar disorder are gradually decreasing, with less attention having been paid to other indications. Methods We examined lithium prescriptions between 1994 and 2017 in data provided by the Drug Safety in Psychiatry Program AMSP, including psychiatric hospitals in Germany, Austria and Switzerland. We compared lithium use for different diagnoses before and after 2001 and in three periods (T1: 1994–2001, T2: 2002–2009, and T3: 2010–2017). Results In a total of 158,384 adult inpatients (54% female, mean age 47.4±17.0 years), we observed a statistically significant decrease in lithium prescriptions between 1994–2000 and 2001–2017 in patients with schizophrenia spectrum disorder from 7.7% to 5.1% and in patients with affective disorders from 16.8% to 9.6%. Decreases in use were also observed for diagnostic subgroups: schizoaffective disorder (ICD-10 F25: 27.8% to 17.4%), bipolar disorder (F31: 41.3% to 31%), depressive episode (F32: 8.1% to 3.4%), recurrent depression (F33: 17.9% to 7.5%, all: p<0.001) and emotionally unstable (borderline) personality disorder (6.3% to 3.9%, p=0.01). The results in T1 vs. T2 vs. T3 were for F25: 26.7% vs. 18.2% vs. 16.2%, F32: 7.7% vs. 4.2% vs. 2.7%, F33: 17.2% vs. 8.6% vs. 6.6% and for F31: 40.8% vs. 31.7% vs 30.0%, i. e. there was no further decrease for lithium use in bipolar disorder after 2002. Lithium's main psychotropic co-medications were quetiapine (21.1%), lorazepam (20.6%), and olanzapine (15.2%). Discussion In inpatients, the use of lithium has decreased in patients with bipolar disorder and also with various other psychiatric diagnoses. [ABSTRACT FROM AUTHOR]

Rapid development of electronic and grid storage technologies based on lithium-ion batteries are leading to tight supply of lithium resources in the future. Extracting lithium from seawater can completely solve the problem of lithium resource shortage. An electro-deposition method based on a lithium superionic conductive solid-state electrolyte, Li1.5Al0.5Ge1.5(PO4)3 (LAGP), has been reported to obtain metallic lithium from seawater. However, expensive LAGP increases the cost of lithium extraction, while Li1.3Al0.3Ti1.7(PO4)3 (LATP) with relatively lower prices cannot meet the stable requirements. Herein, a low-cost, stable glass–ceramics, Li1.5Al0.3Ti1.7Si0.2P2.8O12 (LATSP), has been prepared for lithium extraction from seawater. The LATSP glass–ceramics show good selectivity towards Li+ and exhibit a high ionic conductivity of 3.98 × 10−4 S cm−1 at 22 °C. After soaking in simulated seawater, LATSP showed much better stability than LATP, comparable to LAGP. The resultant LATSP glass–ceramics was successfully employed in a seawater lithium extraction device, with a high lithium extraction Coulombic efficiency of 94.0%. Moreover, the LATSP exhibits an ionic conductivity of 2.80 × 10−4 S cm−1 and maintains a complete structure after 45 h of lithium extraction. This work presents an effective and practical Li-ion conducting membrane for lithium extraction from seawater. [ABSTRACT FROM AUTHOR]

Background: This study examines the association between the coefficient of variation (%CV) of lithium levels and episode risk and frequency in bipolar patients maintaining serum lithium levels within the therapeutic range. Methods: We retrospectively reviewed patients with bipolar disorder under care from 2018 to 2022. Inclusion criteria were at least 2 years of follow-up, a minimum of three annual lithium level measurements within the therapeutic range. Patients were categorized based on seizure status. We calculated mean lithium levels, standard deviation (SD), and %CV. Results: The study included 75 patients (patients with-without episodes, 39–36). Demographic data revealed no significant differences. While mean lithium levels showed no significant disparity between groups, SD and %CV were notably higher in patients with episodes (P <.05). ROC analysis demonstrated AUC values of 0.722 (95% CI: 0.607–0.836 P =.001) for %CV and 0.709 (95% CI: 0.593–0.826; P =.002) for SD. The optimal %CV cutoff was 17.39, with 67% sensitivity and 69% specificity. A weak correlation was found between %CV and the number of episodes (P =.001, r = 0.376). The post-hoc power analysis for this study was 0.78. Conclusions: Despite acceptable lithium levels, patients with recent episodes exhibited significant lithium level fluctuations. Integrating %CV with real-time lithium measurements during bipolar disorder follow-up may enhance clinical monitoring and seizure prediction. [ABSTRACT FROM AUTHOR]

Energy transitions are reshaping hydrosocial relations. How they will be reshaped, however, depends on location and water's material relationship to other resources and industrial activities embedded within energy transitions. To highlight this, we focus on three different resources—coal, natural gas, and lithium—to signal how the water–energy nexus will be reworked in a transition away from fossil fuels. We examine the water–coal nexus as an example of a resource relationship that is transitioning out, or that is being moved away from in the green energy transition. Natural gas represents the "bridge fuel" used through the transition. Lithium illustrates a resource inside the green transition, as it is a fundamental material for green technologies in the transition to a low‐carbon future. Coal, natural gas, and lithium each have their own material impacts to water resources that stem from their industrial lifecycle and different implications for communities shaped by coal, natural gas, and lithium activities. To explore this, we review each of these resources' connection to water, their legal and regulatory dimensions, and their impact on communities and water justice. We argue that the energy transition is also a hydrosocial transition that will create uneven water‐related benefits and burdens. To maximize sustainability and equity, efforts to decarbonize energy systems must examine the localized, place‐based hydrosocial relations that differentially affect communities. This article is categorized under:Engineering Water > Planning WaterHuman Water > Water GovernanceHuman Water > Rights to Water [ABSTRACT FROM AUTHOR]

As a key ingredient of batteries for electric vehicles (EVs), lithium plays a significant role in climate change mitigation, but lithium has considerable impacts on water and society across its life cycle. Upstream extraction methods—including open‐pit mining, brine evaporation, and novel direct lithium extraction (DLE)—and downstream processes present different impacts on both the quantity and quality of water resources, leading to water depletion and contamination. Regarding upstream extraction, it is critical for a comprehensive assessment of lithium's life cycle to include cumulative impacts related not only to freshwater, but also mineralized or saline groundwater, also known as brine. Legal frameworks have obscured social and ecological impacts by treating brine as a mineral rather than water in regulation of lithium extraction through brine evaporation. Analysis of cumulative impacts across the lifespan of lithium reveals not only water impacts in conventional open‐pit mining and brine evaporation, but also significant freshwater needs for DLE technologies, as well as burdens on fenceline communities related to wastewater in processing, chemical contaminants in battery manufacturing, water use for cooling in energy storage, and water quality hazards in recycling. Water analysis in lithium life cycle assessments (LCAs) tends to exclude brine and lack hydrosocial context on the environmental justice implications of water use by life cycle stage. New research directions might benefit from taking a more community‐engaged and cradle‐to‐cradle approach to lithium LCAs, including regionalized impact analysis of freshwater use in DLE, as well as wastewater pollution, cooling water, and recycling hazards from downstream processes. This article is categorized under:Human Water > Human WaterHuman Water > Water GovernanceHuman Water > Water as Imagined and RepresentedScience of Water > Water and Environmental Change [ABSTRACT FROM AUTHOR]

Background: Older‐age bipolar disorder (OABD) is commonly defined as bipolar disorder in individuals aged 60 or more. There have been no studies to examine temporal trends in the pharmacological treatment of OABD. We aimed to investigate prescription changes among OABD patients discharged from two public mental hospitals in Taiwan from 2006 to 2019. Methods: OABD patients discharged from the two study hospitals, from 1 January 2006 to 31 December 2019 (n = 1072), entered the analysis. Prescribed drugs at discharge, including mood stabilisers (i.e., lithium, valproate, carbamazepine, and lamotrigine), antipsychotics (i.e., second‐ and first‐generation antipsychotics (SGAs and FGAs)), and antidepressants, were investigated. Complex polypharmacy was defined as the use of three or more agents among the prescribed drugs. Temporal trends of each prescribing pattern were analyzed using the Cochran‐Armitage Trend test. Results: The most commonly prescribed drugs were SGAs (72.0%), followed by valproate (48.4%) and antidepressants (21.7%). The prescription rates of SGAs, antidepressants, antidepressants without mood stabilisers, and complex polypharmacy significantly increased over time, whereas the prescription rates of mood stabilisers, lithium, FGAs, and antidepressants plus mood stabilisers significantly decreased. Conclusions: Prescribing patterns changed remarkably for OABD patients over a 14‐year period. The decreased use of lithium and increased use of antidepressants did not reflect bipolar treatment guidelines. Future research should examine whether such prescribing patterns are associated with adverse clinical outcomes. [ABSTRACT FROM AUTHOR]

Introduction: Bipolar disorder is a psychiatric condition commonly treated with lithium. This treatment has various biological effects on the brain; however, variability in the areas and types of changes as a result of lithium treatment has resulted in discourse over lithium's effect. As a result, a comprehensive synthesis is needed to understand lithium's true neurological effect. This review aims to identify a common result of lithium use in the neurobiology of bipolar patients, specifically in the amygdala, to determine whether volumetric changes in the amygdala are a common effect. Methods: We conducted a preliminary search to identify key search terms across electronic databases, including Google Scholar and PubMed. After screening and application of inclusion and exclusion criteria, 9 cross-sectional studies were identified. Results: The evidence from these cross-sectional studies showed either an increase or no change in amygdalar volume. While this fails to identify a definite pattern in amygdalar volume changes, it highlights a need for further research to identify sources of heterogeneity and minimize them to ascertain accurate results. Conclusions: The present review may be used to influence future work concerning neurobiological changes in the amygdala as a result of lithium treatment for bipolar patients by summarizing patterns in the current literature. [ABSTRACT FROM AUTHOR]

The small, lipophilic tetrafluoroborate anion is ubiquitous in the imidazol(in)ium and iminium precursors to N‐heterocyclic carbenes (NHCs), including cyclic (alkyl)(amino)carbenes (CAACs). Its symmetrical distribution of charge over four highly electronegative fluorine atoms confers high stability, attenuating basicity while shielding the boron center. Here we report that this inertness does not withstand the nucleophilicity of free carbenes, when combined with a polarizing lithium cation. Reaction of CAAC ⋅ HBF4 salts with LiN(SiMe3)2, a protocol widely used to liberate free CAACs, generates zwitterionic CAAC‐BF3 adducts within minutes at 80 °C, or hours at room temperature, even for bulky N‐diisopropylphenyl (DIPP) CAACs. Imidazol(in)ium tetrafluoroborates likewise form NHC‐BF3 adducts in excellent yields. [ABSTRACT FROM AUTHOR]

The cycling lifespan of high‐energy‐density lithium–sulfur (Li–S) batteries is dominantly limited by the rapid failure of Li metal anodes. Herein, the evolution of Li metal anode along cycling is systematically investigated in Li–S batteries to clarify the Li plating and stripping behaviors, the generation and accumulation of inactive Li, and the failure mechanism of Li metal anodes. Concretely, plated Li strips preferentially than bulk Li to leave massive stripping Li shells during initial discharge, and the stripping Li shells are refilled by plated Li during the subsequent charge to generate thick Li dendrites. During the following cycles, inactive Li generates and accumulates on top of bulk Li due to solid electrolyte interphase formation and incomplete removal of plated Li. Eventually, the accumulation of inactive Li hinders the diffusion of Li ions through the inactive Li layer to induce cell polarization at the end of the second discharge plateau and rapid decay of discharge capacity. This work elucidates the detailed evolution mechanism of Li metal anode along cycling in working Li–S batteries and highlights the reactivation of inactive Li as an effective strategy to prolong the cycling lifespan of Li–S batteries. [ABSTRACT FROM AUTHOR]

Lithium metal batteries (LMBs) suffer severe capacity deterioration due to sluggish ionic transport kinetics at extremely low temperatures, which limits their practical operation. Selecting solvents with low desolvation energy, and promoting interfacial Li+ transport in solid electrolyte interphase (SEI) are regarded as effective methods to improve electrochemical performances. Herein, 1,3‐dioxolane (DOL) with weak solvating power is adopted for designing a DOL‐based localized high concentration electrolyte (DLHCE) with LiNO3 as a multifunctional additive. The strong coordination between NO3− and DOL molecules not only inhibits the polymerization of DOL at high lithium bis(fluorosulfonyl)imide (LiFSI) concentration, but also reduces the solvent‐diluent miscibility and extends the salt‐solvent solubility. As a result, an anion‐dominated solvation structure is obtained that derives an inorganic‐rich SEI composed of LiF and Li3N, guiding the uniform deposition of Li at low temperature. Remarkably, the Li||LiFePO4 cells retain 53.6% of room temperature capacity at −40 °C, and also present potential application of Li||NCM811 cells under cryogenic environments. [ABSTRACT FROM AUTHOR]

Changes in intracellular concentrations of Na+ and K+ are shown to alter gene expression. Another monovalent cation, Li+, is well known as a medicine for treatment of psychiatric disorders, but mechanism of its action is obscure. Thus, it is important to evaluate the effect of Li+ on gene expression in endothelial cells. Here we studied influence of the increased intracellular Na+ or Li+ concentrations on transcription of Na+i/K+i-sensitive genes. Treatment of the human endothelial cells (HUVEC) with LiCl for 1.5 h resulted in accumulation of Li+ in the cells. This was followed by increase in the FOS and EGR1 mRNAs levels and decrease in the JUN and MYC mRNA levels. Treatment of HUVEC with the Na+-ionophore monensin led to accumulation of Na+ and loss of K+ ions. However, monensin had no significant effect on gene expression. Incubation of HUVEC with elevated extracellular NaCl concentration increased intracellular K+ concentration and transcription of the ATF3 gene, while transcription of the JUN gene decreased. These results indicate that Na+ and Li+ ions have different effects on the gene expression profile in the cells that is likely associated with the fact that they affect differently the intracellular monovalent cations ratio. [ABSTRACT FROM AUTHOR]

Background: Lithium is the gold-standard treatment for Bipolar Disorder (BD) in both adults and adolescents, effectively managing mood episodes and reducing suicide risk. While its efficacy in neurotypical youth is well established, its use in adolescents with Autism Spectrum Disorder (ASD) and comorbid BD remains under-researched. Here, we present the protocol for a study aiming to evaluate the efficacy and tolerability of Extended-Release Lithium Salts in treating adolescents with BD and comorbid ASD compared to neurotypical BD patients. Methods: This longitudinal prospective naturalistic comparative study will enroll lithium-naïve adolescents aged 12–18 with BD, with or without comorbid ASD, from the Department of Child and Adolescent Psychiatry and Psychopharmacology. Participants will be followed for six months while receiving Extended-Release Lithium Salts treatment. Primary outcomes will include mood instability, suicidality, emotional dysregulation, and aggression, assessed through a range of clinical rating scales and diagnostic tools at baseline, three months, and six months. Secondary outcomes will focus on the safety and tolerability of Extended-Release Lithium Salts, with measures including side effect ratings, physical exams, and laboratory tests. Results: We hypothesize that Extended-Release Lithium Salts will demonstrate non-inferiority in treating BD symptoms in adolescents with comorbid ASD compared to those without ASD. Conclusions: This study is poised to fill a significant gap in the literature by providing critical data on the use of lithium for adolescents with BD and ASD. Findings will inform clinical practice and future research, potentially guiding more personalized treatment approaches for this complex and vulnerable population. [ABSTRACT FROM AUTHOR]

In the development of polymer electrolytes, the understanding of the complex interplay of factors that affect ion transport is of importance. In this study, the strongly coordinating and flexible poly (ethylene oxide) (PEO) is compared to the weakly coordinating and stiff poly (trimethylene carbonate) (PTMC) as opposing model systems. The effect of molecular weight (Mn) and end group chemistry on the physical properties: glass transition temperature (Tg) and viscosity (η) and ion transport properties: transference number (T+), ion coordination strength and ionic conductivities were investigated. The cation transference number (T+) showed the opposite dependence on Mn for PEO and PTMC, decreasing at low Mn for PTMC and increasing for PEO. This was shown to be highly dependent on the ion coordination strength of the system regardless of whether the end group was OH or if the chains were end‐capped. Although the coordination is mainly of the cations in the systems, the differences in T+ were due to differences in anion rather than cation conductivity, with a similar Li+ conductivity across the polymer series when accounting for the differences in segmental mobility. [ABSTRACT FROM AUTHOR]

Background: Despite a variability in response and a narrow therapeutic index, Lithium (Li) remains the gold standard treatment for bipolar disorders (BD), and a treatment of choice for unipolar disorders (UD). Red blood cell Li concentration (RBCLiC) and red blood cell/plasma Li ratio (LiR) have been studied in many areas of mood disorders (such as acute or chronic Li efficacy, adherence, side effects (SE), intoxication management) as well as in several research domains. This systematic review aims to synthesize the existing literature. Methods: We conducted a systematic review, based on preferred reporting items for systematic reviews and Metanalysis (PRISMA) guidelines, of articles published between 1972 and February 2023, indexed in the following databases: EMBASE, MEDLINE, Cochrane Library. The search terms were combinations of the following headings: "Lithium AND Plasma AND Erythrocyte AND Mood disorders". The systematic review protocol was published to PROSPERO (CRD42023406154). Results and conclusion: Out of the 252 identified studies, 57 met the selection criteria. The articles investigated the interest of RBCLiC and other blood parameters (PLiC and LiR) in various areas: (i) disease management (31 articles) (compliance/adherence (5 articles), SE/toxicity (13 articles), prediction of Li response/therapeutic efficacy for acute episode or for relapse prevention (17 articles)), (ii) Li blood parameters as trait markers of mood disorders subtypes (UD, BDI, BDII) (16 articles), (iii) Li blood parameters as state markers of mood episodes (11 articles), (iv) factors influencing Li blood parameters (age, gender, ethnicity, dosage and duration of Li treatment, co-medications with other treatments, seasonality) associated with RBCLiC or LiR (24 articles), and (v) potential pathophysiological mechanisms (30 articles). Conclusion: Overall, this review suggests that RBCLiC or LiR could be of interest for tolerance monitoring. However, the heterogeneity of methods and results, coupled with the limited amount of data, does not allow clear conclusions to be drawn in the other areas explored in this literature review. Given the potential interest in exploring brain Li pharmacokinetics (PK)s, this review calls for further research. [ABSTRACT FROM AUTHOR]

Lithium metal batteries (LMBs) are considered as one type of the most promising next‐generation energy storage devices with high‐energy‐density, and stabilizing the lithium metal anodes (LMAs) to overcome LMBs' safety concerns and performance degradation has attracted extensive attention. Introducing advanced polymer materials into the critical components of LMBs has proven to be an effective and promising approach for stabilizing LMAs toward practical application of LMBs. In addressing the lack of a timely review on the emerging progress of advanced polymer materials in LMBs for stabilizing LMAs, a comprehensive article summarizing the most recent developments of multiscale cellulose materials, including micron cellulose (MC) and nanocellulose (NC), in LMBs is reviewed. First, the basic structures of cellulose, characteristics comparison, and the development history of introducing cellulose into LMBs are presented. Furthermore, the roles of multiscale cellulose materials and functional mechanisms in various components of LMBs for stabilizing LMAs are summarized. A general conclusion and a perspective on the current limitations and future research directions of cellulose‐based stable LMBs are proposed. The aim of this review is not only to summarize the recent progress of multiscale cellulose materials in stabilizing LMAs but also to lighten the pathways for realizing LMBs' practical application. [ABSTRACT FROM AUTHOR]

The widespread use of reinforced concrete continues to face challenges, particularly in mitigating alkali-silica reaction (ASR), due to its detrimental effects on concrete strength and durability. This paper investigates the effectiveness of using binary supplementary cementitious materials (SCMs) in mitigating ASR by incorporating metakaolin (MK) and waste glass powder (GP) as partial replacements for cement. Additionally, the potential of a new cement product, "NewCem Plus" (NCM), along with the use of basalt fibers and lithium, was evaluated through a 14-day accelerated mortar bar test following the ASTM C1260. This study also assessed concrete's properties such as its compressive strength and workability using the flow test. The results indicated that MK was effective, reducing expansion by 79%, 84%, and 88% with 10%, 20%, and 30% cement replacement, respectively, compared to the control mixture. On the other hand, GP showed a more modest reduction in expansion, with 10%, 20%, and 30% replacement levels reducing expansion by 20%, 43%, and 75%, respectively. Furthermore, the addition of lithium to MK significantly mitigated ASR, reducing expansion below the ASTM threshold. However, mixtures containing NewCem Plus, lithium, and basalt fibers showed minimal impact on ASR reduction. These findings underscore the viability of using binary or ternary blends of SCMs to mitigate ASR in concrete, encouraging their adoption in future concrete applications. [ABSTRACT FROM AUTHOR]

Lithium holds significant importance in energy storage and can be extracted from geothermal water, making it an additional resource to traditional mining. Combining lithium extraction from geothermal water with electricity generation from geothermal energy offers a compelling strategy to address future energy challenges. Situated in Southeast Sumatra, Indonesia, Way Ratai has considerable geothermal potential and is known for its hot springs. This study primarily aims to characterize lithium enrichment within the Way Ratai geothermal system. Water samples from various sources (one spring, seven hot springs, one well, and seawater) were analyzed for cations, anions, trace elements, and isotopic composition. The results show that Way Ratai is an old geothermal system with sodium-chloride water, where lithium enrichment is attributed to interactions between water and rocks, with some influence from seawater. The discrepancy between calculated and observed magnesium (Mg) concentrations suggests a pre-heating mixing process between rainwater and seawater. The reservoir rock in Way Ratai is mostly andesitic, with temperatures ranging from 182o to 227oC. This study enhances our understanding of thermal water characteristics, reservoir temperatures, and water origins in high enthalpy geothermal systems, offering valuable insights into lithium enrichment in coastal geothermal regions. [ABSTRACT FROM AUTHOR]

Lithium holds significant importance in energy storage and can be extracted from geothermal water, making it an additional resource to traditional mining. Combining lithium extraction from geothermal water with electricity generation from geothermal energy offers a compelling strategy to address future energy challenges. Situated in Southeast Sumatra, Indonesia, Way Ratai has considerable geothermal potential and is known for its hot springs. This study primarily aims to characterize lithium enrichment within the Way Ratai geothermal system. Water samples from various sources (one spring, seven hot springs, one well, and seawater) were analyzed for cations, anions, trace elements, and isotopic composition. The results show that Way Ratai is an old geothermal system with sodium-chloride water, where lithium enrichment is attributed to interactions between water and rocks, with some influence from seawater. The discrepancy between calculated and observed magnesium (Mg) concentrations suggests a pre-heating mixing process between rainwater and seawater. The reservoir rock in Way Ratai is mostly andesitic, with temperatures ranging from 182o to 227oC. This study enhances our understanding of thermal water characteristics, reservoir temperatures, and water origins in high enthalpy geothermal systems, offering valuable insights into lithium enrichment in coastal geothermal regions. [ABSTRACT FROM AUTHOR]

Lithium (Li) metal is considered as a promising anode material for high‐energy batteries; yet, its practical application is hindered by uncontrolled Li dendrite growth, especially at a high rate. Herein, a dual conductive gradient V2CTx/MoO3 (DG‐V2CTx/MoO3) host that integrates electronic/ionic conductive gradients and lithiophilicity is prepared by layer‐by‐layer assembly for dendrite‐free Li anodes. Gradient LiF deriving from different amount of V2CTx endows a good ionic conductive gradient; while, MoO3 is regarded as a spacer to avoid the restacking of V2CTx, increasing space for Li deposition. The dual conductive gradients effectively optimize the current density and Li+ flux distribution at the bottom, achieving fast reduction of Li+ and a "bottom–up" Li deposition mode. Meanwhile, the lithiophilic V2CTx and MoO3 guide the homogeneous Li growth. As a result, the symmetrical half‐cells based on DG‐V2CTx/MoO3@Li anodes conduct 700 h at 5 mAh cm−2 and 20 mA cm−2. The DG‐V2CTx/MoO3@Li||LiFePO4 full‐cells maintain a capacity retention of 85.4% after 1350 cycles at 2 C. Remarkably, the DG‐V2CTx/MoO3@Li||LiNi0.6Co0.2Mn0.2O2 full‐cells can run 150 cycles with 80.6% capacity retention even at harsh conditions. The well‐adjusted materials and structures with both dual conductive gradients and lithiophilic properties will bring inspiration for novel material design of other metal batteries. [ABSTRACT FROM AUTHOR]

Through microscope identitication, X-ray diffraction analysis, scanning electron microscopy analysis, automatic mineral quantitative analysis (AMICS) and LA-ICP-MS micro area analysis, the occurrence status of lithium and titanium elements associated with the ore in Sanchahe bauxite were identified. The ore ss mainly composed of diaspore, illite, chlorite, kaolinite, and a small amount of pyrite, anatase, etc. The bauxite mineral in the ore ss mainly diaspore, while the titanium mineral ss mainly anatase. Lithium does not have an independent mineral, and titanium is mainly present in illite, chlorite, and diaspore, There are two particle size forms of diaspore, over 200 µm granular and less than 1 µm microscopic scaly morphology, illite is mainly tiner than 75 µm small scale-like structures, chlorite is mainly coarser than 150 µm in the form of flakes, and anatase is mainly in tiner than 75 µm granular. The total content of Li2O in the ore is 228.96 x 10-6, the total content of TiO2> in the ore is 5.29%, 54.28,_ exist in the form of independent mineral anatase, and 45.72_ exist in the form of isomorphic or ultrafine grained minerals. [ABSTRACT FROM AUTHOR]

A zeolitic sample, named MT-ZLSH, was synthesized using mining tailings (MT) as the precursor material, resulting in a structure comprising: Linde type A (LTA) and sodalite-hydroxysodalite (ZLSH). This naming convention reflects the material's origin and its structural characteristics. The material was further modified by incorporating lithium, producing MT-ZLSH-Li+. Physicochemical characterizations were performed, and the material was evaluated for its potential to remove methylene blue (MB) from synthetic wastewater through adsorption and photocatalysis. Efficient adsorption was observed under typical wastewater pH conditions, with a maximum adsorption capacity of 23.4 mg·g−1, which fit well with the Langmuir isotherm model. The key mechanisms governing MB adsorption were identified as ion exchange, electrostatic attraction, and hydrogen bonding. The adsorption process was exothermic, with kinetic data fitting both the pseudo-second order and intraparticle diffusion models, achieving 82% removal and a maximum adsorption capacity of 40 mg·g−1 over 12 h. MB adsorption followed a two-step process, initially involving film diffusion, followed by intraparticle diffusion. Additionally, photocatalytic degradation of MB achieved 77% degradation within 180 min. However, a decrease in reusability was observed during a second cycle of MB adsorption and photodegradation, highlighting the need for further optimization to enhance the material's long-term performance. [ABSTRACT FROM AUTHOR]

Background: Optimising maintenance drug treatment selection for people with bipolar disorder is challenging. There is some evidence that clinical and demographic features may predict response to lithium. However, attempts to personalise treatment choice have been limited. Method: We aimed to determine if machine learning methods applied to electronic health records could predict differential response to lithium or olanzapine. From electronic United Kingdom primary care records, we extracted a cohort of individuals prescribed either lithium (19,106 individuals) or olanzapine (12,412) monotherapy. Machine learning models were used to predict successful monotherapy maintenance treatment, using 113 clinical and demographic variables, 8,017 (41.96%) lithium responders and 3,831 (30.87%) olanzapine responders. Results: We found a quantitative structural difference in that lithium maintenance responders were weakly predictable in our holdout sample, consisting of the 5% of patients with the most recent exposure. Age at first diagnosis, age at first treatment and the time between these were the most important variables in all models. Discussion: Even if we failed to predict successful monotherapy olanzapine treatment, and so to definitively separate lithium vs. olanzapine responders, the characterization of the two groups may be used for classification by proxy. This can, in turn, be useful for establishing maintenance therapy. The further exploration of machine learning methods on EHR data for drug treatment selection could in the future play a role for clinical decision support. Signals in the data encourage further experiments with larger datasets to definitively separate lithium vs. olanzapine responders. [ABSTRACT FROM AUTHOR]

High-yielding synthetic routes to five new extremely bulky aminopyridine pro-ligands were developed, viz. (C5H3N-6-Ar1)N(H)Ar2-2; Ar1 = Trip, Ar2 = TCHP (HAmPy1), Ar* (HAmPy2) or Ar† (HAmPy3); Ar1 = TCHP, Ar2 = Ar* (HAmPy4) or Ar† (HAmPy5) (Trip = 2,4,6-triisopropylphenyl, TCHP = 2,4,6-tricyclohexylphenyl, Ar* = C6H2(CHPh2)2Me-2,6,4, Ar† = C6H2(CHPh2)2Pri-2,6,4. Four of these were deprotonated with LiBun in diethyl ether to give lithium aminopyridinate complexes which were dimeric for the least bulky ligand, [{Li(AmPy1)}2] or monomeric for the bulkier aminopyridinates, i.e., in [Li(AmPy2−4)(OEt2)]. One aminopyridine was deprotonated with MeMgI to give monomeric [Mg(AmPy3)I(OEt2)2]. When treated with sodium or potassium mirrors or 5% w/w Na/NaCl, over-reduction occurred, leading to the alkali metal aminopyridinates, [M(AmPy3)(η6-toluene)] (M = Na or K) or [{Na(AmPy3)}∞]. An attempted reduction of [Mg(AmPy3)I(OEt2)2] with a dimagnesium(I) compound led only to partial loss of diethyl ether and the formation of [(AmPy3)Mg(μ-I)2Mg(AmPy3)(OEt2)]. All prepared complexes have potential as ligand transfer reagents in salt metathesis reactions with metal halide complexes. [ABSTRACT FROM AUTHOR]

Aim: Lithium, even at low doses, appears to offer neuroprotection against a wide variety of insults. In this controlled pilot, we examined the safety (i.e., side‐effect profile) of lithium in a sample of young people identified at ultra‐high risk (UHR) for psychosis. The secondary aim was to explore whether lithium provided a signal of clinical efficacy in reducing transition to psychosis compared with treatment as usual (TAU). Methods: Young people attending the PACE clinic at Orygen, Melbourne, were prescribed a fixed dose (450 mg) of lithium (n = 25) or received TAU (n = 78). The primary outcome examined side‐effects, with transition to psychosis, functioning and measures of psychopathology assessed as secondary outcomes. Results: Participants in both groups were functionally compromised (lithium group GAF = 56.6; monitoring group GAF = 56.9). Side‐effect assessment indicated that lithium was well‐tolerated. 64% (n = 16) of participants in the lithium group were lithium‐adherent to week 12. Few cases transitioned to psychosis across the study period; lithium group 4% (n = 1); monitoring group 7.7% (n = 6). There was no difference in time to transition to psychosis between the groups. No group differences were observed in other functioning and symptom domains, although all outcomes improved over time. Conclusions: With a side‐effect profile either comparable to, or better than UHR antipsychotic trials, lithium might be explored for further research with UHR young people. A definitive larger trial is needed to determine the efficacy of lithium in this cohort. [ABSTRACT FROM AUTHOR]

Asymptotic giant branch (AGB) stars can experience proton ingestion events (PIEs), leading to a rich nucleosynthesis. During a PIE, the intermediate neutron capture process (i-process) develops, leading to the production of trans-iron elements. It is also suggested that lithium is produced during these events. We investigate the production of lithium and trans-iron elements in AGB stars experiencing a PIE with 1 < M ini / M ⊙ < 3 and − 3 < [ Fe / H ] < 0 . We find that lithium is produced in all PIE models with surface abundances 3 < A(Li) < 5 . The surface enrichment and overall AGB lithium yield increases with decreasing stellar mass. The lithium enrichment is accompanied by a production of 13C with 3 < 12 C/13C < 9 at the surface just after the PIE. AGB stars experiencing PIE may be related to J-type carbon stars whose main features are excesses of lithium and13C. In addition to Li and 13C, heavy elements (e.g., Sr, Ba, Eu, Pb) are significantly produced in low-metallicity stars up to [Fe/H] ≃ − 1 . The yields of our models are publicly available. Additionally, of interest to the Li nucleosynthesis, we provide an updated fitting formula for the 7Be( e − , ν e )7Li electron capture rate. [ABSTRACT FROM AUTHOR]

Low expansion Li2O-Al2O3-SiO2 (LAS) glass-ceramics were prepared using sintering method. The effect of ZnO partially substitution for Li2O on the microstructure, sintering behavior, crystallization behavior and properties of LAS glass-ceramics was investigated. The results show that the substitution of ZnO for Li2O reduces the initial crystallization temperature of LAS glass-ceramics, leading to significant amount of Li2Al2 Si3O10 phase precipitating out after holding at 800 °C for 10 min, which hinders the sintering shrinkage of glass. In contrast, the LAS glass-ceramics without ZnO exhibits slower crystallization at 800 °C, which is beneficial for sintering densification process. When the sintering temperature is 1 100 °C, the main crystalline phase present in glass-ceramics is identified as β-spodumene. The coefficient of thermal expansion of glass-ceramics without ZnO is 1. 747 x 10-6 K-1, the flexural strength is 138. 4 MPa, the dielectric constant is 3. 52 and the dielectric loss is 0. 0016. [ABSTRACT FROM AUTHOR]

Lithium (Li) is the lightest metal in existence. Its effects on higher plants are still under discussion because both positive and toxic results have been reported in different species. In the last decade, the use of Li has increased considerably, and it is projected that Li waste will be an environmental problem in the near future, such that various organisms, including plants, may be altered by its presence. Interestingly, Li can trigger hormesis, with beneficial effects at low doses and inhibitory or harmful effects at high doses. Currently, numerous research groups are focusing their studies on agriculture to obtain crops fortified with Li, which represents a nutritional advantage in food if adequate concentrations are used. However, more studies are still needed in order to understand the biochemical mechanisms of the effects of Li on plants. This review describes the natural and anthropogenic sources of Li, as well as the concentrations of this element in different environments. Regarding the uses of Li in different areas, topics related to doses that cause toxicity and lethality in humans are addressed. Given its impact on crop production, mechanisms of Li uptake and transport in higher plants are reviewed, as well as the effects on plant metabolism and physiology. Likewise, the perspective on the controlled use of Li in biostimulation and biofortification of crops is addressed. [ABSTRACT FROM AUTHOR]

Lithium sulfide was produced in a plasma system by the reaction of plasma-ionized sulfur with lithium metal. Thermodynamic calculations and optical emission spectroscopy were used to investigate the chemical behavior and reaction mechanism of lithium metal in sulfur plasma atmosphere. The effects of radiofrequency (RF) power and radiofrequency (RF) time on the properties of lithium sulfide prepared by the cold plasma method were investigated. The macroscopic morphology, microscopic morphology, elemental distribution and phase of the sulfide product (lithium sulfide) were further tested and analyzed. The results show that under the conditions of power ≥ 210 W and time ≥ 15 min, Li2S2-free lithium sulfide with high purity is generated; with the enhancement of power, lithium oxide is transformed into lithium sulfide. Subsequently, its electrochemical performance as a battery anode was tested. The test obtained: the specific capacity of charging is up to 216.9 mAh/g, and the specific capacity of discharging is up to 182.8 mAh/g; the impedance has a double capacitance to resist arcing, which can be carried out normally in the charging and discharging process, and it has a certain degree of electrochemical performance. [ABSTRACT FROM AUTHOR]

The availability of lithium resources is of great significance for the development of modern technologies, as well as for civil and military industries. The Qinghai-Tibet Plateau is a region known for its abundance of lithium-rich salt lakes. However, the specific origin of lithium in these lakes is still unknown, which hinders the advancement of the lithium resource business in this region. To research this issue, this study involved the collection of 20 samples from Lakkor Co Salt Lake on Qinghai-Tibet Plateau, encompassing samples of surface brine, cold springs, fresh lakes, and recharge rivers. The composition of anions and cations in these samples was determined. Furthermore, the analysis extensively utilized the Piper three-line diagram, Gibbs model, and ion proportion coefficient. The findings of this study indicate that as the moves from the recharge water system to salt lake, there is a transition in water type from strong carbonate to moderate carbonate and weak carbonate, as well as Na sulfate. This research based on a similar source of both lithium and boron, utilized ion correlation analysis and boron isotope study in the Lakkor Co area, and analyzed the source and transporting process of lithium. The main origin of lithium in Lakkor Co is the dissolution of lithium-rich rocks, recharge water systems, and deep hydrothermal fluids. These findings are highly significant in enhancing the foundational data of lithium-rich brine resources in the Qinghai-Tibet Plateau and are beneficial for assessing the future development of such deposits. [ABSTRACT FROM AUTHOR]

Lithium hexafluorophosphate (LiPF6), the most commonly used lithium battery electrolyte salt, is vulnerable to heat and humidity. Quantitative and qualitative determination the variation of LiPF6 have always relied on advanced equipment. Herein, we develop a fast, convenient, high-selective fluorescence detection method based on metal--organic cages (MOC), whose emission is enhanced by nearly 20 times in the presence of LiPF6 with good stability and photobleaching resistance. The fluorescent probe can also detect moisture in battery electrolyte. We propose and verify that the luminescence enhancement is due to the presence of hydrogen bond-induced enhanced emission effect in cages. Fluorescent excitation-emission matrix spectra and variable-temperature nuclear magnetic resonance spectroscopy are employed to clarify the role of hydrogen bonds in guest-loaded cages. Density functional theory (DFT) calculation is applied to simulate the structure of host-guest complexes and estimate the adsorption energy involved in the system. The precisely matched lock-and-key model paves a new way for designing and fabricating novel host structures, enabling specific recognition of other target compounds. [ABSTRACT FROM AUTHOR]

The energies of an electron in a one-dimensional crystal are studied with both the Schrödinger and Dirac equations using the plane wave expansion method. The crystalline potential sensed by the electron in a cell was calculated by accounting for the Coulombic (electrostatic) interaction between the electron and the surrounding cores (immobile positive ions at the center of the crystal cells). The energies and wave functions of the electron were calculated as a function of four parameters: the period a p of the lattice, the dimension n d i m of the matrix in the momentum space, the partition number l p a in which the unit cell is divided to calculate the potential and the number of cores n c o that affect the electron. It was found that 8000 cores (surrounding the electron) were needed to reach our convergence criterion. An analytical equation that accurately describes the behavior of the energies in function of the cores that affect the electron was also found. As case studies, the energies for pseudo-lithium and pseudo-graphene were obtained as a first approximation for one-dimensional lattices. Subsequently, the energies of an isolated dimer nanoparticle were also calculated using the supercell method. [ABSTRACT FROM AUTHOR]

This study, based on the analysis of existing experimental data, presents a third generation Calphad description of lithium, covering all temperature ranges, using nonlinear least squares in Matlab. We have expanded the SGTE database's description of lithium phases (face-centered cube, body-centered cube, liquid) down to 0 K with reasonable accuracy, taking into account the significant effort required to reconstruct the database for each element. During the evaluation process, it was determined that the low-temperature phase of lithium is fcc. The heat capacity of crystalline Li was accurately described using the extended Debye model. The third generation Calphad description of lithium utilized the two-state model and the extended Einstein model, leading to improved agreement with experimental data compared to previous assessments. [ABSTRACT FROM AUTHOR]

Mixed matrix lithium adsorbents have attracted much interest for lithium recovery from brine. However, the absence of an interfacial interaction between the inorganic lithium-ion sieves (LISs) and the organic polymer matrix resulted in the poor structural stability and attenuated lithium adsorption efficiency. Here, a novel hollow hemispherical mixed matrix lithium adsorbent (H-LIS) with high interfacial compatibility was constructed based on mussel-bioinspired surface chemistry using a solvent evaporation induced phase transition method. The effects of types of functional modifiers, LIS loading amount, adsorption temperature and pH on their structural stability and lithium adsorption performance were systematically investigated. The optimized H-LIS adsorbent with the LIS loading amount of 50 wt.% possessed the structural merit that the LIS functionally modified by dopamine exposed on both the inner and outer surfaces of the hollow hemispheres. At the best adsorption pH of 12.0, it showed a comparable lithium adsorption capacity of 25.68 mg·g−1 to the powdery LIS within 4 h, favorable adsorption selectivity of Mg/Li and good reusability that could maintain over 90% of lithium adsorption capacity after the LiCl adsorption—0.25 M HCl pickling-DI water cleaning cycling processes for three times. The interfacial interaction mechanism of H-LIS for lithium adsorption was innovatively explored via advanced microcalorimetry technology. It suggested the nature of the Li+ adsorption process was exothermic and dopamine modification could reduce the activation energy for lithium adsorption from 15.68 kJ·mol−1 to 13.83 kJ·mol−1 and trigger a faster response to Li+ by strengthening the Li+-H+ exchange rate, which established the thermodynamic relationship between the structure and Li+ adsorption performance of H-LIS. This work will provide a technical support for the structural regulation of functional materials for lithium extraction from brine. [ABSTRACT FROM AUTHOR]

Lithium is a strategic metal due to its use in green technologies, particularly battery manufacturing. It is on the US List of Critical Minerals and the European Union's List of Critical Raw Materials. In Mongolia, there are three major types of potentially economic Li deposits: (1) Deposits related to granites, granitic pegmatites and associated rocks; (2) Li-rich clay deposits; (3) Salar (Li brine) deposits. The first type of mineralization is associated with the lithium–fluorine-rich peraluminous A-type granites and related rocks (greisens, pegmatites, ongonites, ongorhyolites). The mineralization includes Li and also Sn, W, Ta and Nb. Lithium is hosted in Li-rich micas, unlike the world-class Li-bearing pegmatite deposits where the bulk of Li is in spodumene. In Mongolia, particularly promising are Li brines of endorheic basins in the Gobi Desert with an arid environment, high evaporation rates and low precipitation. [ABSTRACT FROM AUTHOR]

Membranes with precise Li+/Na+ and Li+/K+ separations are imperative for lithium extraction from brine to address the lithium supply shortage. However, achieving this goal remains a daunting challenge due to the similar valence, chemical properties, and subtle atomic‐scale distinctions among these monovalent cations. Herein, inspired by the strict size‐sieving effect of biological ion channels, a membrane is presented based on nonporous crystalline materials featuring structurally rigid, dimensionally confined, and long‐range ordered ion channels that exclusively permeate naked Li+ but block Na+ and K+. This naked‐Li+‐sieving behavior not only enables unprecedented Li+/Na+ and Li+/K+ selectivities up to 2707.4 and 5109.8, respectively, even surpassing the state‐of‐the‐art membranes by at least two orders of magnitude, but also demonstrates impressive Li+/Mg2+ and Li+/Ca2+ separation capabilities. Moreover, this bioinspired membrane has to be utilized for creating a one‐step lithium extraction strategy from natural brines rich in Na+, K+, and Mg2+ without utilizing chemicals or creating solid waste, and it simultaneously produces hydrogen. This research has proposed a new type of ion‐sieving membrane and also provides an envisioning of the design paradigm and development of advanced membranes, ion separation, and lithium extraction. [ABSTRACT FROM AUTHOR]

Background: The effect of an immune-boosting beverage (SAM) containing Sambucus Nigra, an energy beverage (ENE), an in-office bleaching (BLE) agent with 25% hydrogen peroxide superior, glazing (GLA) or polishing (POL) methods, and professional dental prophylaxis (PDP) on the color of CAD-CAM restorative materials is unknown. Methods: In total 210 specimens were prepared, consisting of CAD-CAM feldspathic (FC), zirconia-reinforced lithium disilicate ceramic (ZLS) and hybrid ceramic (HC). The ceramic specimens were divided according to the polishing methods of glazing (GLA) and mechanical polishing (POL). All materials were divided into two groups: with and without BLE. A 25% hydrogen peroxide superior (HPS) gel was used for BLE. After the baseline (BAS) measurement, the specimens were immersed in 3 different beverages (distilled water (DIS), SAM, ENE). After 28 days, a fine-grained (RDA 7) prophylaxis paste was applied. Statistical analysis of ∆E00 color difference values was performed by 3-way ANOVA and Bonferroni test (α = 0.05). Results: The effect of all other actions except material-BLE-beverage on color for BAS-Day 28 was statistically different (p < 0.05). The effect of material, material-BLE, beverage on color for Day 28-PDP was statistically different (p < 0.05). After 28 days, the lowest color change was found in FC-GLA and HC immersed in DIS (p = 0.0001) and the highest in FC-POL immersed in ENE (p = 0.0002). PDP was efficient in color recovery in HC immersed to DIS, ENE and SAM (p = 0.0010). For FC, HC and ZLS, BLE caused a higher color change (p < 0.0001). Regardless of the material, the highest color change for BLE-beverage was found in BLE-treated specimens immersed in ENE (p = 0.0496) and the lowest color change was found in non-BLE-treated specimens immersed in SAM (p = 0.0074). Conclusions: In materials pre-exposed to 25% HPS, the effect of PDP on color recovery was lower than in unexposed materials. After 28 days, mechanical polishing produced higher color change in FC than glazing, however, in ZLS effects of glazing and mechanical polishing on color were similar. For material/polishing method, HC was the most effective. ENE caused higher color change than DIS and SAM. PDP was more effective than ENE in restoring color to DIS- and SAM-immersed specimens. [ABSTRACT FROM AUTHOR]

This study aimed to investigate the behavioral responses and circadian rhythms of mice to both rapid and gradual increases in photoperiod, mimicking the transition from winter to summer, which is associated with a heightened prevalence of hospitalizations for mania and suicidal behavior. Behavioral tests were performed in C57BL/6 male mice exposed to a transitional photoperiod, from short to long durations. To determine if circadian rhythms are affected, we measured spontaneous locomotor activity and body temperature. Mice exhibited heightened exploratory and risk‐taking behaviors compared with equatorial and static long (16:8 h of light–dark cycle for several days) groups. These behaviors were prevented by lithium. Spontaneous locomotor activity and body temperature rhythms persisted and were effectively synchronized; however, the relative amplitude of activity and interdaily stability were diminished. Additionally, the animals displayed increased activity during the light phase. Photoperiodic transition modulates behavior and circadian rhythms, mirroring certain features observed in bipolar disorder patients. This study introduces an animal model for investigating mania‐like behavior induced by photoperiodic changes, offering potential insights for suicide prevention strategies and the management of mood disorders. [ABSTRACT FROM AUTHOR]

Background: Partial coverage concepts have met the main goal of conservative dentistry. Vonlays, which combine features of veneers and onlays, are a recent alternative to full coverage designs and overlay partial coverage restorations. This in vitro study was conducted to compare the fracture resistance of the newly introduced pressable zirconia-reinforced lithium silicate with pressable lithium disilicate ceramic and to determine the optimal preparation design for partial coverage on upper premolars. Methods: Fifty-two duplicated epoxy resin dies were prepared following vonlay and overlay preparation guidelines. For each preparation (n = 26), the specimens were divided into two subgroups to be restored with lithium disilicate (IPS e.max Press) or zirconia-reinforced lithium silicate (Vita Ambria) (n = 13 each). Ceramic vonlays and overlays were bonded using dual cure resin cement, subjected to thermomechanical fatigue, and the load to fracture was tested by using a universal testing machine. The specimens were fractographically analyzed via scanning electron microscopy (SEM). The normality of the fracture resistance data was checked using the Shapiro‒Wilk test and Q‒Q plots, and two-way ANOVA was used to assess the effect of the type of preparation and ceramic material on the fracture resistance. Results: The group of overlays restored with zirconia-reinforced lithium silicate showed the highest mean fracture load (1218.69 N), while the group of vonlays restored with lithium disilicate had the lowest mean fracture resistance (967.15 N). The effect of preparation design and material type on fracture resistance was significant for both factors, p = 0.003 and p < 0.0001, respectively. Different features of the fracture surfaces, such as arrest lines, hackles, and directions of crack propagation, were observed. Conclusions: Zirconia-reinforced lithium silicate exhibited greater resistance to fracture compared to lithium disilicate, making it a potential substitute for partial coverage restorations. Additionally, the overlay showed superior fracture resistance when compared to the vonlay preparation design. [ABSTRACT FROM AUTHOR]

Dual‐ion batteries (DIBs) represent a promising alternative for lithium ion batteries (LIBs) for various niche applications. DIBs with polymer‐based active materials, here poly(2,2,6,6‐tetramethylpiperidinyl‐N‐oxyl methacrylate) (PTMA), are of particular interest for high power applications, though they require appropriate electrolyte formulations. As the anion mobility plays a crucial role in transport kinetics, Li salts are varied using the well‐dissociating solvent γ‐butyrolactone (GBL). Lithium difluoro(oxalate)borate (LiDFOB) and lithium bis(oxalate)borate (LiBOB) improve cycle life in PTMA||Li metal cells compared to other Li salts and a LiPF6‐ and carbonate‐based reference electrolyte, even at specific currents of 1.0 A g−1 (≈10C), whereas LiDFOB reveals a superior rate performance, i. e. ≈90 % capacity even at 5.0 A g−1 (≈50C). This is attributed to faster charge‐transfer/mass transport, enhanced pseudo‐capacitive contributions during the de‐/insertion of the anions into the PTMA electrode and to lower overpotentials at the Li metal electrode. [ABSTRACT FROM AUTHOR]

The recovery of spent lithium‐ion batteries by traditional acid leaching is limited by serious pollution, complicated technology, and the low purity of Li2CO3. To address the problems of the traditional acid leaching process and increasing demand for decarbonization, a technique for the selective carbonation leaching of Li and the recovery of battery‐grade Li2CO3 by a simple concentration precipitation process without acids or bases was developed. The coupling of CO2 and reducing agents could effectively promote the precipitation of MCO3 (M=Ni/Co/Mn) and the selective leaching of Li by decreasing the reducing capability needed for transition metals and decreasing the pH of the solution. The optimal selective leaching process of Li was obtained under 1 MPa CO2 with 20 g/L Na2S2O3 at an L/S ratio of 30 mL/g for 1.5 h. FT‐IR, XRD, ICP‐MS and other methods were used to reveal the multiphase interfacial reaction mechanism of the carbonation reduction of layered cathode materials, which indicated that the reducing agent Na2S2O3 could promote lattice distortion of the cathode materials and effective separation of Li. In summary, a green and economical method for the selective recovery of battery‐grade Li2CO3 using a one‐step method of CO2 carbonation recovery in a near‐neutral environment was proposed. [ABSTRACT FROM AUTHOR]

Uneven lithium (Li) metal deposition typically results in uncontrollable dendrite growth, which renders an unsatisfactory cycling stability and coulombic efficiency (CE) of Li metal batteries (LMBs), preventing their practical application. Herein, a novel carbon cloth with the modification of ZnO nanosheets (ZnO@CC) is fabricated for LMBs. The as‐prepared ZnO@CC with a cross‐linked network significantly reduces the local current density, and the design of ZnO nanosheets can promote the uniform deposition of Li metal as lithiophilic sites. As a result, the Li metal anodes (LMAs) based on ZnO@CC (ZnO@CC@Li) enables a long cycle life over 640 hours with a low overpotential of 65 mV at a current density of 4 mA cm−2 with a capacity of 1 mAh cm−2 in the symmetric cell. Moreover, when coupling the ZnO@CC@Li with a LiFePO4 cathode, the assembled full cell exhibits excellent long cycle and rate performance, highlighting its promising practical application prospect. [ABSTRACT FROM AUTHOR]