双功能
电催化剂
材料科学
析氧
兴奋剂
纳米技术
碳纤维
化学工程
过电位
异质结
电极
催化作用
化学
电化学
光电子学
有机化学
复合数
复合材料
工程类
物理化学
作者
Sa Liu,Luyuan Wang,Guoxiang Wang,Ping Zhu,Zhouyang Long,Xinsheng Zhao
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2025-01-01
卷期号:17 (24): 14772-14780
被引量:5
摘要
Controllable preparation of advanced electrocatalysts with well-designed architecture and desirable active sites for rechargeable Zn-air batteries (ZABs) is challenging. Herein, a hollow urchin-like bifunctional oxygen electrocatalyst (HCoPNC@Co/Co2P-PNCNTs) was developed by assembling P, N-doped carbon nanotubes with confined Co/Co2P heterojunctions on heteroatom-doped carbon hollow spheres via in situ polymerization/deposition, pyrolysis and topical phosphorization strategy. According to the analysis of experiments and theoretical calculations, the Co/Co2P@NC core-shell structure at the top of each CNT was verified to facilitate the electron transfer and the conversion between the adsorbed intermediates, guaranteeing outstanding intrinsic catalytic activity. Meanwhile, the urchin-like hierarchical frameworks led to the formation of a desirable conductive and mass transport network, ensuring the efficient exposure of the electrocatalytic active sites and excellent structural stability. Therefore, the "framework-active sites" endowed HCoPNC@Co/Co2P-PNCNTs with superior catalytic activities towards the oxygen reduction reaction (ORR, half-wave potential of 0.83 V) and oxygen evolution reaction (OER, overpotential of 350 mV@10 mA cm-2) in alkaline electrolyte. Expectedly, the as-assembled ZABs based on HCoPNC@Co/Co2P-PNCNTs delivered a large peak power density of 250 mW cm-2 and a robust charge-discharge cycling stability with negligible voltage decay for 110 h at 2 mA cm-2, illustrating its great practical application in advanced metal-air batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI