反键分子轨道
材料科学
电催化剂
反铁磁性
铁磁性
硫黄
催化作用
锂(药物)
凝聚态物理
化学物理
自旋(空气动力学)
离子
无机化学
磁矩
氧化还原
电子
八面体
联轴节(管道)
纳米技术
充电顺序
自旋极化
电极
作者
Qing Li,Jianghong ZHANG,Siyu Zhu,Ailing Song,Zhipeng Ma,Lei Dai,Yizhong Huang,Imran Shakir,Guangjie Shao,Yuxi Xu
标识
DOI:10.1002/adfm.202528894
摘要
ABSTRACT The spin‐state engineering of transition‐metal catalysts plays a decisive role in enhancing electrocatalytic activity in lithium‐sulfur batteries. While high/low‐spin transitions are accessible for 3 d 4 ‐3 d 7 ions in octahedral fields, Ni 2+ (3 d 8 ) has long been considered spin‐inert under such coordination. Herein, we demonstrate that ferromagnetic NiF 2 effectively circumvents this limitation through exchange‐mediated spin alignment. In contrast to antiferromagnetic NiO, the parallel spin ordering in NiF 2 generates a permanent magnetic moment and upshifts the d‐band center, thereby promoting the injection of spin‐polarized electrons into the antibonding π* orbital of S─S bonds in lithium polysulfides. This strong d‐π coupling significantly reduces the S─S bond order and facilitates sulfur reaction kinetics. As a result, Li‐S batteries with the NiF 2 catalyst deliver an initial capacity of 842.7 mAh g −1 at 1 C and exhibit exceptional cycling stability, with a capacity increase to 941.6 mAh g −1 after 500 cycles. Moreover, a high areal capacity of 7.2 mAh cm −2 is achieved under elevated sulfur loading (8 mg cm −2 ). This work breaks the conventional spin blockade in Ni 2+ catalysts and offers a strategic approach to spin‐level electrocatalyst design for efficient sulfur redox reactions.
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