Investigation on the solidification effect and mechanism of loess utilizing magnesium oxysulfate cement as a curing agent.

In this study, magnesium oxysulfate cement (MOS) was used as a binder for curing loess. The changes in bulk density, porosity, mineral structure and microstructure of the consolidated loess were systematically studied and verified. The porosity decreased from 40.97 % in pure loess to 28.75 % in 13 % MOS solidified sample. Scanning electron microscopy, energy spectrum analysis and thermogravimetric analysis revealed that the addition of MOS binder resulted in the formation of hydrated products, including Mg(OH)2, MgO·mSiO2·nH2O (M-S-H), and 3Mg(OH)2·MgSO4·8H2O (3·1·8 phase), which effectively filled the voids between the grains and facilitated strong bonding among them. After a curing period of 28 days, the compressive strength of loess stabilized with 13 % MOS exhibited an increase to 7.9 MPa. Moreover, following immersion in water for 24 h, the softening coefficient K remained at 0.66. Furthermore, after undergoing five cycles of freeze-thaw cycling, the rate of change in compressive strength RP was only 6.3 %. All the results indicate that MOS exhibits promising potential as a binder for soil stabilization applications.

Biochar-enhanced three-dimensional conductive network thick electrodes for efficient lithium extraction from salt lake brines with high Magnesia-lithium ratios.

Enhancing the kinetic performance of thick electrodes is essential for improving the efficiency of lithium extraction processes. Biochar, known for its affordability and unique three-dimensional (3D) structure, is utilized across various applications. In this study, we developed a biochar-based, 3D-conductive network thick electrode (∼20 mg cm-2) by in-situ deposition of LiFePO4 (LFP) onto watermelon peel biomass (WB). Utilizing Density Functional Theory (DFT) calculations complemented by experimental data, we confirmed that this The thick electrode exhibits outstanding kinetic properties and a high capacity for lithium intercalation in brines, even in environments where the Magnesia-lithium ratios are significantly high. The electrode showed an impressive intercalation capacity of 30.67 mg g-1 within 10 min in a pure lithium solution. It also maintained high intercalation performance (31.17 mg g-1) in simulated brines with high Magnesia-lithium ratios. Moreover, in actual brine, it demonstrated a significant extraction capacity (23.87 mg g-1), effectively lowering the Magnesia-lithium ratio from 65 to 0.50. This breakthrough in high-conductivity thick electrode design offers new perspectives for lithium extraction technologies.

Enhanced Cathode Performance: The Heterostructure Construction of LiCoO2@Co3O4@Li6.4La3Zr1.4Ta0.6O12.

In this study, the heterostructure cathode material LiCoO2@Co3O4@Li6.4La3Zr1.4Ta0.6O12 was prepared by coating Li6.4La3Zr1.4Ta0.6O12 on the surface of LiCoO2 through a one-step solid-phase synthesis. The morphology, structure, electrical state, and elemental contents of both pristine and modified materials were assessed through a range of characterization techniques. Theoretical calculations revealed that the LCO@LLZTO material possessed a reduced diffusion barrier compared to LiCoO2, thereby facilitating the movement of Li ions. Electrochemical tests indicated that the capacity retention rate of the modified cathode composites stood at 70.43% following 300 cycles at a 2C rate. This high rate occurred because the Li6.4La3Zr1.4Ta0.6O12 film on the surface enhanced the migration of Li+, and the spinel phase of Co3O4 had better interfacial stability to alleviate the generation of microcracks by inhibiting the phase change from the layered phase to the rock-salt phase, which considerably improved the electrochemical properties.

Nano ZrO2 Modification for Enhancement of the Electrochemical Performance of Li-Rich Manganese-Based Cathodic Materials.

In this work, high-temperature solid-phase techniques have been used to produce both natural and nano ZrO2-modified Li-rich manganese-based cathodic materials. Several characterizations were carried out to evaluate the morphology, structure, electrical state, and elemental content of unmodified as well as nano-modified Li1.2Ni0.13Co0.13Mn0.54O2. The results of electrochemical tests showed that cathodic materials modified with 0.02 mol nano ZrO2 performed extremely well electrochemically, with initial discharge capacity and coulombic efficiency at 0.1 C reaching up to 308.5 mAh g-1 and 95.38%, respectively. After 170 cycles at 0.2 C, a magnitude of 200.2 mAh g-1 for the final discharge capacity was attained, which translates to a capacity retention of 68.68%. Calculations using density functional theory (DFT) show that adding nanoscale ZrO2 speeds up Li-ion diffusion and increases conductivity by lowering the barrier energy for the migration of Li ions. The structural layout of Li-rich manganese-based cathodic materials may therefore be clarified by the proposed modification technique for nano ZrO2.

Effectively Regulating More Robust Amorphous Li Clusters for Ultrastable Dendrite-Free Cycling.

A disordered phase in Li-deposit nanostructure is greatly attractive, but plagued by the uncontrollable and unstable growth, and the nanoscale characterization in the structure. Here, fully characterized in cryogenic transmission electron microscopy (cryo-TEM), more robust amorphous-Li (ALi) clusters are revealed and effectively regulated on heteroatom-activating electronegative sites and an advanced solid electrolyte interphase (SEI) layer. Heteroatom-activating electronegative sites capably enhance the electrostatic interaction of Li+ and heteroatom-doping graphene-like film (HDGs), meaning lower Li diffusion barrier and larger binding energy that is confirmed by small nucleation overpotentials of 13.9 and 10 mV at 0.1 mA cm-2 in the fluoroethylene carbonate-adding ester-based (FEC-ester) and LiNO3 -adding ether-based (LiNO3 -ether) electrolytes. Orderly multilayer SEI structure comprised of inorganic-rich components enables fast ion transports and durable capabilities to construct highly reversible and long-term plating/stripping cycling. ALi cluster anodes exhibit non-crystalline morphologies and perform ultrastable dendrite-free cycling over 2800 times. Stable ALi clusters are also grown in LiFePO4 (LFP) (LFP-ALi-HDGs-N||LiFePO4 [LFP]) full cells with advantageous capacities up to 165.5 and 164.3 mAh g-1 in these optimized electrolytes at 0.1 C; the remarkable capacity retentions maintain to 93% and 91% after 150 cycles at 0.2 C. Structure viability, electrochemical reversibility, and excellent performance in ALi clusters are effectively regulated.

MoS2 Nanosheets Vertically Grown on Carbonized Corn Stalks as Lithium-Ion Battery Anode.

In this study, MoS2 nanosheets are vertically grown on the inside and outside surfaces of the carbonized corn stalks (CCS) by a simple hydrothermal reaction. The vertically grown structure can not only improve the transmission rate of Li+ and electrons but also avoid the agglomeration of the nanosheets. Meanwhile, a new approach of biomass source application is presented. We use CCS instead of graphite powders, which can not only avoid the exploitation of graphite resources, but also be used as a matrix for MoS2 growth to prevent the electrode from being further decomposed during long cycles and at high current densities. Meanwhile, lithium-ion batteries show remarkable electrochemical performance. They demonstrate a high specific capacity of 1409.5 mA g-1 at 100 mA g-1 in the initial cycle. After 250 cycles, the discharge capacity is still as high as 1230.9 mAh g-1. Even at 4000 mA g-1, they show a high specific capacity of 777.7 mAh g-1. Furthermore, the MoS2/CCS electrodes show long cycle life, and the specific capacity is still up to ∼500 mAh g-1 at 5000 mA g-1 after 1000 cycles.

Auto-generated iron chalcogenide microcapsules ensure high-rate and high-capacity sodium-ion storage.

Sodium-ion batteries (SIBs) are regarded as promising alternative energy-storage devices to lithium-ion batteries (LIBs). However, the trade-off of between energy density and power density under high mass-loading conditions restricts the application of SIBs. Herein, we synthesized an FeSe@FeS material via a facile solid-state reaction. A microcapsule architecture was spontaneously achieved in this process, which facilitated electron transport and provided stable diffusion paths for Na ions. The FeSe@FeS material exhibits a high capacity retention (485 mA h g-1 at 3 A g-1 after 1400 cycles) and superior rate capability (230 mA h g-1 at 10 A g-1 after 1600 cycles) in the half-cell test. Furthermore, superior cycling stability is achieved in the full-cell test. The high mass-loaded FeSe@FeS electrodes (8 mg cm-2) realize a high areal capacity retention of 2.8 mA h cm-2 and high thermal stability.

Unique Reversible Conversion-Type Mechanism Enhanced Cathode Performance in Amorphous Molybdenum Polysulfide.

A unique reversible conversion-type mechanism is reported in the amorphous molybdenum polysulfide (a-MoS5.7) cathode material. The lithiation products of metallic Mo and Li2S2 rather than Mo and Li2S species have been detected. This process could yield a high discharge capacity of 746 mAh g-1. Characterizations of the recovered molybdenum polysulfide after the delithiaiton process manifests the high reversibility of the unique conversion reaction, in contrast with the general irreversibility of the conventional conversion-type mechanism. As a result, the a-MoS5.7 electrodes deliver high cycling stability with an energy-density retention of 1166 Wh kg-1 after 100 cycles. These results provide a novel model for the design of high-capacity and long-life electrode materials.