Building a highly concentration responsive optical thermometer via tunable electron transfer pathways supported by intervalence charge transfer states.

The thermal-coupled levels (TCLs) of lanthanides have attracted great attention in the field of optical thermometer, offering an efficient method to achieve non-contect temperatuer feedback in complex environment. However, the iner 4f electrons are shielded, which becomes the core obstacle in improving the sensing performance. This issue is now circumvented by constructing an electron transfer pathway between Tm3+(1D2) and Eu3+(5D0) configurations. As a result, the electron transfer barrier is related to the relative temperature sensitivity, giving an insight into the modulation mechanism. Compared to the conventional TCLs systems, the relative temperature sensitivity of this strategy is highly concentration-responsive, increasing from 5.56 to 10.1 % K-1 as the Eu3+ molar concentration rises from 0.3 to 0.5 mol%. This work reveals the inner emission mechanism based on IVCT-supported emission mode, and presents the highly adjustability of sensing performance.

Reflectance spectroscopy analysis and lithium content estimation in lithium-rich rocks and stream sediments: Insights from Tuanjie Peak, Western Kunlun, China.

Lithium, a rare metal of strategic importance, has garnered heightened global attention. This investigation delves into the laboratory visible-near infrared and short-wavelength infrared reflectance (VNIR-SWIR 350 nm-2500 nm) spectral properties of lithium-rich rocks and stream sediments, aiming to elucidate their quantitative relationship with lithium concentration. This research seeks to pave new avenues and furnish innovative technical solutions for probing sedimentary lithium reserves. Conducted in the Tuanjie Peak region of Western Kunlun, Xinjiang, China, this study analyzed 614 stream sediments and 222 rock specimens. Initial steps included laboratory VNIR-SWIR spectral reflectance measurements and lithium quantification. Following the preprocessing of spectral data via Savitzky-Golay (SG) smoothing and continuum removal (CR), the absorption positions (Pos2210nm, Pos1910nm) and depths (Depth2210, Depth1910) in the rock spectra, as well as the Illite Spectral Maturity (ISM) of the rock samples, were extracted. Employing both the Successive Projections Algorithm (SPA) and genetic algorithm (GA), wavelengths indicative of lithium content were identified. Integrating the lithium-sensitive wavelengths identified by these feature selection methods, A quantitative predictive regression model for lithium content in rock and stream sediments was developed using partial least squares regression (PLSR), support vector regression (SVR), and convolutional neural network (CNN). Spectral analysis indicated that lithium is predominantly found in montmorillonite and illite, with its content positively correlating with the spectral maturity of illite and closely related to Al-OH absorption depth (Depth2210) and clay content. The SPA algorithm was more effective than GA in extracting lithium-sensitive bands. The optimal regression model for quantitative prediction of lithium content in rock samples was SG-SPA-CNN, with a correlation coefficient prediction (Rp) of 0.924 and root-mean-square error prediction (RMSEP) of 0.112. The optimal model for the prediction of lithium content in stream sediment was SG-SPA-CNN, with an Rp and RMSEP of 0.881 and 0.296, respectively. The higher prediction accuracy for lithium content in rocks compared to sediments indicates that rocks are a more suitable medium for predicting lithium content. Compared to the PLSR and SVR models, the CNN model performs better in both sample types. Despite the limitations, this study highlights the effectiveness of hyperspectral technology in exploring the potential of clay-type lithium resources in the Tuanjie Peak area, offering new perspectives and approaches for further exploration.

Cobalt Ditelluride Meets Tellurium Vacancy: An Efficient Catalyst as a Multifunctional Polysulfide Mediator toward Robust Lithium-Sulfur Batteries.

The commercialization of lithium-sulfur batteries (LSBs) faces significant challenges due to persistent issues, such as the shuttle effect of lithium polysulfides (LiPSs) and the slow kinetics of cathodic reactions. To address these limitations, this study proposes a vacancy-engineered cobalt ditelluride catalyst (v-CoTe2) supported on nitrogen-doped carbon as a sulfur host at the cathode. Density functional theory calculations and experimental results indicate that the electron configuration modulation of v-CoTe2 enhances the chemical affinity and catalytic activity toward LiPS. Specifically, v-CoTe2 can strongly interact with PSs through multisite coordination, effectively facilitating the kinetics of the LiPS redox reaction. Furthermore, the introduction of Te vacancies generates a large number of spin-polarized electrons, further enhancing the reaction kinetics of LiPS. As a result, the v-CoTe2@S cathode demonstrates high initial capacity and excellent cyclic stability, maintaining 80.4% capacity after 500 cycles at a high current rate of 3 C. Even under a high sulfur load of 6.7 mg cm-2, a high areal capacity of 6.1 mA h cm-2 is retained after 50 cycles. These findings highlight the significant potential of Te vacancies in CoTe2 as a sulfur host material for LSBs.

A Porphyrin-Phenylalkynyl-Based Conjugated Organic Polymer as a High-Performance Cathode for Rechargeable Organic Batteries.

Organic electrode materials (OEMs) have attracted much attention for rechargeable batteries due to their low cost, environment friendliness, flexibility, and structural versatility. Despite the above advantages, high solubility in electrolyte and low electronic conductivity remain critical limitations for the application of OEMs. In this work, the conjugated organic polymer (COP) poly([5,10,15,20-tetrakis(4-phenylalkynyl)porphyrin]Cu(II)) (PCuTPEP) is proposed as a cathode for high performance in organic lithium batteries. The polymerization inhibits the dissolution of the organic electrodes in the electrolyte, and the porphyrin and ethynyl-phenyl groups greatly expand the conjugated system and result in a high average discharge plateau at 4.0 V (vs Li+/Li). The PCuTPEP cathode exhibits a reversible discharge capacity of 119 mAh g-1 at a current of 50 mA g-1. Even at a high current density of 2.0 A g-1, excellent cycling stability up to 1000 cycles is achieved with capacity retentions of 88.5 and 90.4% at operating temperatures of 25 and 50 °C in organic lithium batteries, respectively. This study provides the approach for the development of organic cathodes for electrochemical energy storage.

Phonon-Lithium Ion Interactions: A Case Study of LiM(SeO3)2 (M = Al, Ga, In, Sc, Y, and La).

Li ion diffusion is fundamentally a thermally activated ion hopping process. Recently, soft lattice, anharmonic phonon, and paddlewheel mechanism have been proposed to potentially benefit the ion transport, while the understanding of vibrational couplings of mobile ions and anions is still very limited but essential. Herein, we accessed the ionic conductivity, stability, and especially, lattice dynamics in LiM(SeO3)2 (M = Al, Ga, In, Sc, Y, and La) with two different types of oxygen anions within a LiO4 polyhedron, namely, edge-shared and corner-shared with MO6 polyhedra, the prototype of which, LiGa(SeO3)2, has been theoretically reported before with the similar structural features to NASICON and later experimentally synthesized with the room temperature conductivity ∼0.11 mS cm-1. It is interesting to note that LiM(SeO3)2 with a higher Li phonon band center shows higher Li conductivity, which is in contradiction to the conventional understanding of the importance for soft lattice to superionic conductors. The anharmonic and harmonic phonon interactions as well as the couplings between the vibration of the edge-bonded or corner-bonded anion in Li polyanions and the Li ion diffusion have been studied in detail. With transition metal M changing from La, Y, In, Ga, Al, and Sc, anharmonic phonons increase with reduced activation energy for Li diffusion. The phonon modes dominated by the edge-bonded oxygen anions contribute more to the migration of the Li ion than those dominated by the corner-bonded oxygen anions because of the greater atomic interaction between the Li ion and the edge-bonded anions. Thus, rather than the overall lattice softness, attention shall be given to reduce the frequency of the critical phonons contributing to Li ion diffusion as well as to increase the anharmonicity, i.e., through asymmetric Li polyhedra, for the design of Li ion superionic conductors for all-solid-state batteries.

A Fast Self-Healing Binder for Highly Stable SiOx Anodes in Lithium-Ion Batteries.

Silicon oxide-based (SiOx-based) materials show great promise as anodes for high-energy lithium-ion batteries due to their high specific capacity. However, their practical application is hindered by the inevitable volumetric expansion during the lithiation/delithiation process. Constructing high-performance binders for SiOx-based anodes has been regarded as an efficient strategy to mitigate their volume expansion and preserve structural integrity. In this work, we propose a green water-solution PAA-LS binder composed of poly(acrylic acid) (PAA) and sodium lignosulfonate (LS) with fast self-healing properties. The designed binder can be restored due to the strong affinity between Fe3+-catechol coordination bonds, thereby effectively alleviating the volumetric strain of SiOx-based anodes. Notably, with an optimized LS content of 0.5%, the SiOx@PAA-LS electrode exhibits excellent performance, delivering a high capacity of 997.3 mAh g-1 after 450 cycles at 0.5 A g-1. Furthermore, the SiOx||NCM622 full cell also demonstrates superior cycling stability, maintaining a discharge capacity of 147.58 mAh g-1 after 100 cycles at 0.5 A g-1, with an impressive capacity retention rate of 82.72%.

Promoting nitrogen-doped porous phosphorus spheres for high-rate lithium storage.

Phosphorus anode has shown great potential for the high-rate and high-energy-density lithium-ion batteries. Nevertheless, it still suffers from possible electrode cracking, ion-transport restrictions, and active-particle decomposition resulting from repeated alloying/de-alloying. To address the aforementioned issues, a nitrogen-doped flower-like porous phosphorus (f-P) sphere has been developed. The abundant micro-mesopores facilitate ion diffusion and enhance the internal bonding strength of the electrode. Concurrently, the doped nitrogen promotes the generation of a favorable solid electrolyte interphase constructed by fast-ion-conductors. As a result, the f-P exhibits a high-rate capacity of 735mAh g-1 at 20 A g-1 and maintains high Coulombic efficiencies over 900 cycles at 10 A g-1. Furthermore, coin full-cells comprising the f-P anode and lithium cobalt oxide cathode demonstrate stable operation at a high current density of 6 mA cm-2. The combination of a porous structure and doping strategy represents a viable approach for strengthening the durability of electrodes and optimizing the ion transport kinetics of advanced alloy anode materials.

Constructing high-throughput and highly adsorptive lithium-sulfur battery separator coatings based on three-dimensional hexagonal star-shaped MOF derivatives.

The electrochemical performance of high-performance lithium-sulfur (Li-S) batteries is affected by many factors such as shuttle effect and lithium dendrites. To effectively solve this problem, a hexagonal star-shaped composite catalyst containing Co-N-C active sites (Co-NC-X) has been rationally developed under the joint action of Zn2+ and Co2+ bimetallic ions. By modifying it to the Li-S battery separator, Co-NC-X can not only act as a physical barrier to effectively prevent the diffusion of lithium polysulfide (LiPS), but also the special morphology can expose more active sites and have a strong chemisorption effect on LiPS, which effectively promotes the redox conversion of LiPS and mitigates the shuttle effect. Li-S battery with Co-NC-X exhibits excellent electrochemical performance. It has a high specific capacity and stable cycling performance, with an initial discharge capacity of 1406.9 mAh·g-1 at 0.2 C and 876.8 mAh·g-1 at 2 C, and a lower capacity decline rate of 0.093 % for 500 cycles.

Importance of salinity on regulating the environmental fate and bioaccumulation of lithium in the Yangtze River Estuary.

The demand of lithium (Li) has increased rapidly in recent decades under carbon neutrality strategies, but the environmental fate and potential risks of Li in aquatic ecosystem are barely known. This study conducted a comprehensive field survey in the Yangtze River Estuary (YRE) and the adjacent East China Sea (ECS), to investigate the spatial distribution of dissolved Li and bioaccumulation of Li in the coastal food web. The dissolved Li increased with salinity (from 7.39 to 189 µg L-1), controlled by the conservative mixing of Li-enriched seawater and Li-poor riverine water. Negative correlation was observed between Li content and stable nitrogen isotope in the coastal biota, indicating bio-diminish of Li in the food web. Furthermore, the Li contents in muscle tissues were significantly higher in bivalves (as filter-feeders; mean: 0.75 ±â€¯0.41 µg g-1) than in fish (as predator; mean: 0.10 ±â€¯0.05 µg g-1) and other biota species, indicating that dissolved uptake might be the major exposure pathway for Li. Importantly, it was noticed that the bioaccumulation factors (BAFs) in fish muscle varied greatly (from 0.17 to 5.82), showing lower BAFs for fish inhabiting in marine and benthic regions (with higher salinity and higher dissolved Li concentration). Such inhibition effects of salinity on Li bioaccumulation could not be explained by the modulation of salinity on Li speciation, but highly attributed to the inhibition of high salinity on the dissolved uptake of Li, which was associated with the co-transportation of Li and Na. Our results illuminate the importance of salinity on regulation the spatial variations of dissolved Li and Li bioaccumulation in the YRE and the adjacent ECS, which could help the understanding of Li biogeochemical cycling and potential risks in estuarine and coastal regions.

Axial compression stress-strain relationship of lithium slag rubber concrete.

Replacing cement with lithium slag and fine aggregate with rubber in concrete solves waste disposal, reduces material consumption, boosts sustainability, and enhances concrete performance. A set of prismatic concrete specimens with varying proportions were designed and experimentally tested in order to study the compressive stress-strain behavior of lithium slag rubber concrete (LSRC). The main factors affecting the specimens were lithium slag substitution ratio (SL=0%, 10%, 20%, 30%) and rubber substitution ratio (SR=0%, 5%, 10%, 15%). The results demonstrated that the LSRC exhibited good integrity during the damage. Furthermore, the incorporation of lithium slag (LS) was found to effectively compensate for the reduction in compressive strength due to the incorporation of rubber. When 10% of the fine aggregate was replaced with rubber and 20% of the cement was substituted with lithium slag, the axial compressive strength, elastic modulus, and peak strain of the tested specimens increased by 21.57%, 6.92%, and 17.26%, respectively. Compared with ordinary concrete, LSRC has good toughness, impact resistance and durability with minimal loss of strength, and has broad application prospects in engineering fields (such as airports, highways, housing expansion joints, concrete floors and railway concrete sleepers, etc.). Based on the experimental data, simplified modified equations to predict the compressive strength, elastic modulus, peak strain and axial stress-strain constitutive model of LSRC were proposed, so as to promote the development of LSRC.

Hygroscopic Nature of Lithium Ions: A Simple Key to Super Tough Atmosphere-Stable Hydrogel Electrolytes.

Gel electrolytes have emerged as a versatile solution to address numerous limitations associated with liquid electrolytes in electrical energy storage (EES) devices, in terms of safety, flexibility, and affordability. Aqueous gel electrolytes, in particular, exhibit exceptional features by offering one of the highest ion solvation capacities and ionic conductivities. The two main challenges with hydrogel electrolytes are their easy freezing at subzero temperatures and rapid dehydration under open conditions, leading to the failure of the EES device. In response, we present an uncomplicated and quick-to-make hydrogel electrolyte system offering impressive mechanical properties (205.5 kPa tensile strength, 2880 kJ/m3 toughness, and 3030% strain at the break), along with antifreezing and antiflammability attributes. Notably, the hydrogel electrolyte demonstrates high ionic conductivity and superior performance in supercapacitor cells over a wide range of temperatures (-40 to 80 °C) and under various deformations. The hydrogel electrolyte maintains its capabilities under open conditions over an extended period of time, even at 50 °C, showcased by powering a wristwatch. The atmospheric stability of the hydrogel electrolyte demonstrated in this study introduces promising prospects for the future of EES devices spanning from production to end-user consumption.

Lithium alleviates paralysis in experimental autoimmune neuritis in Lewis rats by modulating glycogen synthase kinase-3ß activity.

IMPORTANCE: Guillain-Barré syndrome (GBS)-like neuropathy mimics the leading cause of sporadic acute nontraumatic limb paralysis in individuals from developed countries. Experimental autoimmune neuritis (EAN) is an animal model of GBS and of syndromes such as acute canine polyradiculoneuritis, seen in dogs and cats. OBJECTIVE: The involvement of glycogen synthase kinase (GSK)-3ß, a pro-inflammatory molecule, in rat EAN is not fully understood. This study evaluated the potential role of GSK-3ß in EAN through its inhibition by lithium. METHODS: Lewis rats were injected with SP26 antigen to induce EAN. Lithium was administered from 1 day before immunization to day 14 post-immunization (PI). Then the rats were euthanized and their neural tissues were prepared for histological and Western blotting analyses. RESULTS: Lithium, an inhibitor of GSK-3, significantly ameliorated EAN paralysis in rats, when administered from day 1 to day 14 PI. This corresponded with reduced inflammation in the sciatic nerves of EAN rats, where phosphorylation of GSK-3ß was also upregulated, indicating suppression of GSK-3. CONCLUSIONS AND RELEVANCE: These findings suggest that lithium, an inhibitor of GSK-3ß, plays a significant role in ameliorating rat EAN paralysis, by suppressing GSK-3ß and its related signals in EAN-affected sciatic nerves.

Regulating Non-Equilibrium Solvation Structure in Locally Concentrated Ionic Liquid Electrolytes for Wide-Temperature and High-Voltage Lithium Metal Batteries.

The development of high-voltage lithium metal batteries (LMBs) encounters significant challenges due to aggressive electrode chemistry. Recently, locally concentrated ionic liquid electrolytes (LCILEs) have garnered attention for their exceptional stability with both Li anodes and high-voltage cathodes. However, there remains a limited understanding of how diluents in LCILEs affect the thermodynamic stability of the solvation structure and transportation dynamics of Li+ ions. Herein, we propose a wide-temperature LCILEs with 1,3-dichloropropane (DCP13) diluent to construct a non-equilibrium solvation structure under external electric field, wherein the DCP13 diluent enters the Li+ ion solvation sheath to enhance Li+ ion transport and suppress oxidative side reactions at high-nickel cathode (LiNi0.9Co0.05Mn0.05O2, NCM90).Consequently, a Li/NCM90 cell utilizing this LCILE achieves a high capacity retention of 94% after 240 cycles at 4.3 V, also operates stably at high cut-off voltages from 4.4 to 4.6 V and over a wide temperature range from -20 to 60 °C. Additionally, an Ah-level pouch cell with this LCILE simultaneously achieves high-energy-density and stable cycling, manifesting the practical feasibility. This work redefines the role of diluents in LCILEs, providing inspiration for electrolyte design in developing high-energy-density batteries.

Self-Oxidated Hybrid Conductive Network Enables Efficient Electrochemical Lithium Extraction Under High-Altitude Environment.

The electrochemical deintercalation method has been considered as an effective way to address the demand for lithium resources due to its environmental friendliness, high selectivity, and high efficiency. However, the performance of electrochemical lithium extraction is closely dependent on the electrode material and needs to be compatible under plateau environments with high-altitude and low-temperature. Herein, an in situ self-oxidation method is conducted to construct a hybrid conductive network on the surface of LiFePO4 (LFP-HN). The introduction of a hybrid conductive network enhanced the interfacial electron/lithium-ion transfer. In addition, structural stability is strengthened through suppressing the intercalation of impurity cations. Consequently, the LFP-HN delivered extremely high lithium extraction capacity (27.42 mg g-1), low energy consumption (4.91 Wh mol-1), and superior purity (91.05%) in Baqiancuo real brine (4788 m, -10 °C). What's more, LFP-HN-based large-scale prototypes are constructed and operated at Baqiancuo, which is calculated to extract 25 kg Lithium Carbonate Equivalent per cycle (4.55 h, 100 pairs of plates). Based on the excellent performance, the modification strategy developed in this work can be a promising solution for industrial lithium extraction under high-altitude environment.

Surface Coordination of Garnet Fillers Improves the Organic-Inorganic Interfacial Compatibility of Composite Solid Electrolyte.

Composite solid electrolytes (CSEs) have become one of the most promising solid-state electrolytes due to their favorable safety and flexibility. However, the weak interaction between inorganic fillers and polymer matrix leads to poor organic-inorganic interfacial compatibility, which degrades the electrochemical performance of CSEs. Herein, it is demonstrated that Li6.4La3Zr1.4Ta0.6O12 (LLZTO) can be chemically bonded to the polymer matrix by surface coordination of the 1,2-dithiolane group of lipoic acid (LA) with metal atoms on the surface of LLZTO through a combination of experimental investigations and theoretical calculations. The surface coordination not only enhances the interfacial compatibility between LLZTO and the polymer matrix, but also facilitates rapid Li+ transport, which leads to the ionic conductivity of the prepared CSE (P-V-M@LLZTO) as high as 6.1 × 10-4 S cm-1 at 30 °C. The excellent interface compatibility ensures a stable cycle of Li/P-V-M@LLZTO/Li symmetrical cell for more than 3500 h. As a result, LiFePO4/P-V-M@LLZTO/Li cell delivers the discharge capacity of 161 mAh g-1 after 5 cycles with a capacity retention of 81% after 500 cycles at 0.5C under 30 °C. This work demonstrates that surface coordination is an effective strategy to solve the inherent interfacial incompatibility problem in CSEs.

Lithium-induced cognitive dysfunction assessed over 1-year hospitalisation: A case report.

Introduction: Lithium-induced neurotoxicity is almost always reversible but can cause irreversible neurological sequelae, namely the syndrome of irreversible lithium-effectuated neurotoxicity (SILENT). As there is no definitive treatment for SILENT, caution is required when administering lithium. Reports on the effect of lithium-effectuated neurotoxicity on cognitive function are limited. We report a case in which high cognitive function was lost after lithium overdose and hardly recovered, as evaluated using multiple neuropsychological tests during a 1-year hospitalisation period. Patient presentation: A 52-year-old man on lithium medication with bipolar disorder was admitted to the intensive care unit because of lithium overdose. The patient achieved lucid consciousness after continuous haemodiafiltration. However, he could not move his body as desired or produce appropriate verbal expressions; thus, he was moved to our psychiatric ward, where his treatment continued. Management and outcome: After several months, the patient was diagnosed with SILENT owing to persistent motor and cognitive dysfunctions. Multiple neuropsychological tests were performed, and cognitive function was evaluated. The Neurobehavioural Cognitive Status Examination showed a worsening trend, and the full intelligence quotient of the Wechsler Adult Intelligence Scale-Third Edition was in the mild intellectual disability range. Conclusion: This is a clear case of cognitive dysfunction due to SILENT and is difficult to treat. Thus, it is crucial to prevent the onset of SILENT. Contribution: This report is valuable because it is one of the few to track changes in cognitive function over time in a patient with SILENT using objective measures over 1 year of hospitalisation.

Effect of preparation design on fracture resistance of molars restored with occlusal veneers of different CAD-CAM materials: an in vitro study.

BACKGROUND: Occlusal veneer had been evaluated for mechanical properties using lithium disillicate. However, studies evaluating the mechanical properties of occlusal veneer with different preparation designs and ceramic materials are lacking. So, this in vitro study aimed to evaluate the fracture resistance of occlusal veneers with two designs fabricated from two different ceramic materials. MATERIAL AND METHODS: Fourty mandibular third molars were distributed to 2 groups (n = 20) according to preparation design: group (O) anatomical occlusal reduction and group (OA) anatomical occlusal and 1 mm axial reduction. Each group was additionally subdivided into two subgroups (n = 10) according to ceramic materials; in subgroup X, lithium disilicate (e.max CAD, Ivoclar AG, Schaan, Liechtenstein) was used, and in subgroup S, zirconia-reinforced lithium silicate (ZLS) (Vita Suprinity, VitaZahnfabrik, Bad Säckingen, Germany) was used. All specimens were cemented with a light-cure resin cement (Choice 2, Bisco, Schaumburg, USA). 5000 thermocycles were applied to all specimens with both temperatures of 5 °C and 55 °C in two water baths; the dwell time was 30s at each bath, and the transfer time was 10s. Then all specimens were subjected to a fatigue simulation under dynamic loading of 200 N for 250,000 cycles. A universal testing machine (5500R/1123, Instron, Norwood, USA) was used to evaluate the fracture strength with a crosshead speed of 1 mm/min. All data were analyzed statistically by using a two-way ANOVA, and for some violations of assumptions, these results were compared with those obtained by the nonparametric test (Scheirer Ray Hare) (α = 0.05). RESULTS: A statistically significantly higher fracture resistance in the 'OA' (3389 N) compared to the 'O' (2787 N) group regardless of the ceramic material (P < .001) and a statistically significantly higher fracture resistance in the 'X' (3295 N) compared to the 'S' (2881 N) regardless of the preparation design (P = .015). CONCLUSIONS: For occlusal veneers, all preparation designs and materials (such as Vita Suprinity and e.max CAD) had clinically acceptable fracture resistance values that were greater than the maximal biting forces. On the other hand, the e.max CAD with occlusal veneer, including axial reduction design, demonstrated the maximum fracture resistance value. Finally, no relationship between fracture strength and mode of failure was found.

Investigation of polypyrrole based composite material for lithium sulfur batteries.

With the rising demand for electricity storage devices, the performance requirements for such equipment have become increasingly stringent. Lithium-sulfur (Li-S) batteries are poised to be among the next generation of energy storage systems. However, before they can be commercially viable, several challenges must be addressed, including low sulfur conductivity and the shuttle effect. Herein, polypyrrole based sulfur composite was prepared by simple method in hydrothermal teflon lined autoclave for Li-S battery. The S/SP/ppy/PVDF electrode exhibited the initial discharge capacity of 662 mAh g- 1 at 0.5 C and 637 mAh g- 1 after 100 cycles. The Coulombic efficiency was 96% all along charge/discharge cycling. Moreover, Li-S coin cells were assembled and tested to demonstrate the potential application and scale-up of the polypyrrole-sulfur composite.

In Situ Forming Asymmetric Gel Polymer Electrolyte Enhances the Performance of High-Voltage Lithium Metal Batteries.

With the rapid evolution of electric vehicle technology, concerns regarding range anxiety and safety have become increasingly pronounced. Battery systems with high specific energy and enhanced security, featuring ternary cathodes paired with lithium (Li) metal anodes, are poised to emerge as next-generation electrochemical devices. However, the asymmetric configuration of the battery structure, characterized by the robust oxidative behavior of the ternary cathodes juxtaposed with the vigorous reductive activity of the Li metal anodes, imposes elevated requisites for the electrolytes. Herein, a well-designed gel polymer electrolyte with asymmetric structure was successfully prepared based on the Ritter reaction of cyanoethyl poly(vinyl alcohol) (PVA-CN) and cationic ring-opening polymerization of s-Trioxane. With the aid of the sieving effect of separator, the in situ asymmetric gel polymer electrolyte has good compatibility with both the high-voltage cathodes and Li anodes. The amide groups generated by PVA-CN after the Ritter reaction and additional cyano groups can tolerate high voltages up to 5.1 V, matching with ternary cathodes without any challenges. The functional amide and cyano groups participate in the formation of the cathode electrolyte interface and stabilize the cathode structure. Meanwhile, the in situ formed ether-based polyformaldehyde electrolyte is beneficial for promoting uniform Li deposition on anode surfaces. Li-Li symmetric cells demonstrate sustained stability over 2000 h of cycling at a current density of 1 mA cm-2 for 1 mAh cm-2. Furthermore, the capacity retention rate of Li(Ni0.6Mn0.2Co0.2)O2-Li cells with 0.5 C cycling after 300 cycles is 92.2%, demonstrating excellent cycle stability. The electrolyte preparation strategy provides a strategy for the progress of high-performance electrolytes and promotes the rapid development of high-energy-density Li metal batteries.

Dramatic Enhancement Enabled by Introducing TiN into Bread-like Porous Si-Carbon Anodes for High-Performance and Safe Lithium Storage.

Doping modifications and surface coatings are effective methods to slow volume dilatation and boost the conductivity in silicon (Si) anodes for lithium-ion batteries (LIBs). Herein, using low-cost ferrosilicon from industrial production as the energy storage material, a bread-like nitrogen-doped carbon shell-coated porous Si embedded with the titanium nitride (TiN) nanoparticle composite (PSi/TiN@NC) was synthesized by simple ball milling, etching, and self-assembly growth processes. Remarkably, the porous Si structure formed by etching the FeSi2 phase in ferrosilicon alloys can provide buffer space for significant volume expansion during lithiation. Highly conductive and stable TiN particles can act as stress absorption sites for Si and improve the electronic conductivity of the material. Furthermore, the nitrogen-doped porous carbon shell further helps to sustain the structural stability of the electrode material and boost the migration rate of Li-ions. Benefiting from its unique synergistic effect of components, the PSi/TiN@NC anode exhibits a reversible discharge capacity up to 1324.2 mAh g-1 with a capacity retention rate of 91.5% after 100 cycles at 0.5 A g-1 (vs fourth discharge). Simultaneously, the electrode also delivers good rate performance and a stable discharge capacity of 923.6 mAh g-1 over 300 cycles. This research can offer a potential economic strategy for the development of high-performance and inexpensive Si-based anodes for LIBs.