Suppressing hydrogen evolution and promoting dendrite free zinc deposition by fluorinated triazine framework towards robust aqueous zinc ion batteries.

Aqueous zinc-ion batteries (AZIBs) have become a research hotspot, but the inevitable zinc dendrites and parasitic reactions in the zinc anode seriously hinder their further development. In this study, three covalent triazine frameworks (DCPY-CTF, CTF-1 and FCTF) have been synthesized and used as artificial protective coatings, in which the fluorinated triazine framework (FCTF) increases the zinc-philic site, thus better promoting dendritic free zinc deposition and inhibiting hydrogen evolution reactions. Excitingly, both experimental results and theoretical calculations indicate that the FCTF interface adjusts the deposition of Zn2+ along the (002) plane, effectively alleviating the formation of zinc dendrites. As expected, Zn@FCTF symmetric cells exhibit cycling stability of over 4000 h (0.25 mA cm-2), meanwhile Zn@FCTF//NHVO full cells provide a high specific capacity of 280 mAh/g at 1.0 A/g, which are superior to those of bare Zn anode. This work provides new insights for suppressing hydrogen evolution and promoting dendrite-free zinc deposition to construct highly stable and reversible AZIBs.

Investigating the role of non-ionic surfactants as electrolyte additives for improved zinc anode performance in aqueous batteries.

Zinc metal anodes encounter significant challenges, including dendrite growth, hydrogen evolution, and corrosion, all of which impede the rate capability and longevity of aqueous zinc-ion batteries (AZIBs). To effectively tackle these issues, we introduced Tween-80 into the traditional ZnSO4 electrolyte as an additive. Tween-80 possesses electronegative oxygen atoms that enable it to adsorb onto the zinc (Zn) anode surface, facilitating the directional deposition of Zn metal along the (002) orientation. The hydroxyl and ether groups within Tween-80 can displace some of the coordinated water molecules in the Zn2+ inner solvation shell. This disruption of the hydrogen bond network regulates the solvation structure of Zn2+ ions and suppresses the possibility of hydrogen evolution. Moreover, the long hydrocarbon chain present in Tween-80 exhibits excellent hydrophobic properties, aiding in the resistance against corrosion of the Zn anode by water molecules and reducing hydrogen evolution. Consequently, a symmetric cell equipped with the Tween-80 additive can cycle stably for over 4000 h at 1 mA cm-2 and 1 mA h cm-2. When paired with the V2O5 cathode, the full cell demonstrates a high-capacity retention rate exceeding 80 % over 1000 cycles at a current density of 2 A g-1. This study underscores the advantages of utilizing non-ionic surfactants for achieving high-performance aqueous zinc-ion batteries.

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.

Advancing Zinc Anodes: Strategies for Enhanced Performance in Aqueous Zinc-Ion Batteries.

The promising features of aqueous zinc ion batteries (AZIBs), including their inherent safety, environmental friendliness, abundant raw materials, cost-effectiveness, and simple manufacturing process, position them as strong candidates for large-scale energy storage. However, their practical application faces significant challenges, such as uncontrolled dendritic growth, undesirable side reactions, and hydrogen evolution reactions (HER), which undermine the efficiency and longevity of the system. To address these issues, extensive research has been conducted to improve these batteries' energy density and lifespan. This comprehensive review explores the fundamental mechanisms of zinc dendrite formation, its properties, and the interfacial chemistry between the electrode and electrolyte. It also delves into strategies for protecting the zinc anode, with a focus on the modulation of zinc ion deposition dynamics at the electrolyte interface. The discussion concludes with an evaluation of the current challenges and future prospects of AZIB, aiming to enhance their viability for grid-scale energy storage solutions.

Crucial role of Snf7-3 in synaptic function and cognitive behavior revealed by conventional and conditional knockout mouse models.

Snf7-3 is a crucial component of the endosomal sorting complexes required for transport (ESCRT) pathway, playing a vital role in endolysosomal functions. To elucidate the role of Snf7-3 in vivo, we developed conventional-like and conditional Snf7-3 knockout (KO) mouse models using a "Knockout-first" strategy. Conventional-like Snf7-3 KO mice showed significantly reduced Snf7-3 mRNA expression, and older mice (25-40 weeks) exhibited impaired social recognition and increased miniature excitatory postsynaptic currents (mEPSCs). Conversely, conditional KO mice aged 8-24 weeks, with Snf7-3 specifically deleted in forebrain excitatory neurons, displayed impaired object location memory and elevated mEPSC frequency. Enhanced dendritic complexity was observed in the medial prefrontal cortex of these mice, indicating early synaptic disturbances. Our findings underscore the critical role of Snf7-3 in maintaining normal cognitive functions and social behaviors. The observed synaptic and behavioral deficits in both conventional-like and conditional KO mice highlight the importance of Snf7-3 in specific neuronal populations, suggesting that early synaptic changes could precede more pronounced cognitive impairments.

Boosting Fast Charging of Lithium-Metal Batteries via Weak Interactions Between Non-Solvating Solvents and Anions in High-Safety Eutectic Electrolytes.

Proper design of the solvation structure is crucial for the development of lithium metal batteries (LMBs). In this paper, the use of 1,2-Dimethoxyethane (DME) as a non-solvating cosolvent in amide-based eutectic electrolytes is proposed to address challenges related to high viscosity, high polarization, and low conductivity, thus enhancing the compatibility with lithium metal anodes. Through physical characterization combined with simulation calculations the existence of a weak interaction between DME and anions is confirmed, which promotes the dissociation of lithium salts and increases the Li+ transference number and diffusion coefficient, thus improving the fast charging performance of eutectic electrolytes. In addition, stable SEI layer enriched with inorganic components is formed during the cycling process, resulting in uniform and dense lithium deposition. The fast charging performance of the cell can be effectively improved by utilizing the interaction between anions and solvents. The LiFePO4 (LFP)||Li cell has a capacity retention of 97% after 1200 cycles at 5 C and also performs well at high temperature of 50 °C. Overall, the use of a non-solvating cosolvent in eutectic electrolytes presents a promising and innovative approach for enhancing electrolyte performance in LMBs.

Dendrite Growth and Dead Lithium Formation in Lithium Metal Batteries and Mitigation Using a Protective Layer: A Phase-Field Study.

Lithium metal batteries (LMBs) are considered one of the most promising next-generation rechargeable batteries due to their high specific capacity. However, severe dendrite growth and subsequent formation of dead lithium (Li) during the battery cycling process impede its practical application. Although extensive experimental studies have been conducted to investigate the cycling process, and several theoretical models were developed to simulate the Li dendrite growth, there are limited theoretical studies on the dead Li formation, as well as the entire cycling process. Herein, we developed a phase-field model to simulate both electroplating and stripping process in a bare Li anode and Li anode covered with a protective layer. A step function is introduced in the stripping model to capture the dynamics of dead Li. Our simulation clearly shows the growth of dendrites from a bare Li anode during charging. These dendrites detach from the bulk anode during discharging, forming dead Li. Dendrite growth becomes more severe in subsequent cycles due to enhanced surface roughness of the Li anode, resulting in an increasing amount of dead Li. In addition, it is revealed that dendrites with smaller base diameters detach faster at the base and produce more dead lithium. Meanwhile, the Li anode covered with a protective layer cycles smoothly without forming Li dendrite and dead Li. However, if the protective layer is fractured, Li metal preferentially grows into the crack due to enhanced Li-ion (Li+) flux and forms a dendrite structure after penetration through the protective layer, which accelerates the dead Li formation in the subsequent stripping process. Our work thus provides a fundamental understanding of the mechanism of dead Li formation during the charging/discharging process and sheds light on the importance of the protective layer in the prevention of dead Li in LMBs.

Multiscale Defective Interfaces for Realizing Na-CO2 Batteries With Ultralong Lifespan.

Despite their favorable high energy density and potential for CO2 recycling, Na-CO2 batteries have been held back by limitations in cycling capability, stemming from the sluggish CO2 reduction/evolution reaction (CO2RR/CO2ER) kinetics at CO2 cathode and unmanageable deposition/stripping of metallic Na at the anode upon cycling. Herein, a "two-in-one" electrode with multiscale defective FeCu interfaces (CP@FeCu) is presented, which is capable of improving the CO2RR/CO2ER kinetics of CO2-breathing cathode, while modulating sodium deposition behavior. Experimental and theoretical investigations reveal multiscale defective FeCu interfaces are responsible for the enhancement of sodiophilicity and catalytic properties. The defect and valence oscillation effects originate in multiscale defective FeCu interfaces, effectively facilitating the adsorption of reactants and decomposition of Na2CO3 during CO2RR/CO2ER processes, along with exceptional cycling stability of 2400 cycles (4800 h) at 5 µA cm-2. Meanwhile, the CP@FeCu with sodium affinity creates a uniform electric field and robust adsorption for Na, making initial nucleation sites more conducive to Na deposition and achieving dendrite-resistant and durable anodes. This work offers a scientific insight into the functionalization design of "two-in-one" electrodes, which is essential for a unified solution to the challenges in sodium anodes and CO2 cathodes.

Polar Covalent Triazine Frameworks as High-Performance Potassium Metal Battery Cathodes.

The exploration of potassium metal batteries (PMBs) has been intensified, leveraging potassium's abundant availability, low redox potential, and small Stokes radius. Covalent triazine frameworks (CTFs) stand out for their accessible nitrogen sites and customizable structures, making them attractive electrode materials. Nonetheless, there is a lack of established design principles to guide the development of high-performance PMBs using CTFs. In this work, CTFs consisting of different monomers are used as PMB cathodes to investigate the structure-performance correlation. The electronic structure analysis reveals the polar characteristic of a CTF derived from the tetracyanoquinodimethane monomer, setting it apart with superior capacity (161 mAh g-1 at 0.1 A g-1), rate performance (85 mAh g-1 at 5 A g-1), and stability (capacity retention of 81% after 1000 cycles) over three non-polar counterparts in PMBs. Calculations based on density functional theory support the exceptional performance with increased K+ adsorption energy. Ultimately, among multifaceted factors, the polarity of CTF is the leading element that determines the K+ storage capability. These findings pave the way for the development of prudent CTF electrodes for high-performance PMBs.

Ultra-tough Dynamic Supramolecular Ion-conducting Elastomer Induced Uniform Li+ Transport and Stabilizes Interphase Ensures Dendrite-free Lithium Metal Anodes.

Artificial polymer solid electrolyte interphases (SEIs) with microphase-separated structures provide promising solutions to the inhomogeneity and cracking issues of natural SEIs in lithium metal batteries (LMBs). However, achieving homogeneous ionic conductivity, excellent mechanical properties, and superior interfacial stability remains challenging due to interference from hard-phase domains in ion transport and solid-solid interface issues with lithium metal. Herein, we present a dynamic supramolecular ion-conducting poly(urethane-urea) interphase (DSIPI) that achieves these three properties through modulating the hard-phase domains and constructing a composite SEI in situ. The soft-phase polytetrahydrofuran backbone, featuring loose Li+-O coordinating interactions, ensures uniform Li+ transport. Concurrently, sextuple hydrogen bonds in the hard phase dissipate strain energy through sequential bond cleavage, thereby imparting exceptional mechanical properties. Moreover, enriched bis(trifluoromethanesulfonyl)imide anion (TFSI-) in DSIPI promotes the in-situ formation of a stable polymer-inorganic composite SEI during cycling. Consequently, the DSIPI-protected lithium anode (DSIPI@Li) enables symmetric cells with exceptional cyclability exceeding 4,000 hours at an ultra-high current density of 20 mA cm-2, thereby demonstrating excellent cycling stability. Furthermore, DSIPI@Li facilitates stable operation of the pouch cells under the constraints of a high-loading LiNi0.8Co0.1Mn0.1O2 cathode and low negative/positive capacity (N/P) ratio. This work presents a powerful strategy for designing artificial SEIs and high-performance LMBs.

Bi-Functional Interfacial Modification enables Highly-Exposed Zn(002) Crystal Facet towards Durable Zn Metal Batteries.

Zn-ion batteries (ZIBs) have garnered growing interest in large-scale energy storage devices for the high safety, high theoretical capacity and low electrochemical potential. Nevertheless, their widespread applications are significantly impeded by dendrite formation, hydrogen evolution and corrosion reactions of Zn anodes. Herein, a bi-functional polyacrylic acid (PAA) modified-Zn anode (Zn-PAA) is designed to concurrently inhibit Zn dendrite formation and alleviate side reactions. The bi-functional PAA coating not only selectively acid-etches the active Zn crystal facets to guide the planar deposition along the highly-exposed Zn(002) crystal facet, but also facilitate uniform Zn deposition through coordination between the polymer functional groups and Zn2+. Meanwhile, the electrically-insulated PAA protective layer effectively separates Zn anodes from the electrolyte and modulates the solvation structure of Zn2+.6H2O, significantly suppressing side reactions. Consequently, the assembled Zn-PAA//Zn-PAA symmetrical cell delivers an outstanding cycling stability of 1600 h at 1 mA cm-2 and 1 mAh cm-2. The assembled KVO//Zn-PAA full cell shows exceptional cycling stability over 1500 cycles at 2.0 A g-1 with a high Coulombic efficiency approaching 100%. The facile bi-functional surface modification strategy, which enables to finely tune the crystal facet texture and ion distribution manner, opens up a groundbreaking path towards safe and durable ZIBs.

Tailoring Zn2+ Flux by an Ion Acceleration Layer Modified Separator for High-Rate Long-Lasting Zn Metal Anodes.

A large concentration gradient originating from sluggish ion transport on the surface of Zn metal anodes will result in uneven Zn2+ flux, giving rise to severe dendrite growth, especially at high current density. Herein, an ion acceleration layer is introduced by a facile separator engineering strategy to realize modulated Zn2+ flux and dendrite-free deposition. Zinc hexacyanoferrate as the modifying agent featuring strong zincophilicity and rapid diffusion tunnel can enable fast trap for Zn2+ near the electrode surface and immediate transport onto deposition sites, respectively. The ion acceleration effect is substantiated by improved ion conductivity, decreased activated energy, and promoted Zn2+ transference number, which can moderate concentration gradient to guide homogenous Zn2+ flux distribution. As a result, the separator engineering guarantees Zn||Zn symmetrical cells with long-term stability of 2700 h at 2 mA cm-2, and 1770 h at a large current density of 10 mA cm-2. Moreover, cycling stability and rate capability for full cells with different cathodes can be substantially promoted by the modified separator, validating its superior practical feasibility. This study supplies a new scalable approach to tailoring ion flux near the electrode surface to enable robust Zn metal anodes at a high current density.

Pristine NASICON Electrolyte: A High Ionic Conductivity and Enhanced Dendrite Resistance Through Zirconia (ZrO2) Impurity-free Solid-Electrolyte Design.

Sodium batteries are considered a promising candidate for large-scale grid storage at tropical climate zone, and solid-state sodium metal batteries have a strong proposition as high energy density battery. The main challenge is to develop ultra-pure solid-state ceramic electrolyte and compatible metal interface. Here, a scalable and energy-efficient synthesis strategy of sodium (Na) Super Ionic CONductor, Na1+xZr2SixP3-xO12 (x = 2, NZSP) solid electrolyte, has been introduced with the complete removal of unreacted zirconium oxide (ZrO2) impurities. Additionally, the reaction mechanism for the formation of pure phase NZSP is reported for the first time. The NZSP prepared by utilizing the Zr precursor, i.e., tetragonal zirconium oxide (t-ZrO2) derived from the Zr(OH)4 gets quickly and completely consumed in the synthesis process leaving no unreacted monoclinic ZrO2 impurities. The synthesis process only needs a minimum stay of 4 h, which is three times less than the conventional synthesis method. The elimination of ZrO2 impurities results in a 2.5-fold reduction in grain boundary resistivity, showcasing a total ionic conductivity of 1.75 mS cm-1 at room temperature and a relative density of 98%. The prepared electrolyte demonstrates remarkable resistance to dendrite formation, as evidenced by a high critical current density value of 1.4 mA cm-2.

Zincophile Zn2+ Conductor Regulation by Ultrathin Nano MoO3 Coating for Dendrite-Free Zn Anode.

Aqueous battery with nonflammable and instinctive safe properties has received great attention. However, issues related to Zn anode such as side reactions and rampant dendrite growth hinder the long-term circulation of AZMBs. Herein, an ultrathin(35 nm) MoO3 coating is deposited on the Zn anode by means of vacuum vapor deposition for the first time. Due to the peculiar layer structure of MoO3, insertion of Zn2+ in ZnxMoO3 acts as Zn2+ ion conductor, which regulates Zn2+ deposition in an ordered manner. Additionally, the MoO3 coating can also inhibit the hydrogen evolution and corrosion reactions at the interface. Therefore, both Zn//MoO3@Cu asymmetric battery and Zn symmetric battery cells manage to deliver satisfactory electrochemical performances. The symmetric cell assembled with MoO3@Zn shows a significant long cycle life of more than 1600 h at a current density of 2 mA cm-2. Meanwhile, the MoO3@Zn//Cu asymmetric cell exhibits an ultrahigh Zn deposition/stripping efficiency of 99.82% after a stable cycling of 650 h at 2 mA cm-2. This study proposes a concept of "zincophile Zn2+ conductor regulation" to dictate Zn electrodeposition and broadens novel design of vacuum evaporation for nano MoO3 modified Zn anodes.

Ferroelectric Interfaces for Dendrite Prevention in Zinc-Ion Batteries.

Aqueous rechargeable zinc-ion batteries (ZIBs) are increasingly recognized as promising energy storage systems for mini-grid and mini-off-grid applications due to their advantageous characteristics such as high safety, affordability, and considerable theoretical capacity. However, the long-term cycling performance of ZIBs is hampered by challenges including the uncontrolled dendrite formation, the passivation, and the occurrence of the hydrogen evolution reaction (HER) on the Zn anode. In this study, enhancing ZIB performance by implementing oxide material coatings on Zn metal, serving as a physical barrier at the electrode-electrolyte interfaces to mitigate dendrite growth and suppress the HER is concentrated. Specifically, the mechanisms through which the n-type semiconductor TiO2 coated Zn anode establishes ohmic contact with Zn, and the high-dielectric BaTiO3 (BTO) coated Zn anode fosters Maxwell-Wagner polarization with ferroelectric properties, significantly inhibiting dendrite growth and side reactions, thereby resulting in a highly stable Zn anode for efficient aqueous ZIBs is explored. This advanced BTO/Zn electrode demonstrates an extended lifespan of over 700 h compared to bare Zn and TiO2/Zn anodes. Additionally, full-cell aqueous ZIBs incorporating BTO/Zn//VO2 (B) batteries exhibit superior rate capabilities, high capacity, and sustained cycle life.

Heteroatom Immobilization Engineering toward High-Performance Metal Anodes.

Heteroatom immobilization engineering (HAIE) is becoming a forefront approach in materials science and engineering, focusing on the precise control and manipulation of atomic-level interactions within heterogeneous systems. HAIE has emerged as an efficient strategy to fabricate single-atom sites for enhancing the performance of metal-based batteries. Despite the significant progress achieved through HAIE in metal anodes for metal-based batteries, several critical challenges such as metal dendrites, side reactions, and sluggish reaction kinetics are still present. In this review, we delve into the fundamental principles underlying heteroatom immobilization engineering in metal anodes, aiming to elucidate its role in enhancing the electrochemical performance in batteries. We systematically investigate how HAIE facilitates uniform nucleation of metal in anodes, how HAIE inhibits side reactions at the metal anode-electrolyte interface, and the role of HAIE in promoting the desolvation of metal ions and accelerating reaction kinetics within metal-based batteries. Finally, we discuss various strategies for implementing HAIE in electrode materials, such as high-temperature pyrolysis, vacancy reduction, and molten-salt etching and anchoring. These strategies include selecting appropriate heteroatoms, optimizing immobilization methods, and constructing material architectures. They can be utilized to further refine the performance to enhance the capabilities of HAIE and facilitate its widespread application in next-generation metal-based battery technologies.

An In Situ Generated Organic/Inorganic Hybrid SEI Layer Enables Li Metal Anodes with Dendrite Suppression Ability, High-Rate Capability, and Long-Life Stability.

High-quality solid electrolyte interphase (SEI) layers can effectively suppress the growth of Li dendrites and improve the cycling stability of lithium metal batteries. Herein, 1-(6-bromohexanoyl)-3-butylurea is used to construct an organic/inorganic hybrid (designated as LiBr-HBU) SEI layer that features a uniform and compact structure. The LiBr-HBU SEI layer exhibits superior electrolyte wettability and air stability as well as strong attachment to Li foils. The LiBr-HBU SEI layer achieves a Li+ conductivity of 2.75 × 10-4 S cm-1, which is ≈50-fold higher than the value measured for a native SEI layer. A Li//Li symmetric cell containing the LiBr-HBU SEI layer exhibits markedly improved cyclability when compared with the cell containing a native SEI layer, especially at a high current density (e.g., cycling life up to 1333 h at 15 mA cm-2). The LiBr-HBU SEI layer also improves the performance of lithium-sulfur cells, particularly the rate capability (548 mAh g-1 at 10 C) and cycling stability (513 mAh g-1 at 0.5 C after 500 cycles). The methodology described can be extended to the commercial processing of Li metal anodes as the artificial SEI layer also protects Li metal against corrosion.

Dendrite-free zinc metal anode for long-life zinc-ion batteries enabled by an artificial hydrophobic-zincophilic coating.

Considering the desired energy density, safety and cost-effectiveness, rechargeable zinc-ion batteries (ZIBs) are regarded as one of the most promising energy storage units in next-generation energy systems. Nonetheless, the service life of the current ZIBs is significantly limited by rampant dendrite growth and severe parasitic reactions occurring on the anode side. To overcome these issues caused by poor interfacial ionic conduction and water erosion, we have developed a facile strategy to fabricate a uniform zinc borate layer at the zinc anode/electrolyte interface (ZnBO). Such protective layer integrates superhydrophobic-zincopholic properties, which can effectively eliminate the direct contact of water molecules on the anode, and homogenize the interfacial ionic transfer, thereby enhancing the cyclic stability of the zinc plating/stripping. As a result, the as-prepared ZnBO-coated anode exhibits extended lifespan of 1200 h at 1 mA cm-2 and demonstrates remarkable durability of 570 h at 20 mA cm-2 in Zn||Zn symmetric cells. Additionally, when coupled to an NH4V4O10 (NVO) cathode, it also delivers a superior cyclability (203.5 mAh/g after 2000 cycles at 5 A/g, 89.3 % capacity retention) in coin full cells and a feasible capacity of 2.5 mAh at 1 A/g after 200 cycles in pouch full cells. This work offers a unique perspective on integrating hydrophobicity and zincophilicity at the anode/electrolyte interface through an artificial layer, thereby enhancing the cycle lifespan of ZIBs.

Study on an Interpenetrating Artificial SEI for Lithium Metal Anode Modification and Fast Charging Characterization.

Artificial SEI is one of the effective strategies to improve lithium dendrites and suppress side reactions. However, the role of SEI components and distribution on the modification of the lithium metal anode remains unclear. Therefore, in this study, the oxygen-sulfur (O-S) component and its distribution in SEI were modulated by designing experiments, and then the mechanism of its action was deeply investigated. The study is based on an in-depth analysis of the properties of lithium sulfide (Li2S) and lithium oxide (Li2O) as SEI layer materials and effectively combines them in an ether electrolyte environment to form an innovative SEI structure. The experimental results show that the optimal SEI modulation condition is O120-S10. O120-S10 significantly improves the kinetic performance of electrochemical reactions, reduces the film resistance, and achieves cycling stability of up to 2100 h during high-capacity lithium deposition/stripping at 5 mAh cm-2. When used in conjunction with a ternary cathode material (NCM811), the O120-S10 demonstrates excellent performance under high rate charge/discharge conditions at 10C. After 1500 cycle tests, the battery's specific capacity was maintained at 90 mAh g-1 and the Coulombic efficiency reached 98.52%. Through X-ray photoelectron spectroscopy (XPS) analysis, the vertical structure and ratio distribution of components in SEI were revealed in detail, and the optimal component ratios of Li2S 46.48%, Li2O 46.02%, and Li2CO3 7.50% were determined. The mechanism of action is to achieve a 1 + 1 > 2 superlinear synergistic effect and fast charging performance by combining the ability of Li2O's low lithium ion diffusion barrier with Li2S's ability to inhibit the growth of lithium dendrites.

Areal specializations in the morpho-electric and transcriptomic properties of primate layer 5 extratelencephalic projection neurons.

Large-scale analysis of single-cell gene expression has revealed transcriptomically defined cell subclasses present throughout the primate neocortex with gene expression profiles that differ depending upon neocortical region. Here, we test whether the interareal differences in gene expression translate to regional specializations in the physiology and morphology of infragranular glutamatergic neurons by performing Patch-seq experiments in brain slices from the temporal cortex (TCx) and motor cortex (MCx) of the macaque. We confirm that transcriptomically defined extratelencephalically projecting neurons of layer 5 (L5 ET neurons) include retrogradely labeled corticospinal neurons in the MCx and find multiple physiological properties and ion channel genes that distinguish L5 ET from non-ET neurons in both areas. Additionally, while infragranular ET and non-ET neurons retain distinct neuronal properties across multiple regions, there are regional morpho-electric and gene expression specializations in the L5 ET subclass, providing mechanistic insights into the specialized functional architecture of the primate neocortex.