4.7 Article

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

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 630, Issue -, Pages 751-761

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.10.159

Keywords

Oxygen vacancy; Phosphate ions; Surface functionalization; Asymmetric supercapacitors

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Phosphate ion modification and oxygen defects incorporation can enhance the electrochemical kinetics of spinel cobaltite, leading to improved specific capacity and cycling stability for high-performance supercapacitors.
Spinel iron cobaltite (FeCo2O4) 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 FeCo2O4 is obtained in the presence of oxygen vacancies (P-FeCo2O4-x) by a sim-ple metal organic framework gel-derived strategy. Phosphate ions added on the surface of P-FeCo2O4-x 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-FeCo2O4-x electrode delivers a superior specific capacity of 1568.8 F g-1 (784.4 C g-1) 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-FeCo2O4-x and activated carbon which act as positive and negative electrode materials, respectively dis-plays a favorable energy density of 60.2 Wh kg -1 at a power density of 800 W kg -1 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 electro-chemical kinetics of electrode materials.(c) 2022 Elsevier Inc. All rights reserved.

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