过电位
催化作用
材料科学
硫黄
氧化物
电池(电)
密度泛函理论
氧化还原
工作(物理)
动能
化学工程
联轴节(管道)
纳米技术
化学物理
储能
降级(电信)
动力学
电极
能量密度
偶联反应
活化能
多相催化
无机化学
带隙
轨道能级差
分子轨道
复合氧化物
作者
Mingyang Jiang,Jiwei Shi,Yì Wáng,Zhonghao Hu,Chuannan Geng,Qiang Li,Bohan Zhang,Yun Cao,Chuang Xie,Yufei Zhao,Jiaqi Lan,Wei Lv
标识
DOI:10.1002/adma.202520011
摘要
ABSTRACT All‐solid‐state lithium–sulfur batteries (ASSLSBs) offer high theoretical energy density and intrinsic safety, yet their development is hindered by sluggish sulfur redox kinetics at the solid–solid interfaces due to the weak orbital overlap and discontinuous electronic coupling at these regions. Here, we propose rare‐earth oxide catalysts that accelerate the sulfur reduction reaction (SRR) in ASSLSBs by strengthening the f‐d‐p hybridization at catalyst‐sulfur‐electrolyte interfaces. We first define a hybridization‐strength factor, I f‐d , derived from the electron densities of occupied 4 f and unoccupied 5 d states, which quantifies interfacial hybridization and directly correlates with the metal‐sulfur coupling strength. Catalysts with higher I f‐d exhibit lower activation energy ( E a ) and the overpotential ( η ) during SRR, validating its role as a structure‐activity descriptor for catalyst screening and design. Guided by this descriptor, the screened Lu 2 O 3 catalyst minimizes kinetic barriers (0.088 eV), and thus enabling stable cycling for over 20 000 cycles at 5 C, and an ultra‐high areal capacity of 14.48 mAh cm −2 at room temperature, among the highest performances reported for ASSLSBs. This work fills the mechanistic gap between interfacial orbital interactions and battery performance and paves the way toward catalyst design for high‐energy, long‐life ASSLSBs.
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