材料科学
锂硫电池
催化作用
电池(电)
硫黄
转化式学习
锂(药物)
纳米技术
Atom(片上系统)
工程物理
化学工程
冶金
计算机科学
有机化学
工程类
功率(物理)
嵌入式系统
热力学
医学
心理学
教育学
化学
物理
内分泌学
作者
Sandip Maiti,Matthew T. Curnan,Keon‐Woo Kim,Kakali Maiti,Jin Kon Kim
标识
DOI:10.1002/aenm.202401911
摘要
Abstract Theoretically, lithium–sulfur (Li‐S) batteries are highly promising candidates for renewable energy applications, given their scalable energy density and low cost. However, their current practical performance is limited below theoretical expectations, despite attempts to accommodate volumetric expansion and improve electrical conductivity with porous S‐anchoring supports. Battery performance is primarily rate‐limited by the sluggish redox and conversion reaction kinetics of lithium polysulfides (LiPS), which respectively transform into lithium sulfide (Li 2 S) and elemental S through charging and discharging galvanostatic cycles. Given their strong electrocatalytic performance and other pertinent benefits, recent research highlights single‐atom catalysts (SACs) as candidates for enhancing Li‐S batteries. Thus, this review summarizes contemporary advancements regarding SAC implementation in Li‐S batteries, primarily emphasizing catalyst morphology, battery performance, and mechanistic elucidation. More specifically, separators and cathodes can be engineered via SACs to better anchor LiPS and improve their reductive kinetics, thereby inhibiting the “shuttle effect” known to impact Li‐S batteries. In addition, SACs can be modulated with functional groups to synergistically improve performance, enabling higher S loadings and redistributing transferred charge. Overall, SACs conspicuously boost Li‐S battery performance, justifying further research toward their implementation in Li‐S batteries.
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