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用于高性能锂氧电池阴极的非晶态氧化钴包覆碳纳米管上的铱簇修饰

Iridium Cluster Decoration on Amorphous Cobalt Oxide-Coated Carbon Nanotubes for High-Performance Lithium-Oxygen Battery Cathodes.

作者信息

Yao Yuqing, Wang Shang, Ma Xinyang, Han Yuhang, Tong Zirui, Li Geng, Feng Jiayun, Khan Malik Dilshad, Revaprasadu Neerish, Sun Qing, Tian Yanhong

机构信息

State Key Laboratory of Precision Welding & Joining of Materials and Structures, Harbin Institute of Technology, Harbin, 150001, China.

Zhengzhou Research Institute, Harbin Institute of Technology, Zhengzhou, 450000, China.

出版信息

Small. 2025 Aug;21(33):e2503521. doi: 10.1002/smll.202503521. Epub 2025 Jun 23.

DOI:10.1002/smll.202503521
PMID:40545914
Abstract

Lithium-oxygen batteries hold great promise for next-generation energy storage due to their exceptionally high theoretical energy density. However, their practical application is hindered by the sluggish kinetics associated with the oxygen reduction reaction and oxygen evolution reaction, resulting in severe voltage polarization and limited cycling stability. Herein, a simple solvent thermal reaction and a one-step reduction reaction is developed, where amorphous cobalt oxide (CoO) is uniformly coated on multi-walled carbon nanotubes (CNT) and further decorated with highly dispersed iridium (Ir) clusters. The amorphous CoO coatings preferentially nucleate at CNT defect sites, which not only passivates surface defects but also facilitates the homogeneous distribution of Ir clusters. This unique Ir/CoO@CNT architecture provides abundant active sites and promotes efficient electronic and ionic transport, thereby enhancing the electrocatalytic activity and overall battery performance. The synergistic effect between the highly active Ir clusters and the amorphous CoO, which accelerates reaction kinetics and stabilizes the electrode interface. As a result, the Ir/CoO@CNT cathode achieves a high discharge capacity of ≈6700 mAh g, with a low overpotential of 0.96 V and exhibits excellent cycling stability, sustaining over 150 cycles under a limited capacity of 500 mAh g at 500 mA g.

摘要

锂氧电池因其极高的理论能量密度而在下一代储能领域极具潜力。然而,与氧还原反应和析氧反应相关的缓慢动力学阻碍了它们的实际应用,导致严重的电压极化和有限的循环稳定性。在此,我们开发了一种简单的溶剂热反应和一步还原反应,将非晶态氧化钴(CoO)均匀地包覆在多壁碳纳米管(CNT)上,并进一步用高度分散的铱(Ir)簇进行修饰。非晶态CoO涂层优先在CNT缺陷位点成核,这不仅钝化了表面缺陷,还促进了Ir簇的均匀分布。这种独特的Ir/CoO@CNT结构提供了丰富的活性位点,促进了高效的电子和离子传输,从而提高了电催化活性和整体电池性能。高活性Ir簇与非晶态CoO之间的协同效应加速了反应动力学并稳定了电极界面。结果,Ir/CoO@CNT阴极实现了约6700 mAh g的高放电容量,过电位低至0.96 V,并表现出优异的循环稳定性,在500 mA g的电流密度下,在500 mAh g的有限容量下可持续循环150次以上。

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