Low Temperature Rapid Interfacial Kinetics Achieved by Sodium Titanate Anode Co‐Intercalation Storage Mechanism and Stable Solid Electrolyte Interface DOI
Jiaming Zhu, Xiaofeng Yan, Yuhang Jiang

и другие.

Advanced Functional Materials, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 26, 2024

Abstract Quasi‐layered sodium titanates have been extensively studied as anode materials for sodium‐ion batteries (SIBs) owing to their quasi‐zero‐strain intercalative storage chemistry and high theoretical capacity. However, sluggish sodiation kinetics unstable electrode/electrolyte interface lead rapid capacity decay at low temperatures. Herein, the local electronic structure interlayer spacing of Na 2 Ti O 5 are finely regulated by heteroelement Sn‐doping, oxygen rich vacancies, carbon‐confined (Sn‐HNTO@C) improve low‐temperature performance. Theoretical calculations Sn doping concentration control confirm that appropriate concentrations Sn‐doping vacancy defects can redistribute charge density, enhance + adsorption, reduce diffusion energy barriers, endow Sn‐HNTO@C with stable In addition, optimizing electrolyte systems temperatures allows exhibit a ‐solvent co‐intercalation mechanism in ether‐based electrolytes, avoiding desolvent barriers reducing transfer activation energy. Furthermore, thin, solid organic components promotes interfacial kinetics. Consequently, delivers over 500 cycles (177 mAh g −1 ) Sn‐HNTO@C//Na 3 (VPO 4 F full cell presents 91 200 (−15 °C). This study provides unique guidance titanate anodes emphasizes importance SIBs.

Язык: Английский

Challenges and Breakthroughs in Enhancing Temperature Tolerance of Sodium‐Ion Batteries DOI
Chang Che, Feng Wu, Yu Li

и другие.

Advanced Materials, Год журнала: 2024, Номер 36(28)

Опубликована: Апрель 18, 2024

Abstract Lithium‐based batteries (LBBs) have been highly researched and recognized as a mature electrochemical energy storage (EES) system in recent years. However, their stability effectiveness are primarily confined to room temperature conditions. At temperatures significantly below 0 °C or above 60 °C, LBBs experience substantial performance degradation. Under such challenging extreme contexts, sodium‐ion (SIBs) emerge promising complementary technology, distinguished by fast dynamics at low‐temperature regions superior safety under elevated temperatures. Notably, developing SIBs suitable for wide‐temperature usage still presents significant challenges, particularly specific applications electric vehicles, renewable storage, deep‐space/polar explorations, which requires thorough understanding of how perform different By reviewing the development SIBs, influence on parameters related battery performance, reaction constant, charge transfer resistance, etc., is systematically comprehensively analyzed. The review emphasizes challenges encountered both low high while exploring advancements SIB materials, specifically focusing strategies enhance across diverse ranges. Overall, insights gained from these studies will drive that can handle posed harsh climates.

Язык: Английский

Процитировано

39

Topological Design of Highly Conductive Weakly Solvating Electrolytes for Ultrastable Sodium Metal Batteries Operating at −60 °C and Below DOI

Zhiling Wang,

Tao Zheng,

Shuzhan Wang

и другие.

Journal of the American Chemical Society, Год журнала: 2025, Номер unknown

Опубликована: Фев. 6, 2025

Weakly solvating electrolytes (WSE) can favor reversible Na batteries at -40 °C for some extreme applications because of the low desolvation energy. However, it is challenging to enable lower temperatures. Herein, we uncover that ionic conductivity WSE reduces reaction kinetics -60 °C. Accordingly, a highly conductive weakly electrolyte (HCWSE) designed by introducing additives strongly solvents and dilution NaPF6. The additive dominate solvation sheath, increase dissociation NaPF6 fluidity electrolyte, thus greatly improve conductivity. Furthermore, binding energy between Na+ proposed as descriptor determine power solvents, based on which series ultralow-temperature HCWSEs have been topologically facilely strong-solvation ether into weak-solvation solvents. As demonstration, HCWSE showcases long cycling Na||Na cell with an overpotential 42 mV under 1 mA cm-2 1200 h. Na||NNFM (Na0.75Ni0.25Fe0.25Mn0.5O2) exhibits capacity 79.2 mAh g-1 after 160 cycles. cells also achieve impressive performances -70

Язык: Английский

Процитировано

3

The mystic role of high-entropy designs in rechargeable metal-ion batteries: A review DOI
Yi‐Cheng Lin, Shaohua Luo, Wei Zhao

и другие.

Journal of Energy Chemistry, Год журнала: 2024, Номер 98, С. 441 - 471

Опубликована: Июль 4, 2024

Язык: Английский

Процитировано

16

Status and strategies of electrolyte engineering for low-temperature sodium-ion batteries DOI

Su Yang,

Kaipeng Cheng,

Zhenjiang Cao

и другие.

Journal of Materials Chemistry A, Год журнала: 2024, Номер 12(22), С. 13059 - 13080

Опубликована: Янв. 1, 2024

Herein, we summarize the development of low-temperature electrolyte engineering for SIBs, and then propose several strategies to provide guidance systematic design further commercial application SIBs.

Язык: Английский

Процитировано

13

Sole‐Solvent High‐Entropy Electrolyte Realizes Wide‐Temperature and High‐Voltage Practical Anode‐Free Sodium Pouch Cells DOI Open Access
Yanmei Li, Jiawei Wang, Yingyu Wang

и другие.

Advanced Materials, Год журнала: 2025, Номер unknown

Опубликована: Янв. 21, 2025

Abstract Anode‐free sodium batteries (AFSBs) hold great promise for high‐density energy storage. However, high‐voltage AFSBs, especially those can stably cycle at a wide temperature range are challenging due to the poor electrolyte compatibility toward both cathode and anode. Herein, AFSBs with cycling ability in (−20–60 °C) realized first time via sole‐solvent high‐entropy based on diethylene glycol dibutyl ether solvent (D2) NaPF 6 salt. The unique solvent‐ions effect of strong anion interaction weak cation solvation enables entropy‐driven salt disassociation high‐concentration contact ion pairs, thus simultaneously forming stable anion‐derived electrode–electrolyte interphases Moreover, liquid D2 further extends extremes battery. Consequently, ampere‐hour (Ah)‐level anode‐free pouch cells cyclability −20–60 °C realized. Impressively, cell achieves leadingly high cell‐level density 209 Wh kg −1 capacity retention 83.1% after 100 cycles 25 °C. This work provides inspirations designing advanced electrolytes practical AFSBs.

Язык: Английский

Процитировано

2

Sodium-Ion Battery at Low Temperature: Challenges and Strategies DOI Creative Commons
Yanli Zhao, Zhen Zhang,

Yalong Zheng

и другие.

Nanomaterials, Год журнала: 2024, Номер 14(19), С. 1604 - 1604

Опубликована: Окт. 4, 2024

Sodium-ion batteries (SIBs) have garnered significant interest due to their potential as viable alternatives conventional lithium-ion (LIBs), particularly in environments where low-temperature (LT) performance is crucial. This paper provides a comprehensive review of current research on LT SIBs, focusing electrode materials, electrolytes, and operational challenges specific sub-zero conditions. Recent advancements such carbon-based materials titanium-based are discussed for ability enhance ion diffusion kinetics overall battery at colder temperatures. The critical role electrolyte formulation maintaining efficiency stability under extreme cold highlighted, alongside strategies mitigate capacity loss cycle degradation. Future directions underscore the need further improvements energy density durability scalable manufacturing processes facilitate commercial adoption. Overall, SIBs represent promising frontier storage technology, with ongoing efforts aimed overcoming technical barriers enable widespread deployment cold-climate applications beyond.

Язык: Английский

Процитировано

7

Practical and Versatile Sodium‐Ion Batteries Realized With Nitrile‐Based Electrolytes DOI Open Access
Gaopan Liu, Kai Zhang, Yongjie Cao

и другие.

Advanced Energy Materials, Год журнала: 2025, Номер unknown

Опубликована: Янв. 29, 2025

Abstract Sodium‐ion batteries (SIBs) hold tremendous potential in next‐generation energy storage. However, no SIB has yet achieved simultaneous support for high voltage, rapid charging, and all‐climate adaptability due to electrolyte limitations. This study successfully constructs versatile SIBs using an optimized acetonitrile (AN)‐based electrolyte, which offers excellent high‐voltage tolerance, ionic conductivity, anion‐enriched solvation structure, a wide liquidus temperature range. The engineered solid interphase (SEI) exhibits low resistance exceptional stability, effectively supporting fast temperature‐adaptive operation, long‐term cycling stability. Consequently, this tailored combined with robust SEI, enables hard carbon (HC) anodes achieve reversible capacity of 223 mAh g −1 at rate 5 C. When paired NaNi 1/3 Fe Mn O 2 (NFM) cathode, the HC||NFM full cells operate stably cut‐off voltage 4.15 V, sustaining over 1400 cycles Furthermore, practical 3 Ah pouch cell demonstrates retaining 90.7% its after 1000 cycles, shows adaptability, maintaining 56.4% room‐temperature −60 °C 97.3% retention 350 50 °C. work provides valuable insights developing advanced electrolytes SIBs.

Язык: Английский

Процитировано

1

Achieving Enhanced Sodium Storage Performance of Hard Carbon via Rational Modification of a Starch Precursor DOI
Lihong Zhang, Nuo Chen,

Shangjun Zhang

и другие.

ACS Applied Materials & Interfaces, Год журнала: 2025, Номер 17(9), С. 13861 - 13871

Опубликована: Фев. 25, 2025

Chemical modification of starch hydroxyl groups plays a key role in modulating the microstructures and enhancing electrochemical performance hard carbon (HC) anode sodium-ion batteries (SIBs). However, regulation design advanced sodium storage structures are limited by their diverse complex microstructures. Herein, diammonium phosphate (DAP) as cross-linking agent for corn physicochemical properties surface can effectively promote balance between pore structure interlayer spacing constructed HC. The modified HC generally outperformed that unmodified samples. Specifically, optimized HC-10 achieved an improved reversible capacity (344.16 mAh g-1 at 0.03 A g-1), optimal rate capability (134.73 0.3 enduring cycle life (capacity retention 98.5% after 500 cycles g-1). superior originated from operation DAP starch, resulting formation disordered phases structures. On one hand, facilitates growth layers during pyrolysis affects microinterlayer HC, while it also accelerates decomposition precursor catalyst releases gas phase products, which further modulate defects This work provides reference microstructural paving way development biomass-derived materials with exceptional charge/discharge performance.

Язык: Английский

Процитировано

1

Electrolyte Solvation Structure Regulation for Low-Temperature Sodium-Ion Battery DOI

Yangfeng Wang,

Jinglai Duan, Z. Q. Zhu

и другие.

ACS Applied Materials & Interfaces, Год журнала: 2025, Номер unknown

Опубликована: Май 18, 2025

The development of high-performance sodium-ion batteries (SIBs) that can operate effectively in low-temperature environments is essential for large-scale energy storage systems. Due to the sluggish kinetics Na+ desolvation at electrode-electrolyte interface, capacity SIBs decays rapidly low temperatures, which one main challenges are facing present. On basis diethylene glycol dimethyl ether (DEGDME) electrolyte, 1,3-dioxane (DOL) with a melting point and solvation used as cosolvent, trimethylsilyl isocyanate (Si-NCO) LUMO level an additive optimize structure. This optimization facilitates greater participation PF6- anions inner shell structure, thereby improving its stability over certain temperature range. designed electrolyte enables Na||HC half-cell maintain 88.57% room-temperature -40 °C, retention 94.50% after 100 cycles. Additionally, full cell composed O3-type layered oxide sodium nickel iron manganese (NFMN) hard carbon (HC), 83.73% cycles °C. work provides new insights into formulations enhancing electrochemical temperatures.

Язык: Английский

Процитировано

1

Electrolyte Engineering of Hard Carbon for Sodium‐Ion Batteries: From Mechanism Analysis to Design Strategies DOI

Keying Cui,

Ruilin Hou,

Haoshen Zhou

и другие.

Advanced Functional Materials, Год журнала: 2024, Номер unknown

Опубликована: Дек. 4, 2024

Abstract The hard carbon (HC) anodes with desirable electrochemical performances including high initial Coulombic efficiency, superior rate performance and long‐term cycling play an indispensable role in the practical application of sodium ion batteries (SIBs), which are closely related to electrolytes them matched. Fully analyzing mechanism electrolyte engineering for HC is crucial promoting commercialization SIBs, but still lacking. In this review, correlation between physicochemical properties first summarized. And point out properties, conductivity, de‐solvation energy, interface passivation ability Na + storage HC. Then, formation process, composition, as well structure solid interphase (SEI) on surface mainly discussed, structure‐activity relationship SEI analyzed depth. Moreover, based analysis, relevant design strategies have been Finally, challenges future development directions proposed. This review expected provide professional theoretical guidance contribute rational high‐performance anodes, industrialization SIBs.

Язык: Английский

Процитировано

6