Unique Na <sub>5−</sub> <i> <sub>x</sub> </i> SbSe Phase Enables High‐Rate Performance of Sb <sub>2</sub> Se <sub>3</sub> Anodes in Na‐Ion Batteries
Amalie Skurtveit, Andrew Pastusic, Anders Brennhagen, Faduma M. Maddar, Chris E. Mohn, Abhoy Karmakar, Christopher A. O’Keefe, Ivana Hasa, Carmen Cavallo, Bjørnar Arstad, Helmer Fjellvåg, David S. Wragg, Alexey Y. Koposov
Abstract
Abstract Na‐ion batteries (NIBs) need new anode materials to improve energy density. Metal chalcogenides, such as Sb 2 Se 3 , represent a promising alternative to commonly used hard carbon materials, demonstrating high‐rate performance up to 5 A g −1 with minimal capacity losses. However, Sb 2 Se 3 is believed to operate under the conversion/alloying mechanism, typically linked with large structural transformations and volumetric changes—quite contrary to its performance. Herein, by combining multiple operando techniques and atomistic simulations, a new fully sodiated phase, Na 5− x SbSe, is unambiguously revealed as the origin of the high‐rate performance of Sb 2 Se 3 . Na 5− x SbSe is stable within 0.01–0.80 V versus Na/Na + and crystallizes in I 4/ mmm . The remarkable structural flexibility of Na 5 SbSe to changes in Na‐content allows the anode to be (de)sodiated with minimal volumetric changes (≈3.4%). This unique “breathing effect” is intimately linked to high inherent vacancy concentration, disordered, and structurally flexible anion sublattice, providing a stable framework for fast Na diffusion, contributing to the fast‐charging properties of Sb 2 Se 3 . The study showcases the power of operando methods for discovering new phases that are hidden in the mechanistic paths of well‐studied reactions and underlines the intertwined nature of various characterization methods assisted by atomistic insights for a comprehensive understanding of complex (de)sodiation mechanisms.