This thesis develops a thermodynamic and electronic framework for lithium-ion battery cathodes and applies it to a new class of high-capacity sulfides composed exclusively of industrially abundant elements. It introduces lithium-rich cathodes composed of aluminum, iron, and sulfur that leverage reversible multielectron anion redox, in which the formation and cleavage of sulfur-sulfur bonds enable especially high extents of charge storage. A core design framework is established linking delithiated-phase stability to accessible electrochemical redox capacity. The chemical space is expanded with copper-substituted phases, in which unique copper-sulfur electronic interactions delocalize charge compensation beyond sulfur-sulfur bonds, thereby improving the reversibility of anion redox. These materials achieve high energy densities using only industrial elements, offering a promising foundation for next-generation lithium-ion cathodes that address both performance and raw materials constraints. Thus, this thesis advances the long-term goal of building more sustainable energy systems and expanding access to electricity worldwide.
Adrian LindnerSvenja BothSaeed AbdolhosseiniWolfgang MenesklouTimo DannerArnulf LatzUlrike Krewer
CharlesJ. Hansen (8635068)Joshua J. Zak (8635071)Andrew J. Martinolich (1603618)Jesse S. Ko (2930985)Nicholas H. Bashian (4448524)Farnaz Kaboudvand (8635074)Anton Van der Ven (1343688)Brent C. Melot (1712827)Johanna Nelson Weker (8556417)Kimberly A. See (1774297)
Charles HansenJoshua J. ZakAndrew J. MartinolichJesse S. KoNicholas H. BashianFarnaz KaboudvandAnton Van der VenBrent C. MelotJohanna Nelson WekerKimberly A. See