Na-ion Batteries

Na-ion Batteries
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Описание книги

This book covers both the fundamental and applied aspects of advanced Na-ion batteries (NIB) which have proven to be a potential challenger to Li-ion batteries. Both the chemistry and design of positive and negative electrode materials are examined. In NIB, the electrolyte is also a crucial part of the batteries and the recent research, showing a possible alternative to classical electrolytes – with the development of ionic liquid-based electrolytes – is also explored. <p>Cycling performance in NIB is also strongly associated with the quality of the electrode-electrolyte interface, where electrolyte degradation takes place; thus, Na-ion Batteries details the recent achievements in furthering knowledge of this interface. Finally, as the ultimate goal is commercialization of this new electrical storage technology, the last chapters are dedicated to the industrial point of view, given by two startup companies, who developed two different NIB chemistries for complementary applications and markets.

Оглавление

Laure Monconduit. Na-ion Batteries

Table of Contents

List of Illustrations

List of Tables

Guide

Pages

Na-ion Batteries

Introduction

I.1. Why Na-ion batteries?

I.2. From the electrodes to the electrolyte for NIBs. I.2.1.Positive electrodes

I.2.2.Negative electrodes

I.2.3.Electrolytes and the solid electrolyte interphase

I.3. Future commercialization of NIBs

I.4. References

1. Layered NaMO2 for the Positive Electrode

1.1. Research history of layered transition metal oxides as electrode materials for Na-ion batteries until 2009

1.2. Crystal structures of layered materials. 1.2.1.Crystal structures of synthesizable NaxMO2

1.2.2.Structural changes of O3-NaMO2by Na extraction

1.2.3.Structural changes of P2-NaxMO2by Na extraction

1.3. O3-type layered materials. 1.3.1.NaMO2(M = Sc, Ti, V, Cr, Mn, Fe, Co, Ni)

1.3.1.1. O3-NaScO2, O3-NaTiO2and O3-NaVO2

1.3.1.2. O3-NaCrO2

1.3.1.3. O’3-NaMnO2

1.3.1.4. O3-NaFeO2

1.3.1.5. O3-NaCoO2

1.3.1.6. O’3-NaNiO2

1.3.2.O3-Na[M,M’]O2(M, M’ = transition metals)

1.3.2.1. O3-Na[Fe,M]O2

1.3.2.2. O3-Na[Fe,Co,M]O2

1.3.2.3. O3-Na[Ni,Mn,M]O2

1.3.3.Moist air stability of O3-NaMO2and surface coating

1.4. P2-type layered materials. 1.4.1.Practical issues of P2-type materials for Na-ion batteries

1.4.2.P2-Na2/3[Mn,Co,M]O2

1.4.3.P2-Na2/3[Mn,Fe,M]O2

1.4.4.P2-Na2/3[Ni,Mn,M]O2

1.5. Summary and prospects

1.6. Acknowledgments

1.7. References

2. Polyanionic-Type Compounds as Positive Electrodes for Na-ion batteries

2.1. Introduction. 2.1.1.Oxides and polyanionic frameworks as positive electrodes for sodium ion-batteries

2.1.2.NASICONs and Na3V2(PO4)2F3. 2.1.2.1. Structural descriptions and differences

2.1.2.2. Traditional synthesis methods

2.1.2.3. Electrochemical signatures

2.2. NASICON structures as model frameworks in sodium-ion battery applications. 2.2.1.Compositional diversity from solid electrolytes to electrodes

2.2.2.NASICON-typed materials as electrodes for Na batteries. 2.2.2.1. One transition-metal-based NaxM2(XO4)3NASICONs

2.2.2.2. Multitransition-metal-based NaxMM’(PO4)3NASICONs

2.2.3.Na3V2(PO4)3(NVP) 2.2.3.1. Structural modifications as a function of temperature

2.2.3.2. Electrochemical properties and applications of NVP in Na batteries

2.2.3.2.1. Symmetric NASICON NVP//NVP full cells

Box 2.1.Key reactions in NVP symmetric cells

2.2.3.2.2. Recent achievements in NIBs using Na3V2(PO4)3 as positive electrodes

2.3. Na3V2(PO4)2F3used as a model framework in sodium-ion battery applications. 2.3.1.Structural description and compositional diversity

2.3.2.Na3V2(PO4)2F3: a promising active material for positive electrodes in NIBs. 2.3.2.1. A versatile promising material: from LIBs to NIBs

2.3.2.2. A complex phase diagram observed upon cycling, controlled by the charge ordering

2.3.2.3. A paradox related to vanadium redox couples

2.3.3.Oxygen substitution in Na3V2(PO4)2F3and its effects on the electrochemical performance of substituted phases

2.3.4.Paving the way toward Na3V2(PO4)2F3with superior performance

2.3.4.1. Three Na+ions extraction at the extreme cycling conditions

2.3.4.2. Going beyond the extraction of two Na+ions through ionic substitution

2.4. Conclusion and perspectives

2.5. References

3. Hard Carbon for Na-ion Batteries: From Synthesis to Performance and Storage Mechanism

3.1. Introduction

3.2. What is a hard carbon?

3.3. Hard carbon synthesis and microstructure

3.3.1.Synthetic precursors-based hard carbon synthesis

3.3.2.Bio-polymers derived hard carbon synthesis

3.3.3.Biomass-based hard carbon synthesis

3.4. Hard carbon characteristics

3.4.1.Hard carbon structure

3.4.2.Hard carbon porosity

3.4.3.Hard carbon surface chemistry

3.4.4.Hard carbon structural defects

3.5. Electrochemical performance. 3.5.1.Materials performance

3.5.2.Full Na-ion system performance

3.5.3.Sodium insertion mechanisms in hard carbon

3.6. Conclusion

3.7. References

4. Non-Carbonaceous Negative Electrodes in Sodium Batteries

4.1. Introduction

4.2. Insertion materials. 4.2.1.Insertion anodes based on titanium oxide and titanates

4.2.1.1. Titanium oxide TiO2

4.2.1.2. Na2Ti3O7sodium titanate

4.2.1.3. Li4Ti5O12lithium titanate

4.2.1.4. Layered titanates

4.2.2.Insertion anodes based on transition metal chalcogenides

4.2.3.Insertion MXene-based anodes

4.2.4.Insertion organic anodes

4.3. Negative electrode materials based on electrochemical alloying with sodium

4.3.1.Silicon and germanium

4.3.2.Tin

4.3.3.Phosphorus

4.3.4.Antimony

4.3.5.Other post-transition metal elements

4.4. Negative electrode materials based on conversion reactions

4.4.1.Reaction mechanisms of CM

4.4.2.Approaches toward efficient anode CM for NIB

4.5. Conclusion

4.6. References

5. Electrolytes for Sodium Batteries

5.1. Introduction

5.2. Liquid and solid electrolytes for sodium batteries

5.2.1.Organic liquid electrolytes

5.2.2. IL-based electrolytes

5.2.3. Hybrid electrolytes

5.2.4.Effects of additives and impurities

5.2.5.Solid-state electrolytes. 5.2.5.1. Organic ionic plastic crystals

5.2.5.2. Solid polymer electrolytes

5.2.5.3. Gel polymer electrolytes

5.3. Properties of IL-based electrolytes for Na batteries

5.3.1.Physical properties

5.3.2.Thermal stability

5.3.3.Electrochemical stability

5.4. Modeling IL-based electrolytes

5.5. Conclusion and future perspectives

5.6. Abbreviations

5.7. References

6. Solid Electrolyte Interphase in Na-ion batteries

6.1. Introduction. 6.1.1.The solid electrolyte interphase

6.1.2.Characterization of the SEI

6.2. Physical properties of the Na-ion SEI. 6.2.1.Electrochemical stability

6.2.2.Mechanical properties

6.2.3.Dissolution of SEI components

6.3. Comparisons of SEI in sodium- and lithium-based electrolytes. 6.3.1.Formation and composition

6.3.2.Resistance

6.4. Conclusion

6.5. References

7. Batteries Containing Prussian Blue Analogue Electrodes

7.1. Introduction. 7.1.1.Chapter introduction

7.1.2.History of Prussian blue

7.1.3.Physical characteristics: structure, composition and morphology

7.1.4.Synthetic methods

7.2. Electrochemistry of PBAs. 7.2.1.Mechanism and resulting characteristics

7.2.2.Reaction potentials

7.2.3.PBA cathodes

7.2.4. PBA anodes

7.3. Prussian blue batteries. 7.3.1.Cells containing two PBA electrodes

7.3.2.Cells containing one PBA electrode

7.3.3. Challenges for PBA batteries

7.4. Conclusion and future outlook

7.5. References

8. The Design, Performance and Commercialization of Faradion’s Non-aqueous Na-ion Battery Technology

8.1. Introduction

8.2. Experimental. 8.2.1.Active materials

8.2.2.Electrode fabrication

8.2.2.1. Cathode slurry and coating

8.2.2.2. Anode slurry and coating

8.2.2.3. Calendering and slitting

8.2.3.Pouch cell fabrication

8.2.4.Faradion electrolyte

8.3. Cell performance. 8.3.1.Half-cell cycling

8.3.2.Full Na-ion cell cycling: curves and stability

8.3.3.Rate capability

8.3.4.Temperature studies

8.3.5.Three-electrode cell studies

8.4. Safety and zero energy storage and transportation

8.5. Scale-up and prototyping

8.6. Demonstrators: stacks and packs

8.7. Business and IP strategy

8.8. Cost analysis

8.9. Future developments

8.10. Conclusion

8.11. Acknowledgments

8.12. References

List of Authors

Index

A, B, C

D, E, F

H, I, L

M, N, P

S, T, V, X

WILEY END USER LICENSE AGREEMENT

Отрывок из книги

Energy, Field Director – Alain Dollet

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The electrolytes are essential for the proper functioning of any battery technology, with an important focus to minimize interface electrolyte/electrode reactions and enhance both performance and safety. First studies surveyed electrolytes prepared using classical alkyl carbonates solvents and mixtures, in combination with different Na salts (Ponrouch et al. 2012). Their viscosity, ionic conductivity, thermal and electrochemical stability were evaluated to establish some intrinsic trends to identify the first electrolyte formulations with the widest range of applicability for NIBs.

More recently, IL, defined as room temperature molten salts and composed mainly of organic cations and (in)organic anions and presenting a huge versatility of structural variations, were proposed as major alternatives for the development of optimized electrolytes. Indeed, IL offer unique physical and chemical properties associated with low volatility that make them extremely interesting for the development of electrolytes with higher electrochemical and thermal stability. Chapter 5 will give the major trends for the IL-based electrolytes developed for NIBs.

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