4.6 Article

Regulating solid electrolyte interphases on phosphorus/carbon anodes via localized high-concentration electrolytes for potassium-ion batteries

Journal

JOURNAL OF ENERGY CHEMISTRY
Volume 78, Issue -, Pages 589-605

Publisher

ELSEVIER
DOI: 10.1016/j.jechem.2022.12.041

Keywords

Potassium-ion batteries; Phosphorus/carbon anodes; Localized high-concentration electrolytes; Solid electrolyte interphases; Interfacial stability

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By diluting high-concentration ether electrolytes with a non-solvating fluorinated ether, the research team successfully regulated the formation/evolution of solid electrolyte interphases (SEI) on phosphorus/carbon (P/C) anodes. This resulted in improved electrode performance, including reversible capacity, capacity retention rate, and rate capability. This research provides important insights for the development of high-performance potassium-ion batteries.
The resourceful and inexpensive red phosphorus has emerged as a promising anode material of potassium-ion batteries (PIBs) for its large theoretical capacities and low redox potentials in the multielectron alloying/dealloying reactions, yet chronically suffering from the huge volume expansion/shrinkage with a sluggish reaction kinetics and an unsatisfactory interfacial stability against volatile electrolytes. Herein, we systematically developed a series of localized high-concentration electrolytes (LHCE) through diluting high-concentration ether electrolytes with a non-solvating fluorinated ether to regulate the formation/evolution of solid electrolyte interphases (SEI) on phosphorus/carbon (P/C) anodes for PIBs. Benefitting from the improved mechanical strength and structural stability of a robust/uniform SEI thin layer derived from a composition-optimized LHCE featured with a unique solvation structure and a superior K+ migration capability, the P/C anode with noticeable pseudocapacitive behaviors could achieve a large reversible capacity of 760 mA h g(-1) at 100 mA g(-1), a remarkable capacity retention rate of 92.6% over 200 cycles at 800 mA g(-1), and an exceptional rate capability of 334 mA h g(-1) at 8000 mA g(-1). Critically, a suppressed reduction of ether solvents with a preferential decomposition of potassium salts in anion-derived interfacial reactions on P/C anode for LHCE could enable a rational construction of an outer organic-rich and inner inorganic-dominant SEI thin film with remarkable mechanical strength/flexibility to buffer huge volume variations and abundant K+ diffusion channels to accelerate reaction kinetics. Additionally, the highly reversible/durable full PIBs coupling P/C anodes with annealed organic cathodes further verified an excellent practical applicability of LHCE. This encouraging work on electrolytes regulating SEI formation/evolution would advance the development of P/C anodes for high-performance PIBs.(c) 2023 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

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