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High Entropy-Induced Kinetics Improvement and Phase Transition Suppression in K-Ion Battery Layered Cathodes. | LitMetric

High Entropy-Induced Kinetics Improvement and Phase Transition Suppression in K-Ion Battery Layered Cathodes.

ACS Nano

College of Engineering and Applied Sciences, Jiangsu Key Laboratory of Artificial Functional Materials, National Laboratory of Solid-State Microstructures, Collaborative Innovation Center of Advanced Microstructures, Frontiers Science Center for Critical Earth Material Cycling, Nanjing University, Nanjing 210023, China.

Published: January 2024

AI Article Synopsis

  • Layered oxides are promising materials for potassium-ion batteries (KIBs) but face challenges like slow kinetics and structural instability.
  • The introduction of high-entropy design in layered KIB cathodes, exemplified by the HE-KMO compound, improves these issues through multielement doping.
  • HE-KMO shows enhanced electronic properties, better electrochemical stability, and reduced capacity loss over cycles compared to traditional low-entropy materials.

Article Abstract

Layered oxides are widely accepted to be promising cathode candidate materials for K-ion batteries (KIBs) in terms of their rich raw materials and low price, while their further applications are restricted by sluggish kinetics and poor structural stability. Here, the high-entropy design concept is introduced into layered KIB cathodes to address the above issues, and an example of high-entropy layered KMnNiFeCoTiCuMgO (HE-KMO) is successfully prepared. Benefiting from the high-entropy oxide with multielement doping, the developed HE-KMO exhibits half-metallic oxide features with a narrow bandgap of 0.19 eV. Increased entropy can also reduce the surface energy of the {010} active facets, resulting in about 2.6 times more exposure of the {010} active facets of HE-KMO than the low-entropy KMnO (KMO). Both can effectively improve the kinetics in terms of electron conduction and K diffusion. Furthermore, high entropy can inhibit space charge ordering during K (de)insertion, and the transition metal-oxygen covalent interaction of HE-KMO is also enhanced, leading to suppressed phase transition of HE-KMO in 1.5-4.2 V and better electrochemical stability of HE-KMO (average capacity drop of 0.20%, 200 cycles) than the low-entropy KMO (average capacity drop of 0.41%, 200 cycles) in the wide voltage window.

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Source
http://dx.doi.org/10.1021/acsnano.3c06393DOI Listing

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