Electrolytes For Batteries Research Articles

Regulating the Zn electrode/electrolyte interface with lactose additive for high performance Zn anode

The practical utilization of rechargeable aqueous zinc metal batteries (AZMBs) has been constrained by the formation of zinc dendrites and other associated issues. This article introduces lactose, a compound rich in hydroxyl groups, as an electrolyte additive into the aqueous solution of the electrolyte with the objective of suppressing the harmful growth of zinc dendrites. The lactose additive, with its strong zincophilicity, robust intermolecular hydrogen bonding, and a large number of exposed high electronegativity hydroxyl groups, enables lactose to effectively modulate the electrode/electrolyte interface in a dynamic manner, thereby achieving the stability and reversibility of the zinc anode. The findings presented in this work demonstrate the uniform deposition and stripping of zinc in a 2 M ZnSO4 electrolyte with the addition of lactose, thereby enhancing the cycling performance of Zn||Zn batteries. The alteration of the zinc ion environment on the surface of the zinc electrode, in conjunction with the dynamic modulation of the Gouy-Chapman-Stern (GCS) layer by lactose, increases the nucleation overpotential, thereby facilitating to a uniform deposition morphology in lieu of the formation of large-scale dendrites. Furthermore, the formation of hydrogen bonds serves to prevent the occurrence of side reactions. These factors act in concert to enhance the electrochemical performance of AZMBs. The addition of lactose to the electrolyte has resulted in a significant enhancement in the Coulombic efficiency of the card-type Zn||Cu asymmetric battery, reaching 99.7 %. The biodegradability of lactose and the sustainability of its source make this research conducive to the development of environmentally friendly battery electrolyte additives.

Ternary Eutectic Electrolyte for Flexible Wide-Temperature Zinc-Ion Batteries from -20 °C to 70 °C.

Aqueous Zn-ion batteries (ZIBs) have attracted attention for grid applications due to their cost-effectiveness and high security. However, their lifespan decreases at high temperatures due to declining interfacial stability and increased side reactions. To address these challenges, a ternary deep eutectic solvent-based flexible electrolyte, comprised of Zn(ClO4)2 ⋅ 6H2O, butanedinitrile (BD), and LiCl in an amphoteric polymer matrix, was developed to enable wide-temperature ZIBs working from -20 °C to 70 °C. The interactions among BD, Li+, and zinc hydrate alongside the amphoteric groups on the polyelectrolyte matrix could effectively suppress the interfacial side reactions and Zn dendrites formation. Consequently, the symmetric Zn cell demonstrates exceptional stability across a wide-temperature range, with the ability to survive up to 2780 hours (1 mA cm-2) at 50 °C. Furthermore, the flexible Zn||PANI battery can operate stably over 1000 cycles at 50 °C, boasting an initial specific capacity of 124.8 mAh g-1 and capacity retention rate of 87.9 % (3 A g-1). This work presents an effective strategy for designing high-stability energy storage devices with excellent security features that can function reliably across diverse temperature conditions.

Mechanistic Perspectives: Integration and Repairing Adaptation of Self‐Healing Electrolytes for Zinc Ion Batteries

AbstractSelf‐healing is a magical function that endows energy storage devices with extraordinary resilience and has become a promising strategy for advancing battery technology. This short review focus on the recent developments made in self‐healing chemistry for electrolytes in term of extrinsic and intrinsic dynamical concepts. Firstly, the fundamental mechanism of electrolyte self‐healing and repairing adaptation is introduced. The extrinsic self‐healing mechanism adopts capsule‐vascular networking while intrinsic self‐healing lean physical and chemical routes. The Former healing adaptation, generally follows strong physical networking and covalent linkages, which are more prevalent and practical, compared to the latter case of self‐healing. In addition to that, this review also evaluates the estimated healing capabilities and statistics using thermodynamic protocols. Finally, we propose some possible future research directions and development strategies to further apply the self‐healing phenomenon for zinc ion batteries.

Tailored PEO/PEG-PPG Polymer Electrolyte for Solid-State Lithium-Ion Battery

Abstract Solid polymer electrolytes (SPEs) offer a promising avenue for advancing the performance and safety of all-solid-state batteries. In this study, we investigated the effects of blending poly(ethylene oxide) (PEO) with amorphous poly(propylene glycol) (PPG) or poly(ethylene glycol-ran-propylene glycol) (PEG-PPG) to engineer SPEs with enhanced electrochemical properties. By blending PEO with PEG-PPG or PPG, we effectively lowered the crystallinity of PEO, facilitating the diffusion of lithium ions through the SPE and broadening its operational temperature range. This optimization strategy enhanced ionic conductivity and significantly reduced the interfacial resistance between the electrolyte and electrode, thus improving electrochemical stability. The solid-state lithium/lithium iron phosphate (LiFePO4 or LFP) with PEO blended with 7% PEG-PPG showed excellent charge/discharge cycling stability, with maximal discharge capacities of 165 mAh g-1 and 162 mAh g-1 at a current rate of 0.2 C at 60 and 125°C, respectively. The PEG-PPG-based SPE outperformed the PPG polymer-based SPE in terms of better electrochemical performance and a wider temperature range due to its longer polymer chain. This combination offered improved ionic conductivity, interface stability, and electrolyte compatibility with electrodes, making it highly suitable for high-demand applications of lithium-ion batteries.

Localized High-Concentration Electrolyte for All-Carbon Rechargeable Dual-Ion Batteries with Durable Interfacial Chemistry.

Lithium-based rechargeable dual-ion batteries (DIBs) based on graphite anode-cathode combinations have received much attention due to their high resource abundance and low cost. Currently, the practical realization of the batteries is hindered by easy oxidation of the electrolyte at the cathode interface, and solvent co-intercalation at the anode-electrolyte interface. Configuration of a "solvent-in-salt" electrolyte with a high concentration of Li salt is expected to stabilize the electrolyte chemistry versus both electrodes, yet inevitably reduces the mobility of the solvated working ions and increases the cost of the electrolyte. Herein, we propose to build a localized high-concentration electrolyte by adding hydrofluoroether as the diluent to reduce the salt content while improving the solvation structure, allowing more anions to enter the inner solvation sheath. The new electrolyte helps to form uniform and thin interfaces, with elevated contents of inorganic fluorides, on both electrodes, which effectively suppress electrolyte oxidation at the cathode and optimize electrolyte-electrode compatibility at the anode while facilitating charge transfer across the interface. Consequently, the DIBs with graphite as anode and cathode operate for 3000 cycles and retain a high-capacity retention of 95.7%, highlighting the importance of stable interfacial chemistry in boosting the electrochemical performance of DIBs.

Synthesis and characterization of MoS2-carbon based materials for enhanced energy storage applications

The article delves into the synthesis and characterization of MoS2-carbon-based materials, holding promise for applications in supercapacitors and ion batteries. The synthesis process entails the preparation of MoS2 and its carbon hybrids through exfoliation, hydrothermal treatment, and subsequent pyrolysis. Various analytical techniques were employed to comprehensively examine the structural, compositional, and morphological properties of the resulting materials. The article explores the electrochemical performance of these electrode materials in supercapacitors and ion batteries (LiB, SiB, KiB). Electrochemical measurements were conducted in aqueous electrolyte for supercapacitors and various aprotic electrolytes for ion batteries. Results highlight the impact of the synthesis process on electrochemical performance, emphasizing factors such as capacitance, rate capability, and charge/discharge cycle performance. Hydrothermally treated MoS2-carbon exhibited a specific capacitance of approximately 150 F g-1 in supercapacitors, attributed to its high surface area and efficient charge storage mechanisms. Additionally, for Li-ion battery materials without hydrothermal treatment showed impressive capacity retention of around 88% after 500 charge-discharge cycles, starting with an initial specific capacity of about 920 mAh/g. Long-term stability was demonstrated in both supercapacitors and lithium-ion batteries, with minimal capacitance degradation even after extensive charge-discharge cycles. This research underscores the potential of MoS2-based materials as effective energy storage solutions.

La1-xSrxF3-x: A Solid-State Electrolyte for Fluoride Ion Battery with High Ionic Conductivity and Wide Electrochemical Potential Window

Abstract Fluoride ion conductors are developed for use as solid-state electrolytes in fluoride ion batteries which are one of promising candidates for next-generation storage batteries. Ba-doped LaF3 (La0.9Ba0.1F2.9: LBF) is mainly used as a solid-state electrolyte in fluoride ion batteries. However, room temperature conductivity of LBF is considerably low, on the order of 10-6 S cm-1 and it is still unclear the optimal elements to be doped to LaF3. In this study, we have explored La0.9SrxBa0.1-xF2.9 system (x = 0, 0.01, 0.025, 0.05, 0.1), in which Ba in LBF is substituted for Sr and investigated the composition dependence of ionic conductivity. We elucidate that the higher concentration of Sr without Ba can significantly improve the ionic conductivity, and the maximum ionic conductivity of La0.9Sr0.1F2.9 is 1.5 × 10-5 S cm-1 at room temperature, which is one order of magnitude larger than that of LBF. The higher ionic conductivity of LSF is due to the larger grain size and higher sintering density of LSF compared to LBF, which results in lower grain boundary resistance. The LSF total ionic conductivity of 10-4 S cm-1 can be achieved at 350 K, which significantly lowers operating temperature of fluoride ion batteries down to 350 K.

Investigation of the Effects of Cu and Fe/Cu Doping on ZnO Nanoparticles for Application as a Solid Electrolyte Battery

In this work, investigation is done on the effect of doping with copper (Cu) and iron/copper (Fe/Cu) on zinc oxide (ZnO) nanomaterials synthesized through a cost‐effective wet chemical precipitation method for application as a solid‐state electrolyte battery. The scanning electron microscope with energy dispersive X‐ray spectroscopy is used to investigate the morphology and elements presence in Cu and Fe/Cu‐doped ZnO nanoparticles. The X‐ray diffraction data illustrates that the crystallite sizes of pure ZnO, Cu–ZnO, and Fe/Cu–ZnO nanoparticles are 14.86, 13.35, and 10.66 nm, respectively, at the (101) plan calculated by Debye Scherrer's formula. The UV‐Vis absorption spectrum shows that the band gap energies of ZnO, Cu–ZnO, Fe–ZnO, and Fe/Cu–ZnO nanoparticles are identified as 3.382, 3.690, 3.5, and 3.465 eV, respectively. The electrical characterization revealed maximum impedance in Fe/Cu–ZnO nanoparticles with 400 Ω at 1 KHz frequency in comparison to other samples. The current–voltage (I–V) measurement shows that the current sensitivity and electrical conductivity are both enhanced for Fe/Cu–ZnO nanoparticles. Fe and Cu co‐doping improved the electrical characteristics of ZnO, and the Fe/Cu–ZnO nanoparticles are employed as a solid electrolyte in a battery, which achieved a high specific charge capacity of 657.85 mAh g−1.

Phthalocyanine-based solid-state electrolyte for high-capacity and long-life lithium-ion batteries

Phthalocyanine-based solid-state electrolyte for high-capacity and long-life lithium-ion batteries

Simultaneous measurement of temperature and refractive index based on fiber optic Fabry-Pérot cavity in batteries

Abstract A Fabry-Pérot (FP) sensor for simultaneous measurement of refractive index and temperature of an all-fiber synchronous liquid based on the Vernier effect is proposed, special application for internal monitoring of lithium-ion battery electrolytes. The theoretical model of high sensitivity cascade Fabry-Pérot interferometer (PFPI) is established, the sensitivity amplification mechanism of PFPI is analyzed in detail, the perfect matching scheme for measuring the refractive index of the electrolyte inside the battery is designed according to the matching conditions of the optical path, and the corresponding sensors for simultaneous measurement of the temperature and the refractive index are fabricated. The experimental results show that the sensor has a maximum refractive index sensitivity of 15391.5033 nm/RIU, a good linear fit, and can effectively monitor the refractive index change of the electrolyte by 10-4 orders of magnitude during normal charging and discharging of lithium-ion batteries. Compared to traditional epoxy adhesive bonded or laser processed FP sensors, this all-fibre optic structure not only improves temperature and corrosion resistance, but also significantly reduces temperature cross-sensitivity. Its small size and excellent resistance to high temperature and corrosion ensure the sensor's excellent response and broad application prospects in monitoring the refractive index of the electrolyte in 18650 lithium-ion batteries, which provides effective technical support for monitoring the health status of batteries and detecting early safety issues.

3D-Printed Flexible Polyacrylamide/Alginate Gel Polymer Electrolyte for Zinc-Ion Batteries

Flexible and wearable electronics are increasingly popular and utilized in various forms. Batteries have become essential as an energy source for wearable electronics. To meet demands of such electronics, these batteries must remain flexible, lightweight, possess good electrochemical performance, customizable shape, and ensure safety. Zinc-ion batteries (ZIBs) have emerged as a promising energy source for these applications. However, ZIBs encounter challenges due to the lack of flexible electrolytes. Polyacrylamide (PAM) is a polymer widely used as gel polymer electrolytes (GPEs) owing to its versatile electrical conductivity and excellent flexibility. However, PAM alone lacks the mechanical strength required to support flexible and wearable electronics adequately. To address this limitation, alginate (Alg), a polysaccharide with good compatibility with PAM, is incorporated in varying concentrations (0-3 %wt.) to form interpenetrating networks (IPN) hydrogels, with a chemical network of PAM and a physical network of alginate to enhance the overall mechanical properties. Following this, the 3D-printed PAM/Alg hydrogels are immerged in a 2M ZnSO4 electrolyte to create PAM/Alg gel polymer electrolytes (PAM/Alg-GPEs). This process significantly improves the mechanical properties of PAM/Alg-GPEs. Subsequently, the ionic conductivity of these 3D-printed PAM/Alg-GPEs is evaluated using electrochemical impedance spectroscopy (EIS). The results demonstrate that PAM/Alg-GPEs exhibit the desired flexibility along with sufficient electrochemical performance, making them promising candidates for use as wearable electrolytes in zinc-ion batteries.

Functionalized Quasi-Solid-State Electrolytes in Aqueous Zn-Ion Batteries for Flexible Devices: Challenges and Strategies.

The rapid development of wearable and intelligent flexible devices has posed strict requirements for power sources, including excellent mechanical strength, inherent safety, high energy density, and eco-friendliness. Zn-ion batteries with aqueous quasi-solid-state electrolytes (AQSSEs) with various functional groups that contain electronegative atoms (O/N/F) with tunable electron accumulation states are considered as a promising candidate to power the flexible devices and tremendous progress has been achieved in this prospering area. Herein, this review proposes a comprehensive summary of the recent achievements using the AQSSE in flexible devices by focusing on the significance of different functional groups. The fundamentals and challenges of the ZIBs are introduced from a chemical view in the first place. Then, the mechanism behind the stabilization of the flexible ZIBs with the functionalized AQSSE is summarized and explained in detail. Then the recent progress regarding the enhanced electrochemical stability of the ZIBs with the AQSSE is summarized and classified based on the functional groups on the polymer chain. The advanced characterization methods for the AQSSE are briefly introduced in the following sections. Last but not least, current challenges and future perspectives for this promising area are provided from the authors' point of view.

A Computational Review on Localized High‐Concentration Electrolytes in Lithium Batteries

AbstractElectrolyte engineering plays a vital role in improving the battery performance of lithium batteries. The idea of localized high‐concentration electrolytes that are derived by adding “diluent” in high‐concentration electrolytes has been proposed to retain the merits and alleviate the disadvantages of high‐concentration electrolytes, and it has become the focus of attention in high‐voltage lithium batteries, flame‐retardant lithium batteries, and low‐temperature lithium batteries. Extensive efforts have been made to elucidate the fundamentals of localized high‐concentration electrolytes. This review provides an overview of state‐of‐the‐art computational progress in the studies of localized high‐concentration electrolytes, focusing on the application of computational techniques to analyze the redox stability, solvation structures, and interface characteristics of lithium batteries with localized high‐concentration electrolytes. Integrated with experimental approaches, complementing each other, computational methods are believed to be conducive to understanding the working mechanism and designing localized high‐concentration electrolytes for better lithium batteries in the future.

Construction of Ordered and Fast Lithium Ion Channels in Gel Electrolytes for Li-SPAN Batteries.

As one of the most promising battery systems, the lithium sulfur battery is expected to be widely used in fields of high energy density demands. Owing to the unique solid-solid conversion mechanism, there is no shuttle effect for the Li-SPAN (sulfurized polyacrylonitrile) battery. However, the compatibility between Li anode and carbonate electrolyte has not been resolved, which prevents the SPAN from practical applications. Herein, an organic-inorganic gel carbonate electrolyte is proposed to stabilize interphases and structures of both the anode and cathode, where polyimide (PI) is used for electrolyte gelation, which can assist in the uniform distribution of inorganic components at the electrolyte interface. Furthermore, ZnS nanodots loaded on two-dimensional MoS2 flakes provide abundant Li-ion diffusion paths, improve the transfer kinetic of Li ions, and induce uniform nucleation and deposition of Li. This gel electrolyte ensures Li symmetric cells a long-term cycle life of more than 900 h under the condition of deep lithium plating/stripping at 5 mAh cm-1. Li∥Cu cells exhibit a prolonged lifespan of 800 h with a CE of 98.3%. Furthermore, the Li-SPAN battery shows stability of more than 850 cycles, with the capacity retention of 85.1%. This work provides an approach for high-energy Li-SPAN batteries with carbonate-based electrolytes.

Correlation Between Microscopic Current Fluctuations Observed at Ultra-Microelectrodes and Macroscopic Bulk Electrolysis Performance in Redox-Active Microemulsions

Abstract Microemulsions (µEs) have been proposed as redox flow battery (RFB) electrolytes that maximize ionic conductivity and charge capacity by synergizing two immiscible phases. However, charge transfer during electrolysis in µEs is poorly understood. Here, we show that ultramicroelectrode electrolysis of ferrocene-loaded µEs - 20%, 60%, and 90% water - reveals stochastic current fluctuations. These are differentiated in the scanning electrochemical microscopy (SECM) geometry, where power spectral density analysis showed distinct changes in the frequency contributions. SECM in the substrate generation-tip collection mode showed that fluctuations arise under mass-transfer control. Significant differences in the diffusion coefficient of ferrocene species were deducted from SECM approach curves, suggesting phase transfer behavior. Using bulk electrolysis, we calculated the charge accessibility and cycling behavior in the µEs. A decrease in the stochastic behavior of the µEs seems to correlate to a higher accessibility and cycling performance, with the 90% water µE displaying the best reversibility and the 60% the lowest. Altogether, these results suggest that Marangoni-type convection driven by concentration gradients and/or µE restructuring during charge transfer play a role in the electrochemical performance of µEs. This presents opportunities for screening and diagnosing the performance of these emerging RFB electrolytes.

Recent research progress on Li29Zr9Nb3O40-based solid electrolytes for lithium batteries

All-solid-state batteries have become a research hotspot because of their high specific capacity and safety. Solid-state electrolytes are the key material of all-solid-state lithium-ion batteries, and their properties directly affect the overall performance of lithium-ion batteries. So far, many inorganic solid electrolytes have been reported, such as NASICON, LISICON, perovskite, and garnet-type solid electrolyte. However, some lithium-rich rock salt-structured electrolytes, such as Li2ZrO3, LiNbO4, and Li6Zr2O7, have been underappreciated in the field of solid-state electrolytes due to their lower ionic conductivity at room temperature. While investigating solid solution formation, Li6Zr[Formula: see text][Formula: see text]Nb[Formula: see text]O[Formula: see text][Formula: see text][Formula: see text], a new phase known as Li[Formula: see text]Zr9Nb3O[Formula: see text] with a rock-salt structure was discovered. After decades, it was not until a team prepared Li[Formula: see text]Zr9Nb3O[Formula: see text] ceramics by sol-gel method, which exhibited high ionic conductivity (10[Formula: see text]–10[Formula: see text]S cm[Formula: see text]) at room temperature, that the substance showed great potential as a solid electrolyte in all-solid-state lithium-ion batteries. In this paper, the crystal structure, lithium-ion transport mechanism, preparation method, and element doping of Li[Formula: see text]Zr9Nb3O[Formula: see text] are described comprehensively based on research progress in recent years. Then, development prospects and challenges of the concrete application of Li[Formula: see text]Zr9Nb3O[Formula: see text]in all-solid-state lithium-ion batteries are also discussed.

Multisite Crosslinked Poly(ether-urethane)-Based Polymer Electrolytes for High-Voltage Solid-State Lithium Metal Batteries.

Utilizing solid-state polymer electrolytes (SPEs) in high-voltage Li-metal batteries is a promising strategy for achieving high energy density and safety. However, the SPEs face the challenges such as undesirable mechanical strength, low ionic conductivity and incompatible high-voltage interface. Here, a novel crosslinked poly(ether-urethane)-based SPE with a molecular cross-linked structure is fabricated to create high-throughput Li+ transport pathway. The amino-modified Zr-porphyrin-based metal-organic frameworks (ZrMOF) are introduced as multisite cross-linking nodes and polymer chain extenders. The abundant ether/ketonic-oxygen and Lewis acid sites in the SPE achieve high Li+ conductivity (5.7 × 10-4 S cm-1 at 30°C) and Li+ transference number (0.84). The interpenetrating cross-linked structure of SPE with robust mechanical strength results in a record cycle life of 8000h in Li||Li symmetric cell. The high structural stability of ZrMOF and abundant electron-withdrawing urethane/ureido groups in the SPE with high oxidation potential (5.1V) enables a discharge capacity of 182 mAh g-1 at 0.3 C over 500 cycles in a LiNi0.8Co0.1Mn0.1O2||Li cell. Remarkably, a high energy density of 446Wh kg-1 in a 1.5-Ah pouch cell is obtained with high loading cathode (≈4 mAh cm-2), demonstrating a great prospect of the current SPE for practical application in solid-state, high-voltage Li-metal batteries.

Halogen-Bonding Nanoarchitectonics in Supramolecular Plasticizers for Breaking the Trade-Off between Ion Transport and Mechanical Strength of Polymer Electrolytes for High-Voltage Li-Metal Batteries.

The low ionic conductivity of poly(ethylene oxide) (PEO)-based polymer electrolytes at room temperature impedes their practical applications. The addition of a plasticizer into polymer electrolytes could significantly promote ion transport while inevitably decreasing their mechanical strength. Herein, we report a supramolecular plasticizer (SMP) to break the trade-off effect between ionic conductivity and mechanical properties in PEO-based polymer electrolytes. Accordingly, the SMP is constructed by tetraethylene glycol dimethyl ether (G4) and SbF3 through halogen bonds. The SMP-plasticized PEO electrolyte (PEO/SMP) presents a simultaneously enhanced ionic conductivity of 2.4 × 10-4 S cm-1 (25 °C) and a high mechanical strength of 8.1 MPa, compared to those of pristine PEO-based electrolytes. Benefiting from the halogen bonds between G4 and SbF3, the Li-O coordination in PEO/SMP is evidently weakened, and thus rapid Li+ transport is achieved. Furthermore, the PEO/SMP electrolyte possesses a wide electrochemical stability window of 4.5 V and, importantly, derives an inorganic-rich SEI with a low interfacial resistance on a lithium metal surface. By using PEO/SMP, the lithium-metal battery with the LiNi0.5Co0.2Mn0.3O2 cathode exhibits a good rate and long-term cycling performance with a capacity retention of 75.3% (500 cycles). This work offers a rational guideline for the design of polymer electrolytes suitable for high-performance lithium-metal batteries.

Promises and challenges of polyoxometalates (POMs) as an alternative to conventional electrolytes in redox flow batteries (RFBs)

Promises and challenges of polyoxometalates (POMs) as an alternative to conventional electrolytes in redox flow batteries (RFBs)

Li-ion solvation structure at electrified solid-liquid interface: Understanding solvation structure dynamics and its role in electrochemical energy storage through binary ethylene carbonate and dimethyl carbonate solvent.

Binary solvent electrolytes can provide interpretations for designing advanced electrolytes of next generation batteries. This study investigates the adsorption mechanisms of solvated lithium ions in binary solvents near charged electrodes. Molecular dynamic simulations are performed for lithium hexafluorophosphate (LiPF6) in ethylene carbonate and dimethyl carbonate (EC:DMC) solvent sandwiched between two electrodes. Results show that lithium ions form a tetrahedral solvation structure with two EC and two DMC molecules. The solvated lithium ion shows anti-electrostatic interaction with electrodes. This can be attributed to the electrostatic attraction of the polar end of the DMC molecule, which keeps the cation anchored to the positive electrode. Meanwhile, the solvation structure adopts a fix orientation at the negative electrode, which leads to unchanged electrostatic interaction at high charge density. Finally, EC molecules are swapped by DMC molecules near the negative electrode at high charge density. This leads to a decrease in local relative permittivity and, therefore, a decrease in differential capacitance. The differential capacitance of the positive electrode continuously decreases with increasing charge density. This is caused by the partial anchoring of solvent molecules holding the cations, which cancels the adsorption of anions near the positive electrode. This study provides insights into designing better electrolytes for efficient battery performance.