Rational Design of Multinary Metal Chalcogenide Bi 0.4 Sb 1.6 Te 3 Nanocrystals for Efficient Potassium Storage.

Multinary metal chalcogenides hold considerable promise for high-energy potassium storage due to their numerous redox reactions. However, challenges arise from issues such as volume expansion and sluggish kinetics. Here, we present a design featuring a layered ternary Bi 0.4 Sb 1.6 Te 3 anchored on graphene layers as a composite anode, where Bi atoms act as a lattice softening agent on Sb. Benefiting from the lattice arrangement in Bi 0.4 Sb 1.6 Te 3 and structure, Bi 0.4 Sb 1.6 Te 3 /graphene exhibits a mitigated expansion of 28% during the potassiation/de-potassiation process and demonstrates facile K + ion transfer kinetics, enabling long-term durability of 500 cycles at various high rates. Operando synchrotron diffraction patterns and spectroscopies including in-situ Raman, ex situ adsorption, and X-ray photoelectron reveal multiple conversion and alloying/de-alloying reactions for potassium storage at the atomic level. Additionally, both theoretical calculations and electrochemical examinations elucidate the K + migration pathways and indicate a reduction in energy barriers within Bi 0.4 Sb 1.6 Te 3 /graphene, thereby suggesting enhanced diffusion kinetics for K + . These findings provide insight in the design of durable high-energy multinary tellurides for potassium storage. This article is protected by copyright. All rights reserved.