RESUMEN
Reversible oxygen redox (OR) is considered as a paradigmatic avenue to boost the energy densities of layered oxide cathodes. However, its activation is largely coupled with the local coordination environment around oxygen, which is usually accompanied with irreversible oxygen release and unfavorable structure distortion. Herein, it is revealed that the synergistic effect of transition-metal (TM) vacancy and substitution element for modulating the OR activity and reversibility of layered Na0.67 MnO2 through multimodal operando synchrotron characterizations and electrochemical investigations. It is disclosed that TM vacancy can not only suppress the complicated phase transition but also stimulate the OR activity by creating nonbonding O 2p states via the NaâOâvacancy configurations. Notably, the substitution element plays a decisive role for regulating the reversibility of vacancy-boosted OR activity: the presence of strong AlâO bonds stabilizes the Mn-O motifs by sharing O with Al in the rigid MnâOâAl frameworks, which mitigates TM migration and oxygen release induced by TM vacancy, leading to enhanced OR reversibility; while the introduction of weak ZnâO bonds exacerbates TM migration and irreversible oxygen release. This work clarifies the critical role of both TM vacancy and substitution element for regulating the OR chemistry, providing an effective avenue for designing high-performance cathodes employing anionic redox.
RESUMEN
P2-type Mn-based layered oxides are among the most prevalent cathodes for sodium-ion batteries (SIBs) owing to their low cost, resource abundance, and high theoretical specific capacity. However, they usually suffer from Jahn-Teller (J-T) distortion from high-spin Mn3+ and poor cycling stability, resulting in rapid degradation of their structural and electrochemical properties. Herein, a stable P2-type Mn-based layered oxide is realized through a local construction strategy by introducing high-valence Ru4+ to overcome these issues. It has been revealed that the Ru substitution in the as-constructed Na0.6Mg0.3Mn0.6Ru0.1O2 (NMMRO) renders the following favorable effects. First, the detrimental P2-OP4 phase transition is effectively inhibited owing to the robust Ru-O covalency bond. Second, the Mg/Mn ordering is disturbed and the out-of-plane displacement of Mg2+ and in-plane migration of Mn4+ are suppressed, leading to improved structural stability. Third, the redox ability of Mn is increased by weakening the covalence between Mn and O through the local Ru-O-Mn configurations, which contributes to the attenuated J-T distortion. Last, the strong Ru-O covalency bond also leads to enhanced electron delocalization between Ru and O, which decreases the oxidation of oxygen anion and thereby reduces the driving force of metal migration. Because of these advantages, the structural integrity and electrochemical properties of NMMRO are largely improved compared with the Ru-free counterpart. This work provides deeper insights into the effect of local modulation for cationic/anionic redox-active cathodes for high-performance SIBs.
RESUMEN
Utilizing anionic redox activity within layered oxide cathode materials represents a transformational avenue for enabling high-energy-density rechargeable batteries. However, the anionic oxygen redox reaction is often accompanied with irreversible dynamic oxygen evolution, leading to unfavorable structural distortion and thus severe voltage decay and rapid capacity fading. Herein, it is proposed and validated that the dynamic oxygen evolution can be effectively suppressed through the synergistic surface CaTiO3 dielectric coating and bulk site-selective Ca/Ti co-doping for layered Na2/3 Ni1/3 Mn2/3 O2 . The surface dielectric coating layer not only suppresses the surface oxygen release but more importantly inhibits the bulk oxygen migration by creating a reverse electric field through dielectric polarization. Meanwhile, the site-selective doping of oxygen-affinity Ca into Na layers and Ti into transition metal layers effectively stabilizes the bulk oxygen through modulating the O 2p band center and the oxygen migration barrier. Such a strategy also leads to a reversible structural evolution with a low volume change because of the enhanced structural integrality and improved oxygen rigidity. Because of these synergistic advantages, the designed electrode exhibits greatly suppressed voltage decay and capacity fading upon long-term cycling. This study affords a promising strategy for regulating the dynamic oxygen evolution to achieve high-capacity layered cathode materials.
RESUMEN
Utilizing reversible lattice oxygen redox (OR) in battery electrodes is an essential strategy to overcome the capacity limitation set by conventional transition metal redox. However, lattice OR reactions are often accompanied with irreversible oxygen oxidation, leading to local structural transformations and voltage/capacity fading. Herein, it is proposed that the reversibility of lattice OR can be remarkably improved through modulating transition metal-oxygen covalency for layered electrode of Na-ion batteries. By developing a novel layered P2-Na0.6 Mg0.15 Mn0.7 Cu0.15 O2 electrode, it is demonstrated that the highly electronegative Cu dopants can improve the lattice OR reversibility to 95% compared to 73% for Cu-free counterpart, as directly quantified through high-efficiency mapping of resonant inelastic X-ray scattering. Crucially, the large energetic overlap between Cu 3d and O 2p states dictates the rigidity of oxygen framework, which effectively mitigates the structural distortion of local oxygen environment upon (de)sodiation and leads to the enhanced lattice OR reversibility. The electrode also exhibits a completely solid-solution reaction with an ultralow volume change of only 0.45% and a reversible metal migration upon cycling, which together ensure the improved electrochemical performance. These results emphasize the critical role of transition metal-oxygen covalency for enhancing the reversibility of lattice OR toward high-capacity electrodes employing OR chemistry.