Recent Advances in Non-Carbon Dense Sulfur Cathodes for Lithium–Sulfur Battery with High Energy Density

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY ChemElectroChem Pub Date : 2024-11-13 DOI:10.1002/celc.202400481
Viet Phuong Nguyen, Seung-Mo Lee
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Abstract

The seemingly advantageous features of carbon-based materials, such as large pore volume and lightweight structure, could actually lead to low tap density for the sulfur cathode and excessive electrolyte consumption, potentially significantly decreasing the energy density of lithium–sulfur battery. Recently, non-carbon-based materials composed of inorganic matter have emerged as promising candidates for creating dense sulfur cathodes and reducing electrolyte intake. Additionally, inorganic matter exhibits strong interactions with lithium polysulfides, which can address the intrinsic problems of the severe shuttling effect and poor reaction kinetics. In this review, we first discuss the relationship between the tap density of the sulfur cathode and the energy density of lithium–sulfur battery. Subsequently, we systematically summarize recent advances in non-carbon-based materials as sulfur hosts. Finally, we propose future research directions and perspectives for sulfur host materials to inspire the realization of practical lithium–sulfur battery with high energy density.

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高能量密度锂硫电池非碳密硫阴极研究进展
碳基材料表面上的优势,如大孔隙体积和轻结构,实际上可能导致硫阴极的轻接密度低,电解质消耗过多,可能会显著降低锂硫电池的能量密度。最近,由无机物组成的非碳基材料已成为制造致密硫阴极和减少电解质摄入量的有希望的候选者。此外,无机物与多硫化物锂表现出强烈的相互作用,可以解决穿梭效应严重和反应动力学差的内在问题。本文首先讨论了硫阴极接穗密度与锂硫电池能量密度之间的关系。随后,我们系统地总结了非碳基材料作为硫宿主的最新进展。最后,我们提出了硫基质材料未来的研究方向和展望,以启发实现实用化的高能量密度锂硫电池。
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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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