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源自金属有机框架凝胶的磷酸根离子功能化尖晶石铁钴矿用于高性能不对称超级电容器。

Phosphate ions functionalized spinel iron cobaltite derived from metal organic framework gel for high-performance asymmetric supercapacitors.

作者信息

Zhao Yang, Zeng Yun, Tang Wei, Jiang Chenglu, Hu Hengyuan, Wu Xiaoqiang, Fu Junheng, Yan Zhenhua, Yan Minglei, Wang Yong, Qiao Liang

机构信息

College of Water Conservancy and Hydropower Engineering, Sichuan Agricultural University, Ya'an 625014, China.

School of Mechanical Engineering, Chengdu University, Chengdu 610106, China.

出版信息

J Colloid Interface Sci. 2023 Jan 15;630(Pt B):751-761. doi: 10.1016/j.jcis.2022.10.159. Epub 2022 Nov 2.

Abstract

Spinel iron cobaltite (FeCoO) with high theoretical capacity is a promising positive electrode material for building high-performance supercapacitors. However, its inherent poor conductivity and deficient electrochemical active sites hinder the improvement of its electrochemical kinetics behavior. Herein, phosphate ions modified FeCoO is obtained in the presence of oxygen vacancies (P-FeCoO) by a simple metal organic framework gel-derived strategy. Phosphate ions added on the surface of P-FeCoO greatly enhances its surface activity, thus prompting the faster charge storage kinetics of the electrode material. Due to its ample electrochemical active sites and rapid ion diffusion and electron mobility, the optimized P-FeCoO electrode delivers a superior specific capacity of 1568.8 F g (784.4 C g) at a current density of 1 A/g and has an excellent cycling stability with 93.3 % initial capacity retention ratio after 5000 cycles. More impressively, the assembled asymmetric supercapacitor consisting of P-FeCoO and activated carbon which act as positive and negative electrode materials, respectively displays a favorable energy density of 60.2 Wh kg at a power density of 800 W kg and has a long cycling lifespan. These results demonstrate the potential importance of modifying the surface of spinel cobaltite with phosphate ions and incorporating oxygen defects in it as a facile strategy for enhancing the electrochemical kinetics of electrode materials.

摘要

具有高理论容量的尖晶石铁钴矿(FeCoO)是一种很有前景的用于构建高性能超级电容器的正极材料。然而,其固有的低导电性和电化学活性位点不足阻碍了其电化学动力学行为的改善。在此,通过一种简单的金属有机框架凝胶衍生策略,在氧空位存在的情况下获得了磷酸根离子修饰的FeCoO(P-FeCoO)。添加在P-FeCoO表面的磷酸根离子极大地提高了其表面活性,从而促使电极材料的电荷存储动力学更快。由于其丰富的电化学活性位点以及快速的离子扩散和电子迁移率,优化后的P-FeCoO电极在1 A/g的电流密度下具有1568.8 F/g(784.4 C/g)的优异比容量,并且在5000次循环后具有93.3%的初始容量保持率,展现出出色的循环稳定性。更令人印象深刻的是,由P-FeCoO和活性炭分别作为正负极材料组装而成的不对称超级电容器,在800 W/kg的功率密度下显示出60.2 Wh/kg的良好能量密度,并且具有长循环寿命。这些结果证明了用磷酸根离子修饰尖晶石钴矿表面并在其中引入氧缺陷作为增强电极材料电化学动力学的简便策略的潜在重要性。

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