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      Overview of Inorganic Electrolytes for All-Solid-State Sodium Batteries

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          Abstract

          All-solid-state sodium batteries (AS 3B) emerged as a strong contender in the global electrochemical energy storage market as a replacement for current lithium-ion batteries (LIB) owing to their high abundance, low cost, high safety, high energy density, and long calendar life. Inorganic electrolytes (IEs) are highly preferred over the conventional liquid and solid polymer electrolytes for sodium-ion batteries (SIBs) due to their high ionic conductivity (∼10 –2–10 –4 S cm –1), wide potential window (∼5 V), and overall better battery performances. This review discusses the bird’s eye view of the recent progress in inorganic electrolytes such as Na-β”-alumina, NASICON, sulfides, antipervoskites, borohydride-type electrolytes, etc. for AS 3Bs. Current state-of-the-art inorganic electrolytes in correlation with their ionic conduction mechanism present challenges and interfacial characteristics that have been critically reviewed in this review. The current challenges associated with the present battery configuration are overlooked, and also the chemical and electrochemical stabilities are emphasized. The substantial solution based on ongoing electrolyte development and promising modification strategies are also suggested.

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          Most cited references125

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          Sodium-ion batteries: present and future.

          Energy production and storage technologies have attracted a great deal of attention for day-to-day applications. In recent decades, advances in lithium-ion battery (LIB) technology have improved living conditions around the globe. LIBs are used in most mobile electronic devices as well as in zero-emission electronic vehicles. However, there are increasing concerns regarding load leveling of renewable energy sources and the smart grid as well as the sustainability of lithium sources due to their limited availability and consequent expected price increase. Therefore, whether LIBs alone can satisfy the rising demand for small- and/or mid-to-large-format energy storage applications remains unclear. To mitigate these issues, recent research has focused on alternative energy storage systems. Sodium-ion batteries (SIBs) are considered as the best candidate power sources because sodium is widely available and exhibits similar chemistry to that of LIBs; therefore, SIBs are promising next-generation alternatives. Recently, sodiated layer transition metal oxides, phosphates and organic compounds have been introduced as cathode materials for SIBs. Simultaneously, recent developments have been facilitated by the use of select carbonaceous materials, transition metal oxides (or sulfides), and intermetallic and organic compounds as anodes for SIBs. Apart from electrode materials, suitable electrolytes, additives, and binders are equally important for the development of practical SIBs. Despite developments in electrode materials and other components, there remain several challenges, including cell design and electrode balancing, in the application of sodium ion cells. In this article, we summarize and discuss current research on materials and propose future directions for SIBs. This will provide important insights into scientific and practical issues in the development of SIBs.
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            Lithium-sulfur batteries: electrochemistry, materials, and prospects.

            With the increasing demand for efficient and economic energy storage, Li-S batteries have become attractive candidates for the next-generation high-energy rechargeable Li batteries because of their high theoretical energy density and cost effectiveness. Starting from a brief history of Li-S batteries, this Review introduces the electrochemistry of Li-S batteries, and discusses issues resulting from the electrochemistry, such as the electroactivity and the polysulfide dissolution. To address these critical issues, recent advances in Li-S batteries are summarized, including the S cathode, Li anode, electrolyte, and new designs of Li-S batteries with a metallic Li-free anode. Constructing S molecules confined in the conductive microporous carbon materials to improve the cyclability of Li-S batteries serves as a prospective strategy for the industry in the future.
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              Plating a Dendrite-Free Lithium Anode with a Polymer/Ceramic/Polymer Sandwich Electrolyte.

              A cross-linked polymer containing pendant molecules attached to the polymer framework is shown to form flexible and low-cost membranes, to be a solid Li(+) electrolyte up to 270 °C, much higher than those based on poly(ethylene oxide), to be wetted by a metallic lithium anode, and to be not decomposed by the metallic anode if the anions of the salt are blocked by a ceramic electrolyte in a polymer/ceramic membrane/polymer sandwich electrolyte (PCPSE). In this sandwich architecture, the double-layer electric field at the Li/polymer interface is reduced due to the blocked salt anion transfer. The polymer layer adheres/wets the lithium metal surface and makes the Li-ion flux at the interface more homogeneous. This structure integrates the advantages of the ceramic and polymer. With the PCPSE, all-solid-state Li/LiFePO4 cells showed a notably high Coulombic efficiency of 99.8-100% over 640 cycles.
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                Author and article information

                Journal
                Langmuir
                Langmuir
                la
                langd5
                Langmuir
                American Chemical Society
                0743-7463
                1520-5827
                30 July 2024
                13 August 2024
                : 40
                : 32
                : 16690-16712
                Affiliations
                []Electro-Materials Research Laboratory, Centre for Nanoscience and Technology, Pondicherry University , Puducherry 605 014, India
                []College of Materials Science and Engineering, Taiyuan University of Science and Technology , Taiyuan 030024, China
                [§ ]Integrated Composites Laboratory (ICL), Department of Mechanical and Construction Engineering, Northumbria University , Newcastle Upon Tyne NE1 8ST, U.K.
                []Department of Electrical Engineering, Faculty of Engineering, Najran University , Najran 11001, Saudi Arabia
                Author notes
                Author information
                https://orcid.org/0000-0002-8021-8530
                https://orcid.org/0000-0001-6231-5575
                https://orcid.org/0000-0002-6747-2016
                https://orcid.org/0000-0003-0134-0210
                https://orcid.org/0000-0002-0855-752X
                Article
                10.1021/acs.langmuir.4c01845
                11325648
                39078042
                4d09f71e-c6e5-4643-89bc-278d8e58d5cd
                © 2024 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 16 May 2024
                : 04 July 2024
                : 01 July 2024
                Funding
                Funded by: Najran University, doi 10.13039/501100005911;
                Award ID: NU/RG/SERC/12/10
                Funded by: Jiangsu University of Science and Technology, doi 10.13039/501100012216;
                Award ID: NA
                Categories
                Review
                Custom metadata
                la4c01845
                la4c01845

                Physical chemistry
                Physical chemistry

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