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用于锂硫电池的从低熵到高熵的聚硼酸盐及其衍生物

From Low- to High-Entropy PBAs and Their Derivatives for Lithium-Sulfur Batteries.

作者信息

Gonçalves Josué M, Santos Érick A, Amaral Murilo M, Nossol Edson, Figueiredo Rafael O, Zanin Hudson

机构信息

Mackenzie Institute for Research in Graphene and Nanotechnologies (MackGraphe), Mackenzie Presbyterian Institute, Consolação Street 930, São Paulo, São Paulo 01302-907, Brazil.

Advanced Energy Storage Division, Carbon Sci-Tech Laboratories; Center for Innovation on New Energies; School of Electrical and Computer Engineering, University of Campinas, Av Albert Einstein 400, Campinas, São Paulo 13083-852, Brazil.

出版信息

ACS Omega. 2025 Aug 22;10(35):39309-39333. doi: 10.1021/acsomega.5c04943. eCollection 2025 Sep 9.

Abstract

The accelerating global demand for energy has catalyzed the pursuit of advanced, sustainable energy storage systems. Among them, lithium-sulfur (Li-S) batteries stand out for their high theoretical energy density and the abundance and low cost of sulfur. However, their practical deployment remains restricted by issues such as polysulfide dissolution, sluggish redox kinetics, and the notorious shuttle effect. Recent efforts have focused on engineering sulfur host materials and electrocatalysts to overcome these limitations, particularly through the use of polar inorganic compounds that interact strongly with lithium polysulfides (LiPSs) to improve conversion efficiency and cycle stability. In this context, new materials with configurational entropy ranging from low to high entropy have emerged as a new class of functional materials, offering unprecedented structural and compositional tunability. Among them, Prussian blue analogues (PBAs) have gained increasing attention due to their open frameworks, controllable composition, and redox-active sites. Moreover, PBAs represent highly versatile precursors for the rational design and synthesis of advanced catalytic materials, encompassing alloys, metal oxides, metal sulfides, and metal phosphides, among other functional compounds. This review provides a comprehensive and critical assessment of the progress in the application of low-, medium-, and high-entropy PBAs and their derivatives as solid catalysts in Li-S batteries. We clarify the definitions of configurational entropy in PBAs and highlight the current misuse of the term in the literature. The review also addresses synthetic strategies for multielement PBAs, evaluates their physicochemical and catalytic properties, and correlates these features with electrochemical performance. Finally, we identify emerging design trends, key challenges, and future perspectives for the rational development of entropy-tailored PBAs in next-generation Li-S batteries.

摘要

全球对能源的需求不断加速,促使人们追求先进的可持续储能系统。其中,锂硫(Li-S)电池因其高理论能量密度以及硫的丰富性和低成本而脱颖而出。然而,它们的实际应用仍受到多硫化物溶解、氧化还原动力学缓慢以及臭名昭著的穿梭效应等问题的限制。最近的努力集中在设计硫主体材料和电催化剂以克服这些限制,特别是通过使用与多硫化锂(LiPSs)强烈相互作用的极性无机化合物来提高转化效率和循环稳定性。在这种背景下,具有从低到高熵的构型熵的新材料已成为一类新型功能材料,提供了前所未有的结构和组成可调性。其中,普鲁士蓝类似物(PBAs)因其开放框架、可控组成和氧化还原活性位点而受到越来越多的关注。此外,PBAs是用于合理设计和合成先进催化材料的高度通用的前体,包括合金、金属氧化物、金属硫化物和金属磷化物以及其他功能化合物。本文综述全面且批判性地评估了低熵、中熵和高熵PBAs及其衍生物作为Li-S电池固体催化剂应用的进展。我们阐明了PBAs中构型熵的定义,并强调了该术语在文献中的当前误用情况。该综述还讨论了多元素PBAs的合成策略,评估了它们的物理化学和催化性能,并将这些特性与电化学性能相关联。最后,我们确定了下一代Li-S电池中熵定制PBAs合理开发的新兴设计趋势、关键挑战和未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c940/12423821/23f3360027c5/ao5c04943_0010.jpg

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