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Key Electrode Materials for Batteries and Supercapacitors

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Materials Chemistry".

Deadline for manuscript submissions: 30 June 2025 | Viewed by 1351

Special Issue Editors

Key Laboratory of Spin Electron and Nanomaterials of Anhui Higher Education Institutes, Suzhou University, Suzhou 234000, China
Interests: nanomaterials; synthesis; characterization; catalysis; supercapacitor
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

In the 21st century, the escalating global demand for energy, coupled with increasingly severe environmental concerns, has underscored the urgent need for efficient and environmentally friendly energy storage solutions. Batteries and supercapacitors are two kinds of primary energy storage devices, each offering unique advantages in energy density, power density, cycle life, and cost-effectiveness. Batteries are excellent for storing large amounts of energy for gradual release, making them ideal for applications such as electric vehicles and large-scale grid energy storage that require sustained power delivery. On the other hand, supercapacitors stand out in rapid charging and discharging, along with a long cycle life, making them suitable for applications that demand quick power output and fast charging, such as urban traffic signal systems and portable electronic devices.

The advancement of battery technology relies heavily on innovations in novel electrode materials, electrolytes, separators, and other components, especially electrode materials. Lithium-ion batteries (LIBs), renowned for their high energy density and long cycle life, have found widespread applications in consumer electronics and electric vehicles. Currently, the commercial lithium-ion batteries primarily utilize graphite as the anode material and layered oxides as the cathode material. To further enhance battery performance, researchers are exploring novel anode materials including silicon-based materials, as well as cathode materials such as nickel-rich layered oxides, lithium iron phosphate, and solid-state electrolytes. Additionally, sodium-ion batteries have garnered significant attention as a potential low-cost alternative, due to their chemical similarity to LIBs and more abundant and cost-effective resources.

Supercapacitors, also known as electric double-layer capacitors or ultracapacitors, are renowned for their rapid charging and discharging capabilities and long cycle life. Supercapacitors primarily consist of two electrodes, an electrolyte, and a separator, with their performance heavily dependent on the electrode materials to enhance their specific capacitance and power density. While traditional supercapacitors utilize activated carbon as the electrode material, recent research has surged on nanomaterials such as carbon nanotubes, graphene, and low-dimensional transition metal oxides and hydroxides. These nanomaterials offer significantly higher specific surface area and conductivity, enabling a substantial enhancement in energy density without sacrificing the inherent power characteristics of the supercapacitors.

Additionally, to overcome the limitations of single-component electrode materials, researchers have been dedicated to developing functional composite electrode materials. For instance, combining high-capacity metal oxides with highly conductive carbon materials can enhance the energy storage capability of the electrode while maintaining good conductivity. Moreover, modifying the microstructure of electrode materials, such as constructing porous structures or introducing heteroatom doping, can effectively improve their electrochemical performance. These strategies are applicable both to batteries and supercapacitor design.

With advancements in materials science, the development of novel electrode materials and the improvement of existing ones have enabled significant performance enhancements in both batteries and supercapacitors. These technological innovations will not only revolutionize the energy storage field but also contribute significantly to the transformation and sustainability of the global energy system.

Dr. Jin Jia
Prof. Dr. Yucheng Lan
Guest Editors

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Keywords

  • battery
  • supercapacitor
  • electrode material
  • energy storage

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Published Papers (2 papers)

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Research

18 pages, 3782 KiB  
Article
Synergistic Enhancement of Capacitive Performance in Porous Carbon by Phenolic Resin and Boric Acid
by Yingkai Xia, Fengzhi Zhang, Shuo Wang, Shuang Wei, Xu Zhang, Wei Dong, Ding Shen, Shuwei Tang, Fengxia Liu, Yuehui Chen and Shaobin Yang
Molecules 2025, 30(6), 1228; https://doi.org/10.3390/molecules30061228 - 9 Mar 2025
Viewed by 499
Abstract
The study of pore structure regulation methods has always been a central focus in enhancing the capacitance performance of porous carbon electrodes in lithium-ion capacitors (LICs). This study proposes a novel approach for the synergistic regulation of the pore structure in porous carbon [...] Read more.
The study of pore structure regulation methods has always been a central focus in enhancing the capacitance performance of porous carbon electrodes in lithium-ion capacitors (LICs). This study proposes a novel approach for the synergistic regulation of the pore structure in porous carbon using phenol-formaldehyde (PF) resin and boric acid (BA). PF and BA are initially dissolved and adsorbed onto porous carbon, followed by hydrothermal treatment and subsequent heat treatment in a N2 atmosphere to obtain the porous carbon materials. The results reveal that adding BA alone has almost no influence on the pore structure, whereas adding PF alone significantly increases the micropores. Furthermore, the simultaneous addition of PF and BA demonstrates a clear synergistic effect. The CO2 and H2O released during the PF pyrolysis contribute to the development of ultramicropores. At the same time, BA facilitates the N2 activation reaction of carbon, enlarging the small mesopores and aiding their transformation into bottlenecked structures. The resulting porous carbon demonstrates an impressive capacitance of 144 F·g−1 at 1 A·g−1 and a capacity retention of 19.44% at 20 A·g−1. This mechanism of B-catalyzed N2-enhanced mesopore formation provides a new avenue for preparing porous carbon materials. This type of porous carbon exhibits promising potential for applications in Li-S battery cathode materials and as catalyst supports. Full article
(This article belongs to the Special Issue Key Electrode Materials for Batteries and Supercapacitors)
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15 pages, 3083 KiB  
Article
2D Porous Ti3C2 MXene as Anode Material for Sodium-Ion Batteries with Excellent Reaction Kinetics
by Lan Tang, Linlin Zhang, Guohao Yin, Xin Tao, Lianghao Yu, Xiaoqing Wang, Changlong Sun, Yunyu Sun, Enhui Hong, Guangzhen Zhao and Guang Zhu
Molecules 2025, 30(5), 1100; https://doi.org/10.3390/molecules30051100 - 27 Feb 2025
Viewed by 630
Abstract
Sodium-ion batteries (SIBs) are a promising electrochemical energy storage system but face great challenges in developing fast-charging anodes. MXene-based composites are a new class of two-dimensional materials that are expected to be widely used in SIB energy storage due to their excellent electrical [...] Read more.
Sodium-ion batteries (SIBs) are a promising electrochemical energy storage system but face great challenges in developing fast-charging anodes. MXene-based composites are a new class of two-dimensional materials that are expected to be widely used in SIB energy storage due to their excellent electrical conductivity and stable structure. However, MXenes tend to experience interlayer stacking during preparation, which can result in poor electrochemical performance and a lower actual capacity compared to the theoretical value. In this study, the porous structure was created using a chemical oxidation method from a microscopic perspective. The porous MXene (referred to as PM) was prepared by using a low concentration of hydrogen peroxide as the pore-forming solution, which enlarged the interlayer spacing to facilitate the transport of sodium ions in the electrolyte solution. The PM with the addition of hydrogen peroxide solution achieved high-rate performance, with a capacity of 247 mAh g−1 at 0.1 A g−1 and 114 mAh g−1 at 10 A g−1. It also demonstrated long-cycle stability, with a capacity of 117 mAh g−1 maintained over 1000 cycles at 5 A g−1. Full article
(This article belongs to the Special Issue Key Electrode Materials for Batteries and Supercapacitors)
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