Stable Interface 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.

Selective construction of amorphous/crystalline heterostructure high entropy oxide for Li-ion batteries

High entropy oxides (HEO) are widely used as anode for lithium-ion batteries due to their exceptional chemical stability and mechanical strength. However, HEO encounters challenges such as low initial coulomb efficiency (ICE) and poor capacity. To address these issues, a simple mechanochemical method is employed to selectively amorphized and densely embed LiF within the HEO matrix. Taking advantage of the differing chemical properties of LiF and HEO, the transformation of LiF’s crystal structure not only overcomes its poor ionic conductivity but also successfully constructs an amorphous LiF/crystalline HEO heterostructure, which also improves the transport capacity of lithium ions. Additionally, the presence of abundant defects (e.g., oxygen vacancies, dislocations, and stacking faults) boosts the material's lithium transport and storage capacity. Furthermore, LiF facilitates the formation of a stable solid electrolyte interface (SEI) film on the HEO surface, preventing the corrosion of active materials and minimizing side reactions, effectively improving the ICE. The as-prepared LiF/HEO-48 demonstrates a superior initial capacity of 1632.9/1158.5 mAh g−1, along with an ICE of 70.9%. It maintains a high reversible capacity of 552.2 mAh g−1 after 1000 cycles at 0.5 A g−1, and even after 400 cycles at 2 A g−1, it retains 99.4% of its capacity. This study may open up new ways to selectively construct amorphous/heterostructures to improve the ICE and capacity of lithium-ion anodes.

P24-Tango1 interactions ensure ER-Golgi interface stability and efficient transport.

The eukaryotic p24 family, consisting of α-, β-, γ- and δ-p24 subfamilies, has long been known to be involved in regulating secretion. Despite increasing interest in these proteins, fundamental questions remain about their role. Here, we systematically investigated Drosophila p24 proteins. We discovered that members of all four p24 subfamilies are required for general secretion and that their localizations between ER exit site (ERES) and Golgi are interdependent in an α→βδ→γ sequence. We also found that localization of p24 proteins and ERES determinant Tango1 requires interaction through their respective GOLD and SH3 lumenal domains, with Tango1 loss sending p24 proteins to the plasma membrane and vice versa. Finally, we show that p24 loss expands the COPII zone at ERES and increases the number of ER-Golgi vesicles, supporting a restrictive role of p24 proteins on vesicle budding for efficient transport. Our results reveal Tango1-p24 interplay as central to the generation of a stable ER-Golgi interface.

First-Principles Investigation on the Adsorption and Diffusion of Oxygen at the B2(110)–O(001) Interface in Ti2AlNb Alloys

The adsorption and diffusion of oxygen at the B2(110)[1¯11]||O(001)[11¯0] interface in Ti2AlNb alloys were investigated via first-principles calculations. Only a 2.6% interfacial mismatch indicates that B2(110)–O(001) is basically a stable coherent interface. The calculated adsorption energies and diffusion energy barriers show that oxygen prefers to occupy the Ti-rich interstitial sites, and once trapped, it hardly diffuses to other interstitial sites, thus promoting the preferential formation of Ti oxides. Under the premise of a Ti-rich environment, a Nb-rich environment is more favorable for oxygen adsorption than an Al-rich environment. The electronic structures suggest that O 2p orbitals mainly occupy the energy region below −5 eV, bonding with its coordinated atoms of Ti, Al, and Nb. However, Al 3p and Nb 4d orbitals near the Fermi level couple with sparsely distributed O 2p orbitals, forming anti-bonding, which is not conducive to oxygen adsorption. Because Nb 4d electrons are more localized than Al 3p electrons are, Nb–O anti-bonding is weaker. O–Ti has almost no contribution to anti-bonding, suggesting good bonding between them. This is consistent with the experimental observations that TiO2 is the main oxidation product.

Designing Atomic Interface in Sb2S3/CdS Heterojunction for Efficient Solar Water Splitting.

In the emerging Sb2S3-based solar energy conversion devices, a CdS buffer layer prepared by chemical bath deposition is commonly used to improve the separation of photogenerated electron-hole pairs. However, the cation diffusion at the Sb2S3/CdS interface induces detrimental defects but is often overlooked. Designing a stable interface in the Sb2S3/CdS heterojunction is essential to achieve high solar energy conversion efficiency. As a proof of concept, this study reports that the modification of the Sb2S3/CdS heterojunction with an ultrathin Al2O3 interlayer effectively suppresses the interfacial defects by preventing the diffusion of Cd2+ cations into the Sb2S3 layer. As a result, a water-splitting photocathode based on Ag:Sb2S3/Al2O3/CdS heterojunction achieves a significantly improved half-cell solar-to-hydrogen efficiency of 2.78% in a neutral electrolyte, as compared to 1.66% for the control Ag:Sb2S3/CdS device. This work demonstrates the importance of designing atomic interfaces and may provide a guideline for the fabrication of high-performance stibnite-type semiconductor-based solar energy conversion devices.

Highly Conductive Imidazolate Covalent Organic Frameworks with Ether Chains as Solid Electrolytes for Lithium Metal Batteries.

Poly(ethylene oxide) (PEO)-based electrolytes are often used for Li+ conduction as they can dissociate the Li salts efficiently. However, high entanglement of the chains and lack of pathways for rapid ion diffusion limit their applications in advanced batteries. Recent developments in ionic covalent organic frameworks (iCOFs) showed that their highly ordered structures provide efficient pathways for Li+ transport, solving the limitations of traditional PEO-based electrolytes. Here, we present imidazolate COFs, PI-TMEFB-COFs, having methoxyethoxy chains, synthesized by Debus-Radziszewski multicomponent reactions and their ionized form, Li+@PI-TMEFB-COFs, showing a high Li+ conductivity of 8.81 mS cm-1 and a transference number of 0.974. The mechanism for such excellent electrochemical properties is that methoxyethoxy chains dissociate LiClO4, making free Li+, then those Li+ are transported through the imidazolate COFs' pores. The synthesized Li+@PI-TMEFB-COFs formed a stable interface with Li metal. Thus, employing Li+@PI-TMEFB-COFs as the solid electrolyte to assemble LiFePO4 batteries showed an initial discharge capacity of 119.2 mAh g-1 at 0.5 C, and 82.0 % capacity and 99.9 % Coulombic efficiency were maintained after 400 cycles. These results show that iCOFs with ether chains synthesized via multicomponent reactions can create a new chapter for making solid electrolytes for advanced rechargeable batteries.

Highly Conductive Imidazolate Covalent Organic Frameworks with Ether Chains as Solid Electrolytes for Lithium Metal Batteries

AbstractPoly(ethylene oxide) (PEO)‐based electrolytes are often used for Li+ conduction as they can dissociate the Li salts efficiently. However, high entanglement of the chains and lack of pathways for rapid ion diffusion limit their applications in advanced batteries. Recent developments in ionic covalent organic frameworks (iCOFs) showed that their highly ordered structures provide efficient pathways for Li+ transport, solving the limitations of traditional PEO‐based electrolytes. Here, we present imidazolate COFs, PI‐TMEFB‐COFs, having methoxyethoxy chains, synthesized by Debus–Radziszewski multicomponent reactions and their ionized form, Li+@PI‐TMEFB‐COFs, showing a high Li+ conductivity of 8.81 mS cm−1 and a transference number of 0.974. The mechanism for such excellent electrochemical properties is that methoxyethoxy chains dissociate LiClO4, making free Li+, then those Li+ are transported through the imidazolate COFs’ pores. The synthesized Li+@PI‐TMEFB‐COFs formed a stable interface with Li metal. Thus, employing Li+@PI‐TMEFB‐COFs as the solid electrolyte to assemble LiFePO4 batteries showed an initial discharge capacity of 119.2 mAh g−1 at 0.5 C, and 82.0 % capacity and 99.9 % Coulombic efficiency were maintained after 400 cycles. These results show that iCOFs with ether chains synthesized via multicomponent reactions can create a new chapter for making solid electrolytes for advanced rechargeable batteries.

Excellent strength-toughness combination of NiAl–30Cr composites with novel in situ composite microstructure containing NiAl matrix and Cr single-phase

Lightweight NiAl alloys are expected to replace high-density nickel-based superalloys, but their mechanical performance needs to be improved. In this work, NiAl–30Cr composites with a novel heterogeneous microstructure composed of fine NiAl matrix and Cr single-phase was successfully prepared. Nanoscale Cr particles with 15 nm in size precipitated in NiAl matrix are coherent with NiAl matrix owing to very low interplanar and interatomic spacing mismatch. Such a composite microstructure makes NiAl–30Cr exhibit high strength and high toughness. The yield strength (1207 MPa), ultimate compressive strength (2307 MPa), product of strength and plasticity (29.3 GPa%), and fracture toughness (10.76 MPa m1/2) of NiAl–30Cr increased by 96.6%, 85.6%, 55.1% and 19.7% respectively at room temperature compared to the corresponding ones of NiAl. At 1000 °C, the yield strength (144 MPa) of NiAl–30Cr was 85.9% higher than that of NiAl. Solution strengthening and precipitation strengthening were the key strengthening mechanisms at room temperature. The enhancement in toughness was attributed to grain refinement, increased crack propagation paths, weakened Ni–Al covalent bonding and coordinated deformation of Cr single-phase and NiAl matrix. By contrast, the main strengthening mechanism at 1000 °C is the solid solution Cr atoms hindering dislocation climbing and the stable interface bonding between the Cr nanoprecipitation phase and the NiAl matrix. This work provides new ideas for preparing high-strength and tough NiAl alloy.

Hydrophilic polyanionic hydrogel electrolyte for anti-freezing and bending resistant zinc-ion hybrid supercapacitors

Zinc-ion hybrid supercapacitors (ZHSCs) have been widely considered as promising candidates for flexible electrochemical energy storage devices. The key challenge is to develop hydrogel electrolytes with high hydrophilicity, anti-freezing, bending resistance, and stable interface with electrodes. This study reported a hydrogel electrolyte system that can meet the above functions, in which the zincophilic and negatively charged SO3−, migratable Na+, abundant hydrophilic functional groups, gum xanthan, and porous architecture could effectively promote the electrochemical performance of ZHSCs. ZHSCs with such hydrogel electrolytes not only exhibited good low-temperature performance but also showed excellent bending resistance ability. A high specific capacitance could be kept after a long air-working lifespan over 10,000 cycles under a wide operation voltage of 1.85 V at −10 °C. Furthermore, flexible ZHSCs could maintain the capacitance retention of 93.18% even after continuous 500 bends at an angle of 180°. The designed hydrogel electrolytes could be also used for other electrochemical energy storage devices with anti-freezing and bending resistance by changing electrolyte salt.

Lithiated Nafion membrane as a single-ion conducting polymer electrolyte in lithium batteries

AbstractSingle lithium-ion conducting polymer electrolytes are promising candidates for next generation safer lithium batteries. In this work, Li+-conducting Nafion membranes have been synthesized by using a novel single-step procedure. The Li-Nafion membranes were characterized by means of small-wide angle X-ray scattering, infrared spectroscopy and thermal analysis, for validating the proposed lithiation method. The obtained membranes were swollen in different organic aprotic solvent mixtures and characterized in terms of ionic conductivity, electrochemical stability window, lithium stripping-deposition ability and their interface properties versus lithium metal. The membrane swollen in ethylene carbonate:propylene carbonate (EC:PC, 1:1 w/w) displays good temperature-activated ionic conductivities (σ ≈ 5.5 × 10–4 S cm−1 at 60 °C) and a more stable Li-electrolyte interface with respect to the other samples. This Li-Nafion membrane was tested in a lithium-metal cell adopting LiFePO4 as cathode material. A specific capacity of 140 mAhg−1, after 50 cycles, was achieved at 30 °C, demonstrating the feasibility of the proposed Li-Nafion membrane.

High Ionic Conductive, Mechanical Robust Sulfide Solid Electrolyte Films and Interface Design for All‐Solid‐State Lithium Metal Batteries

AbstractAll‐solid‐state lithium batteries (ASSLBs) are considered a promising technology for next‐generation energy storage systems due to their inherent safety. However, the conventional laboratory‐scale ASSLBs reported to date are based on pellet‐type structures with thick solid electrolyte layers, leading to challenges related to low energy densities and poor electrochemical performance. In this study, porous adhesive poly(ethylene vinyl acetate) (PEVA) scaffolds and polytetrafluoroethylene (PTFE) binders are utilized to interweave sulfide solid electrolytes into freestanding films with an ultra‐low thickness of 40 µm, high ionic conductivity of 1.1 mS cm−1, and a high tensile strength of 74 MPa. To mitigate the reduction reaction between the PTFE binder and the lithium metal anode, a Li3N‐rich solid electrolyte interphase (SEI) in situ on lithium metal is formed, and the assembled symmetric cell shows excellent cycling stability within 800 h at the current density of 0.2 mA cm−2 and room temperature. Additionally, the ASSLBs using oxidatively stable Li2ZrCl5F in the composite cathode and the prepared solid electrolyte film demonstrate exceptional cycling performance and fast‐charging capability, with a high cell‐level energy density of 354.4 Wh kg−1. The ASSLBs prepared by coupling E‐LPSCl film and stable interface design exhibit excellent electrochemical performance and a high cell‐level energy density.

Designing a Corrosion Inhibiting Layer to Enhance Cycling Stability of 4.7 V Ni‐Rich Cathode

AbstractThe advent of Ni‐rich cathode promises to increase their energy density of lithium (Li) ion batteries. However, the inherent catalytic activity and resultant decomposition products deteriorate the interfacial stability of Ni‐rich cathode. This case is further exacerbated by a higher operation voltage for delivering more capacity. Here, a facile strategy is reported for coating garnet solid electrolyte as a corrosion inhibiting layer for Ni‐rich cathode, aiming to establish an efficient Li‐conducting and stable interface that reinforces the Li transport and withstands the HF attack, respectively. Benefiting from this design, the interface of modified Ni‐rich cathode exhibits less polarization and fewer side reactions even at a cut‐off voltage of 4.7 V. This difference is mainly attributed to the fast Li transport stemming from the compatibility between Ni‐rich cathode and garnet solid electrolyte. Meanwhile, the stable and dense cathode electrolyte layer, observed by cryo‐transmission electron microscopy characterization, inhibits side reaction between Ni‐rich cathode and liquid electrolyte. This work provides an effective strategy to reinforce the interfacial stability of Ni‐rich cathode and has the potential to advance the commercialization of Ni‐rich cathodes.

Polymer/ceramic interfacial layer enables stable cycling of all-solid-state Li-metal batteries with sulfide electrolyte

The interfacial stability, particularly between lithium metal and the solid electrolyte, as a critical challenge in solid-state batteries leads to rapid lithium-dendrite growth and increased internal resistance. In this study, we tackled these issues by developing a stable interface between sulfide electrolytes Li5.5PS4.5Cl1.5 (LPSCl) and the metallic lithium anode, using a polyethylene oxide (PEO) layer integrated with Li-ion conducting oxide electrolyte Li1.3Al0.3Ti1.7(PO4)3 (LATP). The uniform distribution of LATP within the PEO matrix through a simple stirring process enhanced the mechanical strength of the PEO interlayer and minimizes both the interfacial reactions and lithium dendrite formation. A Li/Li symmetric cell incorporating this LATP-integrated layer exhibited a low interfacial resistance, ensuring stable cycling for 2800 h at a current density of 0.2 mA cm−2 at 60 °C.

Design and fabrication of wearable electronic textiles using twisted fiber-based threads.

Mono-dimensional fiber-based electronics can effectively address the growing demand for improved wearable electronic devices because of their exceptional flexibility and stretchability. For practical applications, functional fiber electronic devices need to be integrated into more powerful and versatile systems to execute complex tasks that cannot be completed by single-fiber devices. Existing techniques, such as printing and sintering, reduce the flexibility and cause low connection strength of fiber-based electronic devices because of the high curvature of the fiber. Here, we outline a twisting fabrication process for fiber electrodes, which can be woven into functional threads and integrated within textiles. The design of the twisted thread structure for fiber devices ensures stable interfacing and good flexibility, while the textile structure features easily accessible, interlaced points for efficient circuit connections. Electronic textiles can be customized to act as displays, health monitors and power sources. We detail three main fabrication sections, including the fabrication of the fiber electrodes, their twisting into electronic threads and their assembly into functional textile-based devices. The procedures require ~10 d and are easily reproducible by researchers with expertise in fabricating energy and electronic devices.

Gold Coated Silver Bonding Wire and Its Consistent Reliability Performances

Thermal aging of gold coated silver bonded ball with aluminium bond pads exhibited a stable interface without Kirkendall voids until 4000h at 200°C for an un-molded device tested under vacuum. Ball and stitch pull remains in strength and remained constant until 4000 hours of aging. The growth of aluminides at the bond interface is about 4.5µm for 4000 hours of aging. The electrical resistance of the bonded ball remains the same until 4000 hours at 175°C for an epoxy molded device, molded with 5 to 7 pH green epoxy molding compound containing low chlorine and sulfur. Interestingly, the bonded ball interface of epoxy molded device has sustained 480h on biased Highly Accelerated Stress Test (bHAST) at +20V bias, 130°C, 85%RH. The bonded ball interface is stable until 1000 hours on unbiased HAST (uHAST) at 130°C, 85% RH as well. Cross-sectional ovservations of the bonded balls revealed the presence of intermetallic phases at the bond interface. However, formation of Kirkendall voids or crack propagatioon due to galvanic corrosions are absent.

Superior Low-Temperature All-Solid-State Battery Enabled by High-Ionic-Conductivity and Low-Energy-Barrier Interface.

All-solid-state batteries (ASSBs) working at room and mild temperature have demonstrated inspiring performances over recent years. However, the kinetic attributes of the interface applicable to the subzero temperatures are still unidentified, restricting the low-temperature interface design and operation. Herein, a host of cathode interfaces are constructed and investigated to unlock the critical interface features required for cryogenic temperatures. The unstable interface between LiNi0.90Co0.05Mn0.05O2 (Ni90) and Li6PS5Cl (LPSC) sulfide solid electrolyte (SE) results in unfavorable cathode-electrolyte interphase (CEI) and sluggish lithium-ion transport across the CEI. After inserting a Li2ZrO3 (LZO) coating layer, the activation energy of the Ni90@LZO/sulfide SE interface can be reduced from 60.19 kJ mol-1 to 41.39 kJ mol-1 owing to the suppressed interfacial reactions. Through replacing the LPSC SE and LZO coating layer by the Li3InCl6 (LIC) halide SE, both a highly stable interface and low activation energy (25.79 kJ mol-1) can be achieved, thus realizing an improved capacity retention (26.9%) at -30 °C for the Ni90/LIC/LPSC/Li-In ASSB. Moreover, theoretical evaluation clarifies that cathode/SE interfaces with high ionic conductivity and low energy barrier are favorable to the Li+ conduction through the interphase and the Li+ transfer across the cathode/interphase interface. These critical understandings may provide guidance for low-temperature interface design in ASSBs.

Stabilization of LiCoO2 Cathodes in High Voltage Lithium Metal Batteries Through 2-(Trifluoromethyl)Benzamide (2-TFMBA) Electrolyte Additives.

Increasing the charging cutoff voltage of LiCoO2 to 4.6V is significant for enhancing battery density. However, the practical application of Li‖LiCoO2 batteries with a 4.6V cutoff voltage faces significant impediments due to the detrimental changes under high voltage. This study presents a novel bifunctional electrolyte additive, 2-(trifluoromethyl)benzamide (2-TFMBA), which is employed to establish a stable and dense cathode-electrolyte interface (CEI). Characterization results reveal that an optimized CEI is achieved through the synergistic effects of the amide groups and trifluoromethyl groups within 2-TFMBA. The resulting CEI not only enhances the structural stability of LiCoO2 but also serves as a high-speed lithium-ion conduction channel, which expedites the insertion and extraction of lithium ions. The Li‖LiCoO2 batteries with 0.5wt% 2-TFMBA achieves an 84.7% capacity retention rate after enduring 300 cycles at a current rate of 1C, under a cut-off voltage of 4.6V. This study provides valuable strategic insights into the stabilization of cathode materials in high-voltage batteries.

Constructing flame retardant microspheres for safe and stable poly (ethylene oxide) based All-Solid-State batteries at high voltage

The development of all-solid-state polymer electrolytes (ASSPE) based on poly (ethylene oxide) (PEO) is facing a series of challenges, such as poor ionic conductivity, low Li+ transference number, flammability, and the limited electrochemical windows of 4 V. Herein, we report our recent effort to meet these challenges by introducing flame retardant microspheres (TH) into PEO-based ASSPE to form stable solid cathode electrolyte interface (CEI) films and enhance safety performance. TH is constructed by reacting tetrabromobisphenol A (TBBA) with hexachlorocyclotriphosphazene (HCCP). With the presence of only 5 wt% TH, the LiNi0.8Mn0.1Co0.1O2 (NCM811)//Li cell achieves a high capacity retention rate of 77.61 % after 100 cycles at the cutoff voltage of 4.3 V and 0.5C, and achieves a capacity retention of 75.7 % at the voltage range of 3–4.5 V after 50 cycles at 0.5C. In addition, the PEO-based ASSPE with TH (TH-PEO/PE) shows excellent flame retardancy, which endows the NCM811//Li pouch cell with good resistance to fire and mechanical abuse. This simple process is compatible with the existing production lines in the battery industry, which exhibits enormous promise in manufacturing commercialized all-solid-state lithium metal batteries (ASSLMBs) with high energy density and safety capabilities.

Metal-heteroatom-doped CoS/MXene nanohybrid for efficient supercapacitor electrode materials

Developing electrode active materials with abundant active sites, hierarchical porous structure, and good chemical/structure stability significantly promote energy density and cycling stability. However, it is not easy to realize all features for a single component, various strategies such as hetero-atom doping, hybridizing route, and defect engineering could provide possible approaches. Herein, FeCoS were hybridized with MXene to achieve high stability and superior electrochemical performance electrode materials, the well-designed heterogeneous nanohybrids have several merits for abundant active sites, exceptional structural durability, excellent electrical conductivity own to the strong interfacial connection and favorable synergistic effect between the two phases. Consequently, the optimal hybrid electrode demonstrated superior electrochemical performance with an excellent specific capacity of 1190 C g−1 at a current density of 2 A g−1 and outstanding rate capability for 900 C g−1 at 10 A g−1. Moreover, the metal-doped with various cations of Fe2+, Al2+, Ni2+ and Sn2+ were separately introduced into the structural phase to evaluate the feasibility, and the strategy not only provides the feasible and universal development of the stable interface between the hybrids, but also paved the way for the design of high-capacity electrodes.

In situ catalytic polymerization of LiNO3-containing PDOL electrolytes for high-energy quasi-solid-state lithium metal batteries

1,3-Dioxolane (DOL) can be induced to form polymer electrolytes by in situ ring opening polymerization at Lewis acid salts. However, the presence of ion–dipole interactions between NO3− and DOL suppresses this polymerization behavior. Herein, we report that the use of Sc(OTf)3 as an initiator can well disrupt this ion–dipole interaction. The in situ ring-opening polymerization of DOL is achieved to form a LiNO3-modified polyDOL-based electrolyte. New mechanism of Li migration in polymer electrolytes have been revealed by molecular dynamics modeling and constructed molecular interface models. It is found that the electrolyte interior is affected by the ion–dipole interactions of Li+ by NO3−, which made it easier for Li+ to be released from the polar ether-oxygen ligands on the polymer chain for rapid migration, thus exhibiting an ionic conductivity of 1.8 mS cm−1 and tLi+ of 0.78. In addition, NO3− preempts the binding sites around Li+, improves the coordination environment, and prioritizes the formation of a kinetically stable anion-derivative interface, which effectively mitigates the interfacial side reactions between the electrodes and the electrolytes. As a result, the assembled solid-state Li||LiFePO4 cell exhibits an impressive 152.3 mAh/g discharge capacity at 0.5C and maintains 80.3 % of the capacity after 450 cycles at 50 °C. This work not only opens a new avenue for designing high-performance gel polymer electrolytes for more metal-based batteries, but also provides valuable insights into understanding the ion migration mechanism.