Overcoming Ion Trapping in Chevrel Phase Compounds via Tailored Anion Substitution: An Integrated Study of Theory, Synthesis, and In Operando Techniques for Reversible Aqueous Zn-Ion Batteries.

Sustainable batteries are key for powering electronic devices of the future, with aqueous zinc-ion batteries (AZIBs) standing out for their use of abundant, readily available elements, and safer production processes. Among the various electrode materials studied for AZIBs, the Chevrel Phase, MoS has shown promise due to its open framework, but issues with zinc ion trapping have limited its practical application. In this work, we employed computational methods to investigate the insertion-deinsertion mechanism in a series of isostructural MoSSe ( = 0-8) solid solutions as materials that could balance the gravimetric capacity and reversible cycling for AZIBs. Density functional theory (DFT) calculations revealed that increasing the Se content would reduce the binding energy of Zn within the structures, enabling Zn deinsertion compared to the MoS structure. Experiments confirmed the formation of MoSSe ( = 0-8) solid solutions, and electrochemical testing showed improved reversibility of Zn insertion/deinsertion as the amount of Se increased, consistent with the computational predictions. Furthermore, combined in operando X-ray diffraction and electrochemical studies revealed a continuous, gradual Zn-insertion process into MoSSe, in stark contrast to the abrupt phase changes observed upon Zn insertion in MoS and MoSe. DFT calculations attributed the stabilization of ZnMoSSe as a prime reason for preventing phase separation, making Se-substituted compounds promising materials for high-performance AZIBs. Overall, this interdisciplinary approach, integrating computational modeling, materials synthesis, and advanced characterization techniques, offers a pathway for fine-tuning anion chemistry that can help create high-performance electrode materials for sustainable energy storage technologies.