材料科学
催化作用
多硫化物
氧化还原
硫黄
工作(物理)
化学工程
锂(药物)
空位缺陷
动力学
氧气
吸附
无机化学
动能
析氧
纳米技术
密度泛函理论
多相催化
化学物理
降级(电信)
作者
Cheng Zhang,Jia Niu,Mengying Xu,Tianwen Bai,Lei Lu,Shan Ji,Lei Zhu,Peng Wang
标识
DOI:10.1002/adfm.202521294
摘要
ABSTRACT Oxygen vacancy (OV)‐engineered catalysts show promise for lithium sulfur batteries (LSBs) by enhancing polysulfide adsorption and conversion, yet most studies focus on total OV concentration while overlooking spatial distribution effects on local catalytic activity and charge transport. This limitation hinders active site utilization and kinetic improvement. To address these issues, we report the successful synthesis of an olive‐shaped In 2 O x nanocatalyst through a straightforward urea‐assisted precursor engineering strategy. This catalyst exhibits a distinctive non‐uniformly distributed OVs, extending the current insights spatially heterogeneous distribution of OVs. Kinetic analysis demonstrates that this distribution enhances catalytic site density and facilitates optimized electron transport pathways. Capitalizing on the synergistic effects of this gradient OV distribution, LSBs incorporating In 2 O x –L deliver superior performance: an initial capacity of 1171 mAh g −1 (0.2 C), robust high‐rate capability, and extended cyclability under demanding conditions (1 C cycling; E/S = 10 µL mg −1 ). This work demonstrates the precise spatial regulation of OVs in electrocatalysts, thereby advancing design principles for next‐generation vacancy‐engineered catalytic systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI