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High-Temperature Electrolysis : From Fundamentals to Applications / edited by Werner Sitte and Rotraut Merkle.

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Format:
Book
Contributor:
Sitte, Werner, editor.
Merkle, Rotraut, editor.
Series:
IOP expanding physics.
IOP Ebooks Series
Language:
English
Subjects (All):
High temperature electrolysis.
Physical Description:
1 online resource (500 pages)
Edition:
First edition.
Place of Publication:
Bristol, England : IOP Publishing Ltd, [2023]
Summary:
This reference text provides a detailed guide to high-temperature electrolysis, including the fundamental and materials aspects of solid oxide and protonic ceramic electrolysis cells, considerations at stack and system levels, recent developments, and important combinations of high-temperature electrolysis with other processes.
Contents:
Intro
Preface
Editor biographies
Werner Sitte
Rotraut Merkle
List of contributors
Chapter 1 High-temperature electrolysis-general overview
1.1 The need for energy conversion and the storage of sustainable energy
1.1.1 From fossil fuels to sustainable energy
1.1.2 Potential conversion and storage technologies
1.2 Electrolysis cells
1.2.1 Thermodynamics of the electrolysis of H2O and CO2
1.2.2 Types of electrolysis cell
1.3 Useful electrochemical concepts for SOC cells
1.3.1 Example of SOC structure and materials
1.3.2 Types of potentials in SOCs
1.3.3 Non-recognized overpotential types in composite electrodes and MIECs
1.4 Recommendations for future work
1.4.1 Stoichiometry of materials
1.4.2 Impurities and segregations
1.4.3 Leaks
1.5 Outlook
Acknowledgments
References
Chapter 2 Electrolyte materials for solid oxide electrolysis cells
2.1 Introduction
2.1.1 Definition of a solid oxide electrolysis electrolyte
2.1.2 Requirements for the electrolyte component
2.2 Materials in common use
2.2.1 Zirconia-based electrolytes
2.2.2 Ceria-based electrolytes
2.2.3 Lanthanum gallate-based perovskite electrolytes
2.2.4 New electrolyte compositions
2.3 Electrolyte degradation mechanisms
2.4 Concluding remarks
Chapter 3 Anode materials for solid oxide electrolysis cells
3.1 Solid oxide electrolysis cell anodes
3.2 Perovskites: a material scientist's playground
3.2.1 Crystal structure of perovskites
3.2.2 The influence of different A- and B-site ions on selected materials properties
3.3 Diffusion in the solid state
3.3.1 Definitions of diffusion coefficients
3.3.2 Measurement of diffusion coefficients and ionic conductivity
3.3.3 Diffusion coefficients of relevant positrode materials.
3.4 Compatibility with electrolyte materials
3.5 Layered rare-earth nickelates
3.5.1 Introduction
3.5.2 Crystal structure
3.5.3 First-order Ruddlesden-Popper phases
3.5.4 Compatibility with electrolyte materials
3.5.5 Higher-order Ruddlesden-Popper phases
3.5.6 SOEC positrode performance
3.6 Concluding remarks
Chapter 4 Cathode materials for solid oxide electrolysis cells
4.1 Fuel electrode processes and requirements
4.2 Ni-YSZ cermet electrodes
4.3 Ceramic electrodes
4.3.1 Ceria
4.3.2 Lanthanum chromites
4.3.3 Ferrite oxides
4.3.4 Strontium titanates
4.3.5 Integration of nanostructured electrocatalysts by infiltration
4.3.6 Integration of nanostructured electrodes by exsolution
4.4 Concluding remarks: from the state of the art to advanced materials design
Chapter 5 Interconnects and coatings
5.1 Introduction
5.2 Theory and characterization methods used to evaluate metallic interconnects
5.2.1 High-temperature oxidation
5.2.2 Volatilization of Cr
5.2.3 Electrical conductivity
5.3 Degradation of interconnects in SOEC atmospheres
5.3.1 Oxygen-rich atmospheres
5.3.2 Hydrogen and hydrogen-steam atmospheres
5.3.3 CO2-CO atmospheres
5.3.4 Other forms of interconnect degradation
5.4 Concluding remarks
Acknowledgment
Chapter 6 Electrode kinetics
6.1 Introduction
6.1.1 Reaction pathways
6.1.2 Model-type thin-film electrodes as a tool to identify reaction pathways
6.2 Three-phase boundary active electrodes
6.2.1 Ni/YSZ as the fuel electrode
6.2.2 Pt/YSZ in an oxygen-containing atmosphere
6.2.3 LaMnO3-based electrodes for oxygen reduction
6.3 Surface active electrodes
6.3.1 The role of electrode defect chemistry in electrode reactions.
6.3.2 The meaning of the electrochemical overpotential in the case of mixed-conducting electrodes
6.3.3 Effect of the electrochemical overpotential on a possible surface potential step
6.3.4 Mechanistic picture of oxygen exchange on MIEC oxide electrodes
6.3.5 The effect of chemical evolution of the electrode surface
6.4 Methods used for the characterization of electrode kinetics
6.4.1 Current-voltage curves
6.4.2 Impedance spectroscopy
6.5 Concluding remarks
Chapter 7 Cell architectures
7.1 Cell geometries
7.1.1 Introduction
7.1.2 Planar cells
7.1.3 Tubular cells
7.2 SOEC configurations
7.2.1 Introduction
7.3 Range of operating conditions
7.4 Mechanical properties
7.5 Concluding remarks
Chapter 8 Metal-supported cells
8.1 Background and motivation
8.2 The manufacture of metal-supported cells
8.2.1 Materials and processing of metal substrates
8.2.2 The manufacture of metal-supported cells
8.3 Operational statuses of MS-SOECs
8.4 Operational statuses of MS-PCECs
8.5 Specific degradation issues of metal-supported cells
8.5.1 Oxidation of the metal substrate
8.5.2 Interdiffusion
8.5.3 Ni migration
8.5.4 Chromium poisoning of the oxygen electrode
8.6 Concluding remarks
Chapter 9 Advanced data analysis
9.1 Introduction
9.2 Electrochemical characterization of SOECs
9.2.1 SOEC testing in general
9.2.2 Electrochemical impedance spectroscopy
9.3 Microstructural analysis and reconstruction
9.3.1 FIB-SEM and μCT
9.3.2 Image processing, segmentation, and reconstruction
9.4 Impedance data analysis
9.4.1 Validity of impedance data
9.4.2 Equivalent circuit modeling
9.4.3 Impedance data deconvolution approaches
9.4.4 DRT-based equivalent circuit modeling and simulation.
9.4.5 Correlation of impedance and physicochemically meaningful parameters
9.5 Concluding remarks
Chapter 10 Long-term stack tests
10.1 Introduction
10.2 General overview of the degradation tests of SOEC stacks
10.3 Long-term SOEC stack tests
10.3.1 Stacks of ESC cells
10.3.2 Stacks of FSC cells
10.4 Degradation mechanisms
10.4.1 Oxidation of the interconnect
10.4.2 Degradation of the YSZ electrolyte
10.4.3 Degradation of the LSC(F) air electrode
10.4.4 Degradation of the Ni-based electrode
10.4.5 Degradation due to contact in stacks
10.5 Concluding remarks
Chapter 11 Proton and mixed proton/hole-conducting materials for protonic ceramic electrolysis cells
11.1 Introduction
11.2 Proton-conducting oxides
11.2.1 Proton incorporation reaction and thermodynamics
11.2.2 Proton transport
11.2.3 Electronic defects in proton-conducting materials
11.2.4 Grain-boundary properties and processing issues
11.2.5 Material examples
11.3 Mixed proton/hole-conducting materials
11.3.1 Proton incorporation reactions and thermodynamics, defect interactions
11.3.2 Proton transport in triple-conducting perovskites
11.3.3 Electronic conductivity, conflicting trends
11.3.4 Surface oxygen exchange kinetics and mechanism
11.3.5 Materials examples
11.4 Concluding remarks
Chapter 12 Thermodynamics, transport, and electrochemistry in protonic ceramic electrolysis cells
12.1 Introduction
12.1.1 SOEC function
12.1.2 PCEC function
12.1.3 Practical tradeoffs
12.2 Electrolyte and electrode compositions
12.3 Faradaic and energy efficiencies
12.4 Electrolyte membrane performance
12.4.1 BCZYYb equilibrium defect chemistry
12.4.2 Defect and charge transport
12.4.3 Half-cell reversible potential and cell voltage.
12.4.4 BCZYYb membrane transport performance
12.5 Electrochemical cells
12.5.1 Pore phase gas-phase transport
12.5.2 Charge conservation within the electron-conducting phase
12.5.3 Defect-incorporation chemistry
12.5.4 Charge-transfer chemistry
12.5.5 Parameter fitting
12.5.6 Defect-incorporation rates
12.6 Concluding remarks
References and additional reading
Chapter 13 Tubular protonic ceramic electrolysis cells and direct hydrogen compression
13.1 Introduction
13.1.1 PCEC operating principles
13.1.2 Cell geometries for pressurized operation
13.2 The thermodynamics and kinetics of pressurized PCECs
13.2.1 Cell-level thermodynamics of pressurized operation
13.2.2 Thermodynamics and kinetics of cell components
13.3 Materials, cell architectures, and assembly
13.3.1 Materials for pressurized operation
13.3.2 Tubular cell fabrication and assemblies
13.4 Status of tubular PCEC technology
13.4.1 Ambient-pressure cell testing
13.4.2 Pressurized tubular PCEs
13.4.3 Future prospects for pressurized tubular PCECs
13.5 Concluding remarks
Chapter 14 Planar protonic ceramic electrolysis cells for H2 production and CO2 conversion
14.1 H2 production and CO2 conversion in PCECs
14.1.1 PCECs for H2 production
14.1.2 CO2 conversion in PCECs
14.1.3 Thermodynamics of H2O electrolysis and CO2 conversion in PCECs
14.1.4 Advantages of employing PCECs for H2 production and CO2 conversion
14.2 Current progress in the field of PCECs for H2 production and CO2 conversion
14.2.1 PCECs for H2 production
14.2.2 PCECs for CO2 conversion
14.3 Challenges and opportunities of H2 production in protonic ceramic electrochemical cells
14.3.1 Faradaic efficiency of PCECs for H2 production
14.3.2 Long-term durability.
14.4 Concluding remarks.
Notes:
Description based on publisher supplied metadata and other sources.
Description based on print version record.
Includes bibliographical references.
ISBN:
0-7503-4596-9

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