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Batteries
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Advances in Electrode Materials for Advanced Batteries
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Advances in Electrode Materials for Advanced Batteries

A special issue of Batteries (ISSN 2313-0105). This special issue belongs to the section "Battery Materials and Interfaces: Anode, Cathode, Separators and Electrolytes or Others".

Deadline for manuscript submissions: 14 February 2025 | Viewed by 6946

Special Issue Editor

Prof. Dr. Xingzhong Guo

E-Mail Website
Guest Editor
State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, China
Interests: porous electrocatalysis and battery materials; flexible thin film electrode materials and devices

Special Issue Information

Dear Colleagues,

Advanced batteries, including lithium-ion batteries, have been attracting growing attention as the most promising commercialized energy storage devices. Reliable safety, high energy density and long service life are the key properties for guaranteeing that advanced batteries penetrate the market. Limited by the inevitable overheating and undesirable electrochemical performance of cathodes and anodes, the need for advanced electrode materials remains urgent. Moreover, other energy storage systems beyond lithium batteries, including sodium, zinc and magnesium batteries, provide new opportunities.

In this Special Issue, we look forward to contributing to solving the above problems in the following three aspects: The understanding of chemical and physical mechanisms of battery degradation is the first step to develop more reliable and durable systems, which will allow us to improve the performance of commercial electrodes or develop new materials based on advanced characterization and theoretical models. Secondly, battery safety is always a prerequisite for the development of lithium-ion battery technology. We must pay attention to the safety of batteries and prevent overheating during charging. Finally, the transition from idealized experiments in the laboratory to industrial commercial production is emphasized.

Topics include, but are not limited to:

  • Improvement of commercialized electrode materials;
  • Development of next-generation electrode materials;
  • Enhancement of battery safety;
  • Advanced characterization methods;
  • Technologies to increase the initial Coulombic efficiency;
  • Fast validation strategies to determine the performance of materials;
  • The gaps between laboratorial and practical batteries.

Prof. Dr. Xingzhong Guo
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Batteries is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • lithium battery
  • cathode
  • anode
  • battery safety
  • advanced characterization
  • prelithiation
  • fast validation
  • practical battery
  • beyond-lithium battery

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Further information on MDPI's Special Issue polices can be found here.

Published Papers (3 papers)

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Research

14 pages, 4084 KiB  
Article
Film Thickness Effect in Restructuring NiO into LiNiO2 Anode for Highly Stable Lithium-Ion Batteries
by Thang Phan Nguyen and Il Tae Kim
Batteries 2024, 10(3), 80; https://doi.org/10.3390/batteries10030080 - 27 Feb 2024
Viewed by 2343
Abstract
The long-term stability of energy-storage devices for green energy has received significant attention. Lithium-ion batteries (LIBs) based on materials such as metal oxides, Si, Sb, and Sn have shown superior energy density and stability owing to their intrinsic properties and the support of [...] Read more.
The long-term stability of energy-storage devices for green energy has received significant attention. Lithium-ion batteries (LIBs) based on materials such as metal oxides, Si, Sb, and Sn have shown superior energy density and stability owing to their intrinsic properties and the support of conductive carbon, graphene, or graphene oxides. Abnormal capacities have been recorded for some transition metal oxides, such as NiO, Fe2O3, and MnO/Mn3O4. Recently, the restructuring of NiO into LiNiO2 anode materials has yielded an ultrastable anode for LIBs. Herein, the effect of the thin film thickness on the restructuring of the NiO anode was investigated. Different electrode thicknesses required different numbers of cycles for restructuring, resulting in significant changes in the reconstituted cells. NiO thicknesses greater than 39 μm reduced the capacity to 570 mAh g−1. The results revealed the limitation of the layered thickness owing to the low diffusion efficiency of Li ions in the thick layers, resulting in non-uniformity of the restructured LiNiO2. The NiO anode with a thickness of approximately 20 μm required only 220 cycles to be restructured at 0.5 A g−1, while maintaining a high-rate performance for over 500 cycles at 1.0 A g−1, and a high capacity of 1000 mAh g−1. Full article
(This article belongs to the Special Issue Advances in Electrode Materials for Advanced Batteries)
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19 pages, 19405 KiB  
Article
High-Performance Full Sodium Cells Based on MgO-Treated P2-Type Na0.67(Mn0.5Fe0.5)1−xCoxO2 Cathodes
by Nermin Taskiran, Sebahat Altundag, Violeta Koleva, Emine Altin, Muhammad Arshad, Sevda Avci, Mehmet Nurullah Ates, Serdar Altin and Radostina Stoyanova
Batteries 2023, 9(10), 497; https://doi.org/10.3390/batteries9100497 - 28 Sep 2023
Cited by 6 | Viewed by 2155
Abstract
Herein, we design a cathode material based on layered Na2/3(Mn1/2Fe1/2)O2 for practical application by combining the Co substitution and MgO treatment strategies. The oxides are prepared via solid-state reactions at 900 °C. The structure, morphology, and [...] Read more.
Herein, we design a cathode material based on layered Na2/3(Mn1/2Fe1/2)O2 for practical application by combining the Co substitution and MgO treatment strategies. The oxides are prepared via solid-state reactions at 900 °C. The structure, morphology, and oxidation state of transition metal ions for Co-substituted and MgO-treated oxides are carefully examined via X-ray diffraction, IR and Raman spectroscopies, FESEM with EDX, specific surface area measurement, and XPS spectroscopy. The ability of oxides to store sodium reversibly is analyzed within a temperature range of 10 to 50 °C via CV experiments, galvanostatic measurements, and EIS, using half and full sodium ion cells. The changes in the local structure and oxidation state of transition metal ions during Na+ intercalation are monitored via operando XAS experiments. It is found that the Co substituents have a positive impact on the rate capability of layered oxides, while Mg additives lead to a strong increase in the capacity and an enhancement of the cycling stability. Thus, the highest capacity is obtained for 2 at.%-MgO-treated Na2/3(Mn1/2Fe1/2)0.9Co0.1O2 (175 mAh/g, with a capacity fade of 28% after 100 cycles). In comparison with Co substituents, the Mg treatment has a crucial role in the improvement of the lattice stability during the cycling process. The best electrode materials, with a chemical formula of 2 at.%-MgO treated Na2/3(Mn1/2Fe1/2)0.9Co0.1O2, were also used for the full cells design, with hard carbon as an anode. In the voltage window of 2–4 V, the capacity of the cells was obtained as 78 mAh/g and 51 mAh/g for applied current densities of 12 mA/g and 60 mA/g, respectively. Full article
(This article belongs to the Special Issue Advances in Electrode Materials for Advanced Batteries)
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13 pages, 4321 KiB  
Article
Constructing a Quasi-Liquid Interphase to Enable Highly Stable Zn-Metal Anode
by Junzhang Wang, Zhou Xu, Tengteng Qin, Jintian Wang, Rui Tian, Xingzhong Guo, Zongrong Wang, Zhongkuan Luo and Hui Yang
Batteries 2023, 9(6), 328; https://doi.org/10.3390/batteries9060328 - 16 Jun 2023
Viewed by 1645
Abstract
Rechargeable aqueous Zn-metal batteries have attracted widespread attention owing to their safety and low cost beyond Li-metal batteries. However, due to the lack of the solid electrolyte interphase, problems such as dendrites, side reactions and hydrogen generation severely restrict their commercial applications. Herein, [...] Read more.
Rechargeable aqueous Zn-metal batteries have attracted widespread attention owing to their safety and low cost beyond Li-metal batteries. However, due to the lack of the solid electrolyte interphase, problems such as dendrites, side reactions and hydrogen generation severely restrict their commercial applications. Herein, a quasi-liquid interphase (QLI) with a “solid–liquid” property is constructed to stabilize the Zn-metal anode. The synergistic effect of solid and liquid behavior ensures the stable existence of QLI and simultaneously enables the interphase dynamic and self-adaptive to the anode evolution. Electrolyte erosion, Zn2+ diffusion and side reactions are inhibited during long-term cycling after introducing QLI, significantly improving the cycling stability and capacity retention of the symmetric and full cells modified with QLI (Zn@QLI), respectively. Constructing an interphase with a quasi-liquid state represents a promising strategy to stabilize the metal anodes in aqueous electrolytes and even extend to organic electrolytes. Full article
(This article belongs to the Special Issue Advances in Electrode Materials for Advanced Batteries)
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