钴
催化作用
碳纳米管
材料科学
锌
碳纤维
化学工程
纳米技术
Atom(片上系统)
化学
冶金
有机化学
复合材料
嵌入式系统
工程类
复合数
计算机科学
作者
Mufei Liu,Hongxing Dong,Guiling Wang,Jing Zhao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-09-19
卷期号:24 (39): 12102-12110
被引量:13
标识
DOI:10.1021/acs.nanolett.4c02820
摘要
Amid the world's escalating energy needs, rechargeable zinc-air batteries stand out because of their environmental sustainability, with their performance being critically dependent on the oxygen reduction reaction (ORR). The inherent slow kinetics of the ORR at air electrodes frequently constrains their operational efficiency. Here, we develop a new self-catalytic approach for in situ growth of carbon nanotubes with new cathode material Co@CoN3/CNTs-800 without external additives. Density functional theory calculation reveals this method integrates nonprecious single-atom catalysis with spatial confinement, facilitating large-scale, in situ fabrication of CNTs, which can support dispersed atomic CoN3 sites and enforce spatial confinement on Co nanoparticles. The Co@CoN3/CNTs-800 electrode achieves an electron transfer number close to ideal (3.9 out of 4.0). In rechargeable zinc-air flow batteries, it achieves a peak power density of 169.5 mW cm-2 and a voltage gap that is only 1.6% larger than the original after 700 h. This work surmounts critical challenges in the ORR kinetics for zinc-air batteries.
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