Anion Of Salt Research Articles

Dynamics of nanofiller–polymer synergy in gel formation via macromolecular crowding: Structure-property relationship of halloysite-integrated hybrid gels with abundant carboxyl groups

Halloysite (Hal) nanotube-reinforced hybrids were designed via mimicing macromolecular crowding for effective adsorption of cationic dyes by copolymerization of N-isopropylacrylamide (NIPA) and pH-responsive methacrylic acid (MA) through thermally initiated free-radical mechanism. A perspective on the synthesis of functional PNIPA-based next-generation hybrids was established using dynamics of nanofiller–polymer synergy in gel formation via incorporation of linear polyacrylamide chains. Since the design of hybrids with high polymer fraction is relatively difficult in gel systems in which the components are simply blended, the optimum gel formation was achieved by combining the advantage of one-pot strategy with the macromolecular crowding created using water-soluble polymer. By interacting with linear polyacrylamide chains via hydrogen bonding interactions, Hal-lumens participate in the formation of hybrid networks and are homogeneously distributed in the polymer matrix, thus significantly improving the physicochemical properties. The reversibility and rapid on-off properties of hybrids with varied Hal-loadings were analyzed depending on pH and ionic strength of surrounding medium. Design of hybrids functionalized with specific groups depends on both the amount of these groups and the nature of their distribution in the network. The swelling of hybrids in pH 9.8 is lower compared to results in 10−5 M KCl solution, while there was an increase in the compressive modulus with a decrease in swelling pH. The effect of potassium salts of different anions on salt-induced swelling and elastic response of hybrids was investigated to understand the interactions between salt ions and hybrid network. The expansion of hybrids was found to follow the reverse order of classical Hofmeister series. Depending on Fick's law, hybrid gels followed non-Fickian kinetics in salt solutions, while Fickian swelling was observed in pH 9.8. The influence of Hal-addition on cationic dye methyl violet (MV) adsorption of hybrids was investigated. While the addition of Hal increased the adsorption capacity, 93.6 % efficiency for MV was obtained in the presence of 5.40 % Hal. The obtained results provided a novel routine for designing alkyl acrylamide-based functional hybrid gels using green one-dimensional tube-like nanoparticles.

Internal Electron-Donation Allocation Design for Intrinsic Solubilization of Lithium Nitrate in Ester Electrolyte for Stable Lithium Metal Batteries.

Lithium metal batteries (LMBs) have become a hot topic in the research of next-generation advanced battery technology due to their high specific energy. However, the high reaction activity between lithium metal and electrolyte is considered one of the key bottlenecks limiting large-scale applications of LMBs. As a classic electrolyte additive, LiNO3 significantly improves the stability of lithium metal in ether-based electrolytes. However, its solubility in carbonate-based electrolytes widely used in lithium-ion batteries is extremely low, and its protective effect on lithium metal is limited, which has become a key obstacle to the commercial application of lithium metal batteries. Here, we enhanced the local negative charge density of carbonyl oxygen atoms in carbonate molecules by introducing electron donors, making it easier for them to coordinate with Li+, thereby weakening the interaction between Li+ and NO3-, and significantly increasing the solubility of LiNO3 in ester electrolytes. The modified ester solvent promotes the derivatization and decomposition of salt anions, leading to the formation of a dense SEI layer rich in LiF and LiNxOy. This significantly improves the stability of lithium metal in ester-based electrolytes. The assembled Li||Li symmetric battery shows excellent cycling performance of over 4000 hours.

In Situ Formed Continuous and Dense Inorganic Borate-Based SEI for High-Performance Li-Metal Batteries.

The practical application of lithium metal batteries (LMBs) is largely hindered by the notorious lithium dendrite growth, low cycle efficiency associated with insufficient electrode-electrolyte interphase dynamics, and electrolyte combustion. Here, an advanced electrolyte using a combination of three kinds of salts dissolved in carbonate-based solvents is developed. The salt anions dominate a primary solvation sheath, resulting in weak interaction between Li+ and the solvents, as well as the in situ formation of an inorganic-rich bilayer solid electrolyte interface (SEI). The designed electrolyte enables high cycle stability in LMBs with a high-loading NMC cathode (approximately 20mg cm-2), exhibiting 89.89% capacity retention after 200 cycles with the cutoff voltage of 4.5V. Cryo-TEM characterization and density-functional theory (DFT) calculations reveal that the borate-based bilayer SEI, characterized by an exceptional dense structure, effectively suppresses lithium dendrite growth, and certify the crucial role of inorganic component continuity and density within the SEI, which surpasses the absorption and migration energy barrier in terms of significance. This profound understanding of SEI structure holds great potential for advancing the development of high-stable LMBs and can be expanded to other battery system.

Tailoring Ce-Centered Metal-Organic Frameworks for Fast Li+ Transport in Composite Polymer Electrolyte.

Regulating metal nodes to innovate the metal-organic framework (MOF) structure is of great interest to boost the performance of MOFs-incorporated composite solid electrolytes. Herein, Ce4+ with a low-lying 4f orbital is selected as metal center to coordinate with organic ligand to prepare MOF of Ce-UiO-66. The unsaturated open metal sites and defected oxygen vacancies furnish Ce-UiO-66 with strengthened Lewis acidity, which promotes Ce-UiO-66 interacting effectively with both poly(ethylene oxide) (PEO) and Li salt anions. Accordingly, Ce-UiO-66 as additive fillers can be uniformly dispersed in PEO matrix to form an advanced composite solid-state electrolyte (Ce-UiO@PEO) with accelerated Li+ transport. The optimized Ce-UiO@PEO displays a boosted ionic conductivity of 4.20 × 10-4 S cm-1 and an improved Li+ transference number of 0.39 at 60 °C, which are highly comparable to those of other MOFs@PEO electrolytes. Combined with the mechanical and thermal stabilities, such a Ce-UiO@PEO electrolyte enables Li/Li symmetric and Li/LiFePO4 full cells with superior cycling stability and rate performance. The Ce-UiO@PEO electrolytes are of great potential to be applied in high-performance lithium metal batteries.

Minimizing solvated water via synergistic effect of salt anion and cosolvent enables stable Zn metal anodes in low-cost acetate electrolyte

Minimizing solvated water via synergistic effect of salt anion and cosolvent enables stable Zn metal anodes in low-cost acetate electrolyte

Bioactivity Modulation: Anionic Influence on Cu(II) Schiff Base Complexes

ABSTRACTThis article explains the synthesis of three Schiff base Cu(II) complexes derived from 3‐hydroxybenzaldehyde and ethylenediamine using three distinct copper anionic salts, and it explores the effects of those salts on the properties of the complexes. Elemental analysis, electronic spectra, FT‐IR, ESR, molar conductance, magnetic measurement, thermogravimetric analysis and PXRD were used to characterize the compounds. The anionic salt has been demonstrated to exhibit distinctive characteristics on Gram‐positive and Gram‐negative bacteria in terms of structure, DNA binding, cell viability, DNA breakage and activity. Furthermore, this ligand L1 and its derivatives indicated positive antifungal efficacy against Aspergillus niger and Trichophyton tonsurans. The study elucidates the manner in which distinct anion salts impacted the properties of complexes and their antifungal, anticancer and antibacterial outcomes.

Tow-way regulation strategy for in-situ electropolymerization additives coordinated by double bonds and boric acid groups in lithium secondary batteries

The stability and cycle life of the cathode material directly affect the electrochemical performance of the secondary battery, and the dendrite problem of the anode material greatly destroys its safety. To solve the above problems, here we report a small organic molecule monomer, 2,2-dimethylvinylboronic acid (DEBA) containing carbon–carbon double bonds and boric acid groups as electrolyte additive for lithium secondary battery. The unsaturated carbon–carbon double bonds in DEBA can undergo in-situ electropolymerization during the electrochemical process, forming a polymer network. The electron-deficient boron element can easily combine with the electron-rich lithium salt anion to form a B-F bond. It can promote the transport rate of Li+, alleviate the Li+ concentration gradient at the interface, and achieve uniform and dense deposition on the Li metal surface. The Li//graphite and Li//LiFePO4 half-cell experiments show that DEBA has an excellent tow-way regulation effect. This rationally designed dual-functional electrolyte additive provides a broad prospect for future electrolyte engineering.

N2H4 Derived Sulfonic Acids: Hydrazine Disulfonate, [(SO3)HNNH(SO3)]2-, and Hydrazine Iso-disulfonate, [H2NN(SO3)2]2.

The reaction of hydrazinium sulfate and chlorosulfonic acid in pyridine leads to the pyridinium salt of the hydrazine disulfonate anion, [(SO3)HNNH(SO3)]2-. The salt is the starting material for the preparation of further hydrazine disulfonates, for example of alkaline metals and barium. In all compounds, the [(SO3)HNNH(SO3)]2- anion adopts the gauche conformation. The conformer is chiral but all of the investigated compounds crystallize as racemates. The disulfonate anion can occur in another constitution with the two sulfonate groups attached to only one nitrogen atom. This so-called hydrazine iso-disulfonate, [H2NN(SO3)2]2-, has been prepared through a substitution reaction between potassium imidodisulfonate, K2[HN(SO3)2], and hydroxylamine-O-sulfonic acid, H2NOSO3H. The hydrazine iso-disulfonate anion has been crystallized as potassium and barium compound, respectively. The compounds were characterized by XRD, vibrational spectroscopy, DFT calculations and thermal analyses.

Solid-State Lithium Batteries with In Situ Polymerized Acrylate-Based Electrolytes Capable of Electrochemically Stable Operation at 100 °C.

Solid polymer electrolytes (SPEs) typically consist of salts with mobile anions that could cause instabilities and parasitic side reactions in solid-state lithium (Li) batteries. To address this challenge, single-Li-ion conducting (SLIC) SPEs, where anions of Li salts are covalently attached to the polymer backbone, have been utilized to reduce the number of mobile anions. This approach improves the cationic transference number but is accompanied by a loss of ionic conductivity. In this work, we investigate a synergetic approach of using both a polymerizable SLIC salt and a conventional Li salt in a polymer matrix by in situ polymerization of the poly(propylene glycol) acrylate (PPGA) monomer. The synthesized hybrid SPEs show a high ionic conductivity of up to ∼2 × 10-4 S cm-1 and a relatively high Li-ion transference number of ∼0.4. With a significantly reduced fraction of mobile anions in the combined salt SPE, in situ polymerized SPE cells with a LiFePO4 (LFP) cathode achieve a stable performance for over 100 cycles at temperatures as high as 100 °C, which is unattainable with conventional Li salts or electrolytes. Furthermore, solid-state nuclear magnetic resonance spectra provide additional insights into differences in Li nucleus environments and emphasize a reduction in activation energy for hybrid SPEs due to their more open structure. This study opens the path for the fabrication of high-performance solid polymer Li batteries capable of operating at high temperatures using commercial battery fabrication equipment, as in situ polymerized acrylate-based polymers provide drop-in compatibility with conventional battery production, ease of acrylate polymerization, and inexpensive, facile SPE chemistry. We expect that further tuning of the acrylate-based SPE composition may allow further increases in its conductivity without sacrificing its electrochemical stability or mechanical properties.

DNA: Novel Crystallization Regulator for Solid Polymer Electrolytes in High-Performance Lithium-Ion Batteries.

In this work, we designed a novel polyvinylidene fluoride (PVDF)@DNA solid polymer electrolyte, wherein DNA, as a plasticizer-like additive, reduced the crystallinity of the solid polymer electrolyte and improved its ionic conductivity. At the same time, due to its Lewis acid effect, DNA promotes the dissociation of lithium salts when interacting with lithium salt anions and can also fix the anions, creating more free lithium ions in the electrolyte and thus improving its ionic conductivity. However, owing to hydrogen bonding between DNA and PVDF, excess DNA occupies the lone pairs of electrons of the fluorine atoms on the PVDF molecular chains, affecting the conduction of lithium ions and the conductivity of the solid electrolyte. Hence, in this study, we investigated the effects of adding different DNA amounts to solid polymer electrolytes. The results show that 1% DNA addition resulted in the best improvement in the electrochemical performance of the electrolyte, demonstrating a high ionic conductivity of 3.74 × 10-5 S/cm (25 °C). The initial capacity reached 120 mAh/g; moreover, after 500 cycles, the all-solid-state batteries exhibited a capacity retention of approximately 71%, showing an outstanding cycling performance.

Cationic Covalent Organic Framework-Modified Polypropylene Separator for High-Performance Lithium Metal Batteries.

As an important component of lithium batteries, the wettability and thermal stability of the separator play a significant role in cell performance. Despite the availability of numerous commercial separators, issues such as low ion selectivity and poor thermal stability continue to limit the efficiency and reliability of the batteries. Herein, two cationic covalent organic frameworks (Br-COF and TFSI-COF) with abundant imidazole cationic groups were designed to modify commercial polypropylene (PP) separators. The strong lithium-ion affinity of the cationic COF enables the effective dissociation of lithium salt ion clusters, simplifying the solvent structure of lithium ions to promote lithium ions transport. Additionally, solvent anions can be anchored to the cationic COF by electrostatic interactions, reducing side reactions on the lithium metal anode surface to form a favorable SEI layer, which can effectively inhibit the growth of lithium dendrites. The rapid dissociation of anions in lithium salts with some organic solvents and cationic COFs was revealed by a molecular dynamics simulation. A LiF-rich SEI layer on the lithium metal anode surface was formed, which can speed up Li+ transport at interfaces, leading to consistent lithium deposition and outstanding battery performance. The ordered porous structure of the cationic COF provides interconnected and continuous channels, improving the wettability between the liquid electrolyte and separators, which is conducive to ion transport. When paired with a LiFePO4 cathode and electrolyte (1.0 M LiTFSI in DEC: EC: DMC = 1:1:1), the LiFePO4/TFSI-COF@PP/Li cell demonstrates a prominent cycling capacity of 148.0 mAh g-1 at 0.5 C with a Coulombic efficiency of 98.0% in the first cycle, and the capacity retention is 82.0% after 100 cycles, showing good cycling stability. Thus, this investigation provides inspiration for the expansion of cationic COF-modified separators for next-generation lithium metal batteries.

Derivatization of Undecahalogenated closo-Dodecaborates [B12X11NH3]- (X = F-I): Attaching Isocyanate, Amidinium, and Formamide Functionalities.

Halogenated closo-dodecaborates are very robust and versatile weakly coordinating anions for numerous applications. The introduction of additional substituents, e.g., pseudohalides, allows the tuning of their chemical and physical properties. In this report, the synthesis of the isocyanate-substituted closo-dodecaborates [B12X11(NCO)]2- (X = H, F-I) was investigated. In an attempt to synthesize the undecahalogenated derivatives, a selective and halogen-dependent reaction yielding boron clusters carrying the functional groups amidinium (-NHCHNMe2) and formamide (-NHC(O)H) was discovered. The halogenated anions were fully characterized by vibrational and NMR spectroscopy, mass spectrometry, and X-ray diffraction. Salts of the formamide-substituted anion [B12X11(NHC(O)H)]2- are surprisingly thermally stable in the condensed phase. In contrast, collision-induced dissociation in the gas phase reveals that the isolated dianion [B12X11(NHC(O)H)]2- in the gas phase preferentially loses water, while the protonated form, which was generated from decomposition of the tetraalkylammonium counterion [B12X11(NHC(O)H)H]-, tends to lose carbon monoxide. Possible reaction mechanisms are discussed.

Bimetal Fluorides with Adjustable Vacancy Concentration Reinforcing Ion Transport in Poly(ethylene oxide) Electrolyte.

The poor ambient ionic transport properties of poly(ethylene oxide) (PEO)-based SPEs can be greatly improved through filler introduction. Metal fluorides are effective in promoting the dissociation of lithium salts via the establishment of the Li-F bond. However, too strong Li-F interaction would impair the fast migration of lithium ions. Herein, magnesium aluminum fluoride (MAF) fillers are developed. Experimental and simulation results reveal that the Li-F bond strength could be readily altered by changing fluorine vacancy (VF) concentration in the MAF, and lithium salt anions can also be well immobilized, which realizes a balance between the dissociation degree of lithium salts and fast transport of lithium ions. Consequently, the Li symmetric cells cycle stably for more than 1400 h at 0.1 mA cm-2 with a LiF/Li3N-rich solid electrolyte interphase (SEI). The SPE exhibits a high ionic conductivity (0.5 mS cm-1) and large lithium-ion transference number (0.4), as well as high mechanical strength owing to the hydrogen bonding between MAF and PEO. The corresponding Li//LiFePO4 cells deliver a high discharge capacity of 160.1 mAh g-1 at 1 C and excellent cycling stability with 100.2 mAh g-1 retaining after 1000 cycles. The as-assembled pouch cells show excellent electrochemical stability even at rigorous conditions, demonstrating high safety and practicability.

Simulating the Competitive Ion Pairing of Hydrated Electrons with Chaotropic Cations.

Experiments show that the absorption spectrum of the hydrated electron (ehyd-) blue-shifts in electrolyte solutions compared with what is seen in pure water. This shift has been assigned to the ehyd-'s competitive ion-pairing interactions with the salt cation relative to the salt anion based on the ions' positions on the Hofmeister series. Remarkably, little work has been done investigating the ehyd-'s behavior when the salts have chaotropic cations, which should greatly change the ion-pairing interactions given that the ehyd- is a champion chaotrope. In this work, we remedy this by using mixed quantum/classical simulations to analyze the behavior of two different models of the ehyd- in aqueous RbF and RbI electrolyte solutions as a function of salt concentration. We find that the magnitude of the salt-induced spectral blue-shift is determined by a combination of the number of chaotropic Rb+ cations near the ehyd- and the number of salt anions near those cations so that the spectrum of the ehyd- directly reflects its local environment. We also find that the use of a soft-cavity ehyd- model predicts stronger competitive interactions with Rb+ relative to I- than a more traditional hard cavity model, leading to different predicted spectral shifts that should provide a way to distinguish between the two models experimentally. Our simulations predict that at the same concentration, salts with chaotropic cations should produce larger spectral blue-shifts than salts with kosmotropic cations. We also found that at high salt concentrations with chaotropic cations, the predicted blue-shift is greater when the salt anion is kosmotropic instead of chaotropic. Our goal is for this work to inspire experimentalists to make such measurements, which will help provide a spectroscopic means to distinguish between simulations models that predict different hydration structures for the ehyd-.

A Trio of Revelations: Weakly Solvating Modulation in Aqueous Electrolytes for Zinc Metal Batteries

The emerging concept of weakly solvating electrolytes in multivalent ion aqueous batteries has garnered attention due to their enhanced kinetic performance at a low cost. This article aims to dissect the concept of "weakly solvating electrolyte" into three revelations, i.e., ion solvation, hydrogen bonding strength, and ionic interactions. It is revealed that a weakly interacting solvent must satisfy the requirements of having a solvation strength weaker than ionic interaction than water molecules, as well as disrupting rather than strengthening hydrogen bonding within them. Moreover, electrolyte chemistry requires balancing multiple factors, and the same weakly interacting solvent exhibits varying effects with the variation of the anions of zinc salts. This study offers quantitative descriptors to the concept of weak solvation, particularly for aqueous electrolytes, and provides insights for future electrolyte advancements for multivalent ion batteries.

Qualitative discrimination and quantitative prediction of salt in aqueous solution based on near-infrared spectroscopy

Freshwater resources have been gradually salinized in recent years, dramatically impacting the ecosystem and human health. Therefore, it is necessary to detect the salinity of freshwater resources. However, traditional detection methods make it difficult to check the type and concentration of salt quickly and accurately in solution. This paper uses a portable near-infrared spectrometer to qualitatively discriminate and quantitatively predict the salt in the solution. The study was carried out by adding ten salts of NaCl, KCl, MgCl2, CaCl2, Na2CO3, K2CO3, CaCO3, Na2SO4, K2SO4, MgSO4 to 2 mL of deionized water to prepare a single salt solution (0.02 %–1.00 %) totaling 100 sets. It was found that the Support vector machine (SVM) model was only effective in discriminating the class of salt anions in the solution. The Partial least squares-discriminant analysis (PLS-DA) model, on the other hand, can effectively discriminate the classes of salt in solution, and the accuracies of the optimal model prediction set and the interactive validation set are 98.86 % and 99.66 %, respectively. Furthermore, the Partial least squares regression (PLSR) models can accurately predict the concentration of NaCl, KCl, MgCl2, CaCl2, Na2CO3, K2CO3, CaCO3, Na2SO4, K2SO4, MgSO4 salt solutions. The coefficients of determination R2 of their model interactive validation sets were 0.99, 0.99, 0.99, 0.97, 0.99, 0.99, 0.98, 0.99, 0.98, and 0.98, respectively. This study shows that NIRS can achieve rapid and accurate qualitative and quantitative detection of salts in solution, which provides technical support for the utilization of safe water resources.

Core-shell nanofiber separator incorporated with PDA-PEI co-modified Li0.33La0.57TiO3 nanowires prepared by co-axial electrospinning for dendrite-free lithium metal batteries

The core-shell nanofibers containing PDA-PEI co-modified Li0.33La0.57TiO3 (LLTO) perovskite nanowires in the shell layer were fabricated by co-axial electrospinning technique to apply as separator in dendrite-free lithium metal batteries. The PVDF-HFP with good mechanical properties and polar C–F bonds was used as the core material, and polyacrylonitrile (PAN) with high thermal stability was employed as the shell layer in nanofibers. The PDA-PEI co-modified Li0.33La0.57TiO3 nanowires, reacting with PF6− anions in LiPF6 salt can not only capture free anions but also provide a lithium-ion migration pathway. Moreover, the core-shell structured nanofibers exhibited high mechanical strength (9.2 N/mm2), robust thermal stability (>0% at 200 °C for 1 h), and favorable electrolyte affinity (electrolyte uptake of 732%). Gelation of PVDF-HFP in liquid electrolyte leads to high-ionic conductivity (3.52 mS/cm), Li+ transference number (tLi+ = 0.68), uniform Li+ flux, and smooth Li deposition. The Li plating/stripping test consisting of Li–Li cells (with CS/LLTO-PDA-PEI) carried out at 0.4 mA/cm2 was conducted for 1000 h without a short circuit. NCM-Li and NCM-Gr coin cells using the CS (core-shell)/LLTO-PDA-PEI separator retained long-term cycle stability and good Coulombic efficiency (CE).

Development of a sensitive high-throughput enzymatic assay capable of measuring sub-nanomolar inhibitors of SARS-CoV2 Mpro

The SARS-CoV-2 main protease (Mpro) is essential for viral replication because it is responsible for the processing of most of the non-structural proteins encoded by the virus. Inhibition of Mpro prevents viral replication and therefore constitutes an attractive antiviral strategy. We set out to develop a high-throughput Mpro enzymatic activity assay using fluorescently labeled peptide substrates. A library of fluorogenic substrates of various lengths, sequences and dye/quencher positions was prepared and tested against full length SARS-CoV-2 Mpro enzyme for optimal activity. The addition of buffers containing strongly hydrated kosmotropic anion salts, such as citrate, from the Hofmeister series significantly boosted the enzyme activity and enhanced the assay detection limit, enabling the ranking of sub-nanomolar inhibitors without relying on the low-throughput Morrison equation method. By comparing cooperativity in citrate or non-citrate buffer while titrating the Mpro enzyme concentration, we found full positive cooperativity of Mpro with citrate buffer at less than one nanomolar (nM), but at a much higher enzyme concentration (∼320 nM) with non-citrate buffer. In addition, using a tight binding Mpro inhibitor, we confirmed there was only one active catalytical site in each Mpro monomer. Since cooperativity requires at least two binding sites, we hypothesized that citrate facilitates dimerization of Mpro at sub-nanomolar concentration as one of the mechanisms enhances Mpro catalytic efficiency. This assay has been used in high-throughput screening and structure activity relationship (SAR) studies to support medicinal chemistry efforts. IC50 values determined in this assay correlates well with EC50 values generated by a SARS-CoV-2 antiviral assay after adjusted for cell penetration.

Effect of the Hofmeister series anion salts on the ice recrystallization inhibition activity of tamarind seed polysaccharide

Tamarind seed polysaccharide (TSP) has been identified as an ice recrystallization inhibition (IRI)-active polysaccharide with potential applications in food cryoprotection. In this study, the IRI performance of TSP was investigated using the splat assay in the presence of different salts containing Hofmeister series anions (Na2SO4, NaH2PO4, NaCl, and NaNO3). The results showed that the IRI activity of TSP in different salt solutions depended on the type of ion present, in agreement with the reverse Hofmeister anion sequence: NO3− > Cl− > H2PO4− > SO42−. It was discovered that the Hofmeister series anion salts modulate the IRI activity of TSP by inducing changes in the aggregation and hydration properties of polysaccharides. In particular, TSP exhibited greater IRI activity when characterized by a lower aggregation and higher hydration degree in the presence of chaotropic ions. These findings highlight the influence of additives present in cryopreservation media and contribute to a fundamental understanding of the mechanism underlying the differential influence on the performance of IRI-active polysaccharides.

Novel DNA-Based Polymer Solid Electrolytes for Lithium-Ion Batteries

Solid electrolytes are becoming increasingly popular due to their safety [1], and the application of organic biomolecules in electrochemical devices is also an important strategy for sustainable development [2]. Recently, we have studied the application of DNA in electrochemical energy storage devices [3]. A novel PVDF@DNA solid polymer electrolyte was designed in this work, we studied the effect of different DNA addition amounts on polymer solid electrolytes. DNA as a plasticizer-like additive, reduces the crystallinity of the polymer solid electrolyte and improves its ionic conductivity [4]. At the same time, due to the Lewis acid effect of DNA, it can promote the dissociation of lithium salt when interacting with lithium salt anions, and it can also fix the anions, causing more free lithium ions in the electrolyte, thus improving its ionic conductivity. The polymer solid electrolyte with DNA shows relatively better performance. Hence, the DNA-based polymer solid electrolyte fabricated in this study has substantial potential for application in LSBs.AcknowledgementThis work was supported by the National Research Foundation of Korea (NRF-2021R1A2C1008272). This work was supported by Ministry of Trade, Industry and Energy, KEIT, under the project title "International standard development of evaluation methods for nano-carbon-based high-performance supercapacitors for electric vehicles" (project # 20016144).