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Jan 1, 2025¡Open MIND
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Development of layered sodium transition metal oxides as cathode materials for sodium-ion batteries

Lukas Fridolin Pfeiffer

With the objective to reach net-zero carbon emissions, mobile and stationary electrical energy storage is gaining significant importance. Currently these applications are dominated by lithium-ion batteries, however, concerns about vulnerable supply chains and potential supply shocks call for a complementary battery technology. Sodium-ion batteries (SIB) are currently developed and commercialized by academia as well as industry and hold the potential as a cost-effective and complementary battery technology to today’s most affordable lithium-ion batteries, if the energy density of sodium-ion batteries can be improved further. This thesis addresses various current challenges of layered oxide cathode materials for the next generation of high-energy sodium-ion batteries in three scientific publications. The first publication, presented in Section 3.1, addresses Na+/vacancy orderings in P2-type layered oxides as cathode active material (CAM) for SIBs. By comparing the closely related materials P2-NaxNi1/3Mn2/3O2 and P2-NaxMn3/4Ni1/4O2, the chemical and structural context of Na+/vacancy orderings are uncovered using various experimental and computational methods. A guideline to estimate the tendency for Na+/vacancy orderings is proposed and crosschecked against various cathode compositions and literature reports. The guideline can serve to design new P2-type layered oxide cathode materials with improved cycling stability based on the absence of Na+/vacancy orderings. The second publication, presented in Section 3.2, takes a closer look at P2-NaxMn3/4Ni1/4O2 addressing the synthesis, structure, electrochemistry and robustness against storage in moist air. This publication explores the relationship between composition, temperature and crystal structure and investigates the synthesis route for a phase pure P2-type material in detail. The as-prepared material exhibits stacking faults, which are described and quantified for the first time and discussed with respect to the synthesis route. The P2-NaxMn3/4Ni1/4O2 CAM exhibits attractive performance in electrochemical half-cells, however, a significant capacity decay occurs during the first cycles. Lastly, a model storage experiment was performed to evaluate the reactivity of the developed P2-NaxMn3/4Ni1/4O2 cathode material with moist air. The third publication, presented in Section 3.3, addresses the origin of capacity fade in P2-NaxMn3/4Ni1/4O2. Three main aging mechanisms are isolated and their origin uncovered, namely surface densification, intra-crystalline cracking and Jahn-Teller distortion. To the best of my knowledge, this is the first scientific report providing proof for surface densification in P2-type layered oxides. The findings are then discussed in Section 4 in the context of recent scientific literature. Guidelines for the design of high-performance layered oxide cathode materials are proposed and as-designed cathode materials are presented. Finally, future directions for the development of powerful layered oxide cathode materials for the next generation of high-energy SIBs are suggested in Section 5.

Open access
Advancements in Battery Materials
X-ray Diffraction in Crystallography
Chemical and Physical Properties of Materials
Original source
Jan 5, 2022¡Angewandte Chemie International Edition
86 cites
A “Blockchain” Synergy in Conductive Polymer‐Filled Metal–Organic Frameworks for Dendrite‐Free Li Plating/Stripping with High Coulombic Efficiency

Yong Ma, Le Wei, Ying He, Xuzhou Yuan ¡ 13 authors

Abstract The performance of lithium‐metal batteries is severely hampered by uncontrollable dendrite growth and volume expansion on the metal anodes. Inspired by the “blockchain” concept in data mining, here we utilize a conductive polymer‐filled metal–organic framework (MOF) as the lithium host, in which polypyrrole (PPy) serves as the “chain” to interlink Li “blocks” stored in the MOF pores. While the N‐rich PPy guides fast Li + infiltration/extrusion and serves as the nucleation sites for isotropic Li growth, the MOF pores compartmentalize bulk Li deposition for 3D matrix Li storage, leading to low‐barrier and dendrite‐free Li plating/stripping with superb Coulombic efficiency. The as‐fabricated lithium‐metal anodes operate over 700 cycles at 5 mA cm −2 in symmetric cells, and 800 cycles at 1 C in full cells with a per‐cycle capacity loss of only 0.017 %. This work might open a new chapter for Li‐metal anode construction by introducing the concept of “blockchain” management of Li plating/stripping.

2 source records
Advanced Battery Materials and Technologies
Advancements in Battery Materials
Advanced Battery Technologies Research
Original source