Solid Electrolyte Interphase Formation Research Articles

Amorphous lithiophilic cobalt‐boride@rGO interlayer for dendrite‐free and highly stable lithium metal batteries

AbstractLithium metal batteries (LMBs) are recognized to be crucial for secondary battery technology targeting electric vehicles and portable electronic devices. However, the undesirable growth of lithium dendrites would result in reduced capacity, short‐circuit, and overheating, seriously hindering the practical applications of LMBs. To address this issue, a neoteric lithiophilic interlayer on a commercial polypropylene separator is presented for the first time, which is constructed by amorphous CoB nanoparticles decorated reduced graphene oxide nanosheets (CoB@rGO). Density Functional Theory calculations and experimental analysis reveal remarkable lithiophilicity features for CoB@rGO and provide multiple Li deposition sites and improved electrolyte wettability, which facilitates the formation of durable solid electrolyte interphase (SEI), reduces side reactions, and improves Li+ flux regulation for long‐term cycling stability in LMBs. Taking advantage of these merits, the symmetric Li//Li cell with CoB@rGO/PP separator exhibits stable cycling for up to 1600 h at 1 mA cm−2 with 1 mAh cm−2. Employed with CoB@rGO separator, the Li//LiFePO4 full cell with a high LiFePO4 loading of 11 mg cm−2 delivers a high initial specific capacity of 115.3 mAh g−1 and a low decay rate of 0.08% per cycle after 200 cycles even at a high rate of 2C.

Inhibiting Residual Solvent induced side reactions in Vinylidene Fluoride-based Polymer Electrolytes enables ultra-stable Solid-State Lithium Metal Batteries.

Residual solvents in vinylidene fluoride (VDF)-based solid polymer electrolytes (SPEs) have been recognized as responsible for their high ionic conductivity. However, side reactions by the residual solvents with the lithium (Li) metal induce poor stability, which has been long neglected. This study proposes a strategy to achieve a delicate equilibrium between ion conduction and electrode stability for VDF-based SPEs. Specifically, 2,2,2-Trifluoro-N, N-dimethylacetamide (FDMA) is developed as the non-side reaction solvent for poly(vinylidene fluoride-co-hexafluoropropylene) (PVHF)-based SPEs, achieving both high ionic conductivity and significantly improved electrochemical stability. The developed FDMA solvent fosters the formation of a stable solid electrolyte interphase (SEI) through interface reactions with Li metal, effectively mitigating side reactions and dendrite growth on the Li metal electrode. Consequently, the Li||Li symmetric cells and Li||LiFePO4 cells demonstrate excellent cycling performance, even under limited Li (20μm thick) supply and high-loading cathodes (>10mg cm-2, capacity >1 mAh cm-2) conditions. The stable Li||LiCoO2 cells operation with a cutoff voltage of 4.48V indicates the high-voltage stability of the developed SPE. This study offers valuable insights into developing advanced VDF-based SPEs for enhanced lithium metal battery performance and longevity. This article is protected by copyright. All rights reserved.

Electric Double Layer Oriented Eutectic Additive Design towards Stable Zn Anodes with A High Depth of Discharge.

ZnSO4-based electrolytes for aqueous zinc ion batteries (AZIBs) fail to meet practical application metrics due to hydrogen evolution reaction (HER) and dendrite growth. In this work, we rationally designed a highly polarized eutectic additive, glycerophosphorylcholine (GPC), to regulate the EDL structure for stable Zn anodes with a high depth of discharge (DOD). On one hand, GPC molecules with abundant hydroxyl groups can precisely regulate the hydrogen bond network in EDL to suppress HER. On the other hand, the enrichment of GPC at the interface is positively responsible for the negative charge density on the Zn surface, which leads to the formation of a robust ZnxPyOz-rich solid-electrolyte interphase (SEI) and terminates dendrite growth in the charge-rich sites. This EDL-oriented eutectic additive engineering enables highly reversible and selectively (002)-textured Zn anodes to operate for over 1450h at a high DOD of 45.3%. Meanwhile, a high-capacity (185.7 mAh g-1) aqueous Zn||VS2 full cell shows remarkable cycling stability over 220 cycles with an excellent capacity retention of 90.4% even at a low current density of 0.1 A g-1 (0.5 C). This work sheds light on electrolyte design and interface engineering for high-performance aqueous batteries. This article is protected by copyright. All rights reserved.

Formation of N‐Doped Carbon Nanofibers Decorated with MoP Nanoflakes for Dendrite‐Free Lithium Metal Anode

AbstractMetallic lithium (Li) is recognized as a promising candidate for anode material of Li‐ion batteries owing to high theoretical specific capacity and low redox potential. However, uncontrollable dendrite growth and huge volume expansion during Li plating/stripping processes hinder its practical application. Herein, N‐doped carbon nanofibers@MoP nanoflakes (NCNF@MoP) is developed as a potential host to address the above challenges. During the formation of solid electrolyte interphase, MoP nanoflakes can be changed into metallic Mo with high lithiophilicity and Li3P with high ionic conductivity. The whole composite host is transformed into a mixed ion/electron conducting network to reduce nucleation overpotential and accelerate diffusion kinetics at the electrode/electrolyte interface. As a proof of concept, the symmetric cell using NCNF@MoP host presents a long‐term cycling up to 2500 h with a low nucleation overpotential of 10 mV at 1 mA cm−2. Additionally, the Li‐NCNF@MoP||LiFePO4 full cell demonstrates a good capacity retention of 92.6% over 2200 cycles at a high current density of 5C (1 C = 169 mA g−1).

Ether vs. Carbonate solvents in Na–CuS Batteries: Impact on anode Morphology, SEI Formation, and desolvation dynamics

Traditionally, electrolyte solvents in batteries have been regarded primarily as carrier for ion transporters. Here, we reveal the critical roles of solvents in transforming microscale anode materials into porous nanostructures and in facilitating the formation of thinner, more efficient solid-electrolyte interphase (SEI) layers. Using machine-learning-assisted molecular dynamics simulations combined with density functional theory calculations on Na–CuS batteries, we unveil the significant yet previously unclear impact of solvent choice on solvation/desolvation dynamics, a complex area that has been difficult to resolve with traditional methods. We demonstrate that solvent choice significantly impacts the capacity, particularly the rate performance, primarily due to the desolvation dynamics, thus establishing a direct correlation between solvent selection and battery performance. Our findings highlight DEGDME as the optimal solvent for Na–CuS half-cells, due to its low Na desolvation energy and favorable Na–O bond energy. This leads to exceptional energy capacity (610 mAh/g at 2C) and ultrafast charging capability (520 mAh/g at 30C). This research marks a significant advancement in energy storage technology by demonstrating the crucial role of solvent selection in anode morphology, SEI formation, and desolvation energy optimization.

Additive-Driven Nanoscale Architecture of Solid Electrolyte Interphase Revealed by Cryogenic Transmission Electron Microscopy.

In Li metal batteries (LMBs), which boast the highest theoretical capacity, the chemical structure of the solid electrolyte interphase (SEI) serves as the key component that governs the growth of reactive Li. Various types of additives have been developed for electrolyte optimization, representing one of the most effective strategies to enhance the SEI properties for stable Li plating. However, as advanced electrolyte systems become more chemically complicated, the use of additives is empirically optimized. Indeed, their role in SEI formation and the resulting cycle life of LMBs are not well-understood. In this study, we employed cryogenic transmission electron microscopy combined with Raman spectroscopy, theoretical studies including molecular dynamics (MD) simulations and density functional theory (DFT) calculations, and electrochemical measurements to explore the nanoscale architecture of SEI modified by the most representative additives, lithium nitrate (LiNO3) and vinylene carbonate (VC), applied in a localized high-concentration electrolyte. We found that LiNO3 and VC play distinct roles in forming the SEI, governing the solvation structure, and influencing the kinetics of electrochemical reduction. Their collaboration leads to the desired SEI, ensuring prolonged cycle performance for LMBs. Moreover, we propose mechanisms for different Li growth and cycling behaviors that are determined by the physicochemical properties of SEI, such as uniformity, elasticity, and ionic conductivity. Our findings provide critical insights into the appropriate use of additives, particularly regarding their chemical compatibility.

Enhanced performance in lithium metal batteries: A dual-layer solid electrolyte interphase strategy via perfluoropolyether derivative additive

The utilization of metallic lithium at the negative electrode is regarded as the most promising approach to enhance the energy density of current lithium battery systems. However, uncontrolled lithium dendrite growth leading to instability and low coulombic efficiency (CE) hinders the practical application of metallic lithium as the negative electrode. This study unveils the synthesis of a perfluoropolyether (PFPE) derivative electrolyte additive, denoted as PPP, through reversible addition-fragmentation chain transfer (RAFT) polymerization involving 2-butylsulfanyl-thiocarbonylsulfanyl-propionic acid (PABTC), PFPE and polydioxolane acrylate (PDXLA) as precursors. This additive incorporates fluorinated segments to enhance lithium ion transport efficiency, along with organic segments to improve battery stability. It facilitates the formation of a distinctive dual-layered solid electrolyte interphase (SEI) in 1,3-dioxolane (DOL) based lithium metal batteries. The upper organic protective layer mitigates volume deformation and suppresses lithium dendrite growth, while the lower dense LiF layer enhances lithium ion transport rates, thus improving battery performance. The resulting dual-layer SEI structured LFP | DOL-PPP | Li cell exhibits a capacity retention of 94.1 % after 150 cycles. Moreover, the Li | DOL-PPP | Li cell demonstrates stable cycling performance exceeding 1800 h at 0.2 mA cm-2. This work underscores the significant potential of PFPE derivatives as electrolyte additives in the design and optimization of lithium batteries.

Mg-Composition Dependent Cycle Stability in Zn<sub>1-x</sub>Mg<sub>x</sub>O Li-ion Battery: Transition from Electronic Transport-Limited to Ionic Transport Limited Cycles

This study explores Mg-composition dependent cycle stability in a Zn<sub>1-x</sub>Mg<sub>x</sub>O Li-ion battery, where battery cycles transition from an electronic transport-limited to an ionic transport limited regime. We investigated the impact of Mg doping in Zn<sub>1-x</sub>Mg<sub>x</sub>O nanocrystals on Li-ion battery performance, focusing on Mg compositions between x=0.05 and x=0.15. Mg composition dependent structural and electrical properties were explored using field effect transistors (FETs) and various microscopic/spectroscopic methods. The electronic conductivity was found to be sensitive to changes in Mg composition. Consistently, the initial capacity decreased with an increase in Mg composition, aligning with the reduction in electronic conductivity due to Mg doping. However, with successive cycles, the capacity became independent of the electronic conductivity, an outcome attributed to the formation of a solid-electrolyte interphase (SEI) and the conversion reactions. Initially, Mg doping reduces electronic conductivity due to increased carrier trapping, leading to lower discharge capacity. However, as cycling progresses, the impact of Mg doping diminishes. The formation of the SEI layer becomes more influential, significantly affecting Li-ion transport. Over time, factors like SEI formation, conversion reaction dynamics, and structural changes within the electrode start to dominate the battery's capacity, rather than the initial electronic conductivity influenced by Mg doping. This understanding can guide the development of materials with lower resistance, facilitating faster charging and discharging rates. More importantly, this study indicates that the initial capacity is closely tied to the conductivity of the Zn<sub>1-x</sub>Mg<sub>x</sub>O material.

LiF-Rich Solid Electrolyte Interphase Formation by Establishing Sacrificial Layer on the Separator.

The formation of a stable solid electrolyte interphase (SEI) layer is crucial for enhancing the safety and lifespan of Li metal batteries. Fundamentally, a homogeneous Li+ behavior by controlling the chemical reaction at the anode/electrolyte interface is the key to establishing a stable SEI layer. However, due to the highly reactive nature of Li metal anodes (LMAs), controlling the movement of Li+ at the anode/electrolyte interface remains challenging. Here, an advanced approach is proposed for coating a sacrificial layer called fluorinated self-assembled monolayer (FSL) on a boehmite-coated polyethylene (BPE) separator to form a stable SEI layer. By leveraging the strong affinity between the fluorine functional group and Li+, the rapid formation of a LiF-rich SEI layer in the cell production and early cycling stage is facilitated. This initial stable SEI formation promotes the subsequent homogeneous Li+ flux, thereby improving the LMA stability and yielding an enhanced battery lifespan. Further, the mechanism behind the stable SEI layer generation by controlling the Li+ dynamics through the FSL-treated BPE separator is comprehensively verified. Overall, this research offers significant contributions to the energy storage field by addressing challenges associated with LMAs, thus highlighting the importance of interfacial control in achieving a stable SEI layer.

Fluorinated Surface Engineering towards High‐rate and Durable Potassium‐ion Battery

Solid electrolyte interphase (SEI) crucially affects the rate performance and cycling lifespan, yet to date more extensive research is still needed in potassium‐ion batteries. We report an ultra‐thin and KF‐enriched SEI triggered by tuned fluorinated surface design in electrode. Our results reveal that fluorination engineering alters the interfacial chemical environment to facilitate inherited electronic conductivity, enhance adsorption ability of potassium, induce localized surface polarization to guide electrolyte decomposition behavior for SEI formation, and especially, enrich the KF crystals in SEI by self‐sacrifice from C‐F bond cleavage. Hence, the regulated fluorinated electrode with generated ultra‐thin, uniform, and KF‐enriched SEI shows improved capacity of 439.3 mAh g‐1 (3.82 mAh cm­‐2), boosted rate performance (202.3 mAh g‐1 at 8.70 mA cm‐2) and durable cycling performance (even under high loading of ~8.7 mg cm‐2). We expect this practical engineering principle to open up new opportunities for upgrading the development of potassium‐ion batteries.

Fluorinated Surface Engineering towards High-rate and Durable Potassium-ion Battery.

Solid electrolyte interphase (SEI) crucially affects the rate performance and cycling lifespan, yet to date more extensive research is still needed in potassium-ion batteries. We report an ultra-thin and KF-enriched SEI triggered by tuned fluorinated surface design in electrode. Our results reveal that fluorination engineering alters the interfacial chemical environment to facilitate inherited electronic conductivity, enhance adsorption ability of potassium, induce localized surface polarization to guide electrolyte decomposition behavior for SEI formation, and especially, enrich the KF crystals in SEI by self-sacrifice from C-F bond cleavage. Hence, the regulated fluorinated electrode with generated ultra-thin, uniform, and KF-enriched SEI shows improved capacity of 439.3 mAh g-1 (3.82 mAh cm--2), boosted rate performance (202.3 mAh g-1 at 8.70 mA cm-2) and durable cycling performance (even under high loading of ~8.7 mg cm-2). We expect this practical engineering principle to open up new opportunities for upgrading the development of potassium-ion batteries.

Coordination polymer-reinforced composite polymer electrolyte for all-solid-state Li-metal batteries

Composite polymer electrolytes (CPEs) have garnered significant interest due to their lightweight, flexible, and suitability for large-scale processing. However, current CPEs still face challenges such as unsatisfactory ionic conductivity (σ), low Li+ transference number (t+), and poor interfacial stability. This study presents the synthesis of a coordination polymer by coordinating Co2+ with terpyridine-end-capped polyethylene glycol (Co(tpy)-PEG). The resulting Co(tpy)-PEG-reinforced PEO-based CPE exhibits exceptional properties, including a high σ of 0.22 mS cm−1, large t+ of 0.75, and superior durability in both Li|Li (1400 h at 0.2 mA cm−2) and Li|LiFePO4 cells (70 % capacity retention after 1000 cycles at 1C) at 60 °C, comparable to the best available CPEs. The incorporation of Co(tpy)-PEG filler plays a vital role in enhancing the σ by disrupting the PEO crystallinity and creating additional Li+ conducting pathways. Additionally, it can free Li+ to increase t+ through Lewis acid-base interactions between Co2+ and TFSI−/O atoms, as well as NO3− and Li+. Furthermore, Co(tpy)-PEG facilitates the formation of a stable multicomponent solid electrolyte interphase containing beneficial Li2Sx, LiF, and Li3N. This work introduces a promising strategy for designing and preparing multifunctional fillers capable of simultaneously reinforcing the σ, t+, and interfacial stability of CPEs.

Topological Defect-regulated Porous Carbon Anodes with fast Interfacial and Bulk Kinetics for High-rate and High-energy-density Potassium-ion Batteries.

Carbonaceous materials are regarded as one of the most promising anodes for potassium-ion batteries (PIBs), but their rate capabilities have been largely limited by the slow solid-state potassium diffusion kinetics inside anode and sluggish interfacial potassium ion transfer process. Herein, high-rate and high-capacity PIBs have been demonstrated by facile topological defect-regulation of the microstructure of carbon anodes. The carbon lattice of the as-obtained porous carbon nanosheets with abundant topological defects (TDPCNSs) holds high potassium adsorption energy yet low potassium migration barrier, thereby enabling efficient storage and diffusion of potassium inside graphitic layers. Moreover, the topological defects can induce preferential decomposition of anions, leading to the formation of high potassium ion conductive solid electrolyte interphase (SEI) film with decreased potassium ion de-solvation and transfer barrier. Additionally, the dominant sp2-hybridized carbon conjugated skeleton of TDPCNSs enables high electrical conductivity (39.4 S cm-1) and relatively low potassium storage potential. As a result, the as-constructed TDPCNSs anode demonstrates high potassium storage capacity (504mA h g-1 at 0.1 A g-1), remarkable rate capability (118mA h g-1 at 40 A g-1) as well as long-term cycling stability. This article is protected by copyright. All rights reserved.

LFO modified separator for the initial anode irreversibility compensation in lithium-ion rechargeable full cells

Lithium-ion batteries (LIBs) dominate portable electronics and electric vehicles for their high energy density and long cycle life. However, a part of active Li loss in the initial charge process for the solid electrolyte interphase (SEI) formation at the anode surface, which reduces the energy density and cycle life of LIBs. Prelithiation attempts have been widely regarded as providing additional active lithium to address this issue. Li5FeO4 (LFO) as a cathode prelithiation additive with high donable lithium ions is very promising. But the residues of the gas release limited its further application due to its low conductivity in the first charge process. Here, we prepared CNT/ Polyacrylonitrile (PAN) /LFO/polypropylene (PP) separator by an electrospinning method, the CNT/PAN/LFO/PP separator can effectively improve cycle performance of LFP batteries, benefiting from Li2O participation in the construction of SEI and higher infiltration rate of the electrolyte resulting in faster interfacial Li+ transfer kinetics. The LFP pouch cell with CNT/PAN/LFO/PP separator can maintain a stable output over 1000 cycles (capacity fade rate per cycle of 0.005 %) with a highercapacity increased by 6.2 %.

Chloro-Functionalized Ether-Based Electrolyte for High-Voltage and Stable Potassium-Ion Batteries.

Ether-based electrolyte is beneficial to obtaining good low-temperature performance and high ionic conductivity in potassium ion batteries. However, the dilute ether-based electrolytes usually result in ion-solvent co-intercalation of graphite, poor cycling stability, and hard to withstand high voltage cathodes above 4.0 V. To address the aforementioned issues, an electron-withdrawing group (chloro-substitution) was introduced to regulate the solid-electrolyte interphase (SEI) and enhance the oxidative stability of ether-based electrolytes. The dilute (~0.91 M) chloro-functionalized ether-based electrolyte not only facilitates the formation of homogeneous dual halides-based SEI, but also effectively suppress aluminum corrosion at high voltage. Using this functionalized electrolyte, the K||graphite cell exhibits a stability of 700 cycles, the K||Prussian blue (PB) cell (4.3 V) delivers a stability of 500 cycles, and the PB||graphite full-cell reveals a long stability of 6000 cycles with a high average Coulombic efficiency of 99.98 %. Additionally, the PB||graphite full-cell can operate under a wide temperature range from -5 °C to 45 °C. This work highlights the positive impact of electrolyte functionalization on the electrochemical performance, providing a bright future of ether-based electrolytes application for long-lasting, wide-temperature, and high Coulombic efficiency PIBs and beyond.

Correlating Graphite Surface with Interphase for Fast‐Charging and Low‐Temperature Operation

AbstractThe properties of graphite surface can not only affect the interaction between graphite and electrolyte but also induce the formation of solid electrolyte interphase (SEI) film. Herein, the graphite surface is purposely treated to incorporate oxygen‐containing functional groups, which facilitates a desired Li2CO3‐rich SEI with high ionic conductivity and good mechanical stability. The modified graphite electrodes exhibit significant enhancement in electrochemical performance during rapid charging at the rate of 15 C, where an impressive capacity of 225 mAh g−1 is still maintained, corresponding to a capacity retention of 60.8%. Moreover, the modified electrodes showcase outstanding performance under wide temperature ranging from −50 to +65 °C, with an amazing capacity retention of 97.6% under −20 °C, the conceivable capacity of 105 mAh g−1 at −50 °C as well as excellent stability at both −20 °C and +65 °C. These findings offer valuable insights into the design of a thin and robust Li2CO3‐rich SEI layer via a facile chemical treatment of the graphite surface.

Optimizing lithium-silver alloy phases for enhanced energy density and electrochemical performance

Lithium (Li) metal batteries though with high energy density are still facing issues like Li dendrite growth, dead Li formation, and thick solid electrolyte interphase (SEI) formation, hindering their long-term stability. Recently, Li-Ag alloys have been reported to potentially address these challenges possibly due to their superior conductivity, lithiophilicity, and mechanical stability. In the pursuit of high-energy-density batteries, Li-Ag alloys typically employ a high Li content phase (γ1). In this study, we applied density functional theory (DFT) calculations to compare the thermodynamic stability, Li adsorption, and Li diffusion of Ag-rich Li-Ag alloy within the γ1 phase (AR-γ1), Ag-poor Li-Ag alloy within the γ1 phase (AP-γ1), and pure Li. AR-γ1 showed better thermodynamic stability and improved Li adsorption and diffusion properties compared to AP-γ1 and pure Li. Electrochemical tests further confirmed the advantages of AR-γ1 in terms of electrode kinetics and cell stability compared to AP-γ1 and pure Li. Our study offers guidance for the selection of the most suitable Li-Ag alloys that can be utilized in high-energy-density lithium batteries.

Reduction‐Tolerance Electrolyte Design for High‐Energy Lithium Batteries

AbstractLithium batteries employing Li or silicon (Si) anodes hold promise for the next‐generation energy storage systems. However, their cycling behavior encounters rapid capacity degradation due to the vulnerability of solid electrolyte interphases (SEIs). Though anion‐derived SEIs mitigate this degradation, the unavoidable reduction of solvents introduces heterogeneity to SEIs, leading to fractures during cycling. Here, we elucidate how the reductive stability of solvents, dominated by the electrophilicity (EPT) and coordination ability (CDA), delineates the SEI formed on Li or Si anodes. Solvents exhibiting lower EPT and CDA demonstrate enhanced tolerance to reduction, resulting in inorganic‐rich SEIs with homogeneity. Guided by these criteria, we synthesized three promising solvents tailored for Li or Si anodes. The decomposition of these solvents is dictated by their EPTs under similar solvation structures, imparting distinct characteristics to SEIs and impacting battery performance. The optimized electrolyte, 1 M lithium bis(fluorosulfonyl)imide (LiFSI) in N‐Pyrrolidine‐trifluoromethanesulfonamide (TFSPY), achieves 600 cycles of Si anodes with a capacity retention of 81 % (1910 mAh g−1). In anode‐free Cu||LiNi0.5Co0.2Mn0.3O2 (NCM523) pouch cells, this electrolyte sustains over 100 cycles with an 82 % capacity retention. These findings illustrate that reducing solvent decomposition benefits SEI formation, offering valuable insights for the designing electrolytes in high‐energy lithium batteries.

Reduction-Tolerance Electrolyte Design for High-Energy Lithium Batteries.

Lithium batteries employing Li or silicon (Si) anodes hold promise for the next-generation energy storage systems. However, their cycling behavior encounters rapid capacity degradation due to the vulnerability of solid electrolyte interphases (SEIs). Though anion-derived SEIs mitigate this degradation, the unavoidable reduction of solvents introduces heterogeneity to SEIs, leading to fractures during cycling. Here, we elucidate how the reductive stability of solvents, dominated by the electrophilicity (EPT) and coordination ability (CDA), delineates the SEI formed on Li or Si anodes. Solvents exhibiting lower EPT and CDA demonstrate enhanced tolerance to reduction, resulting in inorganic-rich SEIs with homogeneity. Guided by these criteria, we synthesized three promising solvents tailored for Li or Si anodes. The decomposition of these solvents is dictated by their EPTs under similar solvation structures, imparting distinct characteristics to SEIs and impacting battery performance. The optimized electrolyte, 1 M lithium bis(fluorosulfonyl)imide (LiFSI) in N-Pyrrolidine-trifluoromethanesulfonamide (TFSPY), achieves 600 cycles of Si anodes with a capacity retention of 81 % (1910 mAh g-1). In anode-free Cu||LiNi0.5Co0.2Mn0.3O2 (NCM523) pouch cells, this electrolyte sustains over 100 cycles with an 82 % capacity retention. These findings illustrate that reducing solvent decomposition benefits SEI formation, offering valuable insights for the designing electrolytes in high-energy lithium batteries.

Constructing an Al3+/Zn2+-Based Solid Electrolyte Interphase to Enable Extraordinarily Stable Al3+-Based Electrochromic Devices.

The interface between the electrochromic (EC) electrode and ionic conductor is crucial for high-performance and extraordinarily stable EC devices (ECDs). Herein, the effect of the ALD-AZO interfacial layer on the performance of the WO3 thin film was examined, revealing that an introduction of the ALD-AZO interfacial layer to the Al3+-based complementary ECDs can lead to improved EC performance and stability, such as an extraordinary cyclability of more than 20,000 cycles, an outstanding coloration efficiency of 109.69 cm2 C-1, and a maximum transmittance modulation of 63.44%@633 nm. The probable explanation is that the introduced ALD-AZO interfacial layer can effectively regulate the band gap of WO3, promote the electron transport process, and induce the formation of a robust solid electrolyte interphase to protect the electrode during cycling. These findings offer valuable insights for enhancing the EC performance of the EC thin films and new space for the construction of advanced multivalent Al3+-based ECDs.