Lithium Distribution Research Articles

Elucidating Heterogeneous Li Insertion Using Single-Crystalline and Freestanding Layered Oxide Thin Film.

The kinetics of interfacial ion insertion govern the uniformity of electrochemical reactions, playing a crucial role in lithium-ion battery performance. In two-dimensional lithium-conducting layered-oxide battery particles, variation in insertion rates across insertion channels remains unclear due to poorly defined crystal orientation at the solid-liquid interface and solid-state-lithium-diffusion length. This ambiguity complicates understanding inhomogeneous lithium-insertion channels activation. A systematic study requires crystallographically predefined interfaces and in situ lithium-concentration mapping. Here, we fabricated a freestanding, (104)-oriented-LiNi1/3Mn1/3Co1/3O2 single-crystal thin film using dissolution-induced release and performed in situ scanning-transmission-X-ray-microscopy to spatially resolve lithium-insertion at well-defined-interfaces. We observed heterogeneous lithium-concentration evolution due to channel-by-channel insertion rate variation, despite the potential for homogeneous lithium distribution via a solid-solution-phase at equilibrium in NMC111. Increasing current density exacerbates this heterogeneity, highlighting channel-by-channel variation. Our findings provide critical insights into battery electrode utilization and lifetime management, potentially guiding the design of more efficient and durable lithium-ion batteries.

Optimization study on the compact thermal neutron imaging system based on portable D-T neutron generator

The distribution of lithium in lithium-ion batteries is critical to their performance and lifespan. Studies have shown that thermal neutron imaging can effectively perform non-destructive testing of this distribution. However, most current thermal neutron imaging systems rely on expensive, bulky, and immobile nuclear reactors or spallation neutron sources, significantly limiting their application scenarios. Therefore, this study adopts a portable D-T neutron generator as the neutron source and uses Monte Carlo simulation methods to optimize the design of key components in the thermal neutron imaging system. Simulation results indicate that the optimized thermal neutron imaging system achieves a thermal neutron flux of 8.36 × 104 n·cm−2·s−1 and a thermal neutron content (TNC) of 14.4% at a collimation ratio of 50. Within an imaging range of Φ100 mm, the non-uniformity of the thermal neutron fluence is approximately 2.07%. Simulation imaging results of lithium and iron step wedges demonstrate that the compact thermal neutron imaging system designed in this study can effectively distinguish between iron and lithium of the same thickness. This finding provides an important reference for subsequent detection of lithium distribution within lithium-ion batteries.

Distribution, enrichment characteristics and prospecting potential of lithium in Uzbekistan: Insights from 1:1 million geochemical mapping

With the world economy gradually shifting to alow‑carbon and greener model in recent years, there is a growing need for developing key metals like lithium in economic development. Economic growth has sped up the country's shift to a green economy along with Uzbekistan's reform and opening up, and the country's developing major mineral resources, such as lithium, have garnered a lot of attention. Owing to lithium resource protential of Uzbekistan is unclear, it is important to examine the possibility of lithium mineralization. The distribution and enrichment characteristics of lithium in the Uzbeksitan Tianshan are studied in this paper, based on geochemical mapping data at a 1:1000000 scale. It's concluded that stream sediments from the Tianshan region of Uzbekistan have higher concentration of lithium than the continental crust, and the South Tianshan has the highest lithium content. Lithium mineralization has been found in the lithium-geochemical anomaly areas in the eastern part of Uzbekistan South Tianshan through field investigation. Spodumene pegmatite, the first instance of pegmatitic type lithium mineralization in this region and even in the Tianshan orogenic belt of Central Asia. In conjunction with the geological background analysis, the metallogenic potential of lithium was assessed, resulting in the identification of four regions with lithium geochemical anomaly, and these sites will serve as target areas for Li deposits prospecting work in the future. This work has significant implications for the advancement of our understanding of the metallogenic theory of pegmatite-type Li deposits, as well as practical guiding significance for lithium ore prospecting in the Tianshan orogenic belt of Central Asia.

Discharging of Ramsdellite MnO2 Cathode in a Lithium-Ion Battery.

We report an application of our unbiased Monte Carlo approach to investigate thermodynamic and electrochemical properties of lithiated manganese oxide in the ramsdellite phase (R-MnO2) to uncover the mechanism of lithium intercalation and understand charging/discharging of R-MnO2 as a cathode material in lithium-ion batteries. The lithium intercalation reaction was computationally explored by modeling thermodynamically significant distributions of lithium and reduced manganese in the R-MnO2 framework for a realistic range of lithium molar fractions 0 < x < 1 in Li x MnO2. We employed interatomic potentials and analyzed the thermodynamics of the resultant grand canonical ensemble. We found ordered or semiordered phases at x = 0.5 and 1.0 in Li x MnO2, verified by configurational entropy changes and simulated X-ray diffraction patterns of partially lithiated R-MnO2. The radial distribution functions show the preference of lithium for homogeneous distributions across the one-dimensional 2 × 1 ramsdellite channels accompanied by alternating reduced/oxidized manganese ions. The occupation of the interstitial sites in the channels is correlated with the calculated voltage profile, showing a sharp voltage drop at x = 0.5, which is explained by the energy penalty of shifting lithium ions from stable tetrahedral to unstable octahedral sites. To facilitate this work, our in-house software, Knowledge Led Master Code (KLMC) was extended to support massive parallelism on high-performance computers.

Ion-Exchange Membranes Extract Lithium From North Sea Oilfield Brines

_ This article, written by JPT Technology Editor Chris Carpenter, contains highlights of paper SPE 215585, “Lithium Extraction From North Sea Oilfield Brines Using Ion-Exchange Membranes,” by Botelho Disu, Roozbeh Rafati, and Amin S. Haddad, University of Aberdeen, et al. The paper has not been peer reviewed. _ The annual demand for lithium for low-carbon technology applications has been growing exponentially. A necessity exists in the current environment for continuous lithium production from both conventional sources and novel extraction sites from alternative brine resources such as oil fields and geothermal sites. in the complete paper, the lithium potentiality of the UK North Sea is evaluated. Identification of North Sea Lithium-Rich Oil and Gas Fields Maps show lithium-ion concentration diffusing from 55 ppm in the western region into low concentrations in the central, northern, and eastern regions of the UK North Sea. Such estimates suggest lithium enrichment in oilfield brine from the Beatrice, Clymore, Gannet, Cly, Auk, and Flumar fields. However, because such map distribution of lithium is achieved based only on one-third of the imputed data, a correlative evaluation with the entire body of data is needed to provide a much more feasible interpretation. When lithium distribution was evaluated simultaneously with strontium/iron/potassium (Sr/Fe/K) total dissolved solids, the rich brine was primarily located across the central, eastern, southern, and western fields. The central and eastern concentrations were estimated to have a lithium-rich brine with concentrations of up to 40 ppm, with lithium-ion presence gradually increasing toward the east. Most of the fields in this region are oil fields, including Montrose, Arbroath, Ula, Nelson, Brisling, Gyda, Ekofisk, and Bream, with Harald possibly being the only gas field with lithium-enriched brine. On the other hand, the lithium-rich fields in the southern and western regions are all gas fields, including the Esmond, Anglia, Lemman, Ann, and Viking fields. Statement of Theory and Definition The economic feasibility of lithium extraction from brine has been observed to be a function of its initial concentration. For oilfield brines, when using novel direct-lithium-extraction (DLE) technologies, the brine concentration economic feasibility for production is reduced to a cutoff benchmark of 50 ppm. However, ongoing developments in DLE technologies envision a feasible, efficient, and highly selective recovery of lithium from brines with low concentrations, even sea water. Manganese ion-sieve powder is a DLE technology that has gathered growing interest. However, one of the main challenges of its application in continuous industrial processes consists of operational challenges that its original powder form can cause. Therefore, forming is necessary if ion-sieve adsorbents are to have an industrial application. This paper has reported and discussed the experimental results of forming the adsorbent powders into different ion-exchange membranes (foam, flat sheet, and granular spherical beads) and their application for lithium extraction from simulated North Sea brine. The complete paper details the description and application of experimental equipment and processes.

Nonequilibrium fast-lithiation of Li4Ti5O12 thin film anode for LIBs

Li4Ti5O12 (LTO) is known for its zero-strain characteristic in electrochemical applications, making it a suitable material for fast-charging applications. Here, we systematically studied the quasi-equilibrium and non-equilibrium lithium-ion transportation kinetics in LTO thin-film electrodes, across a range of scales from the crystal lattice to the microstructured electrodes. At the crystal lattice scale, during the non-equilibrium lithiation process, lithium ions are dispersedly embedded into the 16c position, resulting in more 8a → 16c migration compared with the quasi-equilibrium lithiation, and forming numerous fast lithium diffusion channels inside the LTO lattice. At the microstructural electrode scale, optical spectrum characterizations supported the “nano-filaments” lithiation model in polycrystalline LTO thin-film electrodes during the lithiation process. Our results reveal the patterns of lithium migration and distribution within the LTO thin film electrode under the non-equilibrium and quasi-equilibrium lithiation process, offering profound insights into the potential optimization strategies for enhancing the performance of fast-charging thin film batteries.

Stable Cycling of Ultrahigh Mass Loaded MnO2 for Low-Cost Sodium-Ion Batteries

Achieving cost-effective and sustainable solutions for large-scale energy storage is critical for advancing the global clean energy transition. The intermittent nature of green energy underscores the inadequacy of current large scale energy storage technologies like pumped hydroelectricity which is susceptible to geographic and water resource constraints, making batteries a prime candidate for this role. Although lithium-ion batteries (LIBs) with high energy and power density are a viable solution, the high cost and uneven distribution of lithium reserves limits the widespread application of LIBs for grid energy storage. Considering these developments and the challenges posed by limited lithium reserves, sustainable and low-cost sodium-ion batteries (SIBs) emerge as a promising alternative.Among the various battery electrode materials, manganese dioxide (MnO2) stands out as a promising choice for large-scale energy storage applications due to its earth abundance, cost-effectiveness and non-toxic nature. Although MnO2 is known as a pseudocapacitive material with superior cycling stability in aqueous electrolytes, its dissolution in non-aqueous electrolytes has restricted its widespread use in long lifetime batteries. In this study, we demonstrate that an ether-based electrolyte solution (1M NaClO4 in diglyme) is able to achieve stable cycling of electrodeposited ε-MnO2 as a cathode for SIBs, reaching a over 75% capacity retention over 1000 cycles. This response surpasses conventional ester-based electrolytes (58% of 1M NaClO4 in EC/PC). A comparative cycling stability study, coupled with electrochemical quartz crystal microbalance characterization, validates the efficacy of the ether-based electrolyte in mitigating MnO2 dissolution. Furthermore, the integration of 3D printed graphene aerogel (3D GA) as a scaffold for electrodeposited MnO2 leads to enhanced electrochemical performance of the MnO2 electrode (3D MnO2/GA), resulting in a high areal capacity of 4.4 mAh cm-2 at a current density of 10 mA cm-2. The 3D MnO2/GA electrode possesses scalable electrochemical performance with mass loadings from 20 mg cm-2 to 80 mg cm-2. Using this electrode, a high mass loaded sodium-ion battery (SIB) device was fabricated by using utilizing 58 mg cm-2 3D MnO2/GA as the cathode and 16 mg cm-2 dip-coated TiO2@Cu foam as the anode. This MnO2 | TiO2 device delivered a notable areal capacity of 6.2 mWh cm-2 and a high areal power density of 70.7 mW cm-2. Moreover, the SIB device demonstrates 85% capacity retention after 500 cycles, underscoring the stable cycling of this high-energy and power-density SIB device.

Distribution of lithium in soil from selected states of Brazil: mineral potential and health relationships

Distribution of lithium in soil from selected states of Brazil: mineral potential and health relationships

Geochemical characteristics, Li source and genesis mechanism of thermal mineral water in Sichuan Basin, SW China

Thermal mineral water (temperature >25 °C) is a valuable resource, especially when it contains a certain amount of Li. In this study, an attempt was made to elucidate the factors affecting spatial distribution of lithium (Li) resources and interpret the formation mechanisms of thermal mineral waters in the Sichuan Basin. The spatial distribution, reservoir temperatures, and hydrochemical characteristics of thermal mineral waters were systematically analyzed in the Sichuan Basin, preliminarily revealing Li sources through hydrochemical methods. Results are showed as follows: (1) The Li-bearing (Li ≥ 1 mg/L) thermal mineral waters are mainly distributed in the southwestern part of the Sichuan Basin. There are three sites of thermal mineral waters with Li content greater than 25 mg/L with the hydrochemical type of Cl–Na type: Pengji Well (37.7 mg/L), Foguanghu Well (99.5 mg/L) and Zhougongshan New Well (118.0 mg/L). Among them, the Foguanghu Geothermal Well and the Zhougongshan New Well have high Li content and low Mg/Li (10.7 and 2.5), indicating great potential for utilization. (2) The Li-bearing thermal mineral waters are mainly formed in the fissure and pore reservoirs of the Middle–Lower Triassic. They are mainly affected by the dissolution of halite minerals and the deeply buried ancient seawater of the Triassic. The Li-bearing thermal mineral waters possess high contents of total dissolve solids (TDS) (4.3–230.0 g/L), Cl (0.7–142.9 g/L), Na (0.5–76.7 g/L), K (0.1–52.0 g/L), B (4.1–739.6 mg/L), and Li (1.5–118.0 mg/L). Moreover, the temperature of the geothermal reservoir ranges from 40 to 150 °C. The geothermal reservoir temperatures calculated by K–Mg and Mg–Li geothermometers are positively correlated with the Li content. (3) The Li source of the thermal mineral waters of the Sichuan Basin are dominated by multiple factors: first, Li concentration by evaporation, concentration and deep-seated metamorphism of ancient Triassic seawater; second, water–rock interaction between deep thermal mineral waters and mung bean rock or Emeishan basalt; and third, active tectonic activity and deep faulting induced upward flow of Li in deep fluids. This research enhances understanding of the formation of thermal mineral waters in the Sichuan Basin, offering scientific basis for the exploitation of Li resource.

Laser-induced breakdown spectroscopy for the identification of mineral phases and lithium distribution in refractories used for cobalt metal recovery from spent lithium-ion batteries

Herein, laser-induced breakdown spectroscopy (LIBS) is proposed as an effective strategy for selecting appropriate refractories for recovering valuable metals from spent lithium-ion batteries by determining lithium distributions and identifying mineral phases in refractories. The lithium distributions were obtained by measuring lithium emission line intensities at 610.4 nm under 1000-Pa argon in alumina (Al2O3) and magnesia (MgO) crucibles as refractory models used for recovering cobalt from a model lithium-ion battery containing LiCoO2 and graphite by heating crucibles at 1500 °C in argon atmosphere. The lithium distribution showed the presence of LiAlO2 and unreacted LiCoO2 on the Al2O3 crucible, which was protected from undergoing further damage by LiAlO2. The lithium distribution in the MgO crucible indicated that lithium diffused into the MgO crucible, inducing cracking. Therefore, the experiments with LIBS identified the Al2O3-based refractory as suitable for recovering valuable metals from spent lithium-ion batteries, thus providing an effective strategy for selecting appropriate refractories.

Design of Fluorinated Elastomeric Electrolyte for Solid-State Lithium Metal Batteries Operating at Low Temperature and High Voltage.

This work demonstrates the low-temperature operation of solid-state lithium metal batteries (LMBs) through the development of a fluorinated and plastic-crystal-embedded elastomeric electrolyte (F-PCEE). The F-PCEE is formed via polymerization-induced phase separation between the polymer matrix and plastic crystal phase, offering a high mechanical strain (≈300%) and ionic conductivity (≈0.23 mS cm-1) at -10°C. Notably, strong phase separation between two phases leads to the selective distribution of lithium (Li) salts within the plastic crystal phase, enabling superior elasticity and high ionic conductivity at low temperatures. The F-PCEE in a Li/LiNi0.8Co0.1Mn0.1O2 full cell maintains 74.4% and 42.5% of discharge capacity at -10°C and -20°C, respectively, compared to that at 25°C. Furthermore, the full cell exhibits 85.3% capacity retention after 150 cycles at -10°C and a high cut-off voltage of 4.5V, representing one of the highest cycling performances among the reported solid polymer electrolytes for low-temperature LMBs. This work attributes the prolonged cycling lifetime of F-PCEE at -10°C to the great mechanical robustness to suppress the Li-dendrite growth and ability to form superior LiF-rich interphases. This study establishes the design strategies of elastomeric electrolytes for developing solid-state LMBs operating at low temperatures and high voltages.

Lithium Plating at the Cell Edge Induced by Anode Overhang during Cycling in Lithium-Ion Batteries: Part I. Modeling and Mechanism

The anode overhang is usually cited to prevent lithium plating at the cell edges of lithium-ion batteries. Still, numerous reports in the literature show lithium plating at the cell edge, which is typically referred to as edge plating. Edge plating is often attributed to inhomogeneous lithium distribution, thermal gradients, or pressure-dependent effects. This work presents an easy-to-implement two-dimensional electrochemical model demonstrating inhomogeneous lithiation induced by the anode overhang, which can explain experimentally observed edge plating. First, the mechanism of inhomogeneous lithiation due to the anode overhang is explained in detail. Then, a parameter study on charge protocol and geometric cell properties is presented, and the implications for cell applications are analyzed. Finally, the findings are discussed and put into a broader perspective of cell design, manufacturing, and fast charging application. In Part II of this work, the simulation is validated experimentally using multi-reference electrode single-layer pouch cells.

Lunar Surface Resource Exploration: Tracing Lithium, 7 Li and Black Ice Using Spectral Libraries and Apollo Mission Samples

This is an exercise to explore the concentration of lithium, lithium-7 isotope and the possible presence of black dirty ice on the lunar surface using spectral data obtained from the Clementine mission. The main interest in tracing the lithium and presence of dark ice on the lunar surface is closely related to future human settlement missions on the moon. We investigate the distribution of lithium and 7 Li isotope on the lunar surface by employing spectral data from the Clementine images. We utilized visible (VIS–NIR) imagery at wavelengths of 450, 750, 900, 950 and 1000 nm, along with near-infrared (NIR–SWIR) at 1100, 1250, 1500, 2000, 2600 and 2780 nm, encompassing 11 bands in total. This dataset offers a comprehensive coverage of about 80% of the lunar surface, with resolutions ranging from 100 to 500 m, spanning latitudes from 80°S to 80°N. In order to extract quantitative abundance of lithium, ground-truth sites were used to calibrate the Clementine images. Samples (specifically, 12045, 15058, 15475, 15555, 62255, 70035, 74220 and 75075) returned from Apollo missions 12, 15, 16 and 17 have been correlated to the Clementine VIS–NIR bands and five spectral ratios. The five spectral ratios calculated synthesize the main spectral features of sample spectra that were grouped by their lithium and 7 Li content using Principal Component Analysis. The ratios spectrally characterize substrates of anorthosite, silica-rich basalts, olivine-rich basalts, high-Ti mare basalts and Orange and Glasses soils. Our findings reveal a strong linear correlation between the spectral parameters and the lithium content in the eight Apollo samples. With the values of the 11 Clementine bands and the 5 spectral ratios, we performed linear regression models to estimate the concentration of lithium and 7 Li. Also, we calculated Digital Terrain Models (Altitude, Slope, Aspect, DirectInsolation and WindExposition) from LOLA-DTM to discover relations between relief and spatial distribution of the extended models of lithium and 7 Li. The analysis was conducted in a mask polygon around the Apollo 15 landing site. This analysis seeks to uncover potential 7 Li enrichment through spallation processes, influenced by varying exposure to solar wind. To explore the possibility of finding ice mixed with regolith (often referred to as `black ice’), we extended results to the entire Clementine coverage spectral indices, calculated with a library (350–2500 nm) of ice samples contaminated with various concentrations of volcanic particles.

Unravelling lithium distribution in carbon fibre electrodes for structural batteries with atom probe tomography

Carbon fibres in structural batteries are multifunctional by acting both as structural reinforcement and as lithium (Li)-ion battery electrode. The relationship between the microstructure and mechanical capabilities of carbon fibres are well established, but much remains unexplored regarding their electrochemical properties. Specifically needed is a nanoscale understanding of how Li atoms distribute and interact in the carbon fibres. Atom probe tomography (APT) is uniquely positioned to provide subnanometre resolution in three dimensions. However, it has previously been hampered by undesirable Li migration during analysis. Here, we show that APT is successfully used to analyse electrochemically cycled polyacrylonitrile-based carbon fibres, through electrostatic shielding by means of conductive coating. We measure ∼1.5 at% Li in the carbon fibres after full delithiation, and thus identify trapped Li to constitute a substantial part of the initial capacity fade. After lithiation, Li accounts for ∼9 at% and according to frequency distribution analysis tend to agglomerate on the atomic scale. With nearest neighbour analysis, Li agglomeration is shown independent of heteroatom dopants such as nitrogen. Thus, the agglomeration is more likely induced by differing accessibility for Li in the crystalline and amorphous domains in the carbon fibre. The method used in this study can inform APT experiments on other type of Li-containing carbon electrodes. The findings of the study can be used to guide design of novel carbon fibres for structural batteries with enhanced electrochemical properties.

Heterogeneity of Lithium Distribution in the Graphite Anode of 21700-Type Cylindrical Li-Ion Cells during Degradation

Structural and spatial aspects of cell degradation are studied using a combination of diffraction-and imaging-based tools applying laboratory X-rays, neutron scattering and synchrotron radiation with electrochemical and thermal characterization. Experimental characterization is carried out on cylindrical cells of 21700-type, where four regimes of cell degradation are identified, which are supplemented by an increased cell resistance and surface temperature during cell operation. The amount of intercalated lithium in the fully charged anodes in the fresh and aged states is determined by ex situ X-ray diffraction radiography and in situ X-ray diffraction computed tomography. The qualitatively similar character of the results revealed a loss of active lithium along with the development of a complex heterogeneous distribution over the electrode stripe.

Relaxation Analysis of Silicon Monoxide-Graphite Composite Anode

Relaxation analysis based on X-ray diffraction has been carried out on SiO-graphite composite anode of the lithium-ion battery, focusing on the lithium migration during the relaxation accompanied by the stage change of lithium graphite intercalation compound (Li-GIC). After the termination of electrochemical lithium insertion, XRD peaks of Li-GIC change from stage I into stage II during the relaxation. Due to the slower reaction for lithiation of SiO in comparison with the intercalation of Li-GIC, lithium migration from Li-GIC toward SiO to change the Li-GIC from stages I into II toward the equilibrium lithium distribution. The stage change is more apparent for higher current density at the charging, presumably due to the core–shell model of lithium concentration of SiO after charging.

SPIRAL MRI for in vivo lithium-7 imaging: a feasibility study in mice after oral lithium treatment

Lithium has been the frontline treatment for bipolar disorder for over 60 years. However, its mode of action and distribution in the brain is still incompletely understood. The primary isotope of lithium, lithium-7 (7Li), is a magnetic resonance (MR) active, spin-3/2 nucleus. However, its low MR sensitivity and the small brain size of mice make 7Li MR imaging (MRI) difficult in preclinical research. We tested four MRI sequences (FLASH, RARE, bSSFP, and SPIRAL) on lithium-containing phantoms, and bSSFP and SPIRAL on orally lithium-treated adult C57BL/6 mice. 7Li MR spectroscopy was acquired weekly at 9.4T to monitor the lithium uptake. The in vivo T1 relaxation time of 7Li was estimated in four mice. 4-h SPIRAL 7Li MRI was acquired in ten mice at a resolution of 2 × 2 × 3 mm3. SPIRAL MRI provided the highest signal-to-noise ratio (SNR) per unit acquisition time and the best image quality. We observed a non-homogeneous distribution of lithium in the mouse brain, with the highest concentrations in the cortex, ventricles, and basal brain regions. Almost no lithium signal was detected in the olfactory bulb and the cerebellum. We showed that in vivo 7Li MRI in mice is feasible, although with limited spatial resolution and SNR.

Thermal behaviors during lithium diffusion in Li0.4WO3 bronze studied by elastic and quasi-elastic neutron scattering.

Polycrystalline Li0.4WO3 bronze has been synthesized by solid state reaction carried out in a silica tube at 10-7 MPa and 973 K. The sample is characterized by temperature-dependent neutron elastic and quasielastic scatterings. The room-temperature neutron powder data Rietveld refinement confirmed the space group Im3̄ along with lithium occupancy found predominantly at the 6b crystallographic site. Upon increasing temperature above 300 K lithium at 6b site decreases and at 2a site increases, suggesting Li+ cation diffusion between these two sites demonstrated by quasielastic neutron scattering as well. The lattice thermal expansion anomaly is observed between 380 K and 450 K, which is explained in terms of lithium dynamic disorder (non-equilibrium) as complemented by elastic and quasielastic neutron scatterings. DFT calculations with different lithium distributions at two different crystallographic sites guide to understand the lattice expansion anomaly. The lattice thermal expansion is modeled using Grüneisen first-order approximation, where the Debye-Einstein-Anharmonicity approach provides the temperature-dependent vibrational energy. The DFT-calculated phonon density of states and bulk modulus help extract the characteristic Debye and Einstein frequencies.

Quantification of lithium using handheld instruments: application of LIBS and XRF spectroscopy to assay the lithium content of mineral processing products

Two lithium assay methods have been developed using handheld tools, offering fast and reliable results. These methods are crucial for inline optimization of processes, particularly in the extraction of lithium from hard rock deposits.

Electrochemically Preplated Lithium on Silver Nanoparticle‐Decorated Three‐Dimensional Vertically Aligned Graphene Foam for Rechargeable Lithium Batteries

Graphene‐based materials, which exhibit large surface areas and superior electrical properties, are promising materials as anodes in lithium‐ion batteries (LIBs). However, the formation of a solid electrolyte interphase (SEI) on the large surfaces of these electrodes causes the loss of active lithium, leading to a severe reduction in coulombic efficiency and cycle retention. In this study, we combined an electrochemical lithium deposition (ELD) strategy, wherein active lithium was inserted into an electrode to minimize lithium loss during cycling, with the use of a vertically aligned three‐dimensional (3D) graphene foam. This foam, which was created via freeze‐casting, facilitated uniform lithium distribution during ELD, enhancing active lithium utilization. Consequently, the lithium preplated vertically aligned graphene foam anode could improve charge transfer and stabilize the SEI. It exhibited a superior cycle retention of 86% at a current density of 0.5 C for 200 cycles in LIBs, which is superior to that of preplated film‐type anodes and lithium foils. Moreover, it enabled the easy infiltration of polymer electrolyte through aligned graphene sheets while maintaining its original cell performance with a liquid electrolyte. Furthermore, it exhibited a higher discharge capacity than that of lithium foil anodes with the same negative/positive ratio in high‐areal‐capacity lithium–sulfur batteries. Therefore, this paper indicates the potential of preplated vertically aligned graphene foam as a high safety, high‐areal‐capacity anode for various next‐generation rechargeable lithium batteries.