La1- x K x FeO3-δ: An Anion Intercalative Pseudocapacitive Electrode for Supercapacitor Application

Rakesh Mondal; Neeraj Kumar Mishra; Thandavarayan Maiyalagan; Asha Gupta; Preetam Singh

doi:10.1021/acsomega.1c03902

La_{1- x} K _x FeO_3-δ: An Anion Intercalative Pseudocapacitive Electrode for Supercapacitor Application

ACS Omega. 2021 Nov 1;6(45):30488-30498. doi: 10.1021/acsomega.1c03902. eCollection 2021 Nov 16.

Authors

Rakesh Mondal¹, Neeraj Kumar Mishra¹, Thandavarayan Maiyalagan², Asha Gupta³, Preetam Singh¹

Affiliations

¹ Department of Ceramic Engineering, Indian Institute of Technology (Banaras Hindu University), Varanasi, Uttar Pradesh 221005, India.
² Electrochemical Energy Laboratory, Department of Chemistry, SRM Institute of Science and Technology, Kattankulathur 603203, Tamilnadu, India.
³ Department of Chemistry, Indian Institute of Technology (Banaras Hindu University), Varanasi, Uttar Pradesh 221005, India.

Abstract

The green energy alternative to a fossil fuel-based economy can be provided only by coupling renewable energy solution solutions such as solar or wind energy plants with large-scale electrochemical energy storage devices. Enabling high-energy storage coupled with high-power delivery can be envisaged though high-capacitive pseudocapacitor electrodes. A pseudocapacitor electrode with multiple oxidation state accessibility can enable more than 1e ^- charge/transfer per molecule to facilitate superior energy storage. K-doped LaFeO₃ (La_1-x K _x FeO_3-δ) is presented here as an electrode having a high pseudocapacitance storage, equivalent to 1.32e ^- charge/transfer per molecule, resulting in a capacity equivalent of 662 F/g at 1 mV/s scan rate by introduction of a layered potential over the Fe-ion octahedral to utilize higher redox state energies (Fe⁴⁺→ Fe²⁺). La/K ordering in orthorhombic perovskite (La_1-x K _x FeO_3-δ) made the Fe⁴⁺ oxidation state accessible, and a systematic shift in the redox energies of Fe^4+/3+ and Fe^3+/2+ redox couples was observed with K⁺ ion doping in the A site of the LaFeO₃ perovskite, which resulted in a high faradic contribution to the capacitance, coupled with anionic intercalation of H₂O/OH^- in the host perovskite lattice. The surface capacitive and diffusion control contributions for capacitance are about 42 and 58%, respectively, at -0.6 V, with a scan rate of 1 mV/s. A high gravimetric capacitance, equivalent to 619, 347, 188, 121, and 65 F/g, respectively, at 1, 2, 3, 5, and 10 A/g constant current, was observed for the La_0.5K_0.5FeO_3-δ electrode. Up to 88.9% capacitive retention and 97% Coulombic efficacy were obtained for continuous 5000 cycles of charge/discharge for the La_0.5K_0.5FeO_3-δ electrode. The gravimetric capacitance values of ASCs (activated carbon//La_0.5K_0.5FeO_3-δ) are 348, 290, 228, and 147 F/g at current densities of 1, 2, 3, and 5 A/g, respectively. A maximum specific power of ∼3594 W/kg was obtained when the specific energy reached ∼117 Wh/kg at 5 A/g of current density.