Sodium Ion Transport Research Articles

NaSn2F5 nanocluster composed of nanoparticles with matched lattices induced by dislocations: Accelerated sodium-ion transport via in situ oxidation in solid-state sodium metal battery

Na metal batteries using inorganic solid-state electrolytes (SSEs) have attracted extensive attention due to their superior safety and high energy density. However, their development is plagued by the unclear structural/volumetric evolution of SSEs and the corresponding Na+ migration mechanisms. In this work, NaSn2F5 (NSF) clusters are composed of nanoparticles (NPs) with matched lattices induced by dislocations, which can mitigate the volume swelling/shrinkage of the NPs. NSF behaves like a single ion conductor with a high Na+ transference number (tNa+) of 0.79. Specially, the ionic conductivity (σ) of NSF is increased from 7.64 × 10-6 to 5.42 × 10-5 S cm−1 after partial irreversible oxidation of Sn2+ (0.118 Å) → Sn4+ (0.069 Å) with the shrunk ionic radius during the charge process, giving more spaces for Na+ migration. Furthermore, a poly(acrylonitrile)-NaSn2F5-NaPF6 composite polymer electrolyte (NSF CPE) was fabricated with a σ of 4.13 × 10-4 S cm−1 and a tNa+ of 0.60. The NSF CPE-based symmetric cell can operate over 3000 h due to the couplings between the different components in NSF CPE, which is beneficial for ion transfer and the construction of stable solid electrolyte interface. And the quasi-solid-state Na|NSF CPE|Na3V2(PO4)3 full cell displays excellent electrochemical performance.

Vascular tissue-derived hard carbon with ultra-high rate capability for sodium-ion storage

Vascular tissue helps quickly pass the nutrients and water through the plant. Inspiringly, the transport of electrolyte solutions within such biological tissue may also play an essential role in governing the high-current performance of sodium-ion storage. Herein, we report a facile and efficient approach to fabricate a vascular tissue-derived hard carbon (VHC) by an integrated procedure of leave stripping, carbonization and alkali/acid washing. By meticulously adjusting the pyrolysis temperatures, hierarchical microchannel carbon with abundant turbostratic nanodomains, suitable pore size and special surface functional groups can be obtained, enabling high specific capacity and excellent rate performances. It is believed that the vascular tissue-derived carbon can significantly shorten sodium ion transport paths and further enhance the storage performance on the surface and within the electrode materials, making it a promising candidate for sodium-ion batteries.

The Eleutherococcus senticosus fruits' intractum affects changes in the transepithelial electric potential in the distal section of the rabbit's large intestine and inhibits hyaluronidase

Ethnopharmacological relevanceEleutherococcus senticosus (Rupr. et Maxim.) Maxim. has been used in traditional Russian medicine due to its recognized immunostimulant and anti-inflammatory activities. Compounds present in the fruits have demonstrated the capability to modulate the activity of enzymes such as hyaluronidase, suggesting their potential value in the development of effective therapies for various conditions where anti-inflammatory properties are beneficial, such as gastrointestinal diseases and tumor growth. Aim of the studyIn order to support the use of the fruits in folk medicine, this study is aimed to evaluate, post-mortem, the impact of E. senticosus fruits intractum (40 % extract made from fresh fruits) on the transepithelial electrogenic transport of sodium ions in the colon. The objective of this study was also to examine the impact of the intractum on proinflammatory serum hyaluronidase in children diagnosed with acute leukemia. MethodsThe study employed the Ussing technique to examine electrophysiological characteristics of isolated epithelial tissue, using the distal colon wall isolated from 10 New Zealand white male rabbits. The effect of the intractum on the inhibition of human serum hyaluronidase was examined with turbidimetric screening methods, using the blood samples collected from patients diagnosed with acute leukemia. ResultsFor the first time, we discovered that the intractum used in the stimulation fluid, caused hyperpolarization reactions in colon tissue. Statistical analysis showed that these reactions were significantly different in relation to the control. The intractum significantly inhibited hyaluronidase activity with the mean value by group of 60 %, and 40 % for aescin used as a control. ConclusionThe results support the traditional use of the fruits in inflammatory-related diseases. The use of intractum of E. senticosus on the distal colon wall demonstrates its protective effect on the wall integrity and in a relation to hyaluronidase inhibition may additionally indicate its anti-inflammatory property. Thus, the results mean that the intractum may be used in colon-related diseases.

Multi-interface Combination of Bimetallic Selenide and V4C3Tx MXene for High-Rate and Ultrastable Sodium Storage Devices.

Sodium-ion batteries (SIBs) have great potential as electrochemical energy storage systems; however, their commercial viability is limited by the lack of anode materials with fast charge/discharge rates and long lifetimes. These challenges were addressed by developing a multi-interface design strategy using FCSe (FeSe2/CoSe2) nanoparticles on V4C3Tx MXene nanosheets as conductive substrates. The heterogeneous interface created between the two materials provided high-speed transport of sodium ions, suppressed the chalking-off of nanoparticles, and improved the cycling stability. Additionally, the Fe-Co bonds generated at the interface effectively relieved mechanical stress, further enhancing the electrode durability. The C@FCSe@V4C3 electrode exhibited high-speed charging and discharging characteristics, and maintained a high specific capacity of 260.5 mAh g-1 even after 15,000 cycles at 10 A g-1, with a capacity retention rate of 50.2% at an ultrahigh current density of 20 A g-1. Furthermore, the composite displayed a good cycling capability in the fast discharge and slow charge mode. This demonstrates its promising commercial potential. This multi-interface design strategy provides insights and guidance for solving the reversibility and cycling problems of transformed selenide anode materials.

Enhancing Sodium-Ion Transport by Hollow Nanotube Structure Design of a V5S8@C Anode for Sodium-Ion Batteries.

V5S8 has received extensive attention in the field of sodium-ion batteries (SIBs) due to its two-dimensional (2D) layered structure, and weak van der Waals forces between V-S accelerate the transport of sodium ions. However, the long-term cycling of V5S8 still suffers from volume expansion and low conductivity. Herein, a hollow nanotube V5S8@C (H-V5S8@C) with improved conductivity was synthesized by a solvothermal method to alleviate cracking caused by volume expansion. Benefiting from the large specific surface area of the hollow nanotube structure and uniform carbon coating, H-V5S8@C exhibits a more active site and enhanced conductivity. Meanwhile, the heterojunction formed by a few residual MoS2 and the outer layer of V5S8 stabilizes the structure and reduces the ion migration barrier with fast Na+ transport. Specifically, the H-V5S8@C anode provides an enhanced rate performance of 270.1 mAh g-1 at 15 A g-1 and high cycling stability of 291.7 mAh g-1 with a retention rate of 90.98% after 300 cycles at 5 A g-1. This work provides a feasible approach for the structural design of 2D layered materials, which can promote the practical application of fast-charging sodium-ion batteries.

Enabling Further Organic Electrolyte Infiltration of Cellulose-Based Separators via Defect-Rich Polypyrrole Modification for High Sodium Ion Transport in Sodium Metal Batteries.

Sodium metal batteries (SMBs) have high-density and cost-effective characteristics as one of the energy storage systems, but uncontrollable dendrite growth and poor rate performance still hinder their practical applications. Herein, a nitrogen-rich modified cellulose separator with released abundant ion transport tunnels in organic electrolyte was synthesized by in situ polymerization of polypyrrole, which is based on the high permeability of cellulose in aqueous solution and the interfacial interaction between cellulose and polypyrrole. Meanwhile, the introduction of abundant structural defects such as branch chains, oxygen-containing functional groups, and imine-like structure to disrupt polypyrrole conjugation enables the utilization of conductive polymers in composite separator applications. With the electrolyte affinity surface on, the modified separator exhibits reinforced electrolyte uptake (254%) and extended electrolyte wettability, thereby leading to accelerated ionic conductivity (2.77 mS cm-1) and homogeneous sodium deposition by facilitating the establishment of additional pathways for ion transport. Benefiting from nitrogen-rich groups, the polypyrrole-modified separator demonstrates selective Na+ transport by the data of improved Na+ transference number (0.62). Owing to the above advantages, the battery assembled with the modified separators exhibits outstanding rate performance and prominent capacity retention two times that of the pristine cellulose separator at a high current density under the condition of fluorine-free electrolyte.

Chemical‐Stabilized Aldehyde‐Tuned Hydrogen‐Bonded Organic Frameworks for Long‐Cycle and High‐Rate Sodium‐Ion Organic Batteries

AbstractHydrogen‐bonded organic frameworks (HOFs) are considered as potential choice for future energy storage systems due to their adjustable chemistry, environment friendliness, and cost‐effectiveness. In this study, structurally stabilized and aldehyde‐tuned hydrogen‐bonded organic frameworks (HOFs‐8) are designed and prepared to contain arrayed electronegative sites for sodium‐ion storage. Benefitting from the flexible hydrogen bond and unique structural symmetry, HOFs‐8 can achieve efficient utilization of the active sites and fast transport of sodium ions and electrons. The HOFs‐8 electrode exhibits an impressive lifespan of 5000 cycles at 3.66 A g−1 (20 C). In situ Fourier Transform infrared spectroscopy (in situ FT‐IR) and ex situ X‐ray Photoelectron Spectroscopy (ex situ XPS) analyses are performed to illustrate the mechanism of sodium‐ion storage involving aldehyde‐tuned C═O. Additionally, flexible hydrogen bonds in HOFs materials with unique structural symmetries are investigated to elucidate the mechanism of hydrogen bonding for improving their electrochemical properties. Density functional theory (DFT) simulations verified that HOFs‐8 has excellent Na+ diffusion kinetics, enabling it to demonstrate outstanding rate capability. This work offers insight into the design of new electrodes and improved HOFs, which are expected to have tremendous potential in energy storage systems.

Clinical pathological and genetic mutation characteristics of conjunctival lymphoepithelial carcinoma

Objective: To analyze the clinical pathological and genetic mutation characteristics of conjunctival lymphoepithelial carcinoma. Methods: A retrospective case series study was conducted. Data from three patients diagnosed with conjunctival lymphoepithelial carcinoma and treated with tumor resection surgery at Tianjin Eye Hospital from January 2006 to December 2022 were collected. Four paraffin specimens (including one patient undergoing two surgeries) were subjected to immunohistochemical staining for epithelial antigen and lymphocytic antigen. Epstein-Barr virus (EBV)-encoded RNA (EBER) was detected using in situ hybridization, and whole-exome sequencing was performed on three specimens from two patients using next-generation sequencing methods. Results: All three patients were males aged over 65, with a disease duration ranging from 3 to 44 months. The tumors were unilateral, located on the bulbar or limbal conjunctiva, appearing red, with a maximum diameter of 4-20 mm. Imaging examinations revealed anterior location of the tumors with no involvement of the orbital bone, extraocular muscles, optic nerve, or paranasal sinuses. No local lymph node metastasis was observed in any patient. Pathological findings included undifferentiated carcinoma nests with significant reactive lymphocytic and plasma cell infiltration. Tumor cells were positive for pan-cytokeratin (CK-pan), epithelial membrane antigen (EMA), tumor protein 40 (p40), and tumor protein 63 (p63), with a cell proliferation index (Ki67) exceeding 80%. Cluster of differentiation 20 (CD20), CD3, and CD8 were positive for lymphocytes. In situ hybridization showed partial tumor cell expression of EBER in two specimens of one patient. Whole-exome sequencing revealed 58, 50, and 36 mutated genes in the three specimens, with enriched signaling pathways including melanoma signaling pathway, Notch1 signaling pathway, and RHOQ GTP cycle; enriched biochemical processes included amino acid starvation response, programmed cell death, regulation of lipid synthesis, sodium ion transport, and chromosome segregation. The common mutated gene in all three specimens was SZT2, and SZT2 was involved in the amino acid starvation response. One patient underwent a second complete resection surgery 40 months after partial excision, while the other two underwent complete resection surgery without recurrence. Two patients did not undergo radiation or chemotherapy, and one was lost to follow-up. Conclusions: Conjunctival lymphoepithelial carcinoma is associated with prominent lymphocytic and plasma cell infiltration, some cases are associated with EBV infection, and SZT2 mutations are present in conjunctival lymphoepithelial carcinoma.

Variations in Physiological and Biochemical Characteristics of Kalidium foliatum Leaves and Roots in Two Saline Habitats in Desert Region

Salt stress is a key environmental factor that has adverse effects on plant growth and development. High salinity induces a series of structural and functional changes in the morphological and anatomical features. The physiological and biochemical changes in K. foliatum in response to salt stress in natural environments are still unclear. Based on this, this study compared and analyzed the differences in the physiological and biochemical indicators between the leaf and root tissues in high-salt and low-salt habitats, selecting K. foliatum as the research object. The results showed that the chlorophyll contents in the leaves of K. foliatum decreased in the high-salt habitat, while the thicknesses of the upper and lower epidermises, as well as the thicknesses of the palisade tissue, significantly increased. The high-salt environment led to decreases in the N and P contents in the leaves and root tissues of K. foliatum, resulting in changes in the stoichiometric ratio of elements. The concentrations of C, N, and P in the roots of K. foliatum were lower than those in the leaves. The accumulation of Na+ in the K. foliatum roots was greater than that in the leaves, and the roots could promote the transport of sodium ions to the leaves. The contents of starch and soluble sugar in the leaves showed higher proportions in the high-salt habitat than in the low-salt habitat, while the changes in the roots and leaves were the opposite. As the salt content increased, the proline contents in the leaves and roots of K. foliatum significantly increased, and the proline contents in the roots of K. foliatum were lower than those in the leaves. The leaves and roots exhibited higher levels of peroxidase and superoxide enzymes in the high-salinity habitat than in the low-salinity habitat. The superoxide dismutase (SOD) activity of the K. foliatum leaves and catalase (CAT) activity of the roots were the “central traits” in the high-salt habitat. In the low-salt habitat, the leaf malondialdehyde (MDA) and root C/N were the central traits of the leaves and roots, indicating that K. foliatum adapts to changes in salt environments in different ways.

Potential of Modulating Aldosterone Signaling and Mineralocorticoid Receptor with microRNAs to Attenuate Diabetic Kidney Disease.

Diabetic Kidney Disease (DKD) is a significant complication of diabetes and primary cause of end-stage renal disease globally. The exact mechanisms underlying DKD remain poorly understood, but multiple factors, including the renin-angiotensin-aldosterone system (RAAS), play a key role in its progression. Aldosterone, a mineralocorticoid steroid hormone, is one of the key components of RAAS and a potential mediator of renal damage and inflammation in DKD. miRNAs, small noncoding RNA molecules, have attracted interest due to their regulatory roles in numerous biological processes. These processes include aldosterone signaling and mineralocorticoid receptor (MR) expression. Numerous miRNAs have been recognized as crucial regulators of aldosterone signaling and MR expression. These miRNAs affect different aspects of the RAAS pathway and subsequent molecular processes, which impact sodium balance, ion transport, and fibrosis regulation. This review investigates the regulatory roles of particular miRNAs in modulating aldosterone signaling and MR activation, focusing on their impact on kidney injury, inflammation, and fibrosis. Understanding the complex interaction between miRNAs and the RAAS could lead to a new strategy to target aldosterone signaling and MR activation using miRNAs. This highlights the potential of miRNA-based interventions for DKD, with the aim of enhancing kidney outcomes in individuals with diabetes.

A composite gel polymer electrolyte for sodium metal battery at a wide temperature range

AbstractSodium‐metal batteries (SMBs) are considered a promising alternative to lithium‐metal batteries due to their high‐energy density, low cost, and good low‐temperature performance. However, the serious side reactions and dendrites growth during the process of sodium ions deposition/stripping are the bottleneck that inhibits the further capitalization of SMBs, especially at low temperatures. Herein, a porous framework of 50 μm thickness composite gel‐polymer‐electrolyte (GPE) supported by polyvinylidene difluoride nanowires membrane and Na3Zr2Si2PO12 ceramic particles is proposed to tackle the issues. This GPE not only has high ionic conductivity but also can promote the uniform transportation of sodium ions to form a stable and dense metal‐GPE interfacial layer, which can effectively inhibit the side reactions and dendrites growth in a wide temperature range. The assembled Na//GPE//Na3V2(PO4)3 full battery provides a specific capacity of 100 mAh g−1 at 10 C for more than 3000 cycles calendar life at room temperature. Moreover, the full battery based on this GPE has an extraordinary performance at low temperatures, reaching a specific capacity of 93 and 61 mAh g−1 at 0.5 and 1 C at −20°C, respectively. This work provides a reliable solution for low‐temperature applications of high‐energy density and long‐cycle life SMBs.

Tmprss2 maintains epithelial barrier integrity and transepithelial sodium transport.

The mouse cortical collecting duct cell line presents a tight epithelium with regulated ion and water transport. The epithelial sodium channel (ENaC) is localized in the apical membrane and constitutes the rate-limiting step for sodium entry, thereby enabling transepithelial transport of sodium ions. The membrane-bound serine protease Tmprss2 is co-expressed with the alpha subunit of ENaC. αENaC gene expression followed the Tmprss2 expression, and the absence of Tmprss2 resulted not only in down-regulation of αENaC gene and protein expression but also in abolished transepithelial sodium transport. In addition, RNA-sequencing analyses unveiled drastic down-regulation of the membrane-bound protease CAP3/St14, the epithelial adhesion molecule EpCAM, and the tight junction proteins claudin-7 and claudin-3 as also confirmed by immunohistochemistry. In summary, our data clearly demonstrate a dual role of Tmprss2 in maintaining not only ENaC-mediated transepithelial but also EpCAM/claudin-7-mediated paracellular barrier; the tight epithelium of the mouse renal mCCD cells becomes leaky. Our working model proposes that Tmprss2 acts via CAP3/St14 on EpCAM/claudin-7 tight junction complexes and through regulating transcription of αENaC on ENaC-mediated sodium transport.

Interface Ionic/Electronic Redistribution Driven by Conversion-Alloy Reaction for High-Performance Solid-State Sodium Batteries.

NASICON-type Na+ conductors show a great potential to realize high performance and safety for solid-state sodium metal batteries (SSSMBs) owing to their superior ionic conductivity, high chemical stability, and low cost. However, the interfacial incompatibility and sodium dendrite hazards still hinder its applications. Herein, a conversion-alloy reaction-induced interface ionic/electronic redistribution strategy, constructing a gradient sodiophilic and electron-blocking interphase consisting of sodium-tin (Na-Sn) alloy and sodium fluoride (NaF) between NASICON ceramic electrolyte and Na anode is proposed. The NaxSny alloy-rich layer near the side of the sodium electrode acts as a superior conductor to enhance the anodic sodium-ion transport dynamics while the NaF-rich layer near the side of the ceramic electrolyte serves as an electron insulator to confine the interfacial electron turning ability, achieving uniform and dendrite-free Na deposition during the cycling. Profiting from the synergistic effect of the gradient interphase, the critical current density (CCD) of the assembled Na symmetric cell is significantly increased to 1.7mAcm-2 and the cycling stability of that is as high as 1200h at 0.5mAcm-2. Moreover, quasi-solid-state sodium batteries with both Na3V2(PO4)3 and NaNi1/3Fe1/3Mn1/3O2 cathode display outstanding electrochemical performance.

Enhancing the performance of NaVPO4F cathode materials for sodium-ion batteries through graphite incorporation and polyethylene glycol 6000 modification

An NVPF material with good performance was synthesized, showing a stable structure and efficient and fast sodium ion transport.

Synergistic interface and structural engineering for high initial coulombic efficiency and stable sodium storage in metal sulfides.

Transition metal sulfides (TMS) have gained significant attention as potential anode materials for sodium ion batteries (SIBs) due to their high theoretical capacity and abundance in nature. Nevertheless, their practical use has been impeded by challenges such as large volume changes, unstable solid electrolyte interphase (SEI), and low initial coulombic efficiency (ICE). To address these issues and achieve both long-term cycling stability and high ICE simultaneously, we present a novel approach involving surface engineering, termed as the "dual-polar confinement" strategy, combined with interface engineering to enhance the electrochemical performance of TMS. In this approach, CoS crystals are meticulously coated with polar TiO2 and embedded within a polar S-doped carbon matrix, forming a composite electrode denoted as CoS/TiO2-SC. Significantly, an ether-based electrolyte with chemical stability and optimized solvation properties synergistically interacts with the Co-S-C bonds to create a stable, ultra-thin SEI. This concerted effect results in a notably high ICE, reaching approximately 96%. Advanced characterization and theoretical simulations confirm that the uniform surface modification effectively facilitates sodium ion transport kinetics, restrains electrode pulverization, and concurrently enhances interaction with the ether-based electrolyte to establish a robust SEI. Consequently, the CoS/TiO2-SC electrode exhibits high reversible capacity, superior rate capability, and outstanding cycling stability.

Ion conduction and phase behaviour in dual cation polyelectrolyte blends for sodium-ion batteries

The goal of this work is to develop polymer-based solid-state electrolytes for sodium-ion battery applications. Two polymers are blended in order to reduce the Tg and decouple ionic conductivity from polymer segmental motion. Furthermore, the addition of plasticizers further enhances the ionic conductivity.

Ionic-conductive sodium titanate to boost sodium-ion transport kinetics of hard carbon anode in sodium-ion batteries

Hard carbon with abundant resources, low-cost, and high specific capacity, is a promising anode material for large-scale sodium-ion batteries. However, the poor rate performance of hard carbon suffers from serious challenges due to sluggish ion transport dynamic behavior, especially at low potential, in high power density of sodium-ion batteries. To address this issue, we introduce an ionic-conductive sodium-titanate into hard carbon to boost its sodium-ion transport kinetics via constructing a dual ionic-electronic conducting network in hard carbon anode. Benefiting from our design, the optimized hard carbon-sodium titanate electrode achieves high specific capacity of 137 mAh g−1 at a high current density of 10 A g−1, compared to that of hard carbon of 25 mAh g−1 at 10 A g−1. Remarkably, it also exhibits an excellent capacity retention of 71.4% at the current density of 2.0 A g−1 after 800 cycles. This work presents a practical strategy for high-rate hard carbon design and provides valuable insights into the construction of high-rate anode for advanced sodium-ion batteries.

Reducing Chloride Ion Permeation during Seawater Electrolysis Using Double-Polyamide Thin-Film Composite Membranes.

Low-cost polyamide thin-film composite membranes are being explored as alternatives to expensive cation exchange membranes for seawater electrolysis. However, transport of chloride from seawater to the anode chamber must be reduced to minimize the production of chlorine gas. A double-polyamide composite structure was created that reduced the level of chloride transport. Adding five polyamide layers on the back of a conventional polyamide composite membrane reduced the chloride ion transport by 53% and did not increase the applied voltage. Decreased chloride permeation was attributed to enhanced electrostatic and steric repulsion created by the new polyamide layers. Charge was balanced through increased sodium ion transport (52%) from the anolyte to the catholyte rather than through a change in the transport of protons and hydroxides. As a result, the Nernstian loss arising from the pH difference between the anolyte and catholyte remained relatively constant during electrolysis despite membrane modifications. This lack of a change in pH showed that transport of protons and hydroxides during electrolysis was independent of salt ion transport. Therefore, only sodium ion transport could compensate for the reduction of chloride flux to maintain the set current. Overall, these results prove the feasibility of using a double-polyamide structure to control chloride permeation during seawater electrolysis without sacrificing energy consumption.

Fluorinated and safety-reinforced copolymer solid electrolytes for high-voltage all-solid-state sodium metal batteries

Poly (ethylene oxide)-based all-solid-state electrolytes are extensively regarded as highly promising contenders for the upcoming era of sodium metal batteries. Nevertheless, the intrinsic elevated highest occupied molecular orbital (HOMO) and the strong sodium-ion adsorption energy lead to a narrow electrochemical stability window (ESW) and a sluggish ion transport kinetics, thus retarding its widespread application in high-voltage batteries. About these shortcomings, we propose a strategy of fluorine substitution through a ready UV-initiated free-radical copolymerization to regulate the orbital level sodium-ion adsorption energy of poly (ethylene oxide) electrolytes. The characterization confirmed the success in the introduction of fluorine into the polymer (referred to as P-co-F). DFT calculations demonstrated a lower HOMO (-7.061 eV) in fluorine-substituted polymer electrolyte, which enabled to expand the ESW up to 5.55 V. Besides, the sodium-ion adsorption energy on P-co-F was decreased from −2.78 eV to −3.43 eV, facilitating the rapid transport of sodium ion. In addition, Polyethylene terephthalate (PET) was adopted as a support frame, which would reinforce the mechanical properties of polymer electrolytes. The electrochemical tests suggested P-co-F exhibited a profound interfacial stability in the Na//Na symmetrical system throughout an operational duration of 4690 h at 0.1 mA cm−2. The assembled all-solid-state battery manifested remarkable stability during continuous cycling at room temperature for 200 cycles, retaining an impressive 96.59 % of its initial capacity at 0.1C. The intriguing fluorine-induced effect, coupled with a cost-effective safety substrate, will provide valuable insights for the rational molecular design of innovative electrolytes and easy production scalability for all-solid-state Na metal batteries.

Disclosing the Interfacial Electrolyte Structure of Na-Insertion Electrode Materials: Origins of the Desolvation Phenomenon.

Among a variety of promising cathode materials for Na-ion batteries, polyanionic Na-insertion compounds are among the preferred choices due to known fast sodium transfer through the ion channels along their framework structures. The most interesting representatives are Na3V2(PO4)3 (NVP) and Na3V2(PO4)2F3 (NVPF), which display large Na+ diffusion coefficients (up to 10-9 m2 s-1 in NVP) and high voltage plateaux (up to 4.2 V for NVPF). While the diffusion in the solid material is well-known to be the rate-limiting step during charging, already being thoroughly discussed in the literature, interfacial transport of sodium ions from the liquid electrolyte toward the electrode was recently shown to be important due to complex ion desolvation effects at the surface. In order to fill the blanks in the description of the electrode/electrolyte interface in Na-ion batteries, we performed a molecular dynamics study of the local nanostructure of a series of carbonate-based sodium electrolytes at the NVP and the NVPF interfaces along with careful examination of the desolvation phenomenon. We show that the tightness of solvent packing at the electrode surface is a major factor determining the height of the free energy barrier associated with desolvation, which explains the differences between the NVP and the NVPF structures. To rationalize and emphasize the remarkable properties of this family of cathode materials, a complementary comparative analysis of the same electrolyte system at the carbon electrode interface was also performed.