Ternary Potassium-Bismuth-Telluride Intermetallic Support Promotes Electrochemical Stability in Potassium Metal
Rohit Raj1, Yixian Wang1, Dean Yen2
1Materials Science and Engineering Program, Walker Department of Mechanical Engineering and Texas Materials Institute, The University of Texas at Austin, Austin, TX, 78712, USA.
Abstract:
We employed accumulative roll bonding to fabricate self-standing metallurgical composite of in situ formed alkaline potassium-bismuth-telluride intermetallic K2(Bi2/6Te3/6Vac1/6) embedded in potassium metal. This newly discovered thermodynamically stable potassiophilic crystal, termed "KBT", is fcc antifluorite with K2Te archetype. Symmetric cells achieve 880 h of cycling at 0.5 mA cm-2 and 0.5 mAh cm-2. Potassium metal battery (KMB) with Prussian blue (PB) cathode in carbonate electrolyte retains 80% capacity after 200 cycles at 1C. In ether-based electrolyte with organic cathode, it achieves 80% retention after 900 cycles at 2C. Combined synchrotron X-ray nano-tomography, cryogenic-focused ion beam microscopy (Cryo-FIB) and sputter-down X-ray photoelectron spectroscopy (XPS) demonstrate uniform electrodeposits, versus baseline of potassium filaments intermixed with pores and coarse SEI. Binary K3Bi-K and K2Te-K intermetallic supports also provide improved electrochemical performance, albeit to lesser extent. Multiscale simulation provides insight into role of support structure in adatom energetics, film nucleation, early-stage SEI morphology and interfacial stability.
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