电催化剂
化学
杂原子
电化学
阴极
纳米技术
硫黄
二硫化钼
电池(电)
储能
钼
选择性
氧化还原
极化(电化学)
兴奋剂
分子
组合化学
电化学能量转换
有机自由基电池
自旋态
催化作用
化学物理
电极
作者
Tiansheng Wang,Guobin Yu,Yangyang Wu,Shixin Wang,Yue Zhu,Hongpeng Li,Hongsen Li,Guihua Yu
摘要
Aluminum-sulfur (Al-S) batteries are regarded as promising electrochemical energy storage systems due to their high energy density, cost-effectiveness, and environmental compatibility. However, their practical application is hindered by sluggish sulfur conversion kinetics. Although certain achievements have been made, conventional strategies for modulating the spin state of electrocatalysts, such as heteroatom doping or lattice strain engineering, exhibit inherent limitations in optimizing electron orbital interactions. Herein, we report a novel MoS2 electrocatalyst with spin orientation manipulation achieved through the chiral-induced spin selectivity (CISS) effect. This approach couples chiral molecules with layered MoS2 to regulate the spin polarization of molybdenum atoms, thereby enhancing the sulfur redox kinetics without relying on chemical modification. Electrochemical analyses demonstrated that the cathode with chiral MoS2 delivers a reversible specific capacity of ∼700 mAh g-1 at 2 A g-1 over 3000 cycles, accompanied by improved sulfur utilization efficiency. This work not only provides a paradigm for designing high-performance electrocatalysts in sulfur-based batteries but also highlights the critical role of spin effects in electrocatalytic systems, offering new perspectives for the innovation of electrocatalyst materials in batteries.
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