AI Article Synopsis

  • * MXenes can be easily combined with other materials, like oxides and polymers, enhancing their performance for various applications, particularly in environmental and energy storage uses.
  • * This review focuses on the latest advancements in MXenes for electrochemical energy storage, detailing their synthesis, properties, and applications in supercapacitors and batteries while discussing future research directions.

Article Abstract

A new, sizable family of 2D transition metal carbonitrides, carbides, and nitrides known as MXenes has attracted a lot of attention in recent years. This is because MXenes exhibit a variety of intriguing physical, chemical, mechanical, and electrochemical characteristics that are closely linked to the wide variety of their surface terminations and elemental compositions. Particularly, MXenes are readily converted into composites with materials including oxides, polymers, and CNTs, which makes it possible to modify their characteristics for a variety of uses. MXenes and MXene-based composites have demonstrated tremendous promise in environmental applications due to their excellent reducibility, conductivity, and biocompatibility, in addition to their well-known rise to prominence as electrode materials in the energy storage sector. The remarkable characteristics of 2D MXene, including high conductivity, high specific surface area, and enhanced hydrophilicity, account for the increasing prominence of its use in storage devices. In this review, we highlight the most recent developments in the use of MXenes and MXene-based composites for electrochemical energy storage while summarizing their synthesis and characteristics. Key attention is paid to applications in supercapacitors, batteries, and their flexible components. Future research challenges and perspectives are also described.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9895718PMC
http://dx.doi.org/10.1186/s11671-023-03786-9DOI Listing

Publication Analysis

Top Keywords

energy storage
12
electrochemical energy
8
mxenes mxene-based
8
mxene-based composites
8
mxenes
5
mxene fundamentals
4
fundamentals applications
4
applications electrochemical
4
storage
4
storage sizable
4

Similar Publications

Numerical simulation study on the influence of bend diameter rate on the flow characteristics of nature gas hydrate particles.

Sci Rep

December 2024

Jiangsu Key Laboratory of Oil-Gas Storage and Transportation Technology, Changzhou University, Changzhou, 213164, Jiangsu, China.

Bend pipe is a common part of long distance pipeline. There is very important to study the flow law of hydrate particles in the bend pipe, and pipeline design will be optimized. In addition, the efficiency and safety of pipeline gas transmission will be improved.

View Article and Find Full Text PDF

Bridged emulsion gels from polymer-nanoparticle enabling large-amount biomedical encapsulation and functionalization.

Nat Commun

December 2024

Key Laboratory of Materials Chemistry for Energy Conversion and Storage of Ministry of Education (HUST), School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology (HUST), Wuhan, 430074, China.

Large-amount encapsulation and subsequent expressing are common characteristics for many biomedical applications, such as cosmetic creams and medical ointments. Emulsion gels can accomplish that, but often undergo exclusive, complex, multiple synthesis steps, showing extremely laborious and non-universal. The method here is simple via precisely interfacial engineering in homogenizing a nanoparticle aqueous dispersion and a polymer oil solution, gaining interfacial 45° three-phase-contact-angle for the nanoparticle that can bridge across oil emulsions' interfaces and ultimately form interconnected macroscopic networks.

View Article and Find Full Text PDF

Nanoporous metals have unique potentials for energy applications with a high surface area despite the percolating structure. Yet, a highly corrosive environment is required for the synthesis of porous metals with conventional dealloying methods, limiting the large-scale fabrication of porous structures for reactive metals. In this study, we synthesize a highly reactive Mg nanoporous system through a facile organic solution-based approach without any harsh etching.

View Article and Find Full Text PDF

Amorphous organic-hybrid vanadium oxide for near-barrier-free ultrafast-charging aqueous zinc-ion battery.

Nat Commun

December 2024

Key Laboratory of UV Light-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, Changchun, 130024, China.

Fast-charging metal-ion batteries are essential for advancing energy storage technologies, but their performance is often limited by the high activation energy (E) required for ion diffusion in solids. Addressing this challenge has been particularly difficult for multivalent ions like Zn. Here, we present an amorphous organic-hybrid vanadium oxide (AOH-VO), featuring one-dimensional chains arranged in a disordered structure with atomic/molecular-level pores for promoting hierarchical ion diffusion pathways and reducing Zn interactions with the solid skeleton.

View Article and Find Full Text PDF

Redox-active Co(II) and Zn(II) Pincer Complexes as High-Capacity Anode Materials for Lithium-Ion Batteries.

Adv Sci (Weinh)

December 2024

Department of Chemistry and Research Institute of Molecular Alchemy, Gyeongsang National University, Jinju, 52828, South Korea.

To address the ongoing demand for high-performance energy storage devices, it is crucial to identify new electrode materials. Lithium-ion batteries (LIBs) store energy via the electrochemical redox process, so their electrode materials should have reversible redox properties for rechargeability. On that note, redox-active metal complexes are explored as innovative electrode materials for LIBs.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!