Role In Ion Transport Research Articles

The Transformative Role of Nano-SiO2 in Polymer Electrolytes for Enhanced Energy Storage Solutions

In lithium–polymer batteries, the electrolyte is an essential component that plays a crucial role in ion transport and has a substantial impact on the battery’s overall performance, stability, and efficiency. This article presents a detailed study on developing nanostructured composite polymer electrolytes (NCPEs), prepared using the solvent casting technique. The materials selected for this investigation include poly(vinyl chloride) (PVC) as the host polymer, lithium bromide (LiBr) as the salt, and silica (SiO2) as the nanofiller. The addition of nano-SiO2 dramatically enhanced the ionic conductivity of the electrolytes, with the highest value of 6.2 × 10−5 Scm−1 observed for the sample containing 7.5 wt% nano-SiO2. This improvement is attributed to an increased amorphicity resulting from the interactions between the polymer, salt, and filler components. A structural analysis of the prepared NCPEs using X-ray diffraction revealed the presence of both crystalline and amorphous phases, further validating the enhanced ionic transport. Additionally, the thermal stability of the NCPEs was found to be excellent, withstanding temperatures up to 334 °C, thereby reinforcing their potential application in lithium–polymer batteries. This work explores the electrochemical performance of a fabricated lithium-ion-conducting primary electrochemical cell (Zn + ZnSO4·7H2O|PVC: LiBr: SiO2|PbO2 + V2O5), which demonstrated an open circuit voltage of 2.15 V. The discharge characteristics of the fabricated cell were thoroughly studied, showcasing the promising potential of these NCPEs. With the support of superior morphological and electrical properties, as-prepared electrolytes offer an effective pathway for future advancements in lithium–polymer battery technology, making them a highly viable candidate for enhanced energy storage solutions.

A dual functional Co3O4 thin film with remarkable electrochromic and energy storage performance in the electrolytes of choline chloride and urea

The electrolyte layer plays an important role in ion transport in electrochromic devices, and the optimized preparation of efficient electrolytes can positively affect the conduction process on the electrode surface and at the electrode-electrolyte interface.In this study, we start from a green perspective while improving the performance. Combined with typical eutectic solvents: choline chloride and urea materials. A suitable ratio favorable for the reaction of Co3O4 film is explored and combined with sodium hydroxide, a traditional electrolyte, to enhance the electrochromic performance.The electrochromic and electrochemical properties of Co3O4 films prepared via the sol-gel method in the novel electrolyte were then evaluated. The results show that the performance has been greatly improved, the transmittance rate is 2.5 times higher than the original, the coloration efficiency is 5.8 times higher than the original, and it is more stable and has higher charging and discharging efficiency. This presents a promising avenue for the advancement of oxide films as bifunctional materials for electrochromism and energy storage. The newly developed electrolyte may prove beneficial in enhancing the performance and stability of electrochromic devices through the use of alkaline electrolytes.

Solid-State Electrolytes: Probing Interface Regulation from Multiple Perspectives.

Solid-state electrolytes (SSEs), as the heart of all-solid-state batteries (ASSBs), are recognized as the next-generation energy storage solution, offering high safety, extended cycle life, and superior energy density. SSEs play a pivotal role in ion transport and electron separation. Nonetheless, interface compatibility and stability issues pose significant obstacles to further enhancing ASSB performance. Extensive research has demonstrated that interface control methods can effectively elevate ASSB performance. This review delves into the advancements and recent progress of SSEs in interfacial engineering over the past years. We discuss the detailed effects of various regulation strategies and directions on performance, encompassing enhancing Li+ mobility, reducing energy barriers, immobilizing anions, introducing interlayers, and constructing unique structures. This review offers fresh perspectives on the development of high-performance lithium-metal ASSBs.

Mechanisms of cerebrospinal fluid secretion by the choroid plexus epithelium: Application to various intracranial pathologies.

The choroid plexus (CP) is a small yet highly active epithelial tissue located in the ventricles of the brain. It secretes most of the CSF that envelops the brain and spinal cord. The epithelial cells of the CP have a high fluid secretion rate and differ from many other secretory epithelia in the organization of several key ion transporters. One striking difference is the luminal location of, for example, the vital Na+-K+-ATPase. In recent years, there has been a renewed focus on the role of ion transporters in CP secretion. Several studies have indicated that increased membrane transport activity is implicated in disorders such as hydrocephalus, idiopathic intracranial hypertension, and posthemorrhagic sequelae. The importance of the CP membrane transporters in regulating the composition of the CSF has also been a focus in research in recent years, particularly as a regulator of breathing and hemodynamic parameters such as blood pressure. This review focuses on the role of the fundamental ion transporters involved in CSF secretion and its ion composition. It gives a brief overview of the established factors and controversies concerning ion transporters, and finally discusses future perspectives related to the role of these transporters in the CP epithelium.

From Bulk to Interface: Solvent Exchange Dynamics and Their Role in Ion Transport and the Interfacial Model of Rechargeable Magnesium Batteries.

Multivalent battery chemistries have been explored in response to the increasing demand for high-energy rechargeable batteries utilizing sustainable resources. Solvation structures of working cations have been recognized as a key component in the design of electrolytes; however, most structure-property correlations of metal ions in organic electrolytes usually build upon favorable static solvation structures, often overlooking solvent exchange dynamics. We here report the ion solvation structures and solvent exchange rates of magnesium electrolytes in various solvents by using multimodal nuclear magnetic resonance (NMR) analysis and molecular dynamics/density functional theory (MD/DFT) calculations. These magnesium solvation structures and solvent exchange dynamics are correlated to the combined effects of several physicochemical properties of the solvents. Moreover, Mg2+ transport and interfacial charge transfer efficiency are found to be closely correlated to the solvent exchange rate in the binary electrolytes where the solvent exchange is tunable by the fraction of diluent solvents. Our primary findings are (1) most battery-related solvents undergo ultraslow solvent exchange coordinating to Mg2+ (with time scales ranging from 0.5 μs to 5 ms), (2) the cation transport mechanism is a mixture of vehicular and structural diffusion even at the ultraslow exchange limit (with faster solvent exchange leading to faster cation transport), and (3) an interfacial model wherein organic-rich regions facilitate desolvation and inorganic regions promote Mg2+ transport is consistent with our NMR, electrochemistry, and cryogenic X-ray photoelectron spectroscopy (cryo-XPS) results. This observed ultraslow solvent exchange and its importance for ion transport and interfacial properties necessitate the judicious selection of solvents and informed design of electrolyte blends for multivalent electrolytes.

Attenuated retinoic acid signaling is among the early responses in mouse uterus approaching embryo attachment.

The uterus is transiently receptive for embryo implantation. It remains to be understood why the uterus does not reject a semi-allogeneic embryo (to the biological mother) or an allogeneic embryo (to a surrogate) for implantation. To gain insights, we examined uterine early response genes approaching embryo attachment on day 3 post coitum (D3) at 22 hours when blue dye reaction, an indication of embryo attachment, had not manifested in mice. C57BL/6 pseudo-pregnant (control) and pregnant mouse uteri were collected on D3 at 22 hours for microarray analysis. The self-assembling-manifold (SAM) algorithm identified 21,858 unique probesets. Principal component analysis indicated a clear separation between the pseudo-pregnant and pregnant groups. There were 106 upregulated and five downregulated protein-coding genes in the pregnant uterus with fold change (fc) >1.5 and q value <5%. Gene ontology (GO) analysis of the 106 upregulated genes revealed 38 significant GO biological process (GOBP) terms (P <0.05), and 32 (84%) of them were associated with immune responses, with a dominant natural killer (NK) cell activation signature. Among the top eight upregulated protein-coding genes, Cyp26a1 inactivates retinoic acid (RA) while Lrat promotes vitamin A storage, both of which are expected to attenuate RA bioavailability; Atp6v0d2 and Gjb2 play roles in ion transport and transmembrane transport; Gzmb, Gzmc, and Il2rb are involved in immune responses; and Tdo2 is important for kynurenine pathway. Most of these genes or their related pathways have functions in immune regulations. RA signaling has been implicated in immune tolerance and immune homeostasis, and uterine NK cells have been implicated in immunotolerance at the maternal-fetal interface in the placenta. The mechanisms of immune responses approaching embryo attachment remain to be elucidated. The coordinated effects of the early response genes may hold the keys to the question of why the uterus does not reject an implanting embryo.

Functional nanosheet fillers with fast Li+ conduction for advanced all-solid-state lithium battery

Polymer electrolyte-based solid-state lithium metal batteries can accommodate high energy density and address safety issues, while polymer electrolytes suffer from low lithium ion migration and weak mechanical strength. Hence, as an exceptionally facile and practical strategy, it is of great significance to search for functional fillers to lift the performance of current polymer electrolytes and explore their role in ion transport. Nanosheet materials with a positive charge field, such as VO,NCECN (CeO2 and g-C3N4 composites containing oxygen and nitrogen defects), are outstanding candidates. Combining the calculated and experimental results, we reveal the unique nanosheets structure could achieve the maximum area of contact with PEO, so that the surface of the filler is exposed to more coordination sites to promote the transport of Li+, and improve the ion conductivity (1.08×10−5 S cm−1 at 25°C). As a result, a lithium battery consisting of composite solid electrolyte (CSE) still has a capacity of 135 mAh g−1 after 200 cycles at a current density of 0.3 C when matched with a commercial NCM811 electrode. These findings highlight that functional fillers improve the electrochemical properties of polymers and provide a feasible design solution for high-performance solid electrolytes.

Protonation of Asp116 and distortion of the all-trans retinal chromophore in Krokinobacter eikastus rhodopsin 2 causes a redshift in absorption maximum upon dehydration.

Water is usually indispensable for protein function. For ion-pumping rhodopsins, water molecules inside the proteins play an important role in ion transportation. In addition to amino acid residues, water molecules regulate the colors of retinal proteins. It was reported that a sodium-pumping rhodopsin, Krokinobacter eikastus rhodopsin 2 (KR2), showed a color change from red to purple upon dehydration under crystalline conditions. Here, we applied comprehensive visible and IR absorption spectroscopy and resonance Raman spectroscopy to KR2 in liposomes under hydration-controlled conditions. A large increase in the hydrogen-out-of-plane (HOOP) vibration at 947 (H-C11=C12-H Au mode) and moderate increases at 893 (C7-H and C10-H) and 808 (C14-H) cm-1 were observed under dehydrated conditions, which were assigned by using systematically deuterated retinal. Moreover, the Asn variant at Asp116, which functions as a counter ion for the protonated retinal Schiff base (PRSB), caused a large redshift in the absorption maximum and constitutive increase in the HOOP modes under hydrated and dehydrated conditions. The protonation of a counter ion at Asp116 clearly causes a redshift in the absorption maximum as the all-trans retinal chromophore twists upon dehydration. Namely, the results strongly suggested that water molecules are important for maintaining the hydrogen-bonding network at the PRSB and deprotonation state of Asp116 in KR2.

Research Progress of Shear Thickening Electrolyte Based on Liquid–Solid Conversion Mechanism

As an essential component of the lithium-ion battery system, electrolyte plays a crucial role in ion transport between the electrodes. In the event of thermal runaway, commercial organic electrolytes are prone to internal disturbances and fires; hence, research on safe electrolytes has gradually become a hot topic during recent years. Shear thickening electrolyte, as a new type of smart electrolyte, can exhibit a liquid state in the absence of external force and rapidly converts to a quasi-solid state once the battery is subjected to drastic impact loading. In this paper, the recent progress of shear thickening electrolytes with liquid–solid switching performance is presented, including its working principles, synthesis and preparation procedure, and battery performance. Additionally, the perspective and challenges for practical application are discussed.

Tuning Electrolyte Solvation Structure and CEI Film to Enable Long Lasting FSI−‐Based Dual‐Ion Battery

AbstractDual‐ion battery (DIB) is a promising energy storage system because it can provide high power. However, the stability and rate performance of the battery depend strongly on the type of salt and solvents in the electrolyte. Herein, the use of lithium bis(fluorosulfonyl)imide (LiFSI) is studied, which has better high‐temperature stability, as salt in the DIB and develop a 3 m LiFSI fluoroethylene carbonate/methyl 2,2,2‐trifluoroethyl carbonate (FEC/FEMC) = 3:7 electrolyte, which stabilizes graphite–lithium DIB with 94.1% capacity retention after 2000 cycles at 5C. The DIB also exhibits excellent rate performance with 100.4 mAh g−1 capacity at 30C, with a utilization of 96.3% compared to capacity at 2C. The outstanding electrochemical performance is attributed to the thin cathode electrolyte interface (CEI) layer and fast FSI− transport kinetics, confirmed by X‐ray photoelectron spectroscopy and activation energy calculation. Superior cycle and rate performances are also obtained from a graphite–graphite full cell. Though, increasing salt concentration to 5 and 6 m leads to sluggish FSI− de‐intercalation reaction and lower capacity, which is attributed to solvent co‐intercalation. The research suggests that the electrolyte plays an important role in ion transport, surface film formation, and stability of DIB.

Controlled fabrication of refined mesoporous architectures for enhancement of supercapacitor performance

It is essential to design stable and unique carbon nanostructures for the enhancement of supercapacitor performance, but they still have difficulty with excellent ion transportation, lasting capacitance activity and high rate capability. To pursue the target, herein, a simple co-assembly method is developed to access carbon spheres with large mesopores (MCS). By means of the strengthening force between -OH on Ludox and -NH2 in DAP, silica spheres and poly-2,6-diaminopyridine (PDAP) are assembled into a uniform spherical composite to create a large mesoporous structure for the final MCS product. Changing the pore size of large mesopores plays a key role in ion transport of supercapacitor electrodes. The obtained MCS significantly improve the all-round electrochemical performances with high capacitance, long stability and rate capability, showing its great promise for efficient energy storage.

The Role οf Ion Channels in the Development and Progression of Prostate Cancer.

Ion channels have major regulatory functions in living cells. Apart from their role in ion transport, they are responsible for cellular electrogenesis and excitability, and may also regulate tissue homeostasis. Although cancer is not officially classified as a channelopathy, it has been increasingly recognized that ion channel aberrations play an important role in virtually all cancer types. Ion channels can exert pro-tumorigenic activities due to genetic or epigenetic alterations, or as a response to molecular signals, such as growth factors, hormones, etc. Increasing evidence suggests that ion channels and pumps play a critical role in the regulation of prostate cancer cell proliferation, apoptosis evasion, migration, epithelial-to-mesenchymal transition, and angiogenesis. There is also evidence suggesting that ion channels might play a role in treatment failure in patients with prostate cancer. Hence, they represent promising targets for diagnosis, staging, and treatment, and their effects may be of particular significance for specific patient populations, including those undergoing anesthesia and surgery. In this article, the role of major types of ion channels involved in the development and progression of prostate cancer are reviewed. Identifying the underlying molecular mechanisms of the pro-tumorigenic effects of ion channels may potentially inform the development of novel therapeutic strategies to counter this malignancy.

Onset of Nonlinear Electroosmotic Flow under an AC Electric Field.

Nonlinearity of electroosmotic flows (EOFs) is ubiquitous and plays a crucial role in ion transport, specimen mixing, electrochemistry reaction, and electric energy storage and utilization. When and how the transition from a linear regime to a nonlinear one occurs is essential for understanding, prohibiting, or utilizing nonlinear EOF. However, due to the lack of reliable experimental instruments with high spatial and temporal resolutions, the investigation of the onset of nonlinear EOF still remains in theory. Herein, we experimentally studied the velocity fluctuations of EOFs driven by an alternating current (AC) electric field via ultrasensitive fluorescent blinking tricks. The linear and nonlinear AC EOFs are successfully identified from both the time trace and energy spectra of velocity fluctuations. The transitional electric field (EA,C) is determined by both the convection velocity (U) and AC frequency (ff) as EA,C ∼ ff0.48-0.027U. We hope the current investigation could be essential in the development of both theory and applications of nonlinear EOFs.

The Role of Ion Transport in the Failure of High Areal Capacity Li Metal Batteries

The Role of Ion Transport in the Failure of High Areal Capacity Li Metal Batteries

Considering the Role of Ion Transport in Diffuson‐Dominated Thermal Conductivity

AbstractNext‐generation thermal management requires the development of low lattice thermal conductivity materials, as observed in ionic conductors. For example, thermoelectric efficiency is increased when thermal conductivity is decreased. Detrimentally, high ionic conductivity leads to thermoelectric device degradation. Battery safety and design also require an understanding of thermal transport in ionic conductors. Ion mobility, structural complexity, and anharmonicity have been used to explain the thermal transport properties of ionic conductors. However, thermal and ionic transport are rarely discussed in direct comparison. Herein, the ionic conductivity of Ag+ argyrodites is found to change by orders of magnitude without altering the thermal conductivity. Thermal conductivity measurements and two‐channel lattice dynamics modeling reveal that the majority of Ag+ vibrations have a non‐propagating diffuson‐like character, similar to amorphous materials. It is found that high ionic mobility is not a requirement for diffuson‐mediated transport. Instead, the same bonding and structural traits that can lead to fast ionic conduction also lead to diffuson‐mediated transport. Bridging the fields of solid‐state ionics and thermal transport, it is proposed that a vibrational perspective can lead to new design strategies for functional ionic conducting materials. As a first step, the authors relate the so‐called Meyer–Neldel behavior in ionic conductors to phonon occupations.

Salinity Tolerance Mechanisms in Rice: A Review

Background: Rice (Oryza sativa L.) is one of the most important cereal crop globally and it is the staple food of more than half of world population. Current average yield is 10 to 15% lower than its potential yield. There are many reasons for this yield gap such as biotic and abiotic stresses, management strategies as well as nutrient deficiencies. Salinity is one of the most serious factors limiting the productivity of rice, with adverse effects on germination, plant vigor and crop yield. This salinity may be natural or induced by agricultural activities such as irrigation or the use of certain types of fertilizer. Methods: Salinity induced ionic imbalance and osmotic stress affect water and nutrient uptake, stomatal closure, gas exchange, photosynthesis, transpiration, carbon assimilation and hence decrease in rice yield. Studying the response of rice at physiological, genetic and molecular level is the mandate to develop salt tolerant rice varieties. Conclusion: This review described the impact of salt stress in rice, various types of salt tolerance mechanisms in rice, including the ion homeostasis, production of compatible organic solutes, antioxidative genes, salt responsive regulatory elements, role of ion transporters and channel proteins. Further, the future perspective of developing salt-tolerant varieties using landraces via., marker assisted breeding, genome editing tool, utilization of beneficial microorganisms

Gene regulation at transcriptional and post-transcriptional levels to combat salt stress in plants.

Soil salinity is a major challenge that will be faced more and more by human population in the near future. Higher salt concentrations in the soil limit the growth and production of crops, which poses serious threats to global food production. Various plant breeding approaches have been followed in the past which are reported to reduce the effect of salt stress by inducing the level of protective metabolites like osmolytes and antioxidants. Conventional breeding approaches are time-consuming and not cost-effective. In recent times, genetic engineering has been largely followed to confer salt tolerance through introgressions of single transgenes or stacking multiple transgenes. However, most of such works are limited only at the laboratory level and field trials are still awaited to prove the long-term efficacy of such transgenics. In this review, we attempt to present a broad overview of the current strategies undertaken to develop halophytic and salt-tolerant crops. The salt-induced damages in the plants are highlighted, followed by representing the novel traits, associated with salt stress, which can be used for engineering salt tolerance in glycophytic crops. Additionally, the role of transcriptional and epigenetic regulation in plants for amelioration of salt-induced damages has been reviewed. The role of post-transcriptional mechanisms such as microRNA regulation, genome editing and alternative splicing, during salt stress, and their implications in the development of salt-tolerant crops are also discussed. Finally, we present a short overview about the role of ion transporters and rhizobacteria in the engineering of salt tolerance in crop species.

Role of free volumes and segmental dynamics on ion conductivity of PEO/LiTFSI solid polymer electrolytes filled with SiO2 nanoparticles: a positron annihilation and broadband dielectric spectroscopy study.

The limited ionic conductivity of polymer electrolytes is a major issue for their industrial application. Enhancement of ionic conductivity in the poly(ethylene oxide), PEO, based electrolyte has been achieved by loading passive nanofillers such as SiO2 nanoparticles (NPs). To investigate the role of modifications in free volume characteristics and the polymer chain dynamics induced by the loading of passive fillers on the ionic conductivity of the PEO based ternary electrolyte, a systematic investigation has been carried out using positron annihilation and broadband dielectric spectroscopy. As a result of interfacial interactions, the loading of SiO2 NPs alters the semi-crystalline morphology of PEO resulting in a higher crystallinity at lower loadings due to the surface confinement of PEO chains, and the formation of smaller PEO crystallites at higher loadings due to interparticle nanoconfinement. These modifications are accompanied by a decrease in free volume fraction at the lowest loading (0.5 wt%) followed by an increase at higher loadings (≥2.0 wt%). The Almond-West formalism considering two different universalities in different temperature and frequency ranges has been used to explain the ion-conduction process at different NP loadings. The Li ion conductivity is observed to be maximum for a 5.0 wt% loading of SiO2 NPs. The enhancement in ionic conductivity is observed to be directly correlated with the free volume characteristics and segmental dynamics of the PEO matrix, confirming their role in ion transport in polymer electrolytes.

(Invited) In-Situ X-Ray Imaging Analysis for Dynamic Behavior in All-Solid-State Battery

Next-generation rechargeable batteries are expected to exhibit safety, long life, high power and high energy density. Rechargeable batteries are composed of a positive electrode, a negative electrode, and electrolyte. Improvement of their characteristics themselves, such as capacity, conductivity, or stability by tuning materials, has been one of the main research topics. However, practical batteries are complex system using other functional materials in order to improve battery performance at the pack level. Therefore, the behavior of carrier ions inside the practical battery is also important research topics for the development of rechargeable batteries.For charge/discharge of conventional lithium-ion batteries using an organic electrolyte, an inhomogeneous reaction in composite electrodes related to practical charge/discharge performance has been reported1). Electrodes of lithium-ion batteries are composed of active material, conductive carbon, and binder. Electrolyte is poured into void spaces of composite electrodes, which has a role for ion transport. The electric and ionic conductions must be maintained during charge/discharge. However, these conduction paths depend on the mesoscale structure of composite electrodes, which causes the reaction distribution in composite electrodes. The reaction inhomogeneity is quite related to the practical cell performance of batteries such as safety, cycle life, and rate capability. It has been reported that a reaction distribution forms in the electrode depth direction due to the presence of this nonuniform balance between electric and ionic resistances, and the active area for charge/discharge in composite electrode decreases1). In addition, during high-rate charge/discharge in which a large current flow, not only such an inhomogeneous SOC in electrodes but also concentration change of electrolyte occurs. For electrolyte used for lithium-ion batteries, the lithium-ion transport number is small, about 0.4. Therefore, a salt concentration gradient can be formed in the electrolyte during charge/discharge, and the utilization of lithium-ion is greatly restricted. From the results of NMR measurement, a concentration distribution of 0.78 to 1.27 M is reported2). On the other hand, in the case of the all-solid-state rechargeable battery, the transport number of the carrier ions of the solid electrolyte is 1, so in principle, it is considered that a concentration distribution of carrier is not occurred, and therefore, the high energy density and high rate characteristics are expected. However, direct measurement of concentration distribution in solid electrolyte during battery operation has not been reported.In this study, we introduce examples of the analysis of reaction distribution using synchrotron radiation X-ray in rechargeable batteries. In lithium-ion batteries, nonuniform reaction phenomena of electrode active material were analyzed by two-dimensional imaging XAFS. The results indicate that ion conduction governs the reaction rate inside the composite electrode. In addition, changes in the concentration of the electrolyte solution were investigated by X-ray radiography. For the analysis in all-solid-state battery, the model system was developed using silver ions as probes3), and the characteristics of the all-solid secondary battery were analyzed under charge/discharge conditions.

Molecular‐Scale Interface Engineering of Metal–Organic Frameworks toward Ion Transport Enables High‐Performance Solid Lithium Metal Battery

AbstractMetal–organic frameworks (MOFs) have drawn considerable interest as solid electrolytes (SEs) by virtue of their talents for rational design as ion channels. The crystal interface plays a significant role in ion transport and is thus of vital importance to the performance of solid batteries, however, interface effects of MOFs in SEs are not yet fully understood, especially at the molecular level, and not engineered as well. In this work, MOFs engineered with diverse molecules (Lewis bases) are designed for an optimized interfaces and the impact of interfaces for ion transport is analyzed by using engineered MOFs as SEs. The results show that the ion conductivity of MOFs decorated with a long chain Lewis base (LCLB) has been greatly improved. The interface resistance of the SEs composed of MOFs with LCLB has decreased markedly. Most importantly, the corresponding Li|SE|LiPO4 solid‐state battery (SSB) shows an improved specific capacity of 47% and longer lifetime at 5 C compared with the SSB without interface engineering. Such results shed new light on the understanding of ion transport at interfaces and suggest the feasibility of interface engineered MOFs as advanced SEs.