材料科学
纳米反应器
氧气
催化作用
氧还原
拉曼光谱
电化学
化学工程
纳米技术
析氧
电子结构
密度泛函理论
碳纤维
基质(水族馆)
活动站点
氧化还原
吸附
解吸
活动中心
纳米结构
氧还原反应
无机化学
碳纳米管
作者
Qiaoling Xu,Lei Zhang,Xiayu Li,Weihang Xu,Linyi Ren,Mai Xu,Yingtang Zhou,Hermenegildo Garcı́a
标识
DOI:10.1002/adma.202522781
摘要
ABSTRACT Efficient oxygen reduction reaction (ORR) requires coordination of oxygen adsorption, transport, and catalysis at active sites. Yet most studies address only one step, overlooking whole‐pathway O 2 regulation and thus limiting performance. Here, we report a bioinspired Co‐doped Fe 2 P on N‐doped carbon featuring a hierarchical eucalyptus‐like nanoarchitecture, engineered to regulate oxygen throughout the electrochemical cycle, where Fe–P–Co hetero‐coordinated bridges anchored to the carbon substrate through Fe─N bonds induce strong electronic coupling and polarization. The hierarchical structure generated local electric fields that enriched OH − and O 2 , while multilevel porosity accelerated oxygen transport. This enabled coordinated optimization of oxygen adsorption, transfer, and active‐site electronic configuration. This nanohybrid achieved a half‐wave potential of 0.938 V vs. RHE, sustained discharge in Al‐air batteries for 373 h, and delivered an energy density of 3487 Wh/kg. Theoretical simulations revealed that Co‐doping shortened Fe─P bonds and tuned the Fe electronic environment, lowering the d‐band center and weakening Fe 3d‐O 2p interactions, which reduced the *OH desorption barrier and accelerated ORR kinetics. In situ Raman spectroscopy revealed that Fe–P–Co bridges served as active centers facilitating *OH release during ORR. These findings indicate that integrating hierarchical architecture, hetero‐coordinated Fe–P–Co bridges, and electronic‐state modulation enables whole‐pathway O 2 management for efficient oxygen electrocatalysis.
科研通智能强力驱动
Strongly Powered by AbleSci AI