Mechanism Investigation of High-Performance Li–Polysulfide Batteries Enabled by Tungsten Disulfide Nanopetals

Abstract

Understanding the reaction kinetics and mechanism of Li-polysulfide batteries is critical in designing advanced host materials for improved performance. However, up to now, the reaction mechanism within the Li-polysulfide batteries is still unclear. Herein, we study the reaction mechanism of a high-performance Li-polysulfide battery by in situ X-ray diffraction (XRD) and density functional theory (DFT) calculations based on a multifunctional host material composed of WS₂ nanopetals embedded in rGO-CNT (WS₂-rGO-CNT) aerogel. The WS₂ nanopetal serves as a "catalytic center" to chemically bond the polysulfides and accelerate the polysulfide redox reactions, and the 3D porous rGO-CNT scaffold provides fast and efficient e^-/Li⁺ transportation. Thus, the resulting WS₂-rGO-CNT aerogel accommodating the polysulfide catholyte enables a stable cycling performance, excellent rate capability (614 mAh g^-1 at 2 C), and a high areal capacity (6.6 mAh cm^-2 at 0.5 C). In situ XRD results reveal that the Li₂S starts to form at an early stage of discharge (at a depth of 25% of the lower voltage plateau) during the discharge process, and β-S₈ nucleation begins before the upper voltage plateau during the recharge process, which are different from the conventional Li-S battery. Moreover, the WS₂ itself could be lithiated/delithiated during the cycling, making the lithiated WS₂ (Li _xWS₂, 0 ≤ x ≤ 0.3) a real host material for Li-polysulfide batteries. DFT calculations suggest that Li _xWS₂ (0 ≤ x ≤ 0.3) exhibits moderate binding/anchoring interactions toward polysulfides with adsorption energies of 0.51-1.4 eV. Our work reveals the reaction mechanism of the Li-polysulfide batteries and indicates that the lithiated host plays an important role in trapping the polysulfides.