纳米反应器
电催化剂
氧还原
纳米技术
材料科学
碳纤维
催化作用
方向(向量空间)
氧气
析氧
金属有机骨架
氧还原反应
吸附
工作(物理)
过渡金属
金属
化学
制作
计算机科学
设计要素和原则
功率(物理)
化学工程
作者
Xiaojie Tan,Ning Wang,Qingshan Zhao,Shiyuan Lin,Fengliang Cao,Libo Wang,Cao Y,Ying Liu,Luhai Wang,Shoushi Bo,Han Hu,Mingbo Wu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-07-13
卷期号:26 (28): 9135-9142
标识
DOI:10.1021/acs.nanolett.6c01824
摘要
The precise integration of atomically dispersed active sites into engineered carbon architectures for the oxygen reduction reaction (ORR) remains challenging. Herein, we introduce a novel point-to-point orientation strategy that enables the precise engineering of P-tailored Fe–N 5 motifs within raspberry-like hierarchical carbon nanoreactors (P/Fe–N–HCNCs) for oxygen electrocatalysis in Zn–air batteries. The deliberately designed hierarchical architecture ensures efficient three-dimensional mass transfer, guaranteeing access to active sites. The second-shell P-coordination tailors an electron-asymmetric environment around Fe, optimizing the adsorption free energy of *OOH intermediates and accelerating the ORR kinetics. Consequently, the P/Fe–N–HCNCs delivers an exceptional half-wave potential of 0.94 V vs RHE along with outstanding stability. When deployed in a Zn–air battery, it achieves a peak power density of 271.4 mW cm –2 and an impressive specific capacity of 816 mA h g –1, surpassing most reported nonprecious metal catalysts. This work establishes a general design principle synergizing atomic coordination and nanoarchitecture engineering.
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